craigslist | science/biotech jobs in boston

Director of Product Development Formulation (Carolinas)

2009-11-11T20:12:21-05:00

Great opportunity directing the new formulation group of this highly profitable and fast growing pharmaceutical company. This position reports to the Chief Scientific Officer. Candidates must have a strong background with aseptic liquid formulation of drugs. Advance degree in Pharmaceutical Science, Chemical Engineering, Analytical Chemistry, or related field with 8 + years experience in the pharmaceutical industry.

QA Clerical Support-Part-Time (Burlington, MA)

2009-11-11T16:42:24-05:00

JOB SUMMARY:

This individual will be responsible for data entry/verification and coordination of training files.

JOB RESPONSIBILITIES:

� Data entry and coordination of GMP training files
� Ability to analyze and interpret training data
� Ability to organize daily activities to ensure timely completion of assignments
� Document formatting and processing
� Other duties as assigned

MINIMUM REQUIREMENTS FOR EDUCATION, TRAINING AND EXPERIENCE:
� Must be proficient in the use of word processors and spreadsheets
� Must have strong organizational skills and ability to prioritize and multi-task
� Attention to detail essential
� Knowledgeable in FDA GMPs (21 CFR, 211, 820, and/or 600) a plus
� Knowledgeable in ISO 9001 and 13485 a plus
� One year of industry experience in a GMP or GLP environment preferred
� Work hours part-time 1-5pm.

QA Senior Materials Inspector (Burlington, MA)

2009-11-11T16:37:44-05:00

JOB SUMMARY: The Quality Assurance (QA) Senior Materials Inspector is responsible for the receipt,
inspection, sampling and release of incoming materials.
JOB RESPONSIBILITIES:
1. Overseeing:
�]Incoming material receipt, inspection (visual and mechanical, use of hand measurement verniers or
calipers), sampling and release.
�]Assignment of Hyaluron inventory lot numbers and expiration dates where the manufacturer has not
assigned a date to incoming materials.
�]Segregation of quarantine, release, reject and return materials.
2. Performs QA Review of completed material specifications.
�]Involved in resolving and investigating deviations.
�]Writes procedures.
�]Works on continuous improvement of materials program.
3. Supports QA review of batch records.
MINIMUM REQUIREMENTS FOR EDUCATION, TRAINING AND EXPERIENCE:
�]Bachelor�fs Degree
�]A minimum of 5 years working in medical and/or pharmaceutical environment.
�]Experience in GMP or GLP environment a must.
The above statements are intended to describe the general nature and level of work being performed by people assigned to
this classification. They are not intended t

Research Scientist (Boston, MA)

2009-11-11T16:18:05-05:00

AIR Worldwide

Would you like to work in a fast-paced , results oriented environment while still maintaining a good work life balance? Work on a wide variety of complex problems that allow for creative and innovative solutions.

Development and enhancement of natural hazard models (tropical and extratropical cyclones,earthquakes, severe thunderstorm, etc.)

Manage the collection and analysis of data; integrate the highest quality data into the modeling process
Perform validation and verification analysis of implemented model solutions

Ability to gather, understand, and critically analyze data from all relevant sources of natural hazard information
Solid technical programming skills gained through practical experience (e.g. C, C++, FORTRAN, Python,etc.), FORTRAN experience a big plus
Familiarity with manipulating large data sets, SQL experience a plus
Basic knowledge in statistics, familiarity with statistical packages such as R a plus
Highly motivated and self-directed with demonstrated experience in advancing complex projects
Excellent verbal communication skills
Risk modeling experience and/or GIS skills a plus

Requirements:

2+ years professional experience in a technical environment
MS degree in Physical Science or Engineering

If interested, please apply online at http://track.tmpservice.com/ApplyClick.aspx?id=838034-1857-3739

UST Field Services Tech - Eclipse Division - ECS (Agawam, MA based)

2009-11-11T13:15:36-05:00

Environmental Compliance Services, Inc., (ECS) is an aggressive market leader of business and environmental solutions. This dynamic firm is comprised of more than 200 professionals with offices throughout the Northeast, Southeast and Midwest. Our Eclipse division; a high energy environmental services group specializing in petroleum UST Compliance Services, is seeking a full time Field Services Technician based out of our Agawam, MA office location.

Eclipse is an innovative service line that encompasses such items as total fuel systems management with integrated remote accessing, Automatic Inventory Reconciliation (AIR), 24/7 Emergency Spill response and notification systems, and immediate access to compliance documentation all of which can be tailored to the specific needs of the clients.

The individual for this position will be required to perform routine inspections and evaluations of components involved in the total fuel systems management equipment including dispensers, electronic testing components and monitoring devices, spill bucket installation and repair, installation and O&M of systems components. An understanding of telecommuncations systems functions and operation and maintenance would be extremely beneficial as much of the work with our automated systems involve installation of the components themselves, education of clients and employees, and troubleshooting of those components. There will be close interaction with clientele and general public at site locations.

We are in need of an independent self starter who is willing to learn from the ground up, and has the ability to work on their own with little or not supervision in the future. Mechanical aptitude is a must, must be able to meet physical qualifications including lifting requirements for the job. This position requires extensive travel to job sites on a regular basis as such candidate must be able to meet the ECS Driver�s Safety Policy criteria. Much of the work will be centralized in the eastern part of MA (Bay and Cape Code region), CT, RI and NH.

An important aspect of this position is good organizational and multi-tasking skills and clear and concise communication skills, as well as clear analytical thought processes. Technical understanding and insight in the field is a plus but not necessary, we are looking for an individual who may be starting out on this career path who will be willing to learn the system from the ground up but will quickly be able to function without supervision.

We offer a great work environment and excellent benefits including:
Competitive Salaries in the Marketplace
Employee Stock Ownership Plan (ESOP)
Health & Dental Insurance
Short Term Disability Insurance
Long Term Disability Insurance
Life Insurance
401(k) Plan with company match
Flexible Benefits Account Tuition Reimbursement
Paid sick and vacation time
Paid holidays
Employee Referral Bonus Program
To apply, email, mail, or fax your cover letter and resume
indicating both the position title and branch location you are applying to.

Email: hrmanager@ecsconsult.com
Mail: Mary Russell, ECS, 588 Silver Street, Agawam, MA 01001
Fax: (413) 786-6805
An Equal Opportunity Employer

Associate Scientist - Process Development (Cambridge, MA)

2009-11-11T12:43:50-05:00

We have an immediate need for a Scientific Associate to join our clients Process Science and Production group.

Responsibilities include
* Implementation of analytical methods for biochemical analysis and characterization of recombinant therapeutic proteins.
* Support process development using a variety of analytical methods, analyze and archive analytical data, and collaborate with members of the analytical team as well
as other functional teams.
* Additional responsibilities include timely documentation, presentation in cross-functional project teams.

Skills: Hands-on experience with HPLC and CE techniques is preferred. Experience with LabChip technology would be a plus.
The candidate must have good written and oral communication skills and demonstrate ability to work both independently and as part of a team. The successful candidate should be self-motivated and capable of multi-tasking with strong problem solving skills.

Education: A B.S. or M.S. in Analytical Chemistry, Biochemistry or related life science field with 0-5 years of relevant academic or industrial laboratory experience

Research Associate (Lexington, MA)

2009-11-11T12:37:57-05:00

We are seeking a Research Associate to join our research team focused on ALS and Alzheimer�s disease. The Research Associate will perform routine learning and memory tests with rodents to obtain data for use in memory and memory disorders as well as basic handling and restraint, monitoring animal welfare, body weight and food and water intake, dosing of compounds (SC, IP, PO, IV, etc), dissection, weighing and preservation of tissues and data logging for analysis.
Additional Responsibilities:

� Perform rodent handling, behavioral tests such as operant conditioning & water maze learning

� Administers therapeutic drugs during and prior to learning and memory

� Set up equipment and apparatus for specific laboratory procedures

� Maintain rodent colonies

� Maintain the laboratory and order supplies

The successful candidate will possess demonstrated competency with animal handling, behavioral testing, drug preparation, and dosing (IV, IP and SQ) to rodents. Bachelor degree in biological sciences, neuroscience, or psychology and one year laboratory experience are preferred.

Research Technician II (BWH - Longwood Medical Area)

2009-11-11T12:02:14-05:00

GENERAL SUMMARY/ OVERVIEW STATEMENT:
Working under the general supervision of the supervisor, and in accordance with established hospital policies and procedures, conducts a variety of routine experiments where methodologies are clearly established. The TRA will perform research that is focused on understanding the immune responses in skin including response to vaccination with vaccinia virus. Calculates, transcribes, and analyzes data using basic statistics. The TRA must be organized and capable of considerable independent work with maintenance of detailed, careful records.
PRINCIPAL DUTIES AND RESPONSIBILITIES:
2. Under general supervision, performs a variety of routine tests following established methodologies. Routine tests may include analysis of cells by flow cytometry, PCR, and isolation of lymphocyte subsets using magnetic beads.
3. Prepares and maintains tissue cultures. Maintains long-term tissue cultures of human cell lines and monitors for contamination. Perform tissue culture techniques, including but not limited to maintenance of cultures of fresh cells and cell lines required for research.
4. Works with live vaccinia virus which requires thorough understanding of biosafety procedures. Grows virus in culture and harvests virus for experiments. Infects animals with cultured virus.
5. Harvests animal blood and tissues to study for immune response.
6. Prepares and maintains stock solutions and reagents.
7. Prepares chemicals, instruments and equipment.
8. Discusses progress of work regularly with supervisor.
9. Records data, summarizes, and analyzes results using basic statistics.
10. Maintain detailed laboratory notes with organized records and data.
11. All other duties as assigned.

QUALIFICATIONS:
1. Good organizational skills, detail oriented
2. Ability to methodically record data and to analyze data
3. Computer literacy
4. Good interpersonal and communication skills.

SKILLS/ ABILITIES/ COMPETENCIES REQUIRED:
1. BS in biological/physical science is required.
2. Must have at least two years experience in a directly related research setting including tissue culture and animal experience.
WORKING CONDITIONS: Describe the conditions in which the work is performed.
1. Will work with live virus � this position requires vaccination against smallpox.
2. Will work with human cells and tissues
3. Will work with mouse cells and tissues.

HISTOLOGY TECHNICIAN/11 hrs/days/NSMC

2009-11-11T11:28:22-05:00

SUMMARY
Under the direction of the Histology Coordinator perform a wide variety of duties in the day-to-day operation of the Histology and Pathology Labs.

PRIMARY RESPONIBILITIES
Laboratory Procedures and Protocols
- Under the supervision of the Histology Coordinator, responsible for performing a variety of Histology functions in the Histology Laboratory.
- Responsible for processing, embedding, cutting and mounting on slides all surgical and autopsy tissue specimens.
- Stain all slides; cover slip and clean slides.
- As requested, use special stain; make up special stains from dyes.
- Clean and maintain instruments including autotechnicon, tissue embedding center, microtome and knife sharpener.
- Responsible for general cleaning of all work areas.
- Teach laboratory techniques and protocols to new employees.
- Remain updated on current technology by reading journals and periodicals and by attending workshops /in service presentations as possible.
- Perform other related duties as required or as responsibilities dictate.

Hours can be flexible. Tue and Thurs 7:30a-1p or 8:30a-2p

SKILLS/COMPETENCIES REQUIRED:
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily and be able to demonstrate any knowledge or skills necessary to perform testing in his/her assigned laboratory section. The requirements listed below are representative of the knowledge, skill, and ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Requires intense attention and concentration. Good visual, verbal, hearing, and reasoning skills. Ability to handle several processes concurrently. Ability to deal with a wide range of personalities.

EDUCATION REQUIRED
Require Equivalent to four years of High School and one year's college level training in anatomy, physiology and chemistry; plus 2 years of Histology training in a fully accredited laboratory.

List all LICENSES, CERTIFICATIONS and/or REGISTRATIONS REQUIRED. ASCP certification or equivalent is preferred.

Your decision to join an organization is based on many considerations. At The North Shore Medical Center, we feel our benefit program plays a vital role in demonstrating the organization's commitment to its employees. NSMC's benefits package includes Medical, Dental, Retirement, Earned Time Off, Flexible Spending, Life and Disability Insurances, and Tuition Reimbursement.

NSMC includes Salem Hospital in Salem, Massachusetts, and Union Hospital in Lynn, Massachusetts, both full-service community hospitals, as well as NSMC North Shore Children's Hospital, the NSMC Cancer Center, a freestanding cancer center in Peabody, Massachusetts, the NSMC Heart Center, and the NSMC Women's Center in Danvers, Massachusetts.

The affiliation with Partners, which includes Massachusetts General and Brigham and Women's hospitals, means that NSMC can offer a higher level of expertise and technology to patients on the North Shore.

NSMC Salem Hospital is a 275-bed community teaching hospital that provides a full range of adult and pediatric services, including medicine, surgery, emergency care, ambulatory care, obstetrics, neonatal care, gynecology, and psychiatry services. It is recognized as a regional referral center for cardiology, oncology, neurosurgery, orthopedics, and thoracic surgery services.

NSMC Union Hospital in Lynn is a 130-bed community hospital that provides adult medical and surgical services, including emergency care, ambulatory care, cardiology, psychiatry, oncology, and orthopedic services, as well as a pain center and advanced minimally invasive procedures for the residents of the North Shore.

Northshore Medical Center is an Equal Employment/Affirmative Action Employer.

Please click here to apply.

Part Time Research Asst/Administrator/Editor @Harvard Affiliated Group (Cambridge)

2009-11-11T00:51:39-05:00

While the job requires a bit of ordinary administrative work (about 5 hours a week), most of the work requires a very high level of skill in helping write research papers and grants, editing scientific content for the group's web-site, and editing a web-journal on mathematical biology. Such a job would be suitable for an individual who was in the world of work or academia, but has taken a step away (i.e. is raising a family, or is temporarily in the greater Boston area with a spouse who is in training), wants to work part time, but still wants to do something interesting and demanding. Most of the work can be done from home. The hours are completely flexible, involves interesting people and is interesting intrinsically. The work requires quite high level of skill, especially in writing. A bit of scientific knowledge would be useful, but is not essential.

Brand Ambassado for Science inspired beauty brand

2009-11-10T22:01:13-05:00

Living Proof is looking for a Spokesperson!

Living Proof (www.livingproof.com), the revolutionary beauty company, is looking for a smart, passionate and enthusiastic Spokesperson to represent them on television, the web, live in store and in PR.

Living Proof is a company of world-class scientists from some of the world's leading university and research laboratories, including Drs. Dan Anderson and Bob Langer from MIT, working together with beauty experts towards one common goal: to invent breakthrough formulas that provide beautiful results you can seefrom across the room.

Simply put: Living Proof = Solving Problems.

Our scientists invented the first anti-frizz technology in 30 years. No
Frizz by Living Proof was recognized by the beauty industry as
ground-breaking with the awarding of the prestigious Allure magazine
"Beauty Breakthrough Award" for 2008 - the first-ever recognition of a
beauty product before its introduction on the market. With active skin
and hair programs, Living Proof has many product breakthroughs in
development to launch in the coming years. Today our products are sold
through Sephora, QVC and Livingproof.com with more distribution coming
in the next 6 months.

We are in search of attractive and intelligent men and women with captivating personalities. You must be an excellent communicator and a quick thinker with a great sense of humor and a love for beauty products. Excellent sales skills are a major plus as well as experience in front of the camera.

This is a full time salaried position with bonus and stock options. The position requires frequent travel fro Boston to Philadelphia as well as national travel. If you're interested, please send a recent photo no older than six months, resume and short letter explaining your background and interest to livingproofcasting@gmail.com or hard copies to

Sean De Simone Casting
P.O. Box 20347

GIS Specialist (AIR) (Boston, MA)

2009-11-10T21:37:05-05:00

AIR Worldwide Corporation (AIR) is the scientific leader and most respected provider of risk modeling software and consulting services. AIR founded the catastrophe modeling industry in 1987 and today models the risk from natural catastrophes and terrorism in more than 50 countries. More than 400 insurance, reinsurance, financial, corporate and government clients rely on AIR software and services for catastrophe risk management, insurance-linked securities, site-specific seismic engineering analysis, and property replacement cost valuation. AIR is a member of the ISO family of companies and is headquartered in Boston with additional offices in North America, Europe and Asia. For more information, please visit www.air-worldwide.com.

- Gather, analyze and integrate spatial and non-spatial data from different sources and determine the best way to use, display and store

- Create and edit presentation-quality thematic maps, graphs and charts

- Create and edit presentation-quality, smoothed, interpolated raster maps

- Analyze and manipulate large vector and raster data sets

- Perform various spatial analysis on shapefiles, geodatabases, and ASCII files (text and raster)

- Prepare metadata and other documentation of map data

- Bachelor of Science degree or similar

- Experience with ArcGIS and its various extensions, such as Spatial Analyst); Microsoft Excel; Microsoft Access

- Experience with mapping technologies such as Google Earth/Map, Bing map, etc.

- Knowledge of cartographic and geographic principles, symbology, practices and current trends

- Experience with ArcObjects a plus

- Experience with MapInfo a plus

- Ability to meet rigorous deadlines, work on several projects simultaneously, and work in a team setting

- Excellent analytical, organizational, and communication skills

If interested, please apply online at http://track.tmpservice.com/ApplyClick.aspx?id=838773-1857-6939

RN Patient Support Specialist-0901371 (Rockland, MA)

2009-11-10T16:13:56-05:00

EMD Serono, Inc., an affiliate of Merck KGaA, Darmstadt, Germany, is a leader in the US biopharmaceutical arena, integrating cutting-edge science with unparalleled patient support systems to improve people's lives. The company has strong market positions in neurodegenerative diseases, MS and endocrinology. EMD Serono is also a leader in fertility treatments. With a clear focus on the patient and a leadership presence in the biopharmaceutical industry, EMD Serono's US footprint continues to grow, with more than 1000 employees around the country and fully integrated commercial, clinical and research operations in the company's home state of Massachusetts.

Description

The RN Patient Support Specialist will play an integral role within EMD Serono's Patient Support Call Center (i.e. MS LifeLines) as part of the overall Patient Marketing function within the Neurology Department. The RN Patient Support Specialist will handle direct customer interaction by providing nursing support and assistance to patients, caregivers, family members, nurses, physicians, and pharmacists. A key objective of the role is to achieve customer satisfaction and ensure adherence to therapy. This will be accomplished by listening to the customer needs and utilizing the resources available within the center to provide a customized solution. A geographic territory of patients will be assigned and must be managed to ensure patient adherence of neurology therapies. The RN Support Specialist will manage all customer information according to HIPPA guidelines and other laws and regulations and in the strictest of confidence and will enter all required information accurately and expeditiously into the program database including update of therapy start dates and dose. The RN Support Specialist may be called upon to provide education and support at patient and/or field oriented events.

The shift for this position is: 11:30AM to 8:00PM Monday through Friday, with occasional per diem weekend coverage required.

KEY TASKS AND RESPONSIBILITIES:

Institute and maintain timely patient follow-up via outbound telephone calls to ensure continued product therapy.
Manage an assignment of a geographic territory to reach the greatest number of patients and provide timely follow-up.
Ensure compliance/adherence to therapy through expanded patient support systems.
Provide patient/caregiver teaching as required.
Provide guidance and direction to patients and caregivers in managing therapy side effects.
Maintain communication with outreach nursing agencies and pharmacies to preserve the highest quality of patient handling.
Handle adverse event calls. Triage to United States Product Surveillance (USPS) when appropriate.
Maintain technical expertise in the assigned therapeutic area through continuous education and attendance of periodic internal lectures as well as association meetings for updates of current therapies and industry advancements.
Share unique situations and issues with team members to ensure common response from all RN Support Specialists.
Interact directly with patients, caregivers and Healthcare professionals.
Handle all customer contacts with the highest in professional standards. Each call will be answered promptly, professionally, and compassionately with the end result of meeting the customer's needs (medical information, coordination of homecare requests, fulfillment, general source of information on their assigned therapeutic area, and triage for reimbursement to Reimbursement Specialists).
Timely follow up with registrants of the support programs (e.g., CHAT, MS IN Balance, MS Walks, etc.) to ensure compliance on therapy.
Gather and deliver approved medical information or triage to United States Medical Information (USMI) and/or United States Quality Assurance (USQA) group(s) for advanced medical questions, complaints.
Partner with patient physician/nurses or other healthcare professionals to provide consistent product information.
Ensure timely and effective execution of new customer programs.
Update Managers/Supervisors with feedback from customers to improve services or provide recognition of staff members.
Maintain technical expertise in the assigned therapeutic area through continuous education and attendance of periodic internal lectures as well as association meetings for updates of current therapies and industry advancements.

EDUCATION & LANGUAGES

Must be an active Registered Nurse licensed in the state of Massachusetts.
Fully bilingual capability a plus.
Achieve certification through the International Organization of MS Nurses.

PROFESSIONAL SKILLS & EXPERIENCE

Minimum five years of experience as a Registered Nurse.
Experience in the field of home care or case management a plus but not required.

PERSONAL SKILLS & COMPETENCIES

Must be flexible in working hourly shifts (11:30AM to 8:00PM Tuesday, Wednesday, Thursday, Friday, and 8:45AM to 5:15PM on Saturday), weekends and certain holidays, or holiday weekends. Overtime may be required.
Limited travel will be required. Attendance of certain association meetings during the year may be required to receive updated information or competitive review.
Exceptional customer service and telephone skills.
Strong computer skills (customer contact databases, Windows, Word, and Excel) required.
Data Entry/Typing skills necessary.
Ability to manage multiple and/or repetitive tasks.

Click the link below and open the door to the future by submitting your resume today!

EMD Serono 0901371

Awards & Recognition
June 2009, The Boston Business Journal recognizes EMD Serono as one of the Best Places to Work!
May 2009, The Scientist magazine names EMD Serono one of the best place to work in the life sciences industries!

October 2008, EMD Serono Named as a Top Employer by Science Magazine!

Research Technician, Next-Generation Sequencing (Boston University School of Medicine)

2009-11-10T16:10:58-05:00

Description:
A full-time position is available for an experienced research technician with a background in genomics and/or molecular biology. Experience with next-generation DNA sequencing technologies is a plus but not required. This technician will report to the laboratory supervisor and principle investigator of a shared research core laboratory facility. The individual will be responsible for preparing and characterizing RNA and DNA samples for next-generation sequencing and for operating next-generation sequencing instrumentation. Responsibilities will also include sample inventory, data entry, and general laboratory and instrument maintenance. Excellent competitive salary and benefits.

Qualifications:
Bachelor's degree in life sciences or chemistry with at least 5 year of experience in a laboratory setting required. Strong work ethic, attention to detail, and excellent organizational, documentation, and communication skills are essential requirements for this position.

For more on our lab, visit:
http://pulmonomics.com/tiki-index.php?page=jobs

Contact:
Ms. Erika Langer at pulmonomics@gmail.com
Please put "Sequencing Technician" in the subject heading

Document Control Supervisor (Waltham, MA)

2009-11-10T15:17:59-05:00

The Document Control Specialist is responsible for supporting the internal GLP/GMP auditing program, and assisting in the compilation of regulatory submissions. The candidate will ensure compliance with applicable regulatory requirements by directly working with external manufacturing quality organizations and internal/external partners.

