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document control in Boston

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  1. Logistics Analyst II

    Pharma client seeks a Logistics Analyst II for a 6 month contract.Working in Supply Chain Operations Engineering and Performance, providing technical expertise in the assessment and recommendation of temperature controlled transportation solutions used for Global Distribution of GMP products. The position is within the Project Management function of Supply Chain Operations. Responsibilities include project leadership, prioritization, evaluation of resource requirements and managing contracted ...

  2. Lab Production Technician

    Experience in cGMP environment desirable. HPLC Knowledge. Quality minded and detail oriented. Computer literate. Effective communicator (verbal and written). Highly organized and excellent at multi-tasking. Proactive, hard working and self-motivated. Ability to interpret data and troubleshooting skills. Ability to make decisions in a dynamic environment. Carry out standard operating procedures involving materials measurement, materials handling and inventory control, equipment operation ...

  3. Pharmacovigilance Consultant

     Our client has a lean Pharmacovigilance team and is concerned they will not be able to cover AE/SAE reporting and reconciliation and vendor oversight. PROJECT DETAILS: PV representative on Clinical Trial teams and participate in review of product and study documents. Be responsible for SAE reconciliation activities, SAE tracking and resolution of site specific issues with regard to PV activities. Be involved with quality control activities with regard to SAE narratives, queries, tracking, and ...

  4. Purchasing Specialist I - Job#: 14-01381

      Our client in Cambridge, MA is looking for a Purchasing Specialist I. This is a long term consulting position. If interested, Please apply to this ad. Position: Purchasing Specialist I Location: Cambridge, MA Job#: 14-01381 Job description: The primary purpose of this role is processing purchase orders based on internal purchase requisitions and the resolution of issues related to existing purchase orders. Principal Accountabilities: Responsible for creating and processing purchase ...

  5. Biostatistician

    Allied Search Partners is looking for a candidate for a qualified Biostatistician. Know someone for this position? We offer a $$ bonus if we place your referral in a position. For a complete list of current Allied Search Partners openings Nationwide please go to: http://www.alliedsearchpartners.com/careers.php Position: Biostatistician Schedule: Full Time Permanent/Direct Hire Location: Winchester, MA area To apply: Please send resume to [email removed] or fax to 888 388 7572. No ...

  6. Technical Writer

    Hello,   My name is Sarah and I represent The Fountain Group.  We are a national staffing firm and are currently seeking a Technical Writer for a prominent client of ours.  This position is located in Lexington, MA. Details for the positions are as follows:   Job Description The Global Quality Standards Technical Editor/Writer is responsible for editing and assisting Subject Matter experts with the development, and creation of controlled GMP Global Quality Standards to comply with the new GMP ...

  7. Laboratory Scientist

    Judge Healthcare is currently seeking a Laboratory Scientist for one of America's most well known laboratories in Marlborough, MA!!This job will have the following responsibilities: Follow the laboratory's procedures for specimen handling and processing, test analyses, reporting and maintaining records of patient test result Maintain records that demonstrate that proficiency testing samples are tested in the same manner as patient specimens Analyze specimens using approved testing procedures (see ...

  8. Program Manager – Product Development - Medical Device

      Position Title – WRCHWPM1082014 Program Manager – Product Development - Medical Device – Mass Pike/128 Area, MA – Up to $130K+   Excellent Compensation Package - Base + Bonus + Comprehensive Benefits Local Candidates Only – No Sponsorship   Company   Mid-size ($250M+ in Revenue, 35% Growth), Successful, Global, and Rapidly Growing Boston Area Medical Device firm focused on Implantable Devices - Great Company - Lots of Upside - Excellent Compensation Package - Bonus – Comprehensive Benefits - Join ...

  9. Associate I, Quality Control - Job Ref#: 14-01314

      Our client in Cambridge, MA, is looking for a Associate I, Quality Control. This is a long term consulting position. If interested, Please apply to this ad Job Title: Associate I, Quality Control Job Location: Cambridge, MA, USA Job Ref#: 14-01314 Job Description: Perform cGMP analytical testing of raw materials and support cleaning validation testing. In addition, maintain compliance, support and contribute to general laboratory operations, documentation and quality improvements. DUTIES: 1 ...

  10. Laboratory Technologist

    Our client is currently seeking a Laboratory Technologist in the Marlborough, MA area.This job will have the following responsibilities: Follow the laboratory's procedures for specimen handling and processing, test analyses, reporting and maintaining records of patient test result Maintain records that demonstrate that proficiency testing samples are tested in the same manner as patient specimens Analyze specimens using approved testing procedures (see department SOPs). Review and release test ...

  11. CLIA Lab Supervisior

      ~~Eutropics Inc., located in Cambridge, MA has an immediate opening for a motivated laboratory scientist in the capacity of CLIA Lab Supervisor. Eutropics is currently preparing a CLIA certified predictive diagnostic test for commercial use. The medical oncology diagnostics test relies on assays that leverage the proprietary Praedicare Dx, the core technology platform of mitochondrial priming assessment, to predict hematologic cancer patient response to specific therapies. The path to ...

