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document control in Boston

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    1. Automation Engineer

      This is a contract position that will provide support for a growing automation group. The person in this role will be supporting processes, utilities, and building automation systems used in commercial production. This position requires experience in working within a cGMP operation, especially regarding change control and other quality systems. The candidate must be technically proficient in ...

    2. Sr. Manager (Associate Director) Quality, GLP

       The Sr. Quality Manager of GLP is responsible for assisting with the strategic alignment of projects and activities and refining those projects and/or activities proactively. This role is also responsible for technical development of personnel and ensuring the quality of deliverables within their purview.Key Responsibilities:• Accountable for regulatory compliance and ensuring procedures are ...

    3. Senior Safety Associate II

      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: Senior Safety Associate IIJob ID: 6879Industry: Biotech/PharmaceuticalUnit: Safety and Benefit Risk ManagementLocation: Cambridge, MADuration: 12 months (possible extension ...

    4. Scientist - Formulations

      Kelly Services® has been providing outstanding employment opportunities to the most talented individuals in the marketplace. We are proud to offer a long-term temporary opportunity to work as a Scientist in a prestigious Fortune 500® pharmaceutical company located in Cambridge, MABy working with Kelly in this role, you would be eligible for: - A competitive hourly pay rate with weekly checks ...

    5. Director - Clinical Affairs - Companion Diagnostics - Cambridge, MA

      Fast growing biotech company working on highly specialized products in the oncology field seeking individual with ability to directly oversee clinical trial programs for companion diagnostic products. Activities: *** Develop clinical trial plans for predictive, prognostic and diagnostic tests incorporating requirements from doctors, regulatory agencies and payor groups. *** Execute ...

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      No Contract
      No Internship
      No Freelance
      No Telecommute

    6. Quality Assurance Lead

        Hello,   My name is Christina and I represent The Fountain Group.  We are a national staffing firm and are currently seeking a Quality Assurance Lead for a prominent client of ours.  This position is located in Allston, MA. Details for the position are as follows:   Job Description: The Quality Assurance Lead III reports to the Associate Director, Allston Integrated Remediation ...

    7. Associate Director, Process Automation

       The Client has announced plans for an expansion of its large-scale biologics manufacturing facility. The expansion will create a mammalian cell biologics center of excellence through the introduction of biologics development and clinical trial manufacturing capabilities to the site. Both represent new capabilities the site, a site that in its early years has focused solely on large-scale, ...

    8. Senior Safety Associate II (Adverse Event Reports )

      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: Senior Safety Associate II Job ID: 6879 Industry: Biotech/Pharmaceutical Unit: Safety and Benefit Risk Management Location: Cambridge, MA Duration: 12 months ...

    9. Senior Safety Associate II

      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: Senior Safety Associate II Job ID: 6974 Industry: Biotech/Pharmaceutical Location: Cambridge, MA Duration: 1 Year Contract Pay Rate Range: Depends on Experience (W-2 all ...

    10. Associate Director, Process Automation

       The Client has announced plans for an expansion of its large-scale biologics manufacturing facility. The expansion will create a mammalian cell biologics center of excellence through the introduction of biologics development and clinical trial manufacturing capabilities to the site. Both represent new capabilities the site, a site that in its early years has focused solely on large-scale, ...

    11. Senior Project Manager, Business Operations

      Sr Project Manager - Business Operations Boston, MA $140-$180K + Bonus   Relocation assistance is available for this position Sr. Project Manager to provide business and technical leadership to the Program and Portfolio Management (PPM) team, leading strategic projects and  initiatives within a major bioscience firm, as well as being accountable for “SMART (specific, measurable, ...

    12. Head of Quality Systems IMGN88

        The Opportunity ImmunoGen is seeking an experienced quality professional who will join the management team and provide leadership and direction to the Quality Systems (QS) organization.  The Head of Quality Systems is an important member of the management team at ImmunoGen, and will play an instrumental role driving all the Quality activities relating to ImmunoGen’s manufacturing facility ...