Responsibilities:
Drive, execute and track records and documentation processes throughout the documentation lifecycles including but not limited to:
Generation and control of document change requests
Document formatting and word processing from redlines
Routing, tracking and facilitating timely documentation review, approval and periodic/annual review
Control, distribution and maintenance of internal procedural documentation and records
Indexing, archival and retrieval
Maintenance of product specification files
Maintenance of electronic department directories
Develop and conduct Document Control related training
Creation of Master Batch Records and issuance of Batch Records
Coordinate and compile Batch Record History documents
Release of all raw materials for GMP use and maintain an inventory system
Initiates the creation, review and revision of procedures, specifications and forms
Track and report on document review progress
Track and trend all NCMI�s, Deviations, CAPA�s, and Change Control�s
Assure completeness of all documentation
Track and maintain other internal records including training, Design History Records, equipment records and laboratory notebooks
Assist with the implementation, management and administration of the quality system electronic management systems
Work with subject matter experts on technical subjects in a positive, collaborative manner to prepare controlled documents which conform to Histogenics defined format
Review and proofread documents for consistency of document format and system concerns
Verify and issue production documents and product labels to the manufacturing department
Assign and track lot numbers, material part numbers, change control numbers, issue numbers, equipment numbers and various other unique tracking identification
Provide support for the Quality System during corporate audits
Adhere to and enforce Histogenics policies and procedures related to document control
Perform audits of company areas and processes to confirm compliance with controlled procedures
Prepares and processes status reports, assigns and monitors document numbers, and reviews documents for accuracy and completeness.
Maintains training files and job list for each employee and reports any deviations.
Provides support on various other projects as necessary, ensuring the precision, accuracy, and reliability of the GMP process.
Maintains the GMP change control program by ensuring completeness of change control documents for accuracy and compliance; establish reporting metrics and provide follow up on implementation plan items for change control closure.

Requirements:

Experience with Quality System Documentation and good documentation practices
7 to 10 years of Document Control or other Quality Assurance-related experience in a cGMP environment is a plus.
Experience in the development / implementation of document control and records management procedures in a pharmaceutical or biologics environment.
Prior experience in medical device or other GMP-regulated industry is preferred.
Knowledge of ISO, FDA and cGMP concepts and guidelines.
Ability to lead in a management capacity.
Ability to communicate effectively, verbally and in writing, and demonstrate good interpersonal skills interdepartmentally and with external vendors and contractors
Work on complex assignments in collaboration with various department system owners.
Very Strong analytical problem solving and organizational ability.
Demonstrated ability to work accurately, follow instructions/schedules/timelines and handle multiple priorities.
Professional, well-organized, and eager to learn and be challenged.
Must have excellent MS Office applications Word, Excel, Access, Power Point as well as Adobe Acrobat skills.
Works under minimal supervision
Candidate must be flexible and able to adapt to changes in priorities.

If applying for this position please include salary requirements along with resume

LOCAL CANDIDATES ONLY

SR RESEARCH ASSISTANT / 40 HOURS / DAYS - BWH THORACIC SURG (2195652) (Boston, MA )

2009-11-10T13:34:27-05:00

Brigham and Women�s Hospital (BWH) is internationally known as a leader in cutting-edge research and technology and its commitment to patient-centered care. BWH has a rich legacy of excellence and has been consistently recognized as one of America�s best hospitals by US News and World Report.

GENERAL SUMMARY:
The Clinical Research Associate is responsible for all administrative and operational aspects of clinical research within the Thoracic Surgery Division. He/she monitors patient accrual to surgical trials at the Brigham and Women's Hospital (BWH) and Dana-Farber Cancer Institute (DFCI), including actively recruiting patients on trial, following patients through the protocol treatment program and follow-up, and completing data forms and data management required by the studies.

PRINCIPAL DUTIES AND RESPONSIBILITIES:
1. Responsible for collecting data and maintaining patient information database for studies.
2. Responsible for IRB and other regulatory submissions for protocol submissions and updates, renewals, adverse event reports, deviations, data audits, etc.
3. May be required to do data analysis and run various reports.
4. Interacts with patients/subjects with regard to consenting, data collection, follow-up, and other tasks as assigned. May serves as a liaison between patient and physician.
5. Performs quality control procedures to ensure integrity of data in clinical research database, as determined by Clinical Research Manager.
6. As required, collects biologic samples and specimens and ensures protocol adherence in the operating room, laboratory, and intensive care settings per study guidelines.
7. Answers any phone calls and inquiries regarding clinical research database or study protocol. Refers participants when appropriate to supervisor or clinical staff.
9. All other duties, as assigned.
Requirements
QUALIFICATIONS:
In order to be eligible for an interview the following skills are necessary: previous clinical work including consenting patients AND basic data management.
Master's Degree preferred.

SKILLS/ABILITIES/COMPETENCIES REQUIRED:
1. Experience using Microsoft Excel, Access and Word are required.
2. Experience using Electronic Medical Records for data collection and review is preferred.
3. Knowledge of statistical software required and experience with SAS and or SQL is preferred.
4. Knowledge of clinical research protocols and clinical trials process, with at least 2 years clinical research experience is preferred.
5. Knowledge of medical terminology.
6. Ability to demonstrate professionalism and respect for subjects rights and individual needs.
7. Excellent interpersonal skills are required for working with the study participants.
8. Careful attention to detail.
9. Good oral and written communication skills.

SUPERVISORY RESPONSIBILITIES:
None

WORKING CONDITIONS:
Data office, operating room, and laboratory working conditions include working under pressure to meet deadlines and meetings, moderate stress.

DRESS CODE:
Professional dress code required.
Shift
Day Shift

To apply online, please submit your resume here:
https://careers.partners.org/psc/EA/EMPLOYEE/HRMS/c/HRS_HRAM.HRS_CE.GBL?Page=HRS_CE_JOB_DTL&Action=A&SiteId=2&HRS_JOB_OPENING_ID=2195652

Brigham and Women�s Hospital is an EEO, AA and VEVRAA employer.
http://www.brighamandwomens.org/careers

Study Fleet Field Technician (Gloucester, MA)

2009-11-10T10:42:43-05:00

Integrated Statistics is looking for an individual to work directly with commercial fishermen participating in the National Marine Fisheries Service (NMFS) - Northeast Fisheries Science Center�s (NEFSC) Study Fleet program. We need someone to provide assistance with the installation, training, and trouble shooting of an electronic logbook system and evaluate the quality and completeness of the self-reported data collected by the fishing industry.

Specific duties
1. The incumbent will organize logistical support for industry participants in the Study Fleet program; including recruitment with community leaders, conducting dock-side visits to provide program overviews and determine system constraints. Incumbent will be responsible for the electronic logbook deployment and training, trouble shooting support and data collection. The incumbents will be expected to carry a contractor-issued cell phone and be on call to provide support 24 hours a day d(within reason) during week days and rotationally on weekends.

2. The incumbent will monitor the data collected by participating Study Fleet vessels for quality and completeness, identify areas for improvement in the data collection methods and communicate the results back to the industry and Study Fleet management. The incumbent will maintain records tracking equipment or software failures and circumstances to assist in identifying solutions for recurrent problems or system limitations.

3. The incumbent will sail on participant Study Fleet vessels in order to collect independent catch records for comparison to fisherman hail estimates. Duties at sea may also include collection of biological samples, deployment of additional data collection devices and/or the testing of new equipment or protocols.

4. The incumbent will work with NEFSC Study Fleet staff and other contractors to develop outreach materials, including user manuals, troubleshooting guides, and brochures and letters to fishermen, that will keep them apprised of program accomplishments, challenges and objectives. This will include participation in industry meetings, scientific symposia, and regular visits to fishing ports.

5. The incumbent may conduct independent research to improve the efficacy of Study Fleet data with respect to improving the quality of science used in fisheries stock assessments.

Qualifications
Applicants shall have experience communicating with commercial fishermen and experience collecting fisheries data at-sea, preferably aboard commercial fishing vessels. Preference will be given to applicants with at least one year�s experience working as a certified fisheries observer or extensive experience working on cooperative research projects with the fishing industry. Additionally, applicants shall have the ability to interact with a variety of people including fishermen, technical staff, fisheries managers and other scientists often in stressful situations.

Duties will be focused on field work, meetings with fishermen, troubleshooting hardware/software issues aboard fishing vessels and maintenance of data according to Study Fleet protocols; there will be field and office components to the incumbent�s responsibilities including frequent travel to ports within the Northeast Region and trips to sea aboard participant commercial fishing vessels (~40+ days at sea per year). Applicants shall have moderate to strong computer skills and familiarity with GPS and satellite communications. Preference will be given to those applicants that have demonstrated experience installing electronic hardware/software, use of serial devices, knowledge of electronics, interaction with fishing community members, demonstrated experience in fish identification and quantification procedures, knowledge of relational databases and a background in basic statistics.

Minimum educational requirements include a Bachelors degree in biological or marine sciences that includes at least 6 semester hours in aquatic subjects such as limnology, ichthyology, fishery biology, aquatic botany, aquatic fauna, oceanography, fish culture, or related courses in the field of fishery biology; and at least 12 semester hours in the following areas: general zoology, vertebrate zoology, comparative anatomy, ecology, ecological modeling, computer science, electronics engineering or statistics. Preference will be given to applicants with advanced degrees.

Personnel shall be able to show a demonstrated ability to work independently with little supervision to accomplish program objectives. In some cases, additional training in procedures, equipment, and analytical software that is specific to program requirements will be provided by the NEFSC as tasks develop.

Applicants shall possess a driver's license and passport valid in the US. Valid driver's license required. The successful applicant shall take the online web based security and safety courses, and submit the completed certificate to the COTR.

Additional information on the NEFSC�s Study Fleet program can be found at:
http://www.nefsc.noaa.gov/read/popdy/studyfleet/

BioSkills Technician (BOS)

2009-11-09T18:31:51-05:00

JOB TITLE: Bioskills Technician

STATUS: Full-Time

JOB DESCRIPTION:

The Bioskills Technician�s primary responsibility is to ensure customers� labs run as smoothly and efficiently as possible. The Bioskills Technician works closely with physicians and researchers during labs, receiving & preparing specimens, setting up the lab including proper positioning & draping of the anatomical specimens, assisting during the course, proper repackaging and shipping of specimens and cleaning of lab and instruments. Positive, can do attitude, outstanding problem solving skills, attention to detail, strong communication skills, full time travel and knowledge of anatomy are a must. Previous anatomical specimen lab or �wet lab� experience a plus.

SPECIFICATIONS:

� Be accountable for OSHA compliance
o Ensure proper disposal of biohazard materials
� Maintain adequate surgical and lab supplies for your personal bin.
� Must be extremely flexible team player, adaptable to constant change.
� Excellent customer service abilities.

BioSkills Technician must be able to:
� Stand for extended periods of time.
� Lift up to 70lbs.
� Speak English clearly and fluently
� Complete tasks using computer software at an average skill level
� Provide excellent customer service via all instruments of communication
� Comfortably interact with researchers and physicians.

REQUIREMENTS

Education Bachelors Degree with emphasis on Anatomy/Physiology or verifiable work experience in related field.

Experience Clinical / BioSkills Lab experience preferred.

Please send Cover Letter, Salary History, and Resume for consideration.

DMPK Scientist/ Senior Scientist - (contract assignment)

2009-11-09T16:10:40-05:00

Our client is in search of Scientist to provide hands-on bio-analytical support for preclinical PK/ ADME studies. If you have a strong background and training in PK bio-analytical chemistry, this could be an exciting opportunity for you!

This position requires a Ph.D. or very experienced MS/BS with a minimum of five years industry experience in PK bio-analytical chemistry. The ideal candidate must be proficient in the operation of LC/MS/MS instrumentation, preferably API 4000 for PK, metabolism, and ADME studies. GLP experience is also required since you will assist in transferring methods to support GLP studies to support human trials

You will appreciate the ethics guiding each StratAcuity team member. We build lasting relationships with exceptional scientists and take great care to protect your personal information. Upon receiving your inquiry, you may be directly contacted by a StratAcuity team member to discuss your career goals. We will not share your information with anyone without your direct prior consent.

StratAcuity Scientific, CHEMISTRY IS EVERYTHING.

InVitro Technicians (Bedford, Ma)

2009-11-09T14:52:08-05:00

Toxikon Corporation in Bedford, Ma is seeking entry level candidates for a role within one of our InVitro departments in a growing medical device, pharmaceutical, and biotechnology-testing laboratory. Responsibilities include setting up various tests for the In-Vitro Toxicology department, conducting the studies in a GLP environment. The appropriate candidate will have a bachelor�s degree in an area of the life sciences, and a strong interest in working in a laboratory setting. Candidates will also perform routine laboratory duties; maintain complete documentation of tests and logbooks. Studies are conducted under numerous guidelines, protocols, and Standard Operating Procedures.

Toxikon offers a comprehensive benefits program including paid vacation, sick and personal time, 401K with a company match, medical, dental, vision care, life and short term and long term disability insurance, as well as flexible spending accounts. This facility is not accessible via public transportation; candidates must have their own vehicle or other means of transportation. Hours are Monday � Friday from 8am to 5pm. Toxikon is an equal opportunity employer.

No recruiters please.

Toxicology Technician (Bedford, MA)

2009-11-09T14:40:55-05:00

Toxikon is seeking experienced Technicians for our Pharmaceutical Services facility to support pre-clinical studies alongside research staff under numerous GLP/ other guidelines, protocols, and Standard Operating Procedures and in an AALAC accredited facility. The responsibilities include animal handling / husbandry; data collection and recording; data package preparation; sample preparation; dosing, and; surgical assistance. The successful candidate will also perform materials preparation activities; execute procedures for chemical preparation and characterization; document and validate preparation and characterization procedures, and; maintain laboratory materials inventory. Opportunities for superior training and certification with the American Association for Laboratory Animal Science exist.

A Bachelors degree in a life science (biological sciences, biotechnology, zoology, biochemistry, animal science) with two to four years� experience, or associates degree (science, veterinary technology) with a minimum of five years� experience are required. ALAT certification is preferred. Prior small animal, research, animal husbandry, and/or laboratory experience performing PK and ADME testing are preferred. The successful candidate must have solid experience handling animals (non human primates experience a plus) and performing animal drug administration (p.o., i.v. and i.p.). The candidate will have strong communication and organizational skills and the ability to handle multiple tasks while maintaining attention to detail and quality. The candidate will be working closely with other technicians, scientists, veterinarians, and regulatory affairs personnel.

Research Assistant (Stem Cells) (Children's Hospital Boston)

2009-11-09T13:53:34-05:00

This position is located within the stem cell program of Children's Hospital Boston and calls for a responsible, conscientious and detail-oriented individual. The ideal candidate is a recent graduate (BS) with a passion for stem cell biology and extensive lab experience including mammalian cell culture. Additional experience with virus production, high throughput screening, fluorescence microscopy, laboratory automation / robotics, FACS, image analysis, or programming/databases (e.g., Java, ImageJ, Matlab, FMP) would be a plus.

Duties and responsibilities may include:

* Maintenance of mouse and human embryonic stem cell / iPS cell cultures
* Characterization of stem cell lines via several types of cellular analysis including: immunofluorescence, flow cytometry, DNA / RNA isolation, PCR, and occasional laboratory animal work
* Initiation and Management of orders and inventory, tracking supplies and expenditures for a small sub-group within the laboratory
* Preservation and shipping of reagent requests
* Maintenance of equipment, infrastructure, and space allocation
* Ensure compliance with institutional and federal guidelines in health, safety and animal regulations
* Generation of stock reagents

Requirements:

* Bachelor's Degree, preferable B.S.
* Experience in a laboratory setting (see above for preferred experience)
* Proficiency with Microsoft Office applications (Word, Excel, PowerPoint, etc.)
* Excellent oral and written communication skills
* Willingness to conduct human embryonic stem cell research
* Willingness to commit to at least two years

Be sure to include with your application (incomplete application will be ignored!):

* A detailed cover letter
* CV/resume including GPA, visa status, and relevant experience
* Info on possible start date(s)
* Email your application to: schlaeger@enders.tch.harvard.edu
 

Project Manager - Life Sciences

2009-11-09T13:06:17-05:00

Project Manager with expertise in move and furniture management, vendor and IT coordination. Core competency in construction administration, technology coordination, equipment installation with experience in the life sciences/lab environment. Ability to multitask and perform in high-demand situations. Excellent communication and technical skills. Proficient in Microsoft products including Excel and Project; familiarity with AutoCAD and CAFM programs.

Category Manager, Commercial/Marketing (Biopharmaceutical) 0901373 (Rockland, MA)

2009-11-09T12:35:10-05:00

At EMD Serono, Inc. our strength is our people!

About the Company

EMD Serono, Inc., an affiliate of Merck KGaA, Darmstadt, Germany, is a leader in the US biopharmaceutical arena, integrating cutting-edge science with unparalleled patient support systems to improve people's lives. The company has strong market positions in neurodegenerative diseases, MS and endocrinology. EMD Serono is also a leader in fertility treatments. With a clear focus on the patient and a leadership presence in the biopharmaceutical industry, EMD Serono's US footprint continues to grow, with more than 1000 employees around the country and fully integrated commercial, clinical and research operations in the company's home state of Massachusetts.

Description

The Category Manager is responsible for managing a portfolio of Commercial/Marketing spend categories within a bio-pharmaceutical organization. As a key link between internal customer departments, Procurement, and EMD Serono's external supplier base, the Category Manager is accountable for understanding key business drivers and ensuring that customer requirements are fulfilled. Extensive cross-functional collaboration, and use of strategic sourcing best practices are keys to maximizing value in terms of cost savings/avoidance, risk reduction, quality and supplier performance. The role holder conducts internal and external spend and market analyses, identifies opportunities, develops category strategies, leads sourcing teams, negotiates contracts and manages key supplier relationships. The role holder is an energetic, flexible team player capable of forming strong relationships throughout the entire organization, in addition to successfully leveraging resources, processes and tools to achieve desired outcomes.

KEY TASKS AND RESPONSIBILITIES

Actively work with the business partners to source goods and services in accordance with policies and procedures.
Develop subject matter expertise in order to enhance ability to add value from a procurement perspective.
Ensure the timely execution and delivery of products and services in accordance with business timelines.
Drive value, service and cost savings through optimum vendor selection, management and effective negotiation.
Lead the supplier performance management process for assigned categories.
Provide strategic insight and access to all relevant spend and related data.
Ensure that the business area engages and fully supports the supply base and supplier management strategies that impact their business area.

SKILLS & COMPETENCIES

Willing to diplomatically challenge concepts and tackle large, complex tasks.
Active external learner - can identify new and better ways, and takes advantage of ideas, best practices and solutions
Ability to support/lead and affect transformational change effort
Customer focus and successful management of many internal customers and competing priorities and the need to continually allocate and balance resources across projects, or Account Planning
Strong skills in strategic influencing, collaboration, communications, and conflict management
Strong spend and supplier analysis skills

Qualifications

EDUCATION/PROFESSIONAL EXPERIENCE

Bachelor's degree required (Master's degree preferred)
8 years of relevant work experience with strong preference in a large multi-national bio-pharmaceutical organization
At least 5 years experience in strategic sourcing/category management, conducting cross-functional sourcing projects and negotiating contracts for complex services,li>Project background in most, if not all, key categories of bio-pharmaceutical commercial spend (i.e., Agency, Media, Market Research, Medical Education, Conferences, Print, Premiums and Direct Marketing)
Strategy development experience
C.P.M. or CPIM certificate preferred

EMD Serono 0901373

Awards & Recognition

June 2009, The Boston Business Journal recognizes EMD Serono as one of the Best Places to Work!

May 2009, The Scientist magazine names EMD Serono one of the best place to work in the life sciences industries!

October 2008, EMD Serono Named as a Top Employer by Science Magazine!

Associate Scientist, Upstream Development-0901223 (Rockland, MA)

2009-11-09T12:16:43-05:00

At EMD Serono, Inc. our strength is our people!

About the Company

Description

Manage process development projects under the guidance of the lead manager and/or director. To be an integral team member who designs and develops robust, scaleable fermentation processes. To be proficient in fermentation scale-up and methodologies, fermenter operation, cell lysis and protein recovery operations. To generate reports and group presentations summarizing the data and activities behind experimental work. Liaising with other departmental scientists to keep moving projects forward. To create tech transfer documents, and edit new SOPs and batch records. To monitor, troubleshoot and provide technology support for production runs at scale. To ensure upkeep of equipment required for lab operations. To maintain a substantial knowledge of state-of-the-art principles and theories and may contribute to scientific literature and conferences. To be involved in regulatory filings and participate on project teams. To manage the work of associates under direct line management and cross-resourced on specific projects. To understand GMP requirements and procedures.

KEY TASKS & RESPONSIBILITIES

Manage and/or execute experiments in the role of project or unit operation lead for the development & characterization of upstream unit operations.
Perform and/or manage supporting analytics (in conjunction with direct reports, other lab members or QC).
Record experiments and results using Patentsafe.
Generate reports detailing individual experiments and results. Create and archive BPS cell banks appropriately and ensure cell banks are tested as per project timelines.
Supply BPS Purification with suitable material for downstream studies.
Deal with issues that arise in the PPL in a timely, proactive manner.
Understand PPL requirements for processes transferred into the facility.
Generate development reports for individual and managed activities in the role of project or unit operation lead.
Present experimental results in group meetings, project meetings (CMC and GPT), and other cross-functional team meetings.
Manage and/or create tech transfer documents for unit operations developed.
Participate in teams as required to support MS-BMPD initiatives.
Track and report group KPIs. Provide and support development plan for direct reports and interns
Position requires both domestic and international travel up to 20% of time

EDUCATION & LANGUAGES

A Masters Degree with 3 + years, Doctorate degree or Bachelor's Degree with 6 + years experience.

PERSONAL SKILLS & COMPETENCIES

Has a positive attitude towards customers, understands customer needs, quickly responds to their inquiries and makes sure they are satisfied.
Brings forward creative ideas and makes suggestions for the improvement of existing processes.
Contributes to a positive working climate by demonstrating respect, openness and honesty.
Has good verbal reasoning and presentation skills who seeks a win-win solution through a give-and-take process that recognizes each party's core needs.
Keeps appointments and commitments, allocates appropriate amount of time for completing own work and respects deadlines.
Sets clear goals and has a high expectation level of employees' output and performance.
Supports employee's learning and development by encouraging on the job learning and other development activities.

Click the link below and open the door to the future by submitting your resume today!

EMD Serono 0901223

Awards & Recognition

June 2009, The Boston Business Journal recognizes EMD Serono as one of the Best Places to Work!

May 2009, The Scientist magazine names EMD Serono one of the best place to work in the life sciences industries!

October 2008, EMD Serono Named as a Top Employer by Science Magazine!

Senior Product Manager Reproductive Health 0900567 (Rockland, MA)

2009-11-09T11:56:08-05:00

At EMD Serono, Inc. our strength is our people!

About the Company

Description

In this role you will make a significant contribution to the Reproductive Health marketing Team. The successful candidate will be responsible for developing and implementing marketing initiatives that support the brand strategy and that target both healthcare professionals and patients. This candidate may also be responsible for people management and development.

This is a highly visible role internally and externally. Some of the key interfaces internally are with sales, marketing, medical affairs, supply chain, and regulatory affairs.

Externally you will interact with groups such as: physicians, KOLs, ad agencies, vendors, patient advocacy groups, and professional associations.

