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document control in Boston

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  1. Study Director, Efficacy and Surgical Research Services at Toxikon Corporation

    Our mission is to provide quality pre-clinical research services to Pharmaceutical, Medical Device, and Biotech industries....

  2. Head, Drug Product Process Development at Moderna Therapeutics, Inc

    Interact with other R&D groups (clinical/PK/PD/Tox) to advance the science of RNA pharmaceutics. Experience formulating nucleic acids for in vivo delivery,...

  3. Director/Sr. Director, CMC Regulatory Affairs at Sage Therapeutics

    Bachelor of Science in a scientific discipline (Chemistry, Biochemistry, or related pharmaceutical science), advanced degree preferred....

  4. Associate Director, CMC Regulatory Affairs at Sage Therapeutics

    Bachelor of Science in a scientific discipline (Chemistry, Biochemistry, or related pharmaceutical science), advanced degree preferred....

  5. Research Associate at NantKwest

    BS in biological sciences and a minimum of 2-5 years related academic and/or industry experience, or MS with at least 1 year of work experience preferably in...

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    1. Remote Medical Writer - Oncology

      Hello, My name is Domenic and I represent The Fountain Group.  We are a national staffing firm and are currently seeking a Medical Writer - Oncology for a prominent client of ours.  This is a Remote based position. Details for the position are as follows: Job Description:Overview·         Assisting team to write Clinical and preclinical pharmacology sections of 3 documents.·         Briefing ...

    1. Principal Electrical Engineer at Soft Robotics, Inc.

      Participate in risk management and design control activities; Participate in design reviews and document development activities per established product...

    1. Document Control Coordinator

      Hello, You have been selected because we found your resume in our internal database.  We are currently trying to fill a ­­­­­ ­­­­Document Control Coordinator position in Waltham, MA  for a very prominent Fortune 150 client of ours. You can find the details below.  If you are a fit for this position and are interested in hearing more please email your resume to [email removed] and I will ...

    1. Director/Sr. Director, GMP Quality Assurance at Moderna Therapeutics, Inc

      Initiate and manage the Change Control and Document Control systems. Develop the processes and systems governed by cGXP regulations as well as compliance...

    1. Medical Writer II  (440296)

      OVERVIEW:Assisting team to write Clinical and preclinical pharmacology sections of 3 documents:• Briefing document for the Phase III trial in relapsed refractory multiple myeloma:• Writing of the supporting document and data clinical sections from May to mid-August 2016• PIP:• Writing of the supporting document and data for preclinical and clinical sections - from June to November 2016• ...

    1. Inside Sales Representative at STEMCELL Technologies Inc

      Hands on experience in an academic or biotech laboratory setting. Rigorously document communications and keep up to date the customer relationship management...

    1. Quality Manager – Contractor (9-10 Months)

      The Freudenberg Group, a global technology group with 40.000 employees in some 60 countries, develops leading-edge technologies, and excellent products, solutions and services for more than 30 market segments. Freudenberg Medical is a leading global manufacturer of components for medical devices, complex catheter systems for minimally-invasive surgery and total solutions for the biotech, ...

      No PartTime
      Contract Allowed
      No Internship
      No Freelance
      No Telecommute

    1. Alliance Manager at NantKwest

      3-5 years in the Biotech or Pharmaceutical industry is a must. Provide support to the team with various projects, including compilation and formatting of...

    1. Scientist I

      Hello, My name is Cory and I represent The Fountain Group.  We are a national staffing firm and are currently seeking a Scientist I for a prominent client of ours.  This position is located in Cambridge, MA. Details for the positions are as follows: Job Description:·         Work with the development team on sample processing and NAT assays/ technology platforms/ reagent development.·         ...

    1. Lead Computational Biologist / Data Scientist at Altran

      The team’s comprehensive engineering expertise and technical capabilities include Mechanical, Electrical, Process, Digital Instrumentation and Controls, Civil...

    1. Worth a look... Documentation Analyst

       How are you! My name is John Liotine, I’m a staffing specialist with The Fountain Group a local national staffing firm.  I am currently reaching out to you to fill a new Documentation Analyst position for a very prominent pharmaceutical client of ours. This position is located here in Canton, MA and I would like the opportunity to disclose the client and elaborate on this opportunity in more ...

    1. LAB CORE MT\GENERALIST. Per Diem at Brigham & Women's Faulkner Hospital

      They perform all required Quality Control procedures; Document results accurately and follow through appropriately on all outliers....

    1. Documentation Specialist

      Hello, My name is Scott and I represent The Fountain Group.  We are a national staffing firm and are currently seeking a Documentation Specialist for a prominent client of ours located in Northborough, MA. Details for the positions are as follows:Responsibilities:Maintain the controlled supply of cGMP documents originating within the companyReview documents to determine distribution ...