  12. QA Documentation Associate (Pharma expr, GXP, Document Managment)

    Title: Senior Associate, QA Docs Job ID: 5470 Industry: Biotech/Pharmaceutical Location: Cambridge, MA Duration: 6 Month Contract/1304 hr. Pay Rate Range: Depends on Experience (W-2 all inclusive rate)   Responsibilities: Processing of controlled documentation, lead project and team for final archival of documentation Maintaining appropriate chain of custody for controlled documents submitted to Archivist Maintaining archive index and archive database for conversion to 100% electronic ...

  13. e-Learning Specialist - Job#: 14-01047

     Our client in Cambridge, MA is looking for a e-Learning Specialist. This is a long term consulting position.If interested, Please apply to this ad Job Title: e-Learning Specialist Location: Cambridge, MA Job ID#:14-01047 Job Summary The Learning Specialist maintains close relationships with customers and acquires partners and delivers training needs to R&D personnel. The Learning Specialist acts as Subject Matter Expert in training procedures and processes and partners with R&D personnel to ...

  14. Senior Associate, QA Docs

    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 Associate, QA Docs Job ID: 5470 Industry: Biotech/Pharmaceutical Location: Cambridge, MA Duration: 6 Month Contract/1304 hr. Pay Rate Range: Depends on Experience (W-2 all inclusive rate)   Responsibilities: Processing of controlled documentation, lead project ...

  15. Senior Associate, QA Docs

    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 Associate, QA Docs Job ID: 5470 Industry: Biotech/Pharmaceutical Location: Cambridge, MA Duration: 6 Month Contract/1304 hr. Pay Rate Range: Depends on Experience (W-2 all inclusive rate)   Responsibilities: Processing of controlled documentation, lead project ...

  16. Technical Writer

    Candidates who have experience with Quality Systems editing - (ie. authoring BLA s or NDA s are good indications of these skills) or experience with regulatory publishing would be good candidates for this role. They are looking for candidates with more editorial experience (able to edit already composed/written documents) than the actual writing experience. Would prefer pharma experience. Must have 2-5 years of experience. Primary Duties The Global Quality Standards Technical Editor/Writer is ...

  17. QA Documentation Associate (Pharma expr, GXP, Document Managment)

    Title: Senior Associate, QA Docs Job ID: 5470 Industry: Biotech/Pharmaceutical Location: Cambridge, MA Duration: 6 Month Contract/1304 hr. Pay Rate Range: Depends on Experience (W-2 all inclusive rate)   Responsibilities: Processing of controlled documentation, lead project and team for final archival of documentation Maintaining appropriate chain of custody for controlled documents submitted to Archivist Maintaining archive index and archive database for conversion to 100% electronic ...

  18. Associate I, Quality Control (Cell Biology, Media prep.)

    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 Industry: Biogen/Pharmaceutical Location: Cambridge, MA Hours per Week: 40 Job Details: Lab support function within Quality Control Virology lab to handle biohazard trash decontamination, cell culture media prep, and lab equipment cleaning ...

  19. Biobank Associate Scientist III ( IATA; Pathology Lab experience)

    Title: Associate Scientist III, Technical Development Industry: Biotech/Pharmaceutical Location: Cambridge, MA Duration: 6 Months, possibility converting to FTE Pay Rate Range: Depends on Experience (W-2 all inclusive rate)   Job Details: The Biobank Associate Scientist III will design and manage all Biobank-relevant aspects of a clinical trial project and investigator-initiated pre-clinical research project as related to biospecimens needing to be collected, processed, labeled, shipped and ...

  20. Associate Scientist II, Histotechnologist

    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 Scientist II, Histotechnologist Job ID: 5446 Industry: Biotech/Pharmaceutical Location: Cambridge, MA Duration: 12 Month Contract Pay Rate Range: Depends on Experience (W-2 all inclusive rate) Job Details: • Perform routine and specialized histotechnology-based assays on ...

  21. Quality Administrative Assistant

    Overview: Masy Systems reputation has been 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 growth. In addition, we offer competitive salaries and an excellent benefits package including a matching 401K, health, dental, short term, long term and life insurance.  We also offer holiday pay, sick pay, AAA membership, a ...

  22. Validation Project Leader

    Overview: Masy Systems reputation has been 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 growth. Â In addition, we offer competitive salaries and an excellent benefits package including a matching 401K, health, dental, short term, long term and life insurance. We also offer holiday pay, sick pay, AAA membership, a ...

  23. Clinical Data Manager III-32577

    Type of Role: This is a professional individual contributor role that provides oversight and accountability for multiple low, moderate, and high complexity trials. May be a member of multiple projects of low, moderate, high complexity or a leader of projects of low to moderate complexity. Impact of Decision-Making: This position makes recommendations and decisions that have an impact on specific trials or assignments. The GDM Specialist makes decisions for processes, timing, and structure for trials ...

  24. Quality Assistant

    Masy Systems reputation has been 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 growth. In addition, we offer competitive salaries and an excellent benefits package including a matching 401K, health, dental, short term, long term and life insurance.  We also offer holiday pay, sick pay, AAA membership, a clothing ...