Key Tasks & Responsibilities

Participate in the development of the Gonal F and Reproductive Healthy product portfolio marketing strategy to healthcare professionals and patients. Work with the Director of Marketing to ensure that these strategies fit within the overall US franchise strategy
Proactively develop and execute marketing projects with agencies from concept through implementation. Ensure that all launch milestones are met
Responsible for tactical implementation including but not limited to collateral materials, speaker bureaus, key opinion leader development, etc.
Refine and enhance marketing strategy and tactics based on market experience, new clinical data, and market research/business intelligence findings
Manage budgets and judiciously prioritizes strategies and tactics based on potential value to the Gonal F brand
Build relationships with key internal and external customers to ensure successful execution of projects
Work in close collaboration with Training and Field Sales Management and the Call Center to ensure successful development and implementation of programs, tools, and services with consistent marketing messages
Conduct field visits as necessary to evaluate effectiveness of marketing programs, tools, and services
Collaborate with Business Intelligence and Market Research on the development of research tools and analysis of results to understand market dynamics and trends. Stay abreast of ongoing clinical development for the brand
Collaborate with Medical Affairs and Medical Operations to develop and execute medical education programs
Work with Marketing Advisory team of healthcare providers to develop and adapt plans, support implementation of new and unique customer programs, and value-added services
Partner with key Patient Advocacy Groups to provide education and foster market awareness in the fertility space
Support convention planning and execution of related programs
� Other related duties as assigned

Education & Languages

BA/BS required
MBA or advanced degree preferred

Professional Skills & Experience

Minimum of three to five years related marketing experience in pharmaceutical/biotech industry. Including one to two years managing, leading, and developing people
Strong pharmaceutical marketing experience, requires experience developing marketing programs and materials for healthcare professionals
Experience managing vendors and contractors
Experience managing a marketing budget
Pharmaceutical launch experience strongly preferred
Willing to travel up to 30% of time
Previous pharmaceutical sales or pharmaceutical sales management experience a plus

Personal Skills & Experience

Strong communication skills (written and spoken) and an ability to translate clinical information into succinct and high impact marketing messages
Excellent presentation skills
Ability to work in fast paced environment
Ability to analyze competitive landscape and key brand issues
Must be comfortable with ambiguity common dynamic marketplace
Must possess the ability to multi-task and have superior organizational skills
Excellent interpersonal skills
Ability to demonstrative creative and innovative strategies for business development
Ability to access and influence various functional areas and motivate groups to actions through team building initiatives
Leadership skills in a matrix management environment
Collaborative work style and familiarity with core operating function (sales, marketing, regulatory, legal, medical, global marketing and co-promotion partners)
Business oriented thinking
Relationship management skills

EMD Serono 0900567

Awards & Recognition

June 2009, The Boston Business Journal recognizes EMD Serono as one of the Best Places to Work!

May 2009, The Scientist magazine names EMD Serono one of the best place to work in the life sciences industries!

October 2008, EMD Serono Named as a Top Employer by Science Magazine!

Lab assistant ( entry level) (Lawrence, Ma.)

2009-11-09T10:57:51-05:00

C.I.L. Inc. is an anodize and paint shop

We have a first shift opening for an entry level lab tech/lab assistant.
The ideal candidate would have an appropriate degree ( chemistry, physical sciences ) or laboratory experience.
Please send your resume via email.

Associate Director, Pharmacology, metabolic and inflammatory diseases (Cambridge)

2009-11-09T08:53:49-05:00

Sirtris, a GSK Company, and 2009 winner of American Business Awards Best Overall Company of the Year�up to 100 employees, is developing small molecule drugs that target the sirtuins, a recently discovered family of seven enzymes associated with the aging process. Modulation of these enzymes offers the promise of drug discovery in multiple therapeutic areas.

Join an enthusiastic team in a growing drug discovery company. Sirtris Pharmaceuticals seeks a motivated and team-oriented individual who will be a key contributor to the overall success of the Pharmacology group. The Associate Director, Pharmacology will provide the overall strategic direction of the Pharmacology group as part of Sirtris� ongoing drug discovery efforts in the Sirtuin area.

Primary responsibilities:

o Provide strong leadership and strategic direction to the Pharmacology team.
o Mentor and guide the team through hands on lab work and troubleshooting as required.
o Evaluate the mechanism of action and efficacy of novel Sirtuin agents in the areas of metabolic and inflammatory disease.
o Translate cell-based discovery through in vivo models into the clinic.
o Represent the Pharmacology team at Project Team Meetings demonstrating excellent presentation skills.

PhD in Pharmacology or related discipline and 8-10 years of experience in the pharmaceutical/biotech industry. Must have current and detailed knowledge of in vivo models and PK/PD relationships in metabolic and/or inflammatory disease. Seeking excellent supervisory skills with the ability to influence internal and external decision-making and proven track record of scientific rigor through publications, patents, and speaking engagements. Should enjoy working independently under general direction in a fast-paced environment. Must have strong oral and written communication skills.

Join Sirtris where we are creating revolutionary medicines for diseases of aging. We hope you will see this as a unique opportunity to work in a fun, collaborative, and creative environment with leading edge science.

To apply, please go to: http://sirtrispharma.com/careers-opportunities38.html

Sirtris, a GSK Company, 200 Technology Square, Cambridge, MA 02139

Sirtris will only accept job applications from candidates who are properly documented with authorization to work in the United States.

Note to Employment Agencies: Please do not forward any agency resumes. Sirtris is not responsible for any fees related to resumes that are unsolicited.

Plant Tissue Culture, Research Assistant (Medford, MA)

2009-11-08T23:52:35-05:00
Agrivida is an agricultural biotechnology company developing traits and technology for fuel and chemical production from non-food cellulosic biomass. Our crops and processes enable the production of low cost sugars for use in manufacturing a wide variety of industrial products. Agrivida's innovative products will advance energy independence while reducing greenhouse gas emissions and enhancing the rural economy.

We continue to build a team of experienced plant scientists, molecular biologists, biochemists, chemical engineers and growers with diverse backgrounds and experiences to play key roles in expanding the foundation of our trait biotechnology and bioprocessing capabilities.

Agrivida seeks qualified persons to join our tissue culture team located in Medford, MA. Candidates should possess knowledge and experience in:

o Culture media preparation (calculating concentrations, sterilization, pH adjustment, etc.);
o Plant growth and physiology;
o Aseptic technique; and
o Tissue culture.

Applicants should have a B.S. in biology or a related field, have a strong work ethic, be interested in learning new techniques, be highly motivated, and be able to work well in a team environment or independently. Demonstrated computer literacy and outstanding written, oral, and interpersonal skills are highly desirable. Applicants must be qualified to work in the United States.

Agrivida is an equal opportunity employer.

(Key words: tissue culture, biofuels, ethanol, butanol, biochemicals, traits, plants, agriculture, enzyme, green jobs, renewable energy, corn)

p/t chemist for skin care product development (wellesley)

2009-11-08T17:11:12-05:00
We are a small natural skin care company looking to improve our formulas and extend our product shelf life.
We currently make home-made skin care lotions, lip balms, face creams, oils, astringents, cleansers etc.
We are a non-laboratory environment. We are a small, quiet, low key operation working out of our kitchen warehouse office.

You are interested in part time, after work or weekend hours.
You have Chemistry experience and are interested in formulating great new body, face, skin care products.
You are available to start soon.
Call 617-901-5066

Full time Waste Water Treatment Plant Operator

2009-11-07T17:14:30-05:00
We are seeking a full time waste water treatment plant operator
Minimum of 3 years experience
Full Benefits
Local company

Please respond via email or fax resume to 978-256-1841

Principle Scientist (Philadelphia, PA)

2009-11-07T15:26:21-05:00
Company Info:

Invisible Sentinel is a recently established biotech company focused on developing and commercializing novel diagnostic products for the specific detection of pathogenic bacteria. Invisible Sentinel�s scientific team will integrate existing technologies with innovative and advanced biomedical engineering methods to achieve our objectives. Invisible Sentinel prides itself on not restricting the limits of the career opportunities that employees can pursue as the company realizes its goal of becoming a global diagnostic biotechnology leader. Invisible Sentinel encourages both the professional and personal growth of our employees and is committed to supplying our employees with the resources they need to realize their full potential.

Job Description:

Invisible Sentinel is seeking a talented and highly motivated biomedical scientist with a strong educational and technical background in the fields of bacteriology and immunology. The successful candidate will need to be familiar with the development and characterization of monoclonal antibodies. This position provides the opportunity to be a member of the core design team and as such you will need to demonstrate high levels of enthusiasm, dedication, and innovation. The core responsibility for this position would be the design and development of assays to characterize monoclonal antibodies specific for various bacterial pathogens.

Responsibilities: Will include (but are not limited to) the following:

Establish and Supervise the antibody design and engineering group.
Expression, purification and characterization of monoclonal antibodies.
Represent antibody expertise in project team meetings and provide flexible support to
colleagues working on correlating company projects.
Manage lab resources and assess performance of team members.

Requirements:

Ph.D. in biological sciences with a minimum of 2 to 3 years practice in protein purification
& monoclonal antibody development.
Strong background and expertise in molecular biology, bacteriology and/or immunology.
Experience with expression, purification, and characterization of monoclonal antibodies is required.
Proven track record and in-depth knowledge of current antibody engineering literature and
characterization protocols.
Team-oriented and pro-active attitude; ability to communicate and interact effectively with management as well
as lab personnel.
Constructively contribute to decision-making and optimization of assay design.

TECHNICAL RES ASST I I / 40 HOURS / DAYS - BWH NEUROSURGERY (2194744) (Boston-On Campus/Longwood Area)

2009-11-06T17:49:53-05:00
Brigham and Women�s Hospital (BWH) is internationally known as a leader in cutting-edge research and technology and its commitment to patient-centered care. BWH has a rich legacy of excellence and has been consistently recognized as one of America�s best hospitals by US News and World Report.

GENERAL SUMMARY:
In collaboration with senior member of the research team, assist in projects to elucidate the in vitro and in vivo functions of dysregulated microRNAs in Huntington's disease (HD). Working under very general supervision, execute protocols involving a variety of routine and non-routine experiments at a professional level. Develop modification of existing techniques, as appropriate. Calculate, transcribe, and analyze data using statistical techniques.

PRINCIPAL DUTIES AND RESPONSIBILITIES:
1. Perform routine and non-routine experiments, which are moderate to complex. (Experiments may include RT-PCR, western blot, immunohistochemistry, DNA & RNA isolation, purification and quantification, transformation and transfection.)
2. Mouse husbandry, breeding, tail vein injection, and behavioral observation.
3. Maintain long-term tissue cultures of mammalian cell lines, stem cells and culture of primary neuron. Monitor cell viability, proliferation and cytotoxicity (MTS, LDH assay).
4. Calculate, transcribe and analyze data using advanced statistical techniques.
5. Perform literature searches and help to prepare presentations.
6. Other duties as assigned.
Requirements
QUALIFICATIONS:
BS or Master in biology or related science. Good background in molecular biology, cell biology, and working experience with small animals. 1-2 years of experience at molecular level and in vivo small animal studies in neuroscience/cell biology is a plus. Previous experience with mice tail vein injection is preferred but not necessary.

SKILLS/ABILITIES/COMPETENCIES REQUIRED:
1. Sound analytical and organizational skills.
2. Good oral and written communication skills.
3. Ability to logically and effectively structure tasks and set priorities.
4. Ability to identify potential problems and trouble-shoot solutions.
5. Demonstrated ability to analyze data statistically and to logically present it.

SUPERVISORY RESPONSIBILITIES:
None

WORKING CONDITIONS:
Basic biomedical research lab.

Shift
Day Shift

To apply online, please submit your resume here:
https://careers.partners.org/psc/EA/EMPLOYEE/HRMS/c/HRS_HRAM.HRS_CE.GBL?Page=HRS_CE_JOB_DTL&Action=A&SiteId=2&HRS_JOB_OPENING_ID=2194744

Brigham and Women�s Hospital is an EEO, AA and VEVRAA employer.
http://www.brighamandwomens.org/careers

RESEARCH LAB MANAGER / 40 HOURS / DAYS - BWH SURGERY (2195579) (Boston-On Campus/Longwood Area)

2009-11-06T17:46:45-05:00
Brigham and Women�s Hospital (BWH) is internationally known as a leader in cutting-edge research and technology and its commitment to patient-centered care. BWH has a rich legacy of excellence and has been consistently recognized as one of America�s best hospitals by US News and World Report.

GENERAL SUMMARY:
Working under the general direction of the Principal Investigator, oversees the daily operations of a research laboratory, including fiscal/budget management, supervision of staff, inventory management, compliance, etc. Participates with the principal investigator in the design of experimental protocols. Manages all aspects of funded research including the preparation of grant reports, protocols and financial statements. Participates with PI and fellows in development of grant proposals and submissions. Helps compile and write up research results for presentations and papers.

PRINCIPAL DUTIES AND RESPONSIBILITIES:
1. Supervises the daily activities of all laboratory staff and supervises the daily operation of the lab to ensure smooth running of the laboratory. Evaluates annually the work of the support staff.

2. Trains and/or oversees the training of all personnel regarding the appropriate use of specialized lab techniques and processes.

3. Orders all equipment, and supplies as well as keeping up to date equipment service/maintenance contracts.

4. Manages research grants and budgets of the laboratory. Prepares grant reports and participates in aspects of grant proposal and submission.

5. Ensures that all hospital, state, and federal regulations regarding, general laboratory, fire, biohazard, chemical and needle safety are met.

6. Plans research protocols with investigators and research fellows as indicated and reviews all protocols to be carried out in the laboratory. Performs and help develop sophisticated experimental procedures.

7. Collects and reviews experimental data and assists with data analysis and interpretation.

8. Helps write scientific papers especially those sections dealing with methods, materials and results.

9. Performs other duties as requested by the principal investigator(s)
Requirements
QUALIFICATIONS:

BS Required.
Minimum of 5 years of progressively more responsible research work experience. Prior supervisory experience required.

SKILLS/ABILITIES/COMPETENCIES REQUIRED:
1. Must be able to make independent, effective decisions in appropriate situations.
2. Must possess a scientific imagination commensurate with the independent execution of research projects.
3. Must have aptitude for technical problem solving.
4. Ability to effectively supervise others.
5. Excellent organizational skills to ensure smooth functioning of lab.
6. Demonstrated analytical skills and ability to logically sequence experiments to maximize research.
7. Must possess aptitude for budget management.
8. High level of computer literacy.

SUPERVISORY RESPONSIBILITIES:
Responsible for supervising staff including hiring, firing, evaluating and disciplining. Will orient and train new staff members.

WORKING CONDITIONS:
Busy animal laboratory environment.

Shift
Day Shift

To apply online, please submit your resume here:
https://careers.partners.org/psc/EA/EMPLOYEE/HRMS/c/HRS_HRAM.HRS_CE.GBL?Page=HRS_CE_JOB_DTL&Action=A&SiteId=2&HRS_JOB_OPENING_ID=2195579

Brigham and Women�s Hospital is an EEO, AA and VEVRAA employer.
http://www.brighamandwomens.org/careers

TECHNICAL RES ASST I I / 40 HOURS / DAYS - BWH RHEUMATOLOGY, IMMUNOLOG ( Boston- Off Campus )

2009-11-06T17:35:29-05:00
Brigham and Women�s Hospital (BWH) is internationally known as a leader in cutting-edge research and technology and its commitment to patient-centered care. BWH has a rich legacy of excellence and has been consistently recognized as one of America�s best hospitals by US News and World Report.

GENERAL SUMMARY/ OVERVIEW STATEMENT:

Manages the Confocal Core, and oversees its daily operation. Works very independently, with little guidance from the Director, and coordinates all Core-associated research activities including but not limited to: supervising the activities of scientists using the facility, participating in the design and modification of research protocols, and follows up on novel or anomalous results, composes and presents research reports and manuscripts. Troubleshoots software (Nikon C1 plus) and hardware (Microscopy, custom-designed environmental chamber), and assists users of the facility by providing specialized media and culture conditions to allow extended (1-2 day) time-lapse confocal viewing of cells. Provides image analysis services and training in image analysis software, including Metamorph and Image J.

PRINCIPAL DUTIES AND RESPONSIBILITIES:

1. Maintains equipment in good working order, troubleshoots both hardware and software, arranges and oversees repairs and service calls. Interfaces with vendors in the development of new software for custom applications. Tests and evaluates new equipment under consideration for use in the Core. Compares equipment from different vendors and makes recommendations as to which best serves our needs.

2. Designs and maintains website, scheduling calendar, and facilitates communication with users.

3. Trains users to properly use the system, evaluates user expertise, and determines which users are allowed unsupervised access to the equipment.

4. Collaborates with other labs, provides advice and input regarding experimental design and execution. Recommends staining techniques using established biomarkers, identifies and assesses the stage of different subcellular structures.

5. Totals hours and calculates monies owed by different clients on a monthly basis, communicates this information to the business manager for billing and collection. May be asked (by the Director) to suspend user privileges from clients whose accounts remain unpaid for more than 3 months. Assists in monitoring grant budget.

6. Oversees the collection of data and insures the integrity of same.

7. Plans, designs and performs statistical analyses.

8. Implements and provides quality assurance procedures and systems.

9. Provides post-acquisition image processing for publication, to fit the specific needs of different journals. Prepares data and may present data at scientific meetings, in addition to preparing articles for publication.

10. All other duties, as assigned.
Requirements
QUALIFICATIONS:

B.S. degree in Biological Sciences, excellent computer skills, good communication skills and mechanical skills.

SKILLS/ ABILITIES/ COMPETENCIES REQUIRED:

1. High degree of computer literacy, including web design and management (Fireworks, Dreamweaver), image analysis (Image J, Metamorph), scientific illustration (Adobe Photoshop, Illustrator).
2. Sound analytical and organizational skills
3. Good oral and written communication skills
4. Must be able to logically and effectively structure tasks, set priorities, and multitask.
5. Must be able to identify potential and developing problems and to troubleshoot solutions, often through interfacing with off-site experts and technical service providers (e.g. Nikon, Inc).
6. Some microscopy and photomicroscopy skills, including multicolor immunostaining using different fluorescent dyes, and mounting.
7. Experience with mammalian tissue culture, including preparation of specialized media, understanding of the requirements of different cell lines, cloning by limiting dilution, drug-selection of stable cell lines following transfection, and sorting by flow cytometry.
8. Demonstrated ability to analyze data statistically and present it logically,
9. Must have a broad knowledge of scientific principles, biological structures, and general laboratory techniques.
10. Must have sound interpersonal skills and the ability to train, advise, and interface with client scientists.
11. 1-2 years experience

WORKING CONDITIONS:

Lab environment. Some office work.
Shift
Day Shift

To apply online, please submit your resume here:
https://careers.partners.org/psc/EA/EMPLOYEE/HRMS/c/HRS_HRAM.HRS_CE.GBL?Page=HRS_CE_JOB_DTL&Action=A&SiteId=2&HRS_JOB_OPENING_ID=2193656

Brigham and Women�s Hospital is an EEO, AA and VEVRAA employer.
http://www.brighamandwomens.org/careers

RESEARCH SPECIALIST / 40 HOURS / DAYS - BWH INFECTIOUS DISEASE (Boston-On Campus/Longwood Area)

2009-11-06T17:28:16-05:00
Brigham and Women�s Hospital (BWH) is internationally known as a leader in cutting-edge research and technology and its commitment to patient-centered care. BWH has a rich legacy of excellence and has been consistently recognized as one of America�s best hospitals by US News and World Report.

GENERAL SUMMARY/ OVERVIEW STATEMENT:

The Research Specialist will need to function very independently and with general direction/supervision from the Research Manager and Principal Investigator(s). This candidate will provide primary support to the Unit�s conduct of clinical research trials, including systems and processes. Daily activities include maintaining quality assurance procedures, performing statistical analyses, and designing research protocols.

The Research Specialist will routinely work together with the physicians, research assistants, data managers, laboratory personnel, and the research manager. Effective interactions with external representatives (i.e. monitors) of the various program sponsors will also be required. He/she must be able to consistently ensure adherence to hospital/department policies and established clinician procedures/ standard practices.

This may partly be a federally funded grant (research) position.

PRINCIPAL DUTIES AND RESPONSIBILITIES:

1. Researches, develops, designs, executes and interprets clinical research protocols, ensuring adherence to regulatory requirements.
2. Investigates, creates, and develops new methods and technologies for research advancement.
3. Coordinates all (or portion) of research study activities. Function as a resource for all study issues. Identifies problems and develops solutions.
4. Interacts with patients/subjects in regard to studies, including patient education, procedural instruction, and follow-up. May serve as liaison between patient and physician.
5. Implements quality management activities, including data validation, quality control, and facilitation of sponsor monitoring/audit visits.
6. Responsible for training and orienting new staff. May serve as team lead, or as oversight supervisor for smaller projects and tasks.
7. Contributes to scientific literature, reports, journals and presentations.
8. All other duties, as assigned.
Requirements
QUALIFICATIONS:

PhD preferred. MS degree or equivalent education in a scientific field of research.

Five to seven years of direct research experience. Sound independent judgment and competence in research methodologies.

SKILLS/ ABILITIES/ COMPETENCIES REQUIRED:

� Strong research design and analytical skills
� Strong database statistical skills
� In-depth knowledge of field of research
� Excellent time management/organizational skills
� Strong written and verbal presentation skills

WORKING CONDITIONS:

The Research Specialist will conduct research activities in the outpatient/inpatient setting of the Division of Infectious Disease, BWH/DFCI.

New hires to the Division of Infectious Disease will share office space with other clinicians and research assistants, in a typical hospital/clinic environment.

SUPERVISORY RESPONSIBILITY:
Possible oversight of research assistant work.

To apply online, please submit your resume here:
https://careers.partners.org/psc/EA/EMPLOYEE/HRMS/c/HRS_HRAM.HRS_CE.GBL?Page=HRS_CE_JOB_DTL&Action=A&SiteId=2&HRS_JOB_OPENING_ID=2191600

Brigham and Women�s Hospital is an EEO, AA and VEVRAA employer.
http://www.brighamandwomens.org/careers

TECHNICAL RES ASST I I / 40 HOURS / DAYS - BWH NEUROSURGERY (2194744) (Boston-On Campus/Longwood Area)

2009-11-06T17:24:39-05:00
Brigham and Women�s Hospital (BWH) is internationally known as a leader in cutting-edge research and technology and its commitment to patient-centered care. BWH has a rich legacy of excellence and has been consistently recognized as one of America�s best hospitals by US News and World Report.

Responsibilities
GENERAL SUMMARY:
In collaboration with senior member of the research team, assist in projects to elucidate the in vitro and in vivo functions of dysregulated microRNAs in Huntington's disease (HD). Working under very general supervision, execute protocols involving a variety of routine and non-routine experiments at a professional level. Develop modification of existing techniques, as appropriate. Calculate, transcribe, and analyze data using statistical techniques.

PRINCIPAL DUTIES AND RESPONSIBILITIES:
1. Perform routine and non-routine experiments, which are moderate to complex. (Experiments may include RT-PCR, western blot, immunohistochemistry, DNA & RNA isolation, purification and quantification, transformation and transfection.)
2. Mouse husbandry, breeding, tail vein injection, and behavioral observation.
3. Maintain long-term tissue cultures of mammalian cell lines, stem cells and culture of primary neuron. Monitor cell viability, proliferation and cytotoxicity (MTS, LDH assay).
4. Calculate, transcribe and analyze data using advanced statistical techniques.
5. Perform literature searches and help to prepare presentations.
6. Other duties as assigned.
Requirements
QUALIFICATIONS:
BS or Master in biology or related science. Good background in molecular biology, cell biology, and working experience with small animals. 1-2 years of experience at molecular level and in vivo small animal studies in neuroscience/cell biology is a plus. Previous experience with mice tail vein injection is preferred but not necessary.