    1. LAB MT\BLOOD BANK Per diem at Brigham & Women's Faulkner Hospital

      Baccalaureate Degree in a Science required. They perform all required Quality Control procedures; Document results accurately and follow through appropriately...

    1. Sr. Statistician - Pharmaceutical Research & Manufacturing

      Seeking individual with experience at a pharmaceutical company as a statistician who can support diverse individual projects in multiple functional areas including Clinical Research, Manufacturing, and Post Marketing. Shall: *** Advise scientists and management in each of these settings on the best ways to collect, manage, analyze, decipher, and report results. *** Collect and normalize ...

      No PartTime
      No Contract
      No Internship
      No Freelance
      No Telecommute

    1. LAB MEDICAL TECHNOLOGIST\GENERALIST Fulltime at Brigham & Women's Faulkner Hospital

      They perform all required Quality Control procedures; Document results accurately and follow through appropriately on all outliers....

    1. Project Manager-Operations & Maintenance (O&M)

      PROJECT MANAGER – ENVIRONMENTAL OPERATIONS & MAINTENANCE (O&M) Job DescriptionProvide project management and technical support for Operations, Maintenance, and Monitoring project work with federal and private clients throughout New England and Mid-Atlantic regions. RequirementsExperience in the management of environmental Operations, Maintenance, and Monitoring projects for the Department of ...

    1. Senior Backend Developer (Python/Django) at Gecko Health Innovations (CareTRx)

      An ability to clearly document features and technical and infrastructure requirements. An ability to set up and use a version control system such as Git....

    1. Technical Writer

      We are seeking a talented Technical Writer to work on specific project assignments and provide deliverables as needed for a growing Life Science service provider. Responsibilities include:Ensure timely and efficient creation/review of Label & Pack documents: standard operating procedures, batch records, technical protocols and reports, etc. to maintain quality and readabilityWork with diverse ...

    1. Head of Global Sales - (Market Research Software) at Eli Global

      Pharma Database is a decision making tool (workflow tool) to be used by decision makers in Pharma and Biotech companies....

    1. Quality Control Testing Technician

      $25/HR Bachelors 2 years GMP Documentation QC Microbiology assay Experience with LIMS and electronic enterprise systems preferred. QCM assays and activities and experience reviewing GMP data and identifying aberrant data. environmental monitoring, -water data including bioburden, endotoxin, TOC and conductivity. -in process testing including bioburden, endotoxin, viral testing

      No PartTime
      No Contract
      No Internship
      No Freelance
      No Telecommute

    2. Controller

      Reporting to the Chief Financial Officer, the Controller will play a key role in building a dynamic financial organization. The Controller will be responsible for all internal financial reporting and SEC reporting, and will ensure that the financial organization delivers timely and accurate financials in accordance with GAAP. Also, the controller will ensure that internal controls are ...

    3. Quality Control Analyst

      Hello, My name is Shannon and I represent The Fountain Group. We are a national staffing firm and are currently seeking a Quality Control Analyst / Analytical Chemist for a prominent client of ours. This position is located near Princeton, NJ Details for the position are as follows: RESPONSIBILITIES QC Chemist background. Microbio techniques are a plus.Chromatography data systems (Empower) ...

    4. Medical Writer III (438893)

      OVERVIEW:Assisting team to write Clinical and preclinical pharmacology sections of 3 documentsBriefing document for the Phase III trial in relapsed refractory multiple myelomaWriting of the supporting document and data clinical sections from May to mid-August 2016PIPWriting of the supporting document and data for preclinical and clinical sections - from June to November 2016Briefing document ...

    5. Microbiologist

      $25/HR Microbiological experience GMP experience Bioburden Bachelor?s Degree in Microbiology, Biology or related scientific discipline. 1 - 2 years of experience in biopharmaceutical industry, preferably working in a quality control microbiology laboratory. Working knowledge of traditional microbiological techniques such as spread plating, pour plating, bioburden (membrane filtration) and ...

      No PartTime
      Contract Allowed
      No Internship
      No Freelance
      No Telecommute

      1. Financial Administrator at The First Church of Christ, Scientist

        Gives consistent attention to approval protocols outlined by the Treasurer’s Office in conformity with TMC/CSPS procurement practices and auditing controls....

      2. Metrology and Validation Services Lead at Toxikon Corporation

        Our mission is to provide quality pre-clinical research services to Pharmaceutical, Medical Device, and Biotech industries....

      3. Business Development Representative at Toxikon Corporation

        Minimum Qualifications Degree in life sciences, chemistry or biology Strong understanding of the testing and service industry, including regulatory agencies, as...

      4. Study Director, Ocular Services at Toxikon Corporation

        Our mission continues to focus on providing quality pre-clinical services, competitively priced, with on-time delivery for the Pharmaceutical, Medical Device...

      5. Associate Director, Medical Writing at Biogen

        Provides guidance to MW staff, ensuring that quality and timing of documents meet program, SMT, Development Sciences goals and objectives....