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document control in Boston

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    1. Sr Associate Quality Control

      Manager will conduct in person interviews on Thursday and Friday of this week-please ensure your candidates are available for those 2 days The position is open as it is a backfill for another candidate-it is an immediate need-person can start immediately Candidate will ...

    2. Senior Quality Control Associate

      Industry leading pharmaceutical company is seeking a Senior Associate, Quality Control to work in Woburn, MA. This is a six (6) month contract position. Max pay is $26.00/hour. SUMMARY: The Senior Quality Control (QC) Associate will be responsible for; Assist the Quality ...

    3. Project Manager, Pharmacovigilance & Risk Management

      Project Manager- Pharmacovigilance & Risk Management (PVRM) Location: Cambridge, MA Now hiring at one of the Northeast's fastest growing pharmaceutical companies!  Seeking a pharmaceutical PM with PVRM experience and familiarity with ICH and other international guidelines. ...

    4. Quality Specialist

      Overview: Masy Systems has a reputation built around the quality and experience of our staff. We have carefully built a dynamic team whose members possess diverse professional skills. We offer a casual, friendly atmosphere, promoting individual development and career ...

    5. Calibration Technician

       PLEAS HAVE THIS TYPE OF EXPERIENCE .... 6-8 MONTH CONTRACT ... COULD BE EXTENDED Duties Performs operations necessary for calibration of equipment that may include testing, adjusting, and maintaining measuring and indicating instruments to conform to set standards. May ...

    6. Software QA

      Our client is currently seeking a Data Analyst to join their Research Analytics team. They are seeking a highly motivated, meticulous and detail-oriented individual for a rapidly growing multi-disciplinary team. The candidate should: Be instrumental in quality control ...

    7. Brand Protection Senior Specialist - Pharma

      Title: Brand Protection Senior Specialist Job ID: 5796 Industry: Biotech/Pharmaceutical Location: Cambridge, MA Duration: 13 Month Contract Pay Rate Range: Depends on Experience (W-2 all inclusive rate)   Job Details: The individual will be responsible for developing ...

    8. Senior Safety Associate (Pharmacovigilance; AERS, and/or ARISg)

      Title: Senior Safety Associate: Global Case Management Industry: Biotech/Pharmaceutical Location: Cambridge, MA Duration: 1 Year Contract Pay Rate Range: Depends on Experience (W-2 all inclusive rate)   Job Details: The Safety and Benefit Risk, Global Case Management ...

    9. QC Associate I, Product Complaints (GMP, Pharma)

      Streffco Consultants, Inc., is an international staffing and systems integration organization. We provide technology and business operations resources on a project, contract, contract-to-hire or direct hire basis.   Title: Associate I, Quality Control (Product Complaints) ...

    10. QC Associate I, Product Complaints (GMP, Pharma)

      Streffco Consultants, Inc., is an international staffing and systems integration organization. We provide technology and business operations resources on a project, contract, contract-to-hire or direct hire basis.   Title: Associate I, Quality Control (Product Complaints) ...

    11. Quality Control Analyst

      1) Shift : Tues to Sat 1st Shift  2) Shift: Tues to Sat second shift Performs operations necessary for quality testing and plays a role in implementing new technology within quality control. At more senior levels, provides an investigative or technological orientation in ...

    12. Documentation Specialist

      My name is Bell and I represent The Fountain Group.  We are a national staffing firm and are currently seeking a Documentation Specialist II for a prominent client of ours.  This position is located in Northborough, MA. Details for the positions are as follows:   Job ...

    13. Cleaning Validation Engineer - Consultant

      Grow with ProPharma Group!    We work with clients in the pharmaceutical, biotechnology and medical device industries to provide the best solutions for their unique challenges and concerns. At ProPharma Group, we build successful long-term relationships with clients by ...

    14. QA Contractor

        The Quality Assurance Contractor will be responsible for assisting in the management of cGMP operations for day to day support of drug substance and drug product manufacturing, including exceptions management, change control, and batch record review. Specifically, the QA ...

    15. QA Consultant

      The Quality Assurance Contractor will be responsible for assisting in the management of cGMP operations for day to day support of drug substance and drug product manufacturing, including exceptions management, change control, and batch record review. Specifically, the QA ...

    16. QC Associate I, Product Complaints

      Streffco Consultants, Inc., is an international staffing and systems integration organization. We provide technology and business operations resources on a project, contract, contract-to-hire or direct hire basis.   Title: Associate I, Quality Control (Product Complaints) ...

    17. Associate I, Quality Control (Product Complaints)

      Streffco Consultants, Inc., is an international staffing and systems integration organization. We provide technology and business operations resources on a project, contract, contract-to-hire or direct hire basis.   Title: Associate I, Quality Control (Product Complaints) ...

    18. QC Associate I, Product Complaints (GMP, Pharma)

      Streffco Consultants, Inc., is an international staffing and systems integration organization. We provide technology and business operations resources on a project, contract, contract-to-hire or direct hire basis.   Title: Associate I, Quality Control (Product Complaints) ...

    19. Manufacturing Associate

       GREAT OPPORTUNITY ...  URGENT NEED Operates general manufacturing equipment under close supervision in accordance with current GMPs or standardized procedures and within safety guidelines. Requires good documentation skills and attention to detail. Tasks to be completed ...

    20. Quality Control Analyst I

       Quality Control Analyst I Position Location: Framingham, MA 2:00pm-10:00pm Shift Estimated End Date: 03/03/2015 Job Responsibilities: Performs operations necessary for quality testing and plays a role in implementing new technology within quality control. At more senior ...

    21. Senior Manager Process Engineers & Development - Downstream (boston)

        Providing daily on-the-floor technical support. · Providing technical leadership in process-related investigations. · Overseeing and leading data management & monitoring/SPC review processes. · Developing strategy for process validation activities. · Maintaining the ...

    22. Process Validation Consultant

      Here at ProPharma Group, we work with clients in the pharmaceutical, biotechnology and medical device industries to provide the best solutions for their unique challenges and concerns. We build successful long-term relationships with clients by providing leading industry ...

    23. Quality Control Analyst I

      Quality Control Analyst I Position Location: Allston, MA 7:00am-3:30 pm shift Estimated end date 12/19/2014 **(note Contract will be extended)** Job Number: 4054067 Job Duties: This individual will report to the QC shift Supervisor in the Allston Quality Control ...

    24. Senior Manager Process Engineers & Development - Downstream

        Providing daily on-the-floor technical support. · Providing technical leadership in process-related investigations. · Overseeing and leading data management & monitoring/SPC review processes. · Developing strategy for process validation activities. · Maintaining the ...