SKILLS/ABILITIES/COMPETENCIES REQUIRED:
1. Sound analytical and organizational skills.
2. Good oral and written communication skills.
3. Ability to logically and effectively structure tasks and set priorities.
4. Ability to identify potential problems and trouble-shoot solutions.
5. Demonstrated ability to analyze data statistically and to logically present it.

SUPERVISORY RESPONSIBILITIES:
None

WORKING CONDITIONS:
Basic biomedical research lab.
Shift
Day Shift

To apply online, please submit your resume here:
https://careers.partners.org/psc/EA/EMPLOYEE/HRMS/c/HRS_HRAM.HRS_CE.GBL?Page=HRS_CE_JOB_DTL&Action=A&SiteId=2&HRS_JOB_OPENING_ID=2194744

Brigham and Women�s Hospital is an EEO, AA and VEVRAA employer.
http://www.brighamandwomens.org/careers

RESEARCH ASSISTANT II / 40 HOURS / DAYS - BWH ANESTHESIA (2194893) ( Boston-On Campus/Longwood Area )

2009-11-06T17:21:20-05:00
Brigham and Women�s Hospital (BWH) is internationally known as a leader in cutting-edge research and technology and its commitment to patient-centered care. BWH has a rich legacy of excellence and has been consistently recognized as one of America�s best hospitals by US News and World Report.

GENERAL SUMMARY:
Working under the supervision of the Principal Investigator, conducts computerized image processing and a variety of routine laboratory methodologies for a structural biology laboratory.

PRINCIPAL DUTIES AND RESPONSIBILITIES:
1. Will work in a research team focused on the three-dimensional reconstruction of macromolecules using electron microscopy and image processing
2. Under direct training and supervision of the Principal Investigator, performs computerized image processing and optimizes computer scripts
3. Under general supervision, performs a variety of routine laboratory tests following established methodologies. These may include protein assays, electrophoresis, Western blotting, PCR, chromatography, and general molecular biology techniques
4. Executes protocols for research experiments
5. Prepares laboratory reagents and chemicals
6. Discusses progress of work regularly with supervisor
7. Assists the Principal Investigator with preparation for presentation and written published articles
8. All other duties as assigned
Requirements
QUALIFICATIONS:
BA or BS

SKILLS/ABILITIES/COMPETENCES REQUIRED:
1. Computer literacy. Desirable computer skills include knowledge of unix language, shell scripts, Awk and Perl.
2. Attention to detail and reliability.
3. Ability to analyze data methodically.
4. Capacity and willingness to learn new techniques.
5. Good analytical and organizational skills.
6. Good oral and written communication skills.

SUPERVISORY RESPONSIBILITIES:
None

WORKING CONDITION:
Normal laboratory environment. Work is performed in a research laboratory on-site at the Brigham and Women's Hospital and at a computer facility at Harvard Medical School
Shift
Day Shift

To apply online, please submit your resume here:
https://careers.partners.org/psc/EA/EMPLOYEE/HRMS/c/HRS_HRAM.HRS_CE.GBL?Page=HRS_CE_JOB_DTL&Action=A&SiteId=2&HRS_JOB_OPENING_ID=2194893
BWH is an Equal Opportunity Employer. Qualified Applicants are considered for positions without regard to race, color, religion, sex, national origin, age, marital status, sexual orientation, status as a disabled veteran or a Vietnam Era veteran or the presence of a disability where otherwise qualified.

Science instructors wanted... teach and tutor the MCAT! $21-24/hr! (BU, BC, Tufts, Harvard, Northeastern)

2009-11-06T16:29:46-05:00
The Princeton Review is seeking energetic men and women who have backgrounds in the humanities or hard sciences to teach our Medical College Admissions Test (or MCAT) prep courses in and around Greater Boston!

Trainings are coming up in the forthcoming weeks for the following test types:

MCAT Physics training dates: Fri, January 15th (eve. only), January 16th-17th (full days) (possible December training dates TBD)
MCAT General Chemistry training dates: Fri, January 15th (eve. only), January 16th-17th (full days) (possible December training dates TBD)
MCAT Organic Chemistry training dates: Fri, January 15th (eve. only), January 16th-17th (full days)
MCAT Biology training dates: Fri, January 15th (eve. only), January 16th-17th (full days) (possible December training dates TBD)

The Princeton Review is the dominant global force in test prep. We have recently revamped our compensation policies to provide teachers with more support than ever before, including but not limited to higher starting wages and raise opportunities, paid training and preparation time, excellent travel reimbursement policies, part-time medical, dental, and life insurance, and a competent full-time staff, many of whom are teachers themselves. We pride ourselves on the superior quality of our product - and that product begins and ends with YOU! Here's how to get involved:

1. Register. Let us know you�re interested by filling out our online application or by emailing ChrisJ@review.com directly. You may also call us at 617-558-2828 to speak with a local representative.

2. Audition. We will invite you to one of several local group teaching auditions, where we will quiz you on relevant material and ask you and other prospective instructors to present on a topic of your choosing for 5 minutes at a time. Auditions will be run several times per month in multiple locations, such as Newton, Boston, Worcester, Concord (NH) and Providence (RI). At this group interview, you will have the opportunity to learn about the job itself and ask questions pertinent to your role in the company.

3. Train. Once approved by your audition leader, you may train for any subject in which you have a background or proclivity. Our most immediate trainings are filling up fast! We are always accepting applications for other subject types as well, including GMAT, GRE, LSAT, and SAT.Trainings are often held out of our Newton, MA office, so appropriate transportation is required; we can often host out-of-state residents at local hotels.

4. Start teaching! A new SAT teacher will generally teach one or two nights per week, or about 4-10 hours. (Those who want more work, however, usually get it!). Classes are run in and around the Boston area, with particular attention paid to major suburbs and the North and South Shores.

If you�re eager to start right away, please contact Chris Jacobs at 617-558-2828 or ChrisJ@review.com with your resume and test results; if you've chosen to use our online recruiting system, the information will come automatically. Start the process now and you can be teaching in just a short time! Best of luck!!

Telephone Interviewer (Part-time, Flexible Hours) (Watertown, MA)

2009-11-06T15:21:19-05:00
New England Research Institutes, Inc. (NERI) is a dynamic, independent company specializing in clinical trials management, public health research, survey research and media development. (NERI) offers clients exceptional capabilities as a first rate Contract Research Organization together with the deep knowledge and broad experience of one of the nation's premier public health research institutes.
We are currently looking for a male Telephone Interviewer for a project concerning men�s health, including sexual health. In that position, the Telephone Interviewer will conduct and audio-record in-depth, telephone interviews with a racially and ethnically diverse population of pre-screened male respondents. The Interviewer should be comfortable discussing sensitive health issues with respondents. As this position requires interviews with a culturally and racially diverse population, minorities are encouraged to apply. Hours are flexible and will average about 15 hours per week, and may change from week to week. This is a project-specific position lasting from January 15th through April 30th.
Qualifications:

B.A./B.S. degree and 3 years of directly relevant experience or M.A. degree in a related discipline preferred (e.g. Sociology, Anthropology, Public Health, Community Studies);

Previous experience conducing research interviews is desirable;

Ability to comfortably discuss sensitive issues with respondents;

Excellent interpersonal skills and good listening skills;

Ability to adhere to specific study protocols and procedures;

Ability to debrief with supervisor regarding information from interviews conducted;

Fluency in English and Spanish is ideal but not required;

Ability to use open-ended, non-biased qualitative interviewing techniques;

Knowledge of and familiarity with qualitative research methods;

Ability to work independently;

Curiosity about people and their lives;

Morning and/or afternoon work is required.
If interested, please send your resume and cover letter to Human Resources at humanresources@neriscience.com or visit us at www.neriscience.com

NERI is an Equal Opportunity/Affirmative Action Employer M/F/D/V

Medical Technologist and Manufacturing Technician (Billerica, MA)

2009-11-06T12:45:23-05:00
2 Positions

Position Title: Medical Technologist
Location: Billerica, MA
Education Required: Bachelors Degree in Science

Job Responsibilities:
Following testing protocols, run routine laboratory tests of samples
Perform data reduction and data summaries
Follow and document SOPs
Maintenance of laboratory instruments
Housekeeping of laboratory
Manufacturing of intermediate reagents for laboratory testing
Maintenance of retained samples

Job Requirements:
Bachelor�s degree in Science
At least one year of clinical laboratory experience is required
Academic or industrial laboratory experience required
Laboratory techniques such as ELISA, electrophoresis are desirable
Basic knowledge of science (immunology, biology and chemistry)and basic skills of mathematics
Team oriented interpersonal skills
Proficient in the use of Microsoft Excel and Word
Strong organizational skills
Excellent time management
Detail Oriented

2nd position
Position Title: Manufacturing Technician
Location: Billerica, MA

Position Description:
Working in a biotech manufacturing environment, you will work with a team of other technicians in this setting.
Job Responsibilities:

Routine manufacturing reagents
Documentation
Maintenance and running of manufacturing equipments
Kit assembly
Position Requirements:

Certificate or Associate degree in the biotechnology area
At least 5 years of biotech manufacturing experience
GMP environmental experience a plus
Interpersonal communication skill (oral and written)
Should be able handle multiple task simultaneously
Strong organizational ability and independent
Detail oriented
Must be able to lift up to 30 lbs
This position is eligible for overtime.

Send resumes to dmacneil@staffusmart.com

Biochemistry Research Associate

2009-11-06T11:52:22-05:00
Our client is in need of a Biochemistry Research Associate to help with the development of a diagnostic for a specific human parasitic infection. The position requires a MS in biochemistry, immunology or related field, with a minimum of three years bench experience developing biochemical assays, as well as experience with general serology and infectious disease experience.

Responsibilities will include purification and characterization of biological compounds, analyses of cellular biochemistry and development of non-immunological enzyme assays. Successful candidates will have demonstrated ability to troubleshoot scientific protocols and be able to take the initiative to independently analyze biochemical data and problem solve. The ideal candidate would have prior experience with blood components, manual microtiter plate assays, working knowledge of protein chemistry, enzymology and microbiology, and have familiarity with biochemical purification techniques and assays.

You will appreciate the ethics guiding each StratAcuity team member. We build lasting relationships with exceptional scientists and take great care to protect your personal information. Upon receiving your inquiry, you may be directly contacted by a StratAcuity team member to discuss your career goals. We will not share your information with anyone without your direct prior consent.

StratAcuity Scientific, CHEMISTRY IS EVERYTHING.

Postdoctoral Fellow/Research Associate (BIDMC, Harvard Medical School)

2009-11-06T10:41:44-05:00
A Postdoctoral Fellow/Research Associate position in stroke research is available at the Center for Vascular Biology Research, Beth Israel Deaconess Medical Center, to study the regulation of blood brain barrier after ischemia-reperfusion injury in the brain. The candidate must have experience in mouse surgery and especially in the middle cerebral artery occlusion technique. Our research team studies the signaling pathways involved in the regulation of vascular permeability, angiogenesis and vascular inflammation in many pathophysiological settings. We routinely use molecular and cellular biology approaches, as well as several mouse models of vascular disease. The candidate will join a dynamic research team and will have the opportunity to do both basic and translational research in the stroke field.

Applicants must have recently obtained a PhD in Neuroscience/Cardiovascular Research and have publications in stroke research. Individuals who are interested in this position please send 1) your Curriculum Vitae and 2) the names of 2-3 references to Dr. Teresa Sanchez at tsanchez@bidmc.harvard.edu.

Biotech Research Administrative Assistant (Cambridge)

2009-11-05T16:46:20-05:00
We are a growing medical company located in the Boston area and have an open position within our office. We are looking for someone who can interpret scientific information and provide administrative support to the busy research team. This is an administrative position with the opportunity to take on additional duties as the position develops.

Duties include:
Administrative support to the team
Event planning
Database management
Maintaining calendars and scheduling in Outlook
Coordinating travel and meetings

Requirements:
4-year degree is preferable
Hard-working, not afraid to put in extra time to get the job done

We offer competitive salary and benefits. To apply, please forward a copy of your resume to the address above in MS Word.

Assistant Research Professor (Waltham)

2009-11-05T15:56:51-05:00
The Department of Chemistry at Brandeis University invites applications for an assistant research professor to manage the Brandeis University mass spectrometry facility (BUMS). Candidates must have a doctoral degree; postdoctoral training is sought. Applicants with hands-on instrumentation experience, high technical proficiency, and with a publication record in proteomics, MALDI MS imaging, or Fourier Transform mass spectrometry are especially encouraged to apply. The successful applicant will oversee sample analysis of diverse biological samples, and will have many opportunities for instrumentation and methods development and publications. The facility is equipped with four nano-HPLCs, two MALDI-TOF mass spectrometers, sample handling and fraction collecting robots, an ion-trap mass spectrometer, and a MALDI-ESI-9.4T Fourier transform mass spectrometer. To apply, send a curriculum vitae, a statement of research interests, and have three letters of reference sent to: Dr. Jeffrey N. Agar, Department of Chemistry � MS 015, Brandeis University, 415 South Street, Waltham, MA 02453 or email to Jeffrey Agar, agar@brandeis.edu. First consideration will be given to applications received by November 20, 2009. Brandeis University is an equal opportunity employer, committed to building a culturally diverse intellectual community, and strongly encourages applications from women and minority candidates.

Evening and Weekend Bilingual Field/Telephone Interviewer (Watertown, MA)

2009-11-05T15:48:20-05:00
New England Research Institutes, Inc. (NERI) is a dynamic, independent company specializing in clinical trials management, public health research, survey research and media development. (NERI) offers clients exceptional capabilities as a first rate Contract Research Organization together with the deep knowledge and broad experience of one of the nation's premier public health research institutes.
We are currently looking for a full time Bilingual Field/Telephone Interviewer. In that position, the Field/Telephone Interviewer will:

Administer the informed consent and conduct one on one field research interviews with a diverse group of respondents;

Collect physiological data from respondents (blood pressure, height/weight and hip/waist
measurements);

Follow data collection procedures and project specific protocols with respondents;

Enlist respondent participation in follow-up study by telephone;

Use project tracking techniques to help find �lost� respondents;

Complete all necessary paperwork in a thorough and timely manner following specified procedures and protocols for all editing and paperwork;

Attend project meetings and debriefing sessions, while communicating daily with supervisory staff at NERI.
Qualifications:

Must be bilingual (English/Spanish);

Must be willing to travel and conduct interviews throughout the city of Boston and up to a 90 mile radius of Watertown. Business travel mileage will be reimbursed

Bachelor's degree in a related field and two years of related experience; or high school diploma and 4 years� related experience and/or training;

Ability to conduct non-biased interviews and experience with telephone work;

Ability to interview difficult respondents and have strong interpersonal skills;

Evening and/or weekend work is required.

A valid Driver�s License, Car and Valid Auto Insurance are required.

Ease and familiarity with computers is required, experience with database software is required
If interested, please send your resume and cover letter to Human Resources at humanresources@neriscience.com or visit us at www.neriscience.com
NERI is an Equal Opportunity/Affirmative Action Employer M/F/D/V

Intern - Scientific Support (Do you know anti-bodies?) (Cambridge, MA - Kendall Sq)

2009-11-05T15:13:33-05:00

Abcam is a rapidly growing business, specializing in the production and sale of antibodies and related products. We are a web-based business, with offices in Cambridge, UK, Cambridge, USA, Tokyo, Japan and Hong Kong, China.

This would be a great opportunity for a student to learn about antibodies and their use in research. The student will learn while gaining experience by speaking to scientists of varied backgrounds, and contribute to the team by working on projects.

Duties:

Reporting & Planning

Complete a long-term research project over the span of the internship
Become familiar with BLAST searches, SwissProt, ExPASy, and other protein databases
Develop a basic understanding of antibodies and their use in research
Help with Antibody Training for office
Participate in weekly Scientific Support (Sci Sup) meetings to discuss policies, receive updates from others on the team, and give input on departmental decisions
Meet with each member of the Sci Sup team to learn about their education/employment experiences, what led them to choosing a non-bench position in science, and how they chose Abcam for their career
Cross train with Business Development and Marketing (time permitting)

Operational

Speak with other scientists by taking Customer Service (CS) Level 2 calls, first with a member of the CS team then independently
Learn how to troubleshoot experimental problems by answering customer questions and complaints, first with a member of the Sci Sup team then independently
Publish Abreviews, first with a member of the Sci Sup team then independently

Summary of Job Requirements

Essential - Currently enrolled in a degree program toward a BS in a life sciences field. Student must be in either Junior or Senior Year
Desired � A minimum of 2 classes in a laboratory course within area of concentration or research lab experience
Problem solving skills
Extensive experience and comfort using computers, working knowledge of Excel, Powerpoint, and Outlook

Our culture is one that empowers individuals, with responsibility given at an early stage. We place great emphasis on knowledge and experience. The working environment is fun but intense, with everybody working together as a team to deliver great service and the best products to our customers.

To apply please go to www.abcam.com/careers too upload your resume and cover letter.

Research Assistant I (Harvard Medical School, Boston)

2009-11-05T14:53:23-05:00

77 Avenue Louis Pasteur, NRB 1050

Duties And Responsibilities: Under specific direction, the Research Assistant will perform or participate in gene expression analysis in Human Leukocytes within the Immunological Genome Project. Principal duties include the fluorescent staining and purification of cells by flow cytometry, RNA extraction and purification, measurement of specific gene expression (qPCR, or other technologies). Liaise with the microarray core facility for sample flow and tracking. Coordinate with project immunologists in the definition of Standard Operating Protocols. Participate in data entry and management within study databases, and in the computational analysis of data generated in the project, in relation with project specialists or immunologists. Assist in the management of lab stocks, ordering of reagents and general lab maintenance. This is a grant funded position through September 30, 2011.

Basic Qualifications: College background or equivalent work experience, and familiarity with standard computer usage. At least one year related work experience (relevant coursework may count towards experience).

Additional Qualifications: Additional Qualifications: A foundation in immunology and in particular flow cytometry; familiarity with molecular biology techniques; experience in gene expression analysis or in bioinformatics; demonstrated abilities in basic laboratory techniques helpful; good communication, organizational, and interpersonal skills; ability to take specific direction and work independently as appropriate, within specific guidelines.
Click HERE to Apply!

Quality Assurance Auditor (Norwood)

2009-11-05T14:40:25-05:00
� Knowledge of cGMP/GLP Regulatory Requirements.
� Review of documentation for conformance to established procedures and regulatory guidelines.
� Conduct daily auditing, inspecting and reporting on quality functions.
� Perform QA functions in support of cGMP manufacturing as necessary.
� Ensure that work conforms to appropriate regulatory requirements, including SOP�s, US FDA and US EPA Good Laboratory Practices (GLP) and US FDA current Good Manufacturing Practices (cGMP).

Candidates must live local to the Norwood MA area and be a US Citizen or Permanent Resident Green Card Holder

Email resume as a word attachement to: jobs@cwsciences.com

Commonwealth Sciences, Inc.
http://www.cwsciences.com

Senior CMC Chemist / Manager (Norwood)

2009-11-05T14:36:27-05:00
� Responsible for overall supervision of CMC Chemistry department, and direct supervision of CMC Chemists to include training, career development and performing employee reviews.
� Responsible for overall project leadership of studies.
� Accurately record and document raw data, observations and pharmacy usage.
� Ensure that work conforms to appropriate regulatory requirements, including applicable SOP�s, ICH Guidelines, US FDA and US EPA Good Laboratory Practices (GLP) and US FDA and EMEA current Good Manufacturing Practices (cGMP).

Candidates must live local to the Norwood MA area and be a US Citizen or Permanent Residen Green Card Holder

Email resume to: jobs@cwsciences.com

Commonwealth Sciences, Inc.
http://www.cwsciences.com

Senior Scientist In Vitro Pharmacology 0900719 (Rockland, MA)

2009-11-05T13:31:26-05:00
At EMD Serono, Inc. our strength is our people!
About the Company
EMD Serono, Inc., an affiliate of Merck KGaA, Darmstadt, Germany, is a leader in the US biopharmaceutical arena, integrating cutting-edge science with unparalleled patient support systems to improve people's lives. The company has strong market positions in neurodegenerative diseases, MS and endocrinology. EMD Serono is also a leader in fertility treatments. With a clear focus on the patient and a leadership presence in the biopharmaceutical industry, EMD Serono's US footprint continues to grow, with more than 1000 employees around the country and fully integrated commercial, clinical and research operations in the company's home state of Massachusetts.
Description
The candidate will support NCE and NBE Discovery efforts by conducting in vitro experiments using biochemical and cell-based techniques. The individual will support the primary and secondary screening of small molecules and protein therapeutics including developing and supporting screening assays to advance compounds to lead status. The candidate will follow the direction of their supervisor in the In Vitro Pharmacology Group in conducting experiments with the primary goal of identifying small molecule and biological drug candidates.
Key Tasks & Responsibilities:
Develop and validate biochemical and cellular assays for the screening of small molecule and protein drug candidates, including but not limited to binding and enzymatic assays, ELISA, reporter and cellular functional assays.
Develop and validate biophysical assays for the characterization of novel drug candidates.
Screen synthetic compounds in validated biochemical, biophysical and cellular assays.
Express experimental data in tables and graphs.
Analyze and interpret data to derive the necessary information.
Organize data from experiments into spreadsheets for posting in corporate databases.
Document work and write concise reports.
Give oral presentations, to communicate experimental results.
Education:
MS with 2+ years of experience or BS with 5+ years experience in Biochemistry, or Cell Biology.
A working knowledge of molecular pharmacology is an advantage.
Professional Skills & Experience:
Experience in biochemistry and/or cell biology is required.
Experience in developing in vitro biochemical assays in support of drug discovery is required.
Experience in Biacore and other biophysical methods is highly preferred.
A working knowledge of GPCRs, kinases and pharmacology is preferred.
The candidate must be able to work independently and provide data according to established timelines.
The candidate will be highly organized and self-motivated.
Experience with data analysis software.
Experience with databases and data entry.
Experience with MS packages including Word, Excel, and PowerPoint.
Personal Skills & Competencies:
The detail-oriented candidate must be able to work independently and as a team member in the Discovery environment.
Excellent written, oral and collaborative skills are essential to effectively communicate scientific information to team members.
Click the link below and open the door to the future by submitting your resume today!
EMD Serono 0900719

Awards & Recognition
June 2009, The Boston Business Journal recognizes EMD Serono as one of the Best Places to Work!
May 2009, The Scientist magazine names EMD Serono one of the best place to work in the life sciences industries!
October 2008, EMD Serono Named as a Top Employer by Science Magazine!
more

Group Leader- Antibody Engineering-0900481 (Rockland, MA)