    13. Quality Assurance Associate (Biotech/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: Quality Assurance Associate I/II Job ID: 6949 Industry: Biotech/Pharmaceutical Location: Cambridge, MA Duration: 3 Month Contract Pay Rate Range: Depends on ...

    14. Automation Engineer

      This is a contract position that will provide support for a growing automation group.  The person in this role will be supporting processes, utilities, and building automation systems used in commercial production. This position requires experience in working within a  cGMP operation, especially regarding change control and other quality systems. The candidate must be technically proficient ...

    15. Clinical Document Assitant

      A leading pharmaceutical company in Cambridge, MA has an immediate need for a Clinical Document Assistant. The primary purpose of this job is to provide document processing and filing support for Medical Writing in the preparation of clinical documents.Responsibilities: Upload/file/perform quality control on documents to be submitted to the Trial Master File. Assist writers with insertion of ...

    16. Sr. Manager (Associate Director) Quality, GLP

        The Sr. Quality Manager of GLP is responsible for assisting with the strategic alignment of projects and activities and refining those projects and/or activities proactively. This role is also responsible for technical development of personnel and ensuring the quality of deliverables within their purview. Key Responsibilities: • Accountable for regulatory compliance and ensuring ...

    17. Statistical Process Control (SPC) Technician I

      Statistical Process Control (SPC) Technician I Needed in Lexington, MA Every day, Kelly Services connects professionals with opportunities to advance their careers. We currently have a contract opportunity with a global leader in the biotechnology industry in Lexington, MA.Statistical Process Control (SPC) Technician I ASSIGNMENT LENGTH: End of 2015 PAY RATE: ~$14-16/hrSUMMARY This ...

    18. Quality Control Analyst I

        Hello,   My name is Sean and I represent The Fountain Group.  We are a national staffing firm and are currently seeking a Quality Control Analyst I for a prominent client of ours.  This position is located in Allston, MA. Details for the position are as follows:   Job Description: Performs operations necessary for quality testing and plays a role in implementing new technology ...

    19. Quality Control (QC) Inspector

      Summary: Responsible for performing Incoming/Receiving Inspection of mechanical components, elecrical components, intergrated circuity boards, and sub-assemblies. Performs documentation review and product disposition with guidance and supervision. Ensures non-conforming product is identified and appropriately controlled, and conforming product is appropriately dispositioned for use. Reviews ...

    20. Sr. Associate, Controlled Document Management

      Hello,   My name is Sarah and I represent The Fountain Group. We are a national staffing firm and are currently seeking a Senior Associate, Controlled Document Management for a prominent pharmaceutical client of ours located in Cambridge, MA. Details for the position are as follows:   Job Description: This role is focused on QA/QC review of controlled documents. Thus, candidates must ...

    21. Document Control Analyst II

      Sigma Bullhorn ID: 7647 Location: Lexington Area, MA Position/Role: Document Control Analyst II Client Industry: Biotechnology/Pharmaceuticals Classification: 3 Months Contract (Extensions Likely Through To End of 2016 or Conversion to FTP Status)   PLEASE NOTE: Remote Work is NOT allowed. On-Site Only. If you have any questions, I’ll be happy to answer them, but I’ll need to see a copy ...

    22. Quality Control Analyst   4233

      Contract Assignment - short term cover- 2 months   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 designing, executing, interpreting and validating quality procedures and test methods. Completes routine testing of raw materials, in ...

    23. Firmware Engineer

      Principal Embedded SW lead engineer  Reports To: Manager, Software Engineering Department:    General Position Summary: This position is responsible for designing, implementing, and validating the software for Client Ventricular Assistance Device systems (VAD) Essential Functions/Major Responsibilities:  • Designs, codes, and debugs implantable or external embedded software and/or ...

    24. Systems Engineer

      PRINCIPAL SYSTEMS ENGINEER: Our large Medical Device client, based in Middlesex County, Massachusetts, is seeking a Principal Systems Engineer.  This is a full time, permanent role at a very competitive salary.  General Position Summary: This position is responsible for designing, implementing, and validating the Client Ventricular Assistance Device system. Essential Functions/Major ...