2009-11-05T13:21:46-05:00
At EMD Serono, Inc. our strength is our people!
About the Company
EMD Serono, Inc., an affiliate of Merck KGaA, Darmstadt, Germany, is a leader in the US biopharmaceutical arena, integrating cutting-edge science with unparalleled patient support systems to improve people's lives. The company has strong market positions in neurodegenerative diseases, MS and endocrinology. EMD Serono is also a leader in fertility treatments. With a clear focus on the patient and a leadership presence in the biopharmaceutical industry, EMD Serono's US footprint continues to grow, with more than 1000 employees around the country and fully integrated commercial, clinical and research operations in the company's home state of Massachusetts.
Description
EMD Serono is seeking to appoint a motivated and well qualified scientist for the Protein Engineering and Monoclonal Antibody Technologies (PEAT) group within New Biological Entities (NBE) Technologies. He/she will be responsible for the Monoclonal Antibody Engineering needs of the group and head up a laboratory staff of three with a potential to grow.
This individual will report to the Head of PEAT at their facility in suburban Boston and will be part of an energetic team in a key strategic area of the Discovery organization within EMD Serono. In this regard, he/she will play an important role in the overall responsibility of NBE Technologies for the discovery, optimization and progression of the Company's biotherapeutics discovery pipeline.
As Scientist - Antibody Engineering the incumbent will have responsibilities including, but not limited to, the following:
Leading a group of scientist and technicians in the Monoclonal Antibody Engineering laboratory
Assuming responsibility for the humanization and optimization of antibody candidates generated by hybridoma- or phage display-technology.
Managing the group and taking responsibility for its projects by driving and coordinating his/her direct reports in achieving the specific objectives of the respective research projects.
Advancing antibody technologies within his/her own group as well as influencing the strategies on current and future technologies.
Representing the monoclonal antibody department in specific antibody project teams.
Taking responsibility for defining requirements for research projects and identifying potential constraints and risks.
Use of problem solving skills in evaluating issues, and monitoring and initiating corrective actions where necessary.
Taking responsibility for proposing new projects or amendments to existing projects to the Head of PEAT in the US.
Qualifications
The ideal candidate will have a Ph.D. in molecular biology, biochemistry, biotechnology or biological sciences.
This individual will be a highly motivated scientist with a proven track record in antibody engineering and must have several years of post-doctoral experience in an academic or industry setting.
A strong background in molecular biology, with extensive experience in antibody engineering, antibody expression and purification, and biochemical and biophysical methods for the analysis of antibodies is required. An interest to work part-time at the laboratory bench is desirable.
Familiarity with antibody phage display technology and affinity maturation, and interpretation of computational modelling of antibody-antigen interactions would be useful. Further, experience in preclinical development of therapeutic antibodies is desirable.
It is desired that the candidate demonstrate an aptitude to interact constructively with others across multiple cultural backgrounds in a dynamic matrix structure. He/she must have the ability to collaborate with colleagues throughout the organization in research functions i.e., bio-informatics, protein and cell sciences and structural biology and in corporate functions i.e., business development, intellectual property.
Further to this the candidate will possess strong communication skills, both oral and written. He/she should be confident in presentation with parties both small and large.
As leader of a group, the candidate must be committed to its members and foster a teamwork approach. This will partially be accomplished through the facilitation of a positive work environment. He/she should be skilled in motivating and coaching others as well as interacting well in a team.
The candidate will be, above all, a proactive self-starter with a positive "can do" attitude. He/she will have demonstrated success in achieving goals, be strongly results oriented and have the ability to drive tasks through to completion.
The incumbent will be required to focus on multiple issues at one time, and must have the ability to organise and direct diverse activities in a changing environment, often under time pressure.
With a mature, self-confident and well-balanced personality, it is essential that the candidate also possess a high standard of ethical and intellectual integrity.
Finally, the candidate must be strongly computer literate.
Click the link below and open the door to the future by submitting your resume today!
EMD Serono 0900481

EMD Serono, Inc. Named as a Top Employer by Science Magazine
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Senior Scientist, Cell Pharmacology-0900237 (Rockland, MA)

2009-11-05T13:19:10-05:00
At EMD Serono, Inc. our strength is our people!
About the Company
EMD Serono, Inc., an affiliate of Merck KGaA, Darmstadt, Germany, is a leader in the US biopharmaceutical arena, integrating cutting-edge science with unparalleled patient support systems to improve people's lives. The company has strong market positions in neurodegenerative diseases, MS and endocrinology. EMD Serono is also a leader in fertility treatments. With a clear focus on the patient and a leadership presence in the biopharmaceutical industry, EMD Serono's US footprint continues to grow, with more than 1000 employees around the country and fully integrated commercial, clinical and research operations in the company's home state of Massachusetts.
Description
This position will be responsible for the cell culture, plating and automated profiling of compounds and proteins in support of our drug discovery programs.
Key Tasks & Responsibilities
Maintenance of tumor cell lines in support of Hit-to-Lead and HTS projects.
Development of cellular assays for measuring proliferation, survival, cell cycle and apoptosis.
Perform primary and Log Dose Response testing of small molecule and biotherapeutics in tumor cell assays.
Perform FACS-based analysis for mechanistic studies and cell surface binding studies.
Fluorescent based high content analysis for cell assay support
Education/Languages
BS/MS in biological sciences, with 3-5 years of industry experience.
Must be fluent in both written and spoken English.
Professional Skills & Experience
Extensive experience handling multiple types of cancer cell lines as well as primary cells.
Solid background in the development and running of cell-based assays for HTS, Hit-to-Lead support & mechanism of action studies.
Knowledge of FACS-based technologies for mechanistic studies, preferred.
Experience fluorescence based high content analysis is a plus.
Experience in using automated equipment would be beneficial.
Strong written and oral communication skills.
Ability to work in team oriented environment.
Highly motivated with good organizational skills.
Click the link below and open the door to the future by submitting your resume today!
EMD Serono 0900237

Awards & Recognition
June 2009, The Boston Business Journal recognizes EMD Serono as one of the Best Places to Work!
May 2009, The Scientist magazine names EMD Serono one of the best place to work in the life sciences industries!
October 2008, EMD Serono Named as a Top Employer by Science Magazine!
more

Senior Statistical Programmer-0901356 (Rockland, MA)

2009-11-05T13:14:23-05:00
At EMD Serono, Inc. our strength is our people!
About the Company
EMD Serono, Inc., an affiliate of Merck KGaA, Darmstadt, Germany, is a leader in the US biopharmaceutical arena, integrating cutting-edge science with unparalleled patient support systems to improve people's lives. The company has strong market positions in neurodegenerative diseases, MS and endocrinology. EMD Serono is also a leader in fertility treatments. With a clear focus on the patient and a leadership presence in the biopharmaceutical industry, EMD Serono's US footprint continues to grow, with more than 1000 employees around the country and fully integrated commercial, clinical and research operations in the company's home state of Massachusetts.
Description
Independently program (or write validation programs for) and document tables/listings/graphs for clinical trials or portions of clinical trials requiring routine data manipulation and analysis.
Routine data manipulation and analysis with limited direction.
Program (or write validation programs for) and document tables/listings/graphs for clinical trials requiring complex data manipulation and analysis.
Provide input into general standardization efforts and create (or validate) global macros that streamline repetitive operations.
Mentor biostatisticians and statistical programmer/analysts with advance SAS programming techniques.
Interface with SAS technical support to resolve software problems.
Coordinate, validate and implement SAS upgrades and licenses.
Independently provide input into CRF specifications to collect data specified in the protocol and query with SAS technical support to resolve software problems, coordinate, validate and implement SAS upgrades and licenses.
Independently provide input into CRF specifications to collect data specified in the protocol and query check specifications and provide input into analysis plan specifications and data presentations for clinical trials requiring complex data manipulation and analysis.
Independently program (or write validation programs for) patient randomizations.
Independently create (or validate) non-standard complex derived datasets.
Create project and study phase sub-directories ensuring that all project work resides in the correct project and study phase sub-directories.
Validate study phase flags in oracle tables and download study phase records from oracle tables to create analysis datasets.
Audit changes to the database between study phases.
Understand and follow all statistical and statistical programming SOP�s as well as any other relevant SOP.
Lead process improvement teams as required.
Effectively communicate analysis specification and programming/data issues that arise prior to or during analysis in a timely manner.
Professional Skills & Experience
MS, BS (or equivalent).
6 years pharmaceutical/biotech or other relevant experience.
Fundamental knowledge of relevant statistical areas.
Fundamental knowledge of relevant clinical areas.
Advanced knowledge of SAS/Bas, SAS/STAT; knowledge of SAS/Connect, SAS/Macro, SQL.
Excellent communication skills
Ability to independently solve complex problems logically.
Click the link below and open the door to the future by submitting your resume today!
EMD Serono 0901356

Awards & Recognition
June 2009, The Boston Business Journal recognizes EMD Serono as one of the Best Places to Work!
May 2009, The Scientist magazine names EMD Serono one of the best place to work in the life sciences industries!
October 2008, EMD Serono Named as a Top Employer by Science Magazine!
more

Principal Biostatistician-0901059 (Rockland, MA)

2009-11-05T12:39:36-05:00
At EMD Serono, Inc. our strength is our people!
About the Company
EMD Serono, Inc., an affiliate of Merck KGaA, Darmstadt, Germany, is a leader in the US biopharmaceutical arena, integrating cutting-edge science with unparalleled patient support systems to improve people's lives. The company has strong market positions in neurodegenerative diseases, MS and endocrinology. EMD Serono is also a leader in fertility treatments. With a clear focus on the patient and a leadership presence in the biopharmaceutical industry, EMD Serono's US footprint continues to grow, with more than 1000 employees around the country and fully integrated commercial, clinical and research operations in the company's home state of Massachusetts.
Description
Function as a project biostatistician coordinating statistical aspects across clinical trials within a specific project in a therapeutic area
With limited direction, provide statistical input for statistically complex protocol development
With limited direction, write statistical analysis plans and perform statistical analyses for statistically complex clinical trials
With limited direction, write statistical analysis plans and perform statistical analyses for safety and efficacy summaries for regulatory submissions
Independently provide statistical input for statistically routine protocol development
Independently write statistical analysis plans and perform statistical analyses for statistically routine clinical trials
Participate in departmental standardization efforts
Provide support towards statistical research
Key Tasks & Responsibilities
Participate on clinical development teams
Provide statistical input into clinical development plans
With limited direction, participate in the development of statistical standards for clinical development programs
Review statistical analysis plans written by other statisticians on the project
Review statistical analysis results produced by other statisticians on the project
Review statistical methods sections and the interpretation of results written by other statisticians on the project
Provide statistical support for manuscripts and review manuscripts for accurate statistical interpretation
Functional Roles and Responsibilities:
With limited direction, provide statistical input for protocol/CRF development (e.g., trial design; sample size estimation for the most efficient and practical design; patient randomization; accurate, logical, clear, concise and thorough evaluation of results section; effective CRF specifications to collect data specified the protocol)
With limited direction, write statistical analysis plans for clinical trials as well as for integrated safety and efficacy summaries. Analysis plans written include the most appropriate statistical methodology and data presentations.
With limited direction, analyze clinical trials
With limited direction, write accurate, logical, clear, concise, thorough and objective statistical methods sections for clinical trial reports
Review and co-author clinical trial reports ensuring the accuracy of the statistical interpretation
Understand and follow all Global Biostatistics WIs/SOP as well as any other relevant WIs/SOPs. Provide input into all newly developed departmental quality documents
Provide input into general standardization efforts (e.g., CRFs, query checks, statistical methodology, standard statistical programs, data presentations)
With direction, interact with regulatory agencies regarding statistical issues
With direction, develop responses to regulatory agency requests that maintain perspective and are within the appropriate context
Participate effectively on clinical trial teams
With direction, provide solutions for complex issues presenting alternatives and identifying the best solution
With limited direction, communicate routine and complex statistical concepts and results to non-statistical internal and external colleagues in a clear, concise, focused and articulate manner
With limited direction, function as the statistical primary contact with CROs for studies that are outsourced, and ensure the accuracy and timeliness of the CROs analysis alerting management to any unforeseen circumstances
Produce assigned work within the timelines provided ensuring deadlines are met
Education/Languages
Ph.D. or MS in statistics, biostatistics or related discipline
Fluent in English (French or German is a plus)
Professional Skills & Experience
Several years experience in the Pharmaceutical/Biotechnology industry
Working SAS knowledge and proficient in SAS/Stat
Knowledge of ICH Statistical and Clinical Report Guidelines
Familiarization with relevant therapeutic areas
Personal Skills & Competencies
Ability to work in a matrix organization
Ability to work with multi-disciplinary groups
Strong communication, negotiation and issue resolution skills
Balance concurrent tasks and responsibilities
Click the link below and open the door to the future by submitting your resume today!
EMD Serono 0901059

Awards & Recognition
June 2009, The Boston Business Journal recognizes EMD Serono as one of the Best Places to Work!
May 2009, The Scientist magazine names EMD Serono one of the best place to work in the life sciences industries!
October 2008, EMD Serono Named as a Top Employer by Science Magazine!
more

Research Bioengineer

2009-11-05T12:01:04-05:00
SRI International is a world-leading independent research and technology development organization with almost $300 million in annual revenues. SRI performs multidisciplinary, client-sponsored research and development for government agencies, commercial businesses, and private foundations. To help bring its innovations to market, SRI licenses its technologies, fosters strategic partnerships, and creates new companies. Together, SRI and its subsidiary Sarnoff Corporation have spun off about two dozen companies to date.

Innovations from SRI touch our lives every day. Achievements include the invention of the computer mouse, an important role in the birth of the Internet, and automated check processing for banking. Drugs discovered and developed by SRI are improving and saving lives around the world. The institute's education research is helping improve teaching and learning. SRI has met mission-critical national defense needs for decades, from the Cold War to today's war against terrorism.

SRI, a nonprofit corporation, was founded in 1946 as the Stanford Research Institute, and became independent from Stanford University in 1970.

For additional information, please visit us at http://www.sri.com

Chemistry, physics, materials science, mechanics, optics, and nanotechnology - these are areas underlying many new applications and market opportunities. SRI International's Physical Sciences Division (www.sri.com/psd) offers government and commercial clients worldwide the diverse technical expertise needed to address important technical challenges in these and many other fields. Our work ranges from fundamental research and laboratory experiments to computer simulations, pilot-scale testing, systems development and commercialization of products.

For additional information, please visit the Physical Sciences Division website: http://www.sri.com/psd

We have an immediate opening for a Research Bioengineer to work with a multidisciplinary team developing biosensors using novel DNA microarrays. Will be responsible for performing molecular biology experiments using bacteria, yeasts, viruses and fungi. Experience with cell separation, cellular sub component extraction (proteins, mRNA, and DNA), purification of cellular products, and PCR amplification required. Will apply laboratory experience to the development of fieldable sensor systems that are capable of real-time end-to-end processing and detection. Will also work with laboratory managers developing new sensor systems concepts for a variety of DoD applications. Should be proficient in various biosensor technologies.

Requirements:
--BS/MS in Molecular Biology or Bioengineering with six years of hands-on molecular biology experience using a broad range of laboratory techniques.
--Must have a current Top Secret or Q security clearance, or have had an active TS or Q clearance within the last 24 months.
--Proficient in using molecular biology analytical equipment and military biosensor systems.
--Proficient with computers.

A post-offer, pre-laboratory physical examination will be required.

How to apply:
Apply via our web page www.sri.com/jobs to job number 100282
SRI is an equal opportunity employer.
www.sri.com/jobs

Research Analyst -Industry Exposure Database (Boston, MA)

2009-11-04T16:29:34-05:00

Ensure that the IED effectively supports the benchmarking processes that will be used to assess the quality of exposure data in clients' portfolios
Ensure that there is appropriate consistency between aggregate exposure databases and property-specific databases
Develop and enhance databases containing the locations and characteristics of residential, commercial, and industrial properties in different regions of the world
Collect and analyze data pertaining to building characteristics such as size and construction material
Develop economic models for calculating and validating property replacement costs
Use GIS tools to process and analyze spatial data and create presentation-quality maps
Write technical documentation for internal use and distribution to clients
Create and deliver presentations of analysis methods and results to coworkers and senior management
Collaborate with other staff members in dynamic teams to realize project deadlines

Ability to gather, understand, and critically analyze demographic, economic, and/or property-related data and statistics
Familiarity with handling raw data and manipulating large data sets; SQL experience a big plus
Programming experience in a high-level language such as C++ or Fortran a plus
Demonstrated self-directed ability to learn new concepts and skills
Excellent verbal and written communication skills
Experience in economic modeling, risk modeling, and/or GIS a plus
BS degree in a quantitative field such as economics, demographics, statistics, or engineering. MS preferred
If interested, please apply online at http://track.tmpservice.com/ApplyClick.aspx?id=836236-1857-5739

Research Analyst -Industry Exposure Database (Boston, MA)

2009-11-04T16:19:03-05:00

Ensure that the IED effectively supports the benchmarking processes that will be used to assess the quality of exposure data in clients' portfolios
Ensure that there is appropriate consistency between aggregate exposure databases and property-specific databases
Develop and enhance databases containing the locations and characteristics of residential, commercial, and industrial properties in different regions of the world
Collect and analyze data pertaining to building characteristics such as size and construction material
Develop economic models for calculating and validating property replacement costs
Use GIS tools to process and analyze spatial data and create presentation-quality maps
Write technical documentation for internal use and distribution to clients
Create and deliver presentations of analysis methods and results to coworkers and senior management
Collaborate with other staff members in dynamic teams to realize project deadlines

Ability to gather, understand, and critically analyze demographic, economic, and/or property-related data and statistics
Familiarity with handling raw data and manipulating large data sets; SQL experience a big plus
Programming experience in a high-level language such as C++ or Fortran a plus
Demonstrated self-directed ability to learn new concepts and skills
Excellent verbal and written communication skills
Experience in economic modeling, risk modeling, and/or GIS a plus
BS degree in a quantitative field such as economics, demographics, statistics, or engineering. MS preferred
If interested, please apply online at http://track.tmpservice.com/ApplyClick.aspx?id=836869-1857-8439

Manager of Clinical Operations

2009-11-04T15:26:25-05:00
Our client, an exciting Biotech Company located in the Cambridge Massachusetts area, is in need of an experienced Manager of Clinical Operations to join their team. If you have ten years of industry experience in project management/clinical operations with strong leadership skills, as well as experience developing/ensuring compliance with SOPs and guidelines, FDA regulations and current ICH GCP guidelines, this could be the perfect opportunity for you!

In this position you will be primarily responsible for all functional activities related to execution of Clinical Trials. You will oversee the implementation of the clinical development plan by managing the timeline, resources and budget of clinical activities. You will oversee CRO and investigator sites, write clinical operation sections of regulatory documents and develop study feasibility/cost estimates for outsourced work. You will develop and ensure compliance with SOPs and guidelines, FDA regulations and current ICH GCP guidelines. You will play a key role in managing trial costs by interfacing with the finance group to provide financial information related to clinical development, as well as interfacing with the legal department to develop improvements to document templates, standard processes and tools.

This position requires a minimum of a BS degree in a life science discipline with a minimum of ten years directly relevant industry experience.

You will appreciate the ethics guiding each StratAcuity team member. We build lasting relationships with exceptional scientists and take great care to protect your personal information. Upon receiving your inquiry, you may be directly contacted by a StratAcuity team member to discuss your career goals. We will not share your information with anyone without your direct prior consent.

StratAcuity Scientific, CHEMISTRY IS EVERYTHING.

Research Associate, Molecular Biology, RT-PCR (Boston Area)

2009-11-04T14:25:50-05:00
Research Associate, Molecular Biology, RT-PCR

You will be responsible for supporting Molecular Diagnostic assay development, and Research & Development activities. This is a key position leading the successful development of innovative Molecular Diagnostic products utilizing RT-PCR and Capillary Electrophoresis quantitative detection methods. Your scientific activities will involve:

* Contributing to research and development of molecular diagnostic projects including the execution of clinical study plans, regulatory filings, and interfacing with production, manufacturing, & marketing departments.
* Performing assay development and quantitiative methods for the detection of nucleic acids utilizing PCR, RT-PCR (Real-Time PCR), Capillary Electrophoresis, and nucleic acid chemistry.
* Leading verification studies and validation for the development of molecular diagnostic products.
* Contributing to FDA regulatory filings and 510(k) submissions for CE marked products.
* Maintaining, troubleshooting and optimizing laboratory production equipment.

Preferred Candidate Background and Expertise:

* BS degree in Biology, Chemistry, Engineering, Mechanical Engineering, Electrical Engineering, Industrial Engineering or related Scientific/Engineering field.
* 1-3 years of industry experience involving Molecular Biology related R&D.
* Hands-on scientific expertise performing PCR, RT-PCR, Cloning, Sequencing, nucleic acid extraction, Capillary Electrophoresis, oligo synthesis, nucleic acid chemistry, or enzyme chemistry.
* Expertise working within ISO, CE Marked, & FDA compliance and providing required documentation.

PLEASE APPLY HERE - http://bit.ly/1b8Cu0

Senior Manager, Chemistry & Reagents (Cambridge, MA)

2009-11-04T13:57:30-05:00
T2 Biosystems, Inc. is an exciting early stage company whose mission is to revolutionize diagnostic medicine by providing immediate, accurate testing for nearly any health condition, in nearly any setting. We are seeking a talented and highly motivated individual to be part of our Diagnostics Research and Development team as the Senior Manager, Chemistry. The successful candidate will play a key role in our cutting-edge reagents and chemistry group.

The successful candidate will be highly motivated, results driven, exceptionally talented, analytical, and a team player. They will also have attention to detail and a commitment to and track record of high quality work. In addition, they will also have:

� 10+ years of experience in the medical in vitro diagnostics assay industry
� experience in immunoassay reagents development and manufacturing (including antibodies, diluents, particles, critical reagents, etc) under FDA quality system requirements
� experience with reagents stability, process control, and reproducibility
� experience in a supervisory or leadership capacity
� experience with agglutination or particle based assays strongly desired

Responsibilities will include:

� Managing our internal and external teams of chemists
� Overseeing sourcing, syntheses, characterization, and transfer to manufacturing of all critical reagents including nanoparticles, antibodies, and antigens.
� Working closely with our assay development teams in reagent selection, design, and optimization.
� Supervising process control and quality control measures for reagent production and supply
� Implementing reagent stability studies and critical parameter analyses
� Participating in hands-on chemistry and bench work

If this sounds like you, please send your r�sum� and cover letter to careers@t2biosystems.com, and please identify the job title in the subject line.

T2 Biosystems is an equal opportunity employer. We do not discriminate on the basis of race, color, religion, gender, pregnancy, national origin, age, military service eligibility, veteran status, sexual orientation, marital status, disability, or any other protected class.

Senior Research Associate, Diagnostics Research and Development (Cambridge, MA)

2009-11-04T13:51:58-05:00
T2 Biosystems, Inc. is an exciting early stage company whose mission is to revolutionize diagnostic medicine by providing immediate, accurate testing for nearly any health condition, in nearly any setting. We are seeking a talented and highly motivated Research Associate to be part of our Assay Development Group. Responsibilities include performing, optimizing, and developing a variety of quantitative diagnostic bioassays.

If you have experience in the in vitro diagnostics industry setting, this could be a very exciting position for you.

You will have:
 a Bachelor�s degree in Biology, Clinical Lab Science, Chemistry, Biochemistry, or Bioengineering;
 5+ years of experience working in assay development in IVD industry setting;
 experience with ELISA and immunoassay development;
 excellent oral and written communication skills; and
 demonstrated productivity in a laboratory setting.
In addition,
 You must have excellent laboratory, data analysis and organizational, record keeping and communication skills.
 Prior experience in a fast-paced environment.
 A strong work ethic to generate high quality data under tight deadlines, collaborative and proactive attitude a must.
This is a fast-paced startup environment, and you will be working on multiple, simultaneous projects, so your abilities to manage time, interact with a variety of people, and adjust to changes will be important.

To apply, please send your r�sum� and cover letter to careers@t2biosystems.com, and write the job title in the subject line.

T2 Biosystems is an equal opportunity employer. We do not discriminate on the basis of race, color, religion, gender, pregnancy, national origin, age, military service eligibility, veteran status, sexual orientation, marital status, disability, or any other protected class.

Research Associate, Diagnostics Research and Development (Cambridge, MA)

2009-11-04T13:48:44-05:00
T2 Biosystems, Inc. is an exciting early stage company whose mission is to revolutionize diagnostic medicine by providing immediate, accurate testing for nearly any health condition, in nearly any setting. We are seeking a talented and highly motivated Research Associate to be part of our Assay Development Group. Responsibilities include performing, optimizing, and developing a variety of quantitative diagnostic bioassays.

If you have experience in the in vitro diagnostics industry setting, this could be a very exciting position for you.

You will have:
 a Bachelor�s degree in Biology, Chemistry, Biochemistry, or Bioengineering;
 experience working in a laboratory setting;
 excellent oral and written communication skills;
 superior analytical skills; and
 demonstrated productivity in a laboratory setting.
In addition,
 You must have excellent laboratory, data analysis and organizational, record keeping and communication skills.
 Prior experience in a fast-paced environment and experience with nucleic acid assay development.
 A strong work ethic to generate high quality data under tight deadlines, collaborative and proactive attitude a must.
This is a fast-paced startup environment, and you will be working on multiple, simultaneous projects, so your abilities to manage time, interact with a variety of people, and adjust to changes will be important.

To apply, please send your r�sum� and cover letter to careers@t2biosystems.com, and write the job title in the subject line.

T2 Biosystems is an equal opportunity employer. We do not discriminate on the basis of race, color, religion, gender, pregnancy, national origin, age, military service eligibility, veteran status, sexual orientation, marital status, disability, or any other protected class.

Project Coordinator (Burlington, MA)

2009-11-04T10:33:48-05:00
Project Coordinator� Job # 28047

Position Description
Duties will include the following:
� Support ACM/LCP programs nation-wide
� Prepare and update template proposals and reports
� As needed, prepare draft proposals and reports for ACM/LBP sampling and abatement projects
� Book projects into PTS
� Follow up with clients for missing Pos
� Payment of invoices
� Preparation of final abatement reports
� Assist coordination of ACM/LCP abatement projects (which involve significant subcontractor communication and coordination)
� Draft subcontractor agreements
� Engage and schedule subcontractor
� Review subcontractor licenses and qualifications
� Prepare abatement permits
� Research vendors for competitive pricing in new markets and for new service types; assist project coordinators with staffing decisions � based on personnel licensing needs requirements of jobs
� Research state licensing and regulatory requirements for new markets and services
� Obtain Construction Documents and other support documents from clients
� Respond to client manager and other staff requests for Asbestos and Lead project documention.

Education Requirements
Four year college degree + 1-2 years experience in related environmental/industrial hygiene field.

Specify Registration Requirements
Asbestos EPA Inspector Certification, MA asbestos inspector license a plus

Company Overview
EBI Consulting is a rapidly growing, profitable company, headquartered in Burlington, MA. Our employees are the key to maintaining our competitive edge. To attract and retain the best industry talent EBI shares its success with its employees, and is committed to providing a professional work environment where career learning, growth and recognition are highly valued. If you are seeking an opportunity to work in a progressive organization that will offer you diversified challenges and an excellent opportunity for advancement please review our current employment opportunities. For more information about EBI and open positions please visit our website at www.ebiconsulting.com.

Benefits
EBI offers competitive compensation, bonus opportunities, group medical & dental insurance, 401k plan with employer contribution, tuition reimbursement, paid vacation, and progressive career opportunities.
EOE M/W/D/V

Submittal
Please submit a resume and cover letter in Word or PDF format via email to jobs@ebiconsulting.com. You must include the following information:

1. Reference job #, job title and resource
2. Brief summary of past related experience (highlight your experience as it relates to our need & industry);
3. List of your education credentials and professional registrations
4. Salary history

We look forward to hearing from you!

Medical Director, Reproductive Health Medical Affairs-0901272 (Rockland, MA)

2009-11-03T21:35:33-05:00
At EMD Serono, Inc. our strength is our people!
About the Company
EMD Serono, Inc., an affiliate of Merck KGaA, Darmstadt, Germany, is a leader in the US biopharmaceutical arena, integrating cutting-edge science with unparalleled patient support systems to improve people's lives. The company has strong market positions in neurodegenerative diseases, MS and endocrinology. EMD Serono is also a leader in fertility treatments. With a clear focus on the patient and a leadership presence in the biopharmaceutical industry, EMD Serono's US footprint continues to grow, with more than 1000 employees around the country and fully integrated commercial, clinical and research operations in the company's home state of Massachusetts.
Description
As a leader in fertility health, EMD Serono, Inc. is dedicated to providing patient-friendly, innovative products that are used to treat infertility, a common condition that affects approximately 7.3 million people in the US.
EMD Serono, Inc. is the only company to offer recombinant version of three hormones used in the treatment of infertility. These include Gonal-f (follitropin alfa for injection), Ovidrel� Prefilled Syringe (choriogonadotropin alfa injection) and Luveris (lutropin alfa for injection). Rounding out EMD Serono, Inc.'s portfolio of fertility treatments is Cetrotide (cetrorelix acetate for injection) used to control certain hormonal surges.
The Medical Director, US Medical Affairs, in this position will assist in development, conducts and directs the activities of the assigned Reproductive Health Therapeutic Area in the US Medical Affairs Department. The US Medical Affairs group is responsible for Phase IV and Investigator Initiated Clinical Research also called Independent Medical Grants (IMG). The director will serve as a medical expert to the Reproductive Health/Fertility medical community and internally relating to products developed or marketed by EMD Serono, Inc. and advises management on relevant medical issues. The position will have direct and functional reporting responsibilities to the Senior Vice President / Senior Director of US Medical Affairs.
The Medical Director, Reproductive Health is responsible for providing professional medical and clinical services and support for clinical trials with a concentration on provision of medical monitoring and safety management for a project within a specific therapeutic area. The individual will also be integrally involved in business development activities, feasibility assessments, scientific training, design of clinical development programs and study protocols, and management of medical information.
Responsibilities
Direct / oversee the design and implementation of phase IIIb, IV Medical program for approved products. Ensure that the overall scientific and medical content of all Medical programs is sound. Work to secure cross-functional alignment and / or transparent discussion of risks associated with clear plans to further investigate and track through Medical development.
Responsible for the direction, execution of the Independent Medical Grants.
Provides therapeutic and protocol-specific scientific training to the project teams.
Maintains a working knowledge of projects in his/her functional area for which Research is responsible for medical and/or safety monitoring.
Stays abreast of clinical and drug development information relevant to contracted programs by review of literature, attendance at medical/scientific meetings, and personal interchanges with consultants and investigators.
Provide Strategic Planning, Scientific and Medical Oversight in support of the Commercial Strategies for compounds within the Fertility Therapeutic Area.
Collaborates with sponsors and/or internal departments on the design and review of study-related documents and professional manuscripts.
Interacts with other functional units, Clinical Development, regulatory, Medical Operation, Safety, Medical Information, Sales and Marketing, Sales training and Managed Market, to ensure the highest level of stakeholders' satisfaction through successful execution and completion of projects.
Lead Medical representative on the internal Promotional and Educational review committees.
Maintains a high level of expertise with all projects and Key Opinion Leaders developments through reliable participation in internal meetings, including project tracking, and attendance at professional seminars and educational programs.
Provides protocol-related clinical and scientific training to project team staff members.
Participates in medical/scientific education internally and externally through scheduled lectures and seminars on subjects relevant to company projects and on areas of individual interest and expertise.
Participate in the process of peer review, and generation of abstracts, articles, work-shops, books, chapters etc.
The Medical Director must have experience in clinical drug development as a pharmaceutical physician or academician, knowledge of GCPs and regulatory requirements, and relevant management experience. Experience gained working in the CRO industry and/or experience functioning as a Medical Monitor would be of significant added value. Post-graduate training in a clinical specialty relevant to the specific therapeutic area is preferred.
Qualifications
M.D. or M.D. with a Ph.D. with post-graduate training and experience in OB/GYN with focus on Women's Health / Reproductive Health and in Vitro Fertilization, and training in its subspecialty areas, Clinical or research experience in field of specialization is highly desirable.
Hard working, driven to achieve creative and sound results.
Minimum of 3 years of experience in pharmaceutical-related clinical research and patient care/investigational site experience.
Demonstrable experience in writing or editing reports of scientific research, both for regulatory submission and for scientific publication.
Ability to work in a fast-paced, team-oriented environment.
Experience working with personnel who have varied technical and educational backgrounds.
Experience in cultivating novel business contacts and projects.
Incumbent must have excellent spoken and written communication skills in English as well as interpersonal skills.
EMD Serono 0901272

Awards & Recognition
June 2009, The Boston Business Journal recognizes EMD Serono as one of the Best Places to Work!
May 2009, The Scientist magazine names EMD Serono one of the best place to work in the life sciences industries!
October 2008, EMD Serono Named as a Top Employer by Science Magazine!
more

Medical Director Neurology 0901068 (Rockland, MA)

2009-11-03T21:07:10-05:00
At EMD Serono, Inc. our strength is our people!
About the Company
EMD Serono, Inc., an affiliate of Merck KGaA, Darmstadt, Germany, is a leader in the US biopharmaceutical arena, integrating cutting-edge science with unparalleled patient support systems to improve people's lives. The company has strong market positions in neurodegenerative diseases, MS and endocrinology. EMD Serono is also a leader in fertility treatments. With a clear focus on the patient and a leadership presence in the biopharmaceutical industry, EMD Serono's US footprint continues to grow, with more than 1000 employees around the country and fully integrated commercial, clinical and research operations in the company's home state of Massachusetts.
Description
The Field Medical Director is responsible for leadership and management of the Field Medical Associate Director team. They are responsible for developing and maintaining a close relationship with Medical Affairs and producing materials that Field Medical Associate Directors and MSLs can use to communicate the benefits of our products and to explain safety related issues. They will also oversee the implementation of a plan to conduct training activities to internal and external parties (e.g. sales, medical science liaisons, healthcare providers, managed care, etc.). They must be well versed in the advanced science and medicine of the specific disease process, treatment data and safety concerns and share this knowledge appropriately in the conduct of their function relative to EMD Serono's products.
Clinical opinion leaders should perceive the physician in this position as a peer in their area of specialization
This position requires approximately 75% travel to regional or national areas in need of medical support
Specific Responsibilities include:
Participate in leading the direction, planning, execution and interpretation of the medical coverage for the specified therapeutic area. Must be able to discuss and support the ongoing safety issues and support all training activities.
Represent EMD Serono, Inc. at specific educational events, programs, medical meetings, conventions and congresses, managed care presentations and Advisory Boards.
Identify areas for research collaboration with institutions and unsolicited research proposals for studies that would add new information on EMD Serono's science and medicine.
Actively involved in the training of Internal Sales, MSL's, Marketing and Customer Service employees.
Education Professional Skills & Experience
M.D. or D.O. Degree required. Fellowship or residency training and clinical experience in specific therapeutic area is preferred. Previous experience in supporting and/or partnering with Sales, Research and Development, Regulatory and Pharmacovigilence is within the Biopharmaceutical industry is preferred.
Previous experience in analyzing, writing and publishing medical literature is preferred as well as experience in conducting formal presentations to healthcare providers.
Excellent scientific presentation and public speaking skills are essential as are outstanding management skills.
Click the link below and open the door to the future by submitting your resume today!
EMD Serono 0901068

Awards & Recognition
June 2009, The Boston Business Journal recognizes EMD Serono as one of the Best Places to Work!
May 2009, The Scientist magazine names EMD Serono one of the best place to work in the life sciences industries!
October 2008, EMD Serono Named as a Top Employer by Science Magazine!
more

RESEARCH TECHNOLOGIST

2009-11-03T16:35:51-05:00
Position: Research Technologist, Autism Genomics / Molecular Genetics
Job Description: The Neurogenetics Unit in the Massachusetts General Hospital Center for Human Genetic Research (CHGR) invites applications for a full-time Research Technologist position to support studies examining the genomics of autism and related neurodevelopmental disorders in the lab of Dr. James Gusella, Director of the CHGR. A highly motivated individual is needed to support the development of molecular genetics assays, including next-generation sequencing, to investigate the genomics of autism spectrum disorders. The candidate will work directly with investigators in training and optimization of cutting edge genetic techniques. Candidates will be expected to independently implement assays, maintain accurate records, conduct basic quantitative analysis, and perform routine day to day laboratory operations. This position is ideal for candidates interested in the medical application of basic research, and is a unique opportunity to interact in a highly collaborative and dynamic environment with strong career development potential.

Qualifications: Minimum of a Bachelor�s degree in Genetics, Molecular Biology, Biochemistry or related field required, Master�s degree preferred. Candidate should have at least two years of laboratory research experience, preferably in the context of an independent project. Outstanding new graduates may also be considered. Familiarity with the operation of standard lab equipment and experience with basic molecular genetics techniques required. Prior experience conducting DNA and RNA based assays, including genotyping, sequencing, RT-PCR, and microarray are preferred. Candidate will need excellent communication skills and the ability to interact professionally with all levels of staff and faculty. Excellent critical thinking skills and ability to work independently are essential. Flexible hours may be available.

How to Apply:

Please apply online at www.mghcareers.org and search using Job ID 2195628

BIOINFORMATICS SPECIALIST I

2009-11-03T16:33:45-05:00
Position: Bioinformatics Specialist, Autism Genomics / Molecular Genetics
Job Description: The Neurogenetics Unit in the Massachusetts General Hospital Center for Human Genetic Research (CHGR) invites applications for a full-time Bioinformatics / Computational Genetics position to support studies examining the genomics of autism and related neurodevelopmental disorders in the lab of Dr. James Gusella, Director of the CHGR. A highly motivated individual is needed to support efforts in the analysis of whole genome sequencing and genotyping data. The candidate will conduct multi-disciplinary collaborative research of the most recent high throughput genomics data available in the field. The candidate will interact directly with investigators in the CHGR, Harvard Medical School, and the Broad Institute to develop an analysis pipeline for ongoing data collection. The candidate will be responsible for independently conducting high quality analysis of various datasets. This position is ideal for candidates interested in the interface between computational science and medicine, offering a unique opportunity to interact with leaders in both fields in a dynamic environment with strong career development potential.

Qualifications: Outstanding candidates will have a minimum of a Bachelor�s degree in Bioinformatics, Computational Biology, or a related field. Master�s degree preferred. A strong background in programming and statistics is required. Previous experience in genome assembly, multiple-sequence alignment, and / or next-generation sequencing analysis is preferred. Outstanding new graduates may also be considered. Candidate will need good communication skills and the ability to interact professionally with all levels of staff and faculty. Excellent critical thinking skills and ability to work independently are essential. Flexible hours may be available.

How to Apply:

Please apply online at www.mghcareers.org and search using Job ID # 2195623

RESEARCH TECHNICIAN I

2009-11-03T16:28:52-05:00
Tissue culture core at the Center for Human Genetic Research at MGH seeks a laboratory research technician to work with senior technicians performing tissue culture work.

Cell culturing which include lymphoblast transformation, establishing and growing fibroblast cells, culturing tumor samples, DNA extraction from blood and cultured cells, organization and storage of samples, experiments with mice.

Highly motivated with strong organizational and time management skills; experience with basic laboratory skills.

Previous experience with cell culturing and animal handling is preferred.
B.S. B.S., Biology or related field.

How to Apply:

Please apply online at www.mghcareers.org and search using Job ID # 2194829

Hiring Senior Caregivers & CNAs

2009-11-03T16:08:01-05:00
Senior Home Care Agency Positions: Part-time, Full-time, Live-in
Flexible Schedules: Ongoing Assignments

Fill out ONE Online Job Application (Just 10 Quick Multiple Choice ?s) and be considered for Caregiver openings in the Boston area (new clients arrive daily).

Part-Time, Full-Time and Overnight Positions are currently available for self-motivated, trustworthy individuals with either professional or personal experience in providing care for Seniors.

Companion Caregivers, Certified Nursing Aides, Home Health Aides, LPN's Are encouraged to apply

For some cases, no previous Caregiving experience is required as long as you're professional, caring, and compassionate with the ability to work independently.

Must also confidently
perform these essential job functions:
Provide Companionship and Help Enhance Quality of Life . Assist with Meals . Keep Medications on Track . Prevent Falls . Assist with Walking and Light Exercise . Supervise Household Maintenance . Run Errands . Maintain a Positive Attitude and Great Communication Skills . Nursing Aide assignments may require assisting with bathing, toileting and feeding

Compensation: Rates vary per position - all pay rates are competitive
Employee Benefits Packages (packages vary per position: health, vision, dental, performance and referral bonuses)
Background and Reference Checks Required

Scientist/Analytical Chemist (Cambridge)

2009-11-03T15:33:54-05:00
Reporting to the Senior Director of the Analytical Technology Group, this position is responsible for performing existing and developing new analytical test methods using a wide variety of analytical tools to solve materials issues in the development and manufacture of E Ink�s paper-like electrophoretic display technology. This individual will be a member of a team responsible for evaluating, maintaining and implementing new instruments and test methods to satisfy the needs of the research, manufacturing, product development, and external partners thus ensuring the ensuring the quality, performance, and reliability of E Ink products.

Job Responsibilities:
Collaborate with colloid scientists, ink formulators and engineers to develop test methods for the characterization of the components in E Ink�s displays;
Develop test methods that can be transferred to the quality team;
Run Gage R&R on test methods and trouble shoot issues;
Plan, schedule and execute experiments;
Analyze, present and document the results.

Skill Requirements:
B.S., or M.S. in Chemistry with 1 � 3 years of experience;
Demonstrated experimental skills to work at the lab bench;
Technical expertise in Spectroscopy and Chromatography is preferred;
Demonstrated knowledge of these methods is desirable: GPC, GC, GC-MS, FTIR/NIR/UV/Vis, TGA, DSC, DMA, rheology, wet chemistry, particle size analysis, microscopy;
Must have excellent communication skills, a strong sense of urgency and a performance metrics-driven style;
Must have sound analytical skills, attention to details and strong problem solving skills.

E Ink offers a competitive salary, outstanding benefits package and the professional advantages of joining a successful, High Profile Company. We are an equal opportunity employer.

About E Ink Corporation
Founded in 1997 based on research started at the MIT Media Lab, E Ink Corporation is the leading supplier of electronic paper display (EPD) technologies. Products made with E Ink�s revolutionary electronic ink possess a paper-like high contrast appearance, ultra-low power consumption and a thin, light form. E Ink�s technology is ideal for many consumer and industrial applications spanning handheld devices, watches, clocks and public information and promotional signs. Future technology developments will enable many new applications through ultra-tin, lightweight, rugged, flexible, full color displays. For more information about
E Ink, please visit our web site at www.eink.com.

To apply please send your resume to jobs@eink.com

Customer service associate (PT) (Wilmington)

2009-11-03T14:54:55-05:00
We are a medical device manufacturing company who is a world leader in its market. Every day you will be contributing to a technology geared toward providing direct clinical benefit to patients. We are looking to add a part time customer service person to our team who will:

1) Help customers place orders
2) Answer product questions
3) Track orders
4) Handle customer returns

We would like this person to have:

1) Excellent phone presence
2) 1 or more years of related experience
3) HS diploma; BS is a plus

This positions interacts on a regular basis with customers, the sales force and operations management. It is a part time position and the expected hours will be m-f from 12-4PM.

Lab Automation Engineer - In Vitro Drug Discovery for Pharma Co (Boston, MA 02115)

2009-11-03T12:37:35-05:00
Pharma Co Seeking Automation Engineer for Drug Discovery Lab
1 year temporary position!

RESPONSIBILITIES:

This individual will support In Vivo Sciences drug discovery efforts through the development, validation and implementation of preclinical and early-clinical biomarker assays. The successful candidate will participate in the implementation of assays on automated liquid handling equipment and the development and execution of maintenance and QC protocols. The candidate will also participate in the development of standardized processes for laboratory operations, from sample collection and inventory, to data formatting and reporting.

QUALIFICATIONS:
Significant hands-on experience in the programming, operation, and maintenance of automated laboratory equipment, including liquid handlers, microplate readers, barcoding systems, and various microplate-based washing and dispensing systems.
Experience with Biomek FX/NX platforms and ARTEL MVS.
Experience using Visual Basic programming to control Biomek automation.
Experience with scripting to reformat and load large datasets into standard templates and databases highly desired.
Experience using statistical design principles to develop and troubleshoot processes also highly desired.
A B.S or M.S in a relevant field with at least 3 years research experience.

Program Manager, Medical Affairs-0900969 (Rockland, MA)

2009-11-03T12:24:52-05:00
At EMD Serono, Inc. our strength is our people!
About the Company
EMD Serono, Inc., an affiliate of Merck KGaA, Darmstadt, Germany, is a leader in the US biopharmaceutical arena, integrating cutting-edge science with unparalleled patient support systems to improve people's lives. The company has strong market positions in neurodegenerative diseases, MS and endocrinology. EMD Serono is also a leader in fertility treatments. With a clear focus on the patient and a leadership presence in the biopharmaceutical industry, EMD Serono's US footprint continues to grow, with more than 1000 employees around the country and fully integrated commercial, clinical and research operations in the company's home state of Massachusetts.
PURPOSE OF THE ROLE
Through direction from the Senior Director, Medical Affairs Strategy and Scientific Communications, the Program Manager is responsible for working within the US Medical Affairs function to develop, coordinate, maintain, report and ensure the successful completion (milestones) of deliverables within US Medical Affairs in terms of time, cost and process. The successful Program Manager will manage timelines, establish metrics and develop processes to increase visibility, improve decision making and enhance cycle times for the US Medical Affairs team. The Program Manager will also provide financial updates, reports and develop presentations allowing the US Medical Affairs team to provide accurate tracking and forecasting of activities/finances. Specific activities within US Medical Affairs include clinical trials, scientific communications, medical meetings, management presentations and internal medical support.
KEY TASKS & RESPONSIBILITIES
Create project management charts, reports and milestones (i.e. Gantt charts) for all US Medical Affairs activities (new and existing)
Maintain and develop financial reports including monthly forecasts, annual budgets, long range plans, consolidating actuals and variance reporting
Create operational reports to facilitate decision making and identify accomplishments, areas of focus, process improvements, priorities and issue resolution
Communicate frequently with the senior managers within US Medical Affairs including therapeutic area MDs to ensure team is provided information needed to keep projects on track
Develop cost estimates, proposal timelines, and ensure resources are available to execute new projects
Track project progress and resource utilization
Schedule and lead project meetings both internally and externally
Provide meeting minutes to meeting participants as needed
Provide monthly reports to senior management on project status
Participate in meetings
Interact with the management team to propose and develop new processes to improve the program management role and US Medical Affairs function

EDUCATION/LANGUAGES
3-5 years of progressive project management experience
Excellent oral and written skills in English
Must have demonstrated expertise in all aspects of project management
Must have prior experience either with another Biotech/Pharmaceutical company
Possess the ability to anticipate problems/conflicts and provide resolution through creative problem solving
Possess the ability to function well in a multiple project fast paced environment
Must be able to interact with clients and internal management team

PERSONAL SKILLS & COMPETENCIES
Solid communicator
Strong organization and prioritization skills
Advanced presentation and powerpoint skills
Energetic and willingness to learn and advance skills
Critical problem solver and creative thinker
Ability to communicate effectively with Senior Management
Excellent time management and multi-tasking skills
Flexible and mature with the ability to work under timelines and pressure
Excellent negotiation skills
Excellent written and verbal skills
Detail-oriented
Team leadership skills
Highly self-motivated and reliable
Proactive and able to work independently
Willing and able to travel
Competency in Microsoft Excel, PowerPoint and Word

Click the link below and open the door to the future by submitting your resume today!
EMD Serono 0900969

Awards & Recognition
June 2009, The Boston Business Journal recognizes EMD Serono as one of the Best Places to Work!
May 2009, The Scientist magazine names EMD Serono one of the best place to work in the life sciences industries!
October 2008, EMD Serono Named as a Top Employer by Science Magazine!
more

Environmental Engineer (Cambridge)

2009-11-03T10:34:08-05:00
Environmental Engineer sought by Gradient Corporation, environmental and risk science consulting firm, to apply knowledge of environmental regulations and remediation technologies to improve clients' understanding of fate and transport of chemicals; water treatment; bioremediation; solid waste risk assessment and pollution prevention; and contaminated soil/sediment remediation. Requires a Master's degree or equivalent in Environmental Engineering, Engineering Science or a closely related field and advanced study, research or experience in Environmental Engineering including designing, managing and conducting research and development projects on fate and transport, remedial investigations, metal speciation, water treatment technologies for a wide range of contaminants including metals, PAHs and PCBs. If qualified, send resume to Laura Hanson, HR Manager, Gradient Corporation, 20 University Road, Cambridge, MA 02138 or lhanson@gradientcorp.com

Postdoctoral Research Scientist - Molecular Biology and Proteomics (Beverly, MA)

2009-11-02T15:41:35-05:00
Postdoctoral Research Scientist - Molecular Biology and Proteomics

Differential Proteomics, Inc. (DPx) is a startup biotechnology company engaged in discovering and developing innovative proteomics technologies. DPx is currently seeking a talented scientist to join its dynamic and enthusiastic team for a 2-year postdoctoral position (salary $40-50K), funded by an SBIR grant from the NIH and available immediately.

Extensive laboratory experience in general molecular biology and protein chemistry is required. Candidates should also have skills and experience in protein modification and immobilization, affinity purification, and configuration of affinity reagent binding assays (e.g. ELISA). Specifically, the work will involve novel approaches to the use of phage display libraries of peptides and antibodies to derive collections of affinity reagents to complex protein samples (e.g. plasma). The ideal candidate will possess a working knowledge of mass spectrometry and associated data analysis, and a strong interest in the current state-of-the-art and challenges in proteomics technologies and bioinformatics.

This is an exceptional opportunity to work on exciting new approaches to proteomics at Differential Proteomics Inc., located in Beverly, Massachusetts. The position is particularly suitable for a self-motivated postdoctoral scientist, who will use his or her initiative to champion the project and successfully move it forward.

Interested candidates are invited to send their CV, together with a cover letter of introduction, to info@differentialproteomics.com.

TECHNICAL RES ASST I I / 40 HOURS / DAYS - BWH CHANNING LAB (2195595)_ (Boston, MA )

2009-11-02T14:50:46-05:00
Brigham and Women�s Hospital (BWH) is internationally known as a leader in cutting-edge research and technology and its commitment to patient-centered care. BWH has a rich legacy of excellence and has been consistently recognized as one of America�s best hospitals by US News and World Report.

GENERAL SUMMARY/ OVERVIEW STATEMENT:
The Respiratory Functional Genetics Laboratory focuses on biological functional evaluation of genetic variants associated with asthma and chronic obstructive pulmonary disease (COPD). The TRAII will be an active participant in experimental research and will have the opportunity to present his/her lab work. He/she will work independently, and perform non-routine, highly specialized molecular biology experiments. Also participate in the modification of research protocols.

PRINCIPAL DUTIES AND RESPONSIBILITIES:
1) Independently performs molecular biology and cell biology procedures including but not limited to DNA and cDNA cloning, cell transfection, cell culture and reporter assay.

2) Responsible for the coordination of individual projects, including quality assurance, tracking laboratory supplies and scheduling to meet deadlines.

3) Independently performs experiments and analyzes results.

4) Prepares reagents, solutions and buffers for use in procedures.

5) Under supervision of Respiratory Functional Genetics Laboratory Director, establishes new and modifies existing research techniques.

7) All other duties as assigned

QUALIFICATIONS:
1) BS or BA required; MS degree preferred in Biological Science.
2) Minimum 1 year of relevant lab work experience.
3) Experience with molecular cloning, PCR, mini and maxi preparation plasmid, cell culture, transfection, western blot and immunofluorescence.
4) Experience with nuclear protein extraction, reporter assay and RNAi delivery is plus.
5) Experience with mouse models would be desirable.

SKILLS/ ABILITIES/ COMPETENCIES REQUIRED:

1) Ability to attend to detail and to be precise. Sound analytical and organizational skills.

2) Excellent written and verbal communication skills; must be able to thoroughly document experiments, protocols, and data. Must be able to logically structure tasks and set priorities.

3) Knowledge of cell biology and/or molecular biology typically obtained through a bachelors degree program in biology, molecular genetics, biochemistry, or laboratory science. Broad knowledge of scientific principles and laboratory techniques. Ability to identify potential problems, communicate and troubleshoot them effectively.

4) Must be able to operate and maintain delicate electronic equipment and safely use and dispose of toxic chemicals and biohazardous materials.

WORKING CONDITIONS:
Variety of laboratory/office settings. Exposure to toxic chemicals and biohazardous materials. Work may require odd hours to complete experiments.

To apply online, please submit your resume here:
https://careers.partners.org/psc/EA/EMPLOYEE/HRMS/c/HRS_HRAM.HRS_CE.GBL?Page=HRS_CE_JOB_DTL&Action=A&SiteId=2&HRS_JOB_OPENING_ID=2195595

Brigham and Women�s Hospital is an EEO, AA and VEVRAA employer.
http://www.brighamandwomens.org/careers

TECHNICAL RES ASST I I / 40 HOURS / DAYS - BWH NEUROLOGY (2194294) (Boston, MA )

2009-11-02T14:43:52-05:00
Brigham and Women�s Hospital (BWH) is internationally known as a leader in cutting-edge research and technology and its commitment to patient-centered care. BWH has a rich legacy of excellence and has been consistently recognized as one of America�s best hospitals by US News and World Report.

GENERAL SUMMARY/ OVERVIEW STATEMENT:
Under general supervision of the principle investigator, and according to established hospital departmental policies and procedures and/or specific instructions, performs routine laboratory experiments. Records test results and maintains equipment in working order. Should be able to work independently after initial training period.

PRINCIPAL DUTIES AND RESPONSIBILITIES:
1. Will maintain a large variety of genetic mutant mice, including breeding and genotyping

2. Maintains tracking of Mouse Colony

3. Arranges Mouse transfers between institutions (shipping etc)

4. Maintains basic records of methodologies and test results in a log of work performed.

5. Identifies unusual findings and reports such findings to supervisor.

6. Maintains equipment and supplies in a neat orderly manner.

7. Maintains established department policies, procedures, objectives, quality assurance, safety, environmental and infection control.

8. Performs other duties and responsibilities as directed.
Requirements
QUALIFICATIONS:
1. Should have previous experience (1-2 years) of working in a research lab. However, this requirement could be waived if the candidate possesses other qualifications.

2. Familiarity with basic laboratory instruments, equipment and scientific procedures, usually acquired through coursework.

SKILLS/ ABILITIES/ COMPETENCIES REQUIRED:
1. Must have a sound understanding of laboratory practices and procedures, usually acquired through one to three months of on-the-job training.

2. Must have excellent organizational and record keeping skills.

3. Must have good manual dexterity.

4. Must possess careful attention to detail.

5. Must be able to maintain a neat and orderly working environment.

WORKING CONDITIONS:
1. Will be working with mice.

2. Will be working in a normal laboratory environment.
Shift
Day Shift

To apply online, please submit your resume here:
https://careers.partners.org/psc/EA/EMPLOYEE/HRMS/c/HRS_HRAM.HRS_CE.GBL?Page=HRS_CE_JOB_DTL&Action=A&SiteId=2&HRS_JOB_OPENING_ID=2194294

Brigham and Women�s Hospital is an EEO, AA and VEVRAA employer.
http://www.brighamandwomens.org/careers

Environmental Health & Safety Consultant (Boston Area)

2009-11-02T14:22:53-05:00
We are currently recruiting for highly qualified Consulting Safety Officers (CSOs). We will consider both full and part-time candidates.

Our CSO�s provide environmental health & safety (EHS) program development and support consultation services to Safety Partners� clients. Take responsibility for clients� EHS program development and implementation for general safety, chemical safety, biosafety and radiation safety, and/or perform specific EHS tasks as designated by the client boss.

MAIN JOB DUTIES/RESPONSIBILITIES
� On-site client work, with the goal of supporting clients� EHS programs for workplace safety and for local, state and federal regulatory compliance. EHS program development and implementation for general safety, chemical safety, biosafety and radiation safety. Working with clients to implement policies and procedures for procurement, use and disposal of hazardous materials, including, but not limited to:

 Manage, develop, implement radiation safety, biosafety, chemical safety programs - procurement, use, disposal
 Manage, develop, and implement General Safety Program - basic life safety: general fire safety, hazard awareness, emergency preparedness.
 Develop and maintain all OSHA specific safety programs.
 Carry over relevant elements of safety program throughout client site, including: animal facility, machine shop, engineering, warehouse, shipping & receiving, office/admin.
 Coordinate and facilitate safety committee.
 EHS permitting for procurement / storage / use / disposal of hazardous materials: flammables, rDNA, select agents, MWRA, controlled substances, DEP, EPA, radiation, etc. Environmental permitting may be done upon approval of the Director and President.
 Coordinate hazardous waste segregation, collection, disposal. This may include waste pouring.
 Review hazardous materials ordering, usage & storage to maintain compliance and safety.
 Audit operations to confirm that EHS program components are being observed.
 Training client staff to ensure regulatory compliance and to ensure staff and Safety Officers are integrated into the safety program.
 Maintain central safety files.
 Develop & deliver training for all safety programs relevant to client, including, but not limited to Emergency Preparedness, HazCom, Lab Stand, Chem Awareness, Biosafety, Bloodborne Pathogens, Radiation Safety
 Coordinate specialized training, such as RCRA, DOT, IATA, OSHA First Responder, Wastewater Operator, CPR, First Aid, AED.
& Other duties and responsibilities that may be assigned from time to time by the President.

Requirements: While it is not necessary for candidates to be experts in all of the responsibilities and requirements of the CSO position, it is important in our consideration that you be well versed in many areas. The best candidates will have laboratory and/or regulatory experience, as well as experience in the items listed below. We will train the right person, as long as they are willing to learn quickly.

� Minimum 4+ years of professional health and safety or laboratory experience
� B.S. in related field
� Detail oriented, highly motivated, resourceful
� Excellent written and verbal communication skills
� Ability to work independently
� Proficiency in the use of Microsoft Excel and Microsoft Word
� Ability to travel within the Boston area

We offer flexible scheduling, competitive compensation and benefits.

Special Education Teacher

2009-11-02T14:11:38-05:00
This position offers a competitive salary, Paid Time Off, and great benefits including 401k with company matching, medical and prescription, dental, vision, short-term and long-term disability. In addition, you will have the personal rewards of making a difference in children�s lives and ongoing training from top industry professionals.

A minimum of a Bachelors degree and completion of an approved teacher preparation program and passing scores on the National Teacher Examination. A minimum of 18 credits in Special Education. The teacher position requires the following: good interpersonal skills, enjoys working with children with special needs, Autism knowledge and experience, organized, good communication skills, and the belief that they can make a difference in a child�s life through their teaching.

TECHNICAL RESEARCH ASSIST. I / 40 HOURS / DAYS - BWH OB/GYN (2191592) (Boston, MA )

2009-11-02T13:45:46-05:00
Brigham and Women�s Hospital (BWH) is internationally known as a leader in cutting-edge research and technology and its commitment to patient-centered care. BWH has a rich legacy of excellence and has been consistently recognized as one of America�s best hospitals by US News and World Report.

GENERAL SUMMARY/ DESCRIPTION OF DUTIES:
The individual will work under the close supervision of the PI on a variety of funded research projects. One will be focused on identifying gene mutations underlying brain, face and female reproductive tract birth defects as well as assisting with the Women�s Reproductive Health Research involving developmental biology of the female reproductive tract.

PRINCIPAL DUTIES:
1. Responsibilities for maintenance of cell cultures. RNA processing, northern blotting, RT-PCR procedures, preparation of tissues for histological analysis, FACS, immunoassays, and protein biochemistry, including western blotting, immunoprecipitation and gel electrophoresis.

2. Responsibility for maintenance of mouse colony, genotyping of transgenic mice, sterile cell culture technique, processing and immunostaining of tissues for microscopy, DNA processing from tail biopsies, and PCR analysis.

3. Responsibility for molecular biological techniques

4. Responsibility for assisting in routine laboratory maintenance. Activities include ordering of supplies, keeping records of accounts, autoclaving instruments and glassware, routine cleansing of sterile hoods and incubators, cleaning of lab benches, maintenance of laboratory equipment, disposal of biological and radioactive waste.

5. Responsible for making various buffers, reagents, and other solutions needed for various laboratory procedures.

6. Maintenance of departmental policies, procedures, objectives, quality assurance, safety, environmental and infection control.

7. Performance of other duties or responsibilities such as helping to set us new techniques and computer analysis of data.
Requirements
QUALIFICATIONS:
1. BA/BS in biological or biochemical sciences with strong interest in genetics and neuroscience
2. Familiarity with basic laboratory instruments, equipment and procedures.
3. Molecular biology techniques helpful.

SKILLS AND ABILITES REQUIRED:
1. Must have a sound understand of laboratory policies and procedures-usually acquired through one-three of on the job training.
2. Must have good manual dexterity.
3. Must demonstrate careful attention to detail.
4. Must be able to maintain a neat and orderly working environment.
5. Must have good math skills.
6. Must be dependable and hard working.
7. Must be able to work independently once familiar with a particular technique.

WORKING CONDITIONS:
Normal laboratory environment. Will be working with animals (mice) and also will work with radioactive and other hazardous materials under controlled conditions.

To apply online, please submit your resume here:
https://careers.partners.org/psc/EA/EMPLOYEE/HRMS/c/HRS_HRAM.HRS_CE.GBL?Page=HRS_CE_JOB_DTL&Action=A&SiteId=2&HRS_JOB_OPENING_ID=2191592

Brigham and Women�s Hospital is an EEO, AA and VEVRAA employer.
http://www.brighamandwomens.org/careers

Quality Manager (Newton (MA))

2009-11-02T11:23:56-05:00
New England Cryogenic Center (NECC) and New England Cord Blood Bank (NECBB) is a biotech company looking to hire a Quality Manager. NECC and NECBB currently processes and cryopreserves multiple types of tissues for later use.

Main Responsibilities
1. Ensure that all quality activities are performed in compliance with company Quality Plan.
2. Report to Executive Management on the effectiveness of the Quality System.
3. Report on a regular basis to Executive Management on the performance of the Quality System.
4. Establish a schedule for performance of quality monitoring, audits and reports as required for maintenance of Quality Systems.
5. Communicate with department heads to ensure that they maintain department specific Quality Systems.
6. Act as liaison for all matters relating to quality activities.
7. Ensure compliance with document control regarding change control of documents including SOPs, forms and archive of documents that effect change control.
8. Resource for FDA compliance related to tissue activities.
9. Perform other related duties as assigned.

Previous experience working within a Quality System setting is required. Familiarity with FDA regulations (specifically 21 CFR 1271) and AABB Standards and experience working in a cGTP or cGMP environment is preferred.

Some travel, domestic and international, will be required.

Renewable Energy Project Manager (Waltham)

2009-11-02T08:25:45-05:00
Harvest Power is a venture-backed start-up with offices in Waltham, MA and Seattle, WA. We are an organic materials management company that diverts organic waste from landfills and turns it into renewable energy and compost.
Candidate is responsible for managing the development of specific biogas (anaerobic digestion) and biomass gasification facilities as well as organizing project tracking processes and document management for all projects in development within Harvest's portfolio. Project development commences with commercial engagement and runs through financial closing and the start of construction. Primary activities include oversight of the permitting and facility procurement process as well as completion of organic waste feedstock and energy sales agreements. This person will manage, direct and administer internal and external resources related to their assigned projects and reports to the Manager of Project Development.

Qualifications:
� BA or BS in Environmental Science, Engineering, Biology or similar is required, Master�s degree in business or technical field strongly preferred
� Minimum of five years of experience, preferably in waste management, power generation, construction, environmental services, real estate, architecture, mechanical, civil or environmental engineering or related field. Background in and understanding of anaerobic digestion a plus, though not required.
� Well-developed project management skills
� Very strong organizational skills and persistent execution of tasks
� Good interpersonal, written, analytical, and quantitative skills
� Detail-oriented with ability to multi-task and commitment to producing high-quality work
� Self-starter with the ability to work well in a relatively unstructured yet collaborative work environment with little supervision
� Ability to understand and explain technology
� Ability to travel and work overtime on short notice
� Highly proficient with Microsoft Office and Microsoft Project (or equivalent project management software)
� Highly motivated and willing to work in dynamic start-up environment

Become a scientific community catalyst (cambridge)

2009-11-02T01:34:51-05:00
This job perfect for you if you're interested in science, but not sure exactly which field and would like to learn more about the different kinds of research going on in the area first hand from principal investigators.

Are you sick of standing at the bench, but would still like to be involved in science or research? Do you want to meet scientists working at the very edge of innovation, and learn about a wide variety of different research fields? Become a scientific community catalyst for Orwik.

Orwik is an online content management and distribution site for scientists. It is intended to serve as the scientific memory and repository of research for laboratories, foundations and institutions. Our mission is to make science accessible by providing a platform for the safe and secure sharing of research, open access publishing and creating sustainable scientific communities.

You will be in working with local academics to seed and grow scientific communities, and to help scientists integrate user generated content and maintain sustainable wikis. This job involves working with academic groups in universities and colleges and interdisciplinary institutes in the area.

The ideal candidate should be highly energetic, have a genuine interest in science, innovation, information dissemination and novel technologies. Must have great communication skills, experience working with people and a friendly demeanor.

Requirements :
� Research experience
� Strong communication and writing skills
� Knowledge of social marketing tools like Facebook, Blogger, Twitter and the like

Nice to Have:

* Experience with web technologies
* Interest in building communities
* Knowledge of viral dynamics

To apply, email your CV and a writing sample about why you would like to be a scientific community catalyst

Director of business development for a young Web 2.0 startup (cambridge)

2009-11-02T01:26:29-05:00
Are you interested in internet and Web 2.0 technologies as well as in science and communication? Are you a former geek that wants to try his hand at entrepreneurship? Then, become part of a founding sales-team for a revolutionary startup poised to change the dynamics of scientific discourse.

Orwik is an online content management and distribution site for scientists. It is intended to serve as the scientific memory and repository of research for laboratories, foundations and institutions. Our mission is to make science accessible by providing a platform for the safe and secure sharing of research, open access publishing and creating sustainable scientific communities.

You will be responsible for handling major institutional accounts in academic and pharmaceutical space, signing up new clients and helping in all facets of the sales cycle from sourcing leads to closing accounts. Experience with non-profit, government and research foundations a huge plus.

Relevant experience

* Selling technology to consumers and institutional clients
* Experience working in a research environment
* Experience with non-profit and medical research foundations
* Working with governments and higher education

Must have

* Great communication skills
* BS in science or related fields
* An independent streak and a willingness to learn

Negotiable salary + commissions

Please submit a letter saying why you would like to be part of this exciting new effort, include a CV and bio with relevant experience.

Do you have hands-on lab or sales experience in biology or microscopy? (Work from home)

2009-10-31T09:49:52-04:00
Our client, a life sciences company , has an immediate need as it seeks to grow in the cellular imaging/microscopy market. Currently, we seek individuals experienced in the laboratory with cellular imaging/microscopy applications, systems and/or software to conduct outbound calls to researchers as a follow-up to ongoing purchase needs.

The Cellular Science/Imaging consultant will ...
- Work from home as an independent contractor with flexible hours
- make successive outbound calls to researchers from a list of warm leads and previous customers provided by the client
- utilize the client�s preferred pitch in the approach to these leads
- update customer records and confirm interest on behalf of client
- Cellular Imaging Consultant does not need to complete the sales process - only confirm interest and collect related information.

Excellent Cellular Science/Imaging Consultant candidate will meet the following criteria:
- have education, laboratory or sales experience in the field of biology, microbiology, microscopy or cellular sciences
- direct experience in cellular imaging/microscopy hardware, software and/or applications a plus
- MS/PhD not required - but a plus
- Inside sales and/or sales experience a plus
- have a computer with broadband internet access (not provided by, or reimbursed by the company)
- Have availability of 10 to 40 hours per week between the hours of 8am and 6pm eastern time
- have basic computer skills
- have a reasonably quiet setting in which to work
- have excellent phone skills
- be exceptionally diligent and reliable
- be able to work independently

The Cellular Science Consultant will be provided...
- required software and software orientation
- Product/technology orientation
- Lead follow-up techniques orientation

This is an outstanding opportunity for someone that would like to work from home, needs schedule flexibility and who would like to grow with this exciting new business. Please send a resume with a thoughtful description of why you are interested in this opportunity in the body of the email, including your specific experience in cellular sciences.

Director, Business Development (Boston (Home-based))

2009-10-30T18:34:43-04:00
Pharm-Olam International (�POI�) a leading international Contract Research Organization, with employees and offices across the globe, is looking to further expand our business development team. Pharm�Olam is poised for growth, and is seeking exceptionally talented individuals experienced in developing and growing their respective regions.

If you have a proven BD track record within a CRO or pharmaceutical environment, then we would like to speak with you.

Job Duties & Responsibilities:

� The BD Director�s primary responsibilities will be to identify new opportunities and grow existing business through interaction with key players at targeted major pharma and biotech companies.
� Generate new business, meeting or exceeding quarterly and annual sales targets
� Develop and implement individual territory and account strategies that incorporate significant account and industry profiling with pipeline and therapeutic content, business development, acquisition and retention strategies.
� Seek to achieve individual territory sales through proactive sales activity, focused on both new account acquisitions and existing accounts
� Provide comprehensive presentations POI services to clients
� Provide weekly sales activity reports and monthly sales review to management
� Ability to identify and develop sales leads, professionally present capabilities, manage the sales process through close and handle all aspects of contract negotiations

Knowledge & Experience:

� Minimum of 3 years of business development experience, including experience in and knowledge of clinical drug development
� Prior BD sales experience in a CRO environment mandatory

About Us:

POI has one of the largest global footprints of any CRO. We are committed to establishing and maintaining the industry's strongest multi-national presence. Our monitors have the most extensive knowledge of local and regional customs and sites across a broad range of therapeutic areas.

For confidential consideration, please forward your CV to HR@pharm-olam.com, or via fax to +832 202-0564.

Senior Firmware Engineer (Salem, NH)

2009-10-30T16:42:41-04:00
COMPANY
AgaMatrix is a fast-paced life-sciences technology company that develops, manufactures, and sells next generation blood glucose monitoring (BGM) products to serve the needs of the diabetes community. Our proprietary WaveSense biosensor technologies are the foundation of our platform of products. Our technology expertise spans across biology, chemistry, digital signal processing, engineering and manufacturing. You can find more information about us here: www.wavesense.info

DESCRIPTION
We are rapidly expanding our technology team and are seeking a talented Senior Firmware Engineer who will play a crucial role in developing AgaMatrix product. Beside designing and writing firmware for internal and external products, you will work directly with the Director of Engineering and firmware engineering team to develop product architecture, firmware architecture and manufacturing automatic testing system architecture. In this role, you will also contribute to AgaMatrix firmware development process.

You will be expected to be an expert at developing firmware for 8 to 16 bits microcontroller, the expertise shall span from writing code to embedded operating system and system architecture. You must be able to rapidly learn new technologies, be a self-starter, and take initiative to apply your skills to overcome potential technical barriers. An intense passion for learning and expanding your skills and knowledge is essential for you to be part of our team.
You will be expected to have a passion for developing medical device since the product you are going to develop will be used by millions patients and directly affect many people�s life.

RESPONSIBILITIES
Design, develop, maintain, and implement embedded software and algorithms for internal and external products. May need to lead other junior firmware engineer in complete a project.
Main contributor to the product system architecture and firmware architecture. Contribute to write firmware related documents.
Provides analysis, evaluation, and selection of new concepts and approaches for embedded software design of new or improved products and processes.
Constructively collaborate other engineering disciplines and other departments on system design and development.
Participate in verification & validation testing of embedded software and systems.

QUALIFICATIONS
Must has deep knowledge about microcontroller based firmware design and development. This includes development tool such as C/C++ compiler, Debugger/Emulator, Embedded OS Etc.
Must have experience in writing embedded OS or real time scheduler.
Must have experience written low level device driver and associated hardware such as timer, DMA, AD converter, Comparator, UART, I2C.
Must have experience in writing embedded software that has hard real time requirement. WINDOW CE does not count.
Must have solid background in computer science and is knowledgeable about basic electrical engineering.
Must at least has experience with one 8 or 16 bits microcontroller
Require to be able to read circuit design/schematics
Requires a bachelor's degree and minimum 5 years of experience in the field or in a related area. Master�s degree preferred.
Knowledge of signal process programming experience with MATLAB is a plus
Knowledge of electrochemistry is a plus
It would nice to have done VB .net programming and serial communication
It would be nice to have knowledge of wireless communication in general and Bluetooth in specific
It would be nice to have work in a medical device company and do development work following FDA and ISO standard

COMPENSATION
As a pre-IPO, growing company, we offer a competitive compensation package with benefits including health insurance, dental plan, long term disability, life insurance, and 401k.

CONTACT
If you are interested in joining this intense and passionate team, send resumes in e-format to: mailto: hr@agamatrix.com with "Response to job posting � Senior Firmware Engineer" in the subject field. Please include a cover letter with:
One paragraph explaining what experience and technical expertise you would bring to the AgaMatrix team
One paragraph highlighting a recent development project that you were responsible that illustrates your ability to develop firmware.
One paragraph discussing your ambitions for career development at AgaMatrix

Senior Research Engineer (Salem, NH)

2009-10-30T16:31:52-04:00
COMPANY
AgaMatrix is a fast-paced life-sciences technology company that develops and manufactures next generation Blood Glucose Monitoring products to serve the needs of the diabetes community. Our proprietary WaveSense biosensor technologies are the foundation of our platform of products. Our technology expertise spans across biology, chemistry, digital signal processing, engineering and manufacturing. You can find more information about us here: www.wavesense.info

DESCRIPTION
We are rapidly expanding our technology team and are seeking a talented Senior Research Engineer who can successfully bridge and innovate across the different disciplines of engineering, biology, chemistry, and mathematics. You must be able to rapidly learn new technologies, be a self-starter, take initiative to apply your skills to complex research problems, and innovate solutions for real-world problems. An intense passion for learning and expanding your skills and knowledge is essential for you to be part of our team. In this position, you will get the chance to �make theory into practice�. By working with both the Research and Engineering Teams, you will translate biochemically-generated signals into digital electronic signals by building advanced devices that adapt in real time to nano-scale chemical reactions.

RESPONSIBILITIES
� Help create, build, and evaluate next-generation nano-scale biosensors.
� Work with Research Team to translate their ideas into engineering prototypes and implementations.
� Design and develop hardware and firmware for real-time signal processing on hand-held medical devices.
� Design and develop PC-based Windows and web applications to support algorithm development.

QUALIFICATIONS
� Technical Requirements:
o BS in Electrical Engineering (or equivalent) and 4+ years commercial experience.
o 2+ years experience with microcontroller firmware design and development, including experience with development tools such as C/C++ compilers, Debuggers/Emulators, Embedded OS, etc.
o 2+ years experience developing firmware for 8 or 16 bit microcontrollers.
o Proficiency in understanding and creating circuit design diagrams and schematics.
o 1+ year experience in VB .net programming and serial communications.
o Strong analytical skills, including statistics, mathematics and data handling.

� General Requirements:
o Excellent communication and interpersonal skills and ability to present research findings to peers and management.
o Ability to work both independently with minimal direction and as a team player in a flexible and interdisciplinary environment.
o Eagerness to challenge yourself to learn new technologies in a fast-paced research and product-development environment.

� Preferred:
o MS in Electrical Engineering (or equivalent) and 2+ years commercial experience.
o Knowledge of DSP implementation and experience with MATLAB.
o Working knowledge of wireless communication in general, including Bluetooth.
o Experience working in a medical device company and following FDA and ISO development guidelines.
o 1+ years of performing wet chemistry experiments in a commercial or research setting.
o Strong scientific knowledge, including chemistry, biology, electrochemistry, biosensors, and mass transport.

COMPENSATION
As a pre-IPO, growing company, we offer a competitive compensation package with benefits including health insurance, dental plan, long term disability, life insurance, and 401k.

CONTACT
If you are interested in joining this intense and passionate team, send resumes in e-format to: hr@agamatrix.com with "Response to job posting � Senior Research Engineer" in the subject field. Please include a cover letter with:
� One paragraph explaining what experience and technical expertise you would bring to the AgaMatrix team
� One paragraph discussing your ambitions for career development at AgaMatrix
� One paragraph highlighting a recent technical project that illustrates your ability to innovate.

Thank you for considering AgaMatrix.

Senior Program Manager (Salem, NH)

2009-10-30T16:27:54-04:00
COMPANY
AgaMatrix is a fast-paced life-sciences technology company that develops, manufactures, and sells next generation blood glucose monitoring (BGM) products to serve the needs of the diabetes community. Our proprietary WaveSense biosensor technologies are the foundation of our platform of products. Our technology expertise spans across biology, chemistry, digital signal processing, engineering and manufacturing. You can find more information about us here: www.wavesense.info

DESCRIPTION
We are rapidly expanding our technology team and are seeking a talented Senior Program Manager who can successfully manage the product design and development process for all new and existing products. You will work directly with the Director of Engineering to ensure that all products meet the highest standards of technical excellence and quality, and that products are designed and updated, or new product lines are introduced, to meet the Company�s strategic goals.

As a part of your role so, you will facilitate all cross-functional team communication and coordination and serve as the overall project manager overseeing the activities of individual project during all phases of the development process. This will involve working closely with the Marketing, Applied Research, Engineering, Product Management, Product Design, Manufacturing, Legal, Regulatory and Executive teams to bring each product to a successful launch on time and on budget. You will also help set priorities for products based on available resources.

You will be expected to be an expert at communicating across all levels of the organization. You must be able to rapidly learn new technologies, be a self-starter, and take initiative to apply your skills to overcome potential technical, operational, marketing, and financial barriers. An intense passion for learning and expanding your skills and knowledge is essential for you to be part of our team.

RESPONSIBILITIES
� Facilitate all cross-functional team communication and coordination. Serve as the project manager for all phases of the development process, including working closely with manufacturing, Marketing, Technology, Legal, Compliance, and the executive team to bring a product to successful launch on time and on budget.
� Provide leadership and a centralized point of contact for product feature requests, troubleshooting, and change management;
� Closely collaborates with Marketing and Product Design, Product Management, technical team, Operations, Regulatory and Clinical team in order to prioritize, develop, and release new capabilities and features for AgaMatrix products;
� Driving release plans and processes to ensure that new products and changes to existing products are fully tested and Product performance meets original design intent;
� Collaborate with commercial, product management, and technical teams to ensure that the products are fully tested and Product performance meets original design intts and specifications for new products and new generations of existing products
� Chair regular product meetings and facilitate communication across departments to ensure smooth development of new products and continual support of existing products
� Assist department heads and project managers to manage budgets, schedules and resource allocations across all product development initiatives.
� Work with project teams to develop and implement unified standard processes and leverage IT solutions to streamline product development
� Assist in the preparation of documents pertaining to Design History files/Technical files/regulatory submissions of commercial products
� Assist in planning, organizing, and directing project team activities. Evaluates and reports progress and results obtained, recommends major changes to achieve objectives.

QUALIFICATIONS
� Candidates should have at least 5 years experience in Program Management, and direct experience with medical device product life cycle;
� Candidates will be expected to demonstrate they have experience in project management , managing internal and external dependencies, understanding complex technologies, and creating and managing consumer medical device development processes;
� Candidates must have excellent verbal and written communication skill and solid organization and people skills as well as a passion for medical device development;
� Proven ability to analyze, organize, and integrate large amounts of complex, disparate information into clear, concise specs and plans is a must; Candidates must have a strong technical background and be able to contribute usefully to participate in product architectural and product design discussions;
� Proven ability to create, develop and maintain project schedule; Proficient in MS Word, Excel, Visio and Project is required;
� A BA/BS degree in engineering, science or related technical discipline is required; MBA is preferred;
� Candidates must have managed at least a medical device development projects from start to completion, including requirements gathering, scheduling, spec writing, bug tracking, regulatory filing and working with operation and marketing for successful product launch;.
� Experience with issues related to internationalization of product preferred.

COMPENSATION
As a pre-IPO, growing company, we offer a competitive compensation package with benefits including health insurance, dental plan, long term disability, life insurance, and 401k.

CONTACT
If you are interested in joining this intense and passionate team, send resumes in e-format to: mailto: hr@agamatrix.com with "Response to job posting � Senior Program Manager" in the subject field. Please include a cover letter with:
� One paragraph explaining what experience and technical management expertise you would bring to the AgaMatrix team
� One paragraph highlighting a recent development project that you managed that illustrates your ability to innovate at the organizational process level.
� One paragraph discussing your ambitions for career development at AgaMatrix

Thank you for considering AgaMatrix.

Molecular Biologist (Waltham)

2009-10-30T15:56:13-04:00
Data Analyst/Q/C Technician

1+ years of solid working knowledge of molecular biology required (BA, BSc level)
Position includes both lab work and Data Analysis work
Lab techniques: PCR, DNA sequencing, sequence analysis
Production- environment oriented: attention to detail, adherence to procedure, ability to work under time pressure
Good communication skills, ability to work as part of highly integrated team
Responsibilities include data mining of the published scientific literature, creation and maintenance of genetic-variant databases, and support of diagnostic result reporting.
Perform Data Analysis
Review Q/A packs
Release Coordinator Activities

Research Associate (Norton, MA)

2009-10-30T15:35:34-04:00
Growing CRO looking for motivated individual with strong communication skills.
Requirements:
* Capable of working is a fast-paced team-oriented environment.
* Good understanding of cell biology, biochemistry and microbiology, small animal model and histopathology.
* Hands-on experience in various in vivo and in vitro experiments a must!
* Expertise for the design and execution of a variety of in vitro and in vivo studies in a variety of therapeutic areas such as inflammation, oncology, diabesity, CNS, infectious and cardiovascular diseases is a plus.
* B.Sc or M.Sc. degree in life sciences
* At least 2-5 years relevant laboratory experience required
* Good at learning
Responsibities:
* Various cell biology and molecular biology assay development and screening research efforts that will support discovery and optimization of novel molecules in various cell-bases assays, various cell culture techniques, ELISA assays, Cell proliferations assays, cytotoxicity assays (ATP,MTT,etc), HE staining.
* Various molecular biology work
* Bacteria culture and antimicrobial screening
* Various small animal models, basic animal handling
* Data Analysis

QC Associate - Protein

2009-10-30T13:49:55-04:00
QC Associate will perform testing of a protein based therapeutics in a young energetic Biotechnology company. The assignment is a 6 month contract project and has strong potential to convert to a full time employee.

Responsibilities include:
Run assays including HPLC, SDS-PAGE, IEF, ELISA in a GMP QC lab in support of product release and stability.
Assist with data review supporting release and stability
Assist with writing SOP�s
Maintain, calibrate, and troubleshoot equipment

Requirements:
BS in Scientific discipline with 2+ years of GMP QC laboratory experience
Experience with testing protein or biologic products is required
Experience with HPLC, SDS-PAGE and ELISA
Strong attention to detail and ability to meet strict timelines required
You will appreciate the ethics guiding each StratAcuity team member. We build lasting relationships with exceptional scientists and take great care to protect your personal information. Upon receiving your inquiry, you may be directly contacted by a StratAcuity team member to discuss your career goals. We will not share your information with anyone without your direct prior consent.

StratAcuity Scientific, CHEMISTRY IS EVERYTHING.

Research Technician II (BWH - Longwood Medical Area)

2009-10-30T12:51:30-04:00
GENERAL SUMMARY/ OVERVIEW STATEMENT:
Working under the general supervision of the supervisor, and in accordance with established hospital policies and procedures, conducts a variety of routine experiments where methodologies are clearly established. The TRA will perform research that is focused on understanding the immune responses in skin including response to vaccination with vaccinia virus. Calculates, transcribes, and analyzes data using basic statistics. The TRA must be organized and capable of considerable independent work with maintenance of detailed, careful records.
PRINCIPAL DUTIES AND RESPONSIBILITIES:
2. Under general supervision, performs a variety of routine tests following established methodologies. Routine tests may include analysis of cells by flow cytometry, PCR, and isolation of lymphocyte subsets using magnetic beads.
3. Prepares and maintains tissue cultures. Maintains long-term tissue cultures of human cell lines and monitors for contamination. Perform tissue culture techniques, including but not limited to maintenance of cultures of fresh cells and cell lines required for research.
4. Works with live vaccinia virus which requires thorough understanding of biosafety procedures. Grows virus in culture and harvests virus for experiments. Infects animals with cultured virus.
5. Harvests animal blood and tissues to study for immune response.
6. Prepares and maintains stock solutions and reagents.
7. Prepares chemicals, instruments and equipment.
8. Discusses progress of work regularly with supervisor.
9. Records data, summarizes, and analyzes results using basic statistics.
10. Maintain detailed laboratory notes with organized records and data.
11. All other duties as assigned.

QUALIFICATIONS:
1. Good organizational skills, detail oriented
2. Ability to methodically record data and to analyze data
3. Computer literacy
4. Good interpersonal and communication skills.

SKILLS/ ABILITIES/ COMPETENCIES REQUIRED:
1. BS in biological/physical science is required.
2. Must have at least two years experience in a directly related research setting including tissue culture and animal experience.
WORKING CONDITIONS: .
1. Will work with live virus � this position requires vaccination against smallpox.
2. Will work with human cells and tissues
3. Will work with mouse cells and tissues.
SUPERVISORY RESPONSIBILITY:
N/A
FISCAL RESPONSIBILITY:
N/A

Science Education Sales (Boston area)

2009-10-30T12:39:04-04:00
Is Science Education your passion? Join PASCO scientific, a world leader in 21st Century technology solutions for science education. Our products are coveted by science teachers around the world for their quality and ease of use in the classroom. Located in Roseville, CA we have been serving science educators for over 40 years.

Duties and Responsibilities:

This Boston based position will have multi-state responsibility (PA, NY, CT, MA, NH, VT, MA) for selling our 21st Century science solutions directly to educational end-users in the K-12 market. Call on existing and prospective customers in person, by phone, email and fax. Provide consultative services of PASCO equipment, curriculum, software and over-all solutions for State DOE, local science education organizations, district level decision-makers, and teachers. Required to attend trade shows, conferences and workshops. Must be comfortable with public speaking and giving presentations to large groups. Responsible for meeting revenue goals for the region.

Minimum Qualifications:

� BS in science, engineering or related technical field.
� Minimum of 2+ year�s education technology sales experience with proven track record.
� 50% overnight travel required.
� Strong oral and written communication skills.

Preferred Qualifications:

� Strong understanding of effective teaching methods in 21st Century science
� Classroom and school administration experience
� Comfortable in the use of both Mac and PC based operating systems
EOE M/F/D/V

MECHANICAL/ELECTRICAL ENGINEER WITH MEDICAL DESIGN EXPERIENCE (Newton Center MA)

2009-10-30T11:49:51-04:00
A medical device start-up company located near Boston, MA is seeking a �born engineer� who eats and sleeps electro-mechanical design and is intrigued by the idea of developing medical devices that challenge modern medicine. The devices apply to various organs and diseases, starting with the cardiovascular system (chronic ischemia, myocardial infarctions, heart failures, etc). Current and planned technologies will be able to perform both diagnostic maneuvers and therapeutic treatments of a number of conditions, including ischemia, ulcers, tumors, functional disorders, etc.

The market opportunity for the devices is considerable, and the growth potential for the right engineer � both financially and professionally - is enormous.

WHAT THE COMPANY OFFERS:
- a strong and healthy performance-based company culture;
- a place to learn new skills on the fly during a demanding and progressive transition;
- a unique opportunity for the right professional to help build a company from the ground up, and be part of leading it to successfully meeting worldwide medical needs.

YOU SHOULD APPLY IF YOU:
- have a proven track record with medical device start-ups, including leading organizations to maximize profitability;
- can model complex components and assemblies in CAD and create detailed drawings,
- have performed process-related design tasks to support pilot manufacturing efforts;
- can develop and implement a project strategy, with short and long term goals, operating plans and budgets with internal resources, then monitor progress and make adjustments as conditions require;
- can enhance the company�s intellectual property position via invention disclosures and patent applications;
- have built and tested prototype designs for proofs of concept;
- have developed protocols and performed product verification and validation testing;
- can support production of final products by troubleshooting manufacturing processes;
- thrive on technical, scheduling, and budgetary challenges and ever-increasing responsibility; and
- are open-minded, change-welcoming, diligent, and like to continuously hone your abilities.

SKILLS AND QUALIFICATIONS:
- BS in mechanical/electrical engineering or equivalent, MS preferred;
- Experience in medical device designs, in some leadership positions and at least one successful start-up situation;
- Specific experience with catheter-based and endoscopic medical devices is desired;
- Strong understanding of engineering materials and component selection;
- Experience in effectively leading and directing cross-disciplinary teams including engineering and information technology; and
- Knowledge of and able to network within the medical device industry.

RESPONSIBILITIES:
- Design, development, evaluation, validation, and transfer to manufacturing of new products and processes, and improvements to existing products and processes;
- Support projects from initial concept through manufacturing pilot;
- Assure compliance with FDA regulations, ISO standards, and customer specifications;
- Provide engineering / technical support to Quality Control, Manufacturing and customers;
- Assist in setups and assembly of products;
- Assist in testing of products;
- Assist in machine design and building;
- Support product complaints analysis; and
- Create Device Master Records (DMR) documentation.

Analytical Chemist/Membrane Interface Operator (Montpelier, Vermont)

2009-10-30T10:31:47-04:00

Position Summary

The analytical chemist/membrane interface probe (MIP) operator is responsible for working with all aspects of established analytical chemistry methods and testing procedures that are associated with our MIP program. The MIP technique is a direct sensing tool that is used to assess the levels volatile organic compounds (VOCs) in the subsurface and combines the use of direct push, environmental drilling with up-hole analytical chemistry procedures. Primary analytical methods are gas chromatography, (GC) however, experience with GC/mass spectrometry is a plus. Strong mechanical and electrical troubleshooting skills are required for this position. Technical and analytical leadership is expected from this position, as well as familiarity and fluency with advanced scientific concepts within the particular discipline. Record keeping, data management, data analysis, interpretation and presentation as well as competent technical writing skills are required.
The position involves periods of extended travel for field work in New England, throughout the United States and several international locations; as much as 50 to 75% of the work may be located outside of Vermont.

Responsibilities

The person performing this job will be responsible for the following functions:
- Perform MIP testing in accordance with defined methodology and standard operating procedures.
- Maintain and repair various components of Stone�s MIP program.
- Report analytical results to investigation team.
- Manage analytical data
- Ability to travel for 5 to 10 days continuous.

Required Skills

The following skills are required:
- Analytical instrument calibration, maintenance, troubleshooting and repair.
- MIP testing, maintenance, troubleshooting and repair.
- Analytical reference standards preparation.
- Quality control of all data generated.
- Data preparation and compilation
- Data presentation and analysis.
- The ability to work as a member of a team in a fast-paced, dynamic setting.
- Driver's license and ability to pass a Department of Transportation physical exam.

Experience and Education

Minimum requirements for this position are a Bachelors degree in Chemistry or related field; or three years previous experience in an analytical chemistry field

Part Time Intern wanted (Commonwealth Avenue Boston)

2009-10-30T09:38:53-04:00
Looking for a part time intern (about ten hours a week) to work at a small biotech company.

We are located on Commonwealth Avenue near Agganis Arena

Job description
Ordering of chemicals, reagents, and kits.
Labeling them accordingly

Ability to understand Turkish is a plus

Process Engineer with Delta V familiarity (Central MA)

2009-10-30T09:14:10-04:00
Process Engineer with Delta V familiarity:

Process Engineers needed for start up and check out of CIP / SIP systems at Central MASS Biopharmaceutical site.
Job requires working knowledge of CIP / SIP functions, qualification protocols and ability to leverage existing automation platform (Delta V) as demonstrated by your working knowledge based upon past assignments.

Qualification of CIP / SIP Circuits

� Now until end of Feb 2010
� Jobsite conditions require flexibility of shift work and or weekend work
� Delta V expertise critical to check out process

Please send your resume *AND* salary requirements to: ProcessEngineerDeltaV@yahoo.com.
We are an Equal Opportunity Employer providing comprehensive benefits and competitive salary.

Research Assistant-Tissue Bank Coordinator (Boston)

2009-10-29T21:48:27-04:00
Research Assistant-Tissue Bank Coordinator

Tufts Medical Center and Floating Hospital rank among the top 10 percent of the nation�s independent hospitals to receive federal research funds. Our robust research organization includes groundbreaking bench research, clinical trials and developments in health policy, and is funded by the National Institutes of Health, private foundations, industry and private individuals. Externally funded research will top $66M in the coming fiscal year. Our dual mission of advancing knowledge and training our experts to become investigators of the future drives forward with one goal in mind: quickly turning innovative research into pioneering care.

Tufts Medical Center has the following position:

Research Assistant-Tissue Bank Coordinator:
This position requires preparation of fresh human tissue and blood specimens for frozen storage for subsequent research and diagnostic use as well as maintenance of the computerized database for the frozen tissue archive. Under the supervision of the Medical Director of the Tissue Bank and/or surgical pathologists and hematologist/oncologists, the Tissue Bank Coordinator may perform the following tasks and assume the responsibility for duties including the following:

-Sampling fresh human tumor and normal tissue from surgical pathology specimens for cryopreservation under direct supervision of a surgical pathologist.
-Separate buffy coat cells from whole blood samples by density-gradient centrifugation; wash and cryopreserve mononuclear cell samples.
-Preparation of plasma/serum samples for cryopreservation.
-Conduct nucleic acid extraction and storage from tissue and cell samples
-Transfer samples to liquid nitrogen freezers for long-term storage
-Retrieve samples from liquid nitrogen freezers and prepare them for distribution
-Abstract diagnostic data for frozen samples and enter the information into the computerized database

Knowledge of and experience with complex laboratory practices including cell separation and nucleic acid extraction and knowledge of and adherence to infection control procedures. Good organizational skills to maintain careful records of specimen information. Good computer skills required for data entry and database development and management. At least one year working in a biomedical research or clinical research laboratory. Bachelor degree in biological science is required.
Visit our web site: www.tuftsmedicalcenter.org/careers

Jim Mack
Employment Specialist
Tufts Medical Center
800 Washington Street
Box 795
Boston MA 02111
Jmack1@tuftsmedicalcenter.org