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document control in Boston

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  1. 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,...

  2. Associate Director, CMC Regulatory Affairs at Sage Therapeutics

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

  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. Senior Manager, Clinical Operations and Development at Sage Therapeutics

    Roles and Responsibilities Lead the evaluation, selection and management of Contract Research Organizations (CROs) and other external vendors to ensure...

  5. Director of cGMP Manufacturing at PixarBio Corporation

    Statistical process control (SPC). Investigations, deviations, OOSs, and change control. Communications will be both written documents, and in formal and...

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    1. Validation Specialist III (Support LIMS Project)

      Primary Responsibilities:The Validation / Tech Writer will need to be dedicated 100% to LWLIMS associated project/activitiesWorking with Sanofi ITS Project Leader (IPL) and Sanofi Validation Expert (VEX) to develop validation deliverables as per agreed validation and test strategyValidation deliverables: Validation Plan (contribute), Test Strategy/Cases (contribute), Risk Assessment ...

    1. Senior C++ Software Developer at iPROMOTEu

      BS in Computer Science or equivalent work experience. Drive comprehensive project and product design document requirements, as well as create functional and...

    1. Quality Control Analyst III

      Quality Control Chemistry is responsible for testing intermediate and final product  samples to demonstrate that all products  meet all standards required  for cGMP operations. Various techniques are utilized  in Quality Control including HPLC, GC, Gel Electrophoresis  and multiple types of spectrophotometry. Additional functions  include, stability testing, assay transfers and the ...

    1. ERP HR Senior Consultant at isg

      Document business requirements and processes. Bachelor of Arts or Science degree in a technical or scientific field desirable....

    1. Senior Statistician

      Job Number: 3022852GENERAL SUMMARY/ OVERVIEW STATEMENT: This position will work with the NIH funded Accelerating Medicines Partnership, which brings high-level government, industry and non-profit foundation partners together to identify and validate the most promising biological targets for therapeutics. This network will focus specifically on Rheumatoid Arthritis and Systemic Lupus ...

    1. LabWare Validation/Training at LabAnswer

      Opportunities to work across a variety of laboratory environments (analytical testing, biotech, clinical trials, forensics, medical device, pharmaceutical,...

    1. Research Associate

      The ideal candidate must possess a sound knowledge of the chemical principles and concepts of preparing buffers and tissue culture media and aseptic techniques.Use established procedures (SOP’s) and based on experience, training, and education, interpret complex methodologies (Protocols) provided by scientists.Utilize good laboratory practices while applying technical expertise to formulate ...

    1. Back of House Staff - No weekends! at Sodexo @ Shire

      Come join Sodexo at an exciting biotech account in Lexington, MA! Enjoy a creative, inspiring Catering & Retail environment while exceeding high-end customer...

    1. Validation Specialist III - QC Microbiology

      We're hiring!Azzur Group is a GxP compliance and consulting organization dedicated to providing high quality, expertly backed, assistance that drives life science companies to success. We are seeking highly motivated and talented individuals to join our incredible team of skilled problem solvers. Qualified candidates must have a desire to learn, apply, engage, and adapt in the ever- changing ...

    1. Front of House Staff - No weekends! at Sodexo @ Shire

      Come join Sodexo at an exciting biotech account in Lexington, MA! Enjoy a creative, inspiring Catering & Retail environment while exceeding high-end customer...

    1. Quality Control Analyst III

      We're hiring!Azzur Group is a GxP compliance and consulting organization dedicated to providing high quality, expertly backed, assistance that drives life science companies to success. We are seeking highly motivated and talented individuals to join our incredible team of skilled problem solvers. Qualified candidates must have a desire to learn, apply, engage, and adapt in the ever- changing ...

    1. Protocol Integrator - Part Time at JoVE

      Preparing science manuscripts in MS Word and removing formatting errors. Working with character entities, especially science related Greek characters, to ensure...

    1. Serialization Support Engineer

      Part time (~18 hrs a week) Support serialization project for biological product supply chain by managing and executing various aspects of the project including: Computerized systems validation Process validation of packaging and labeling operations Generation of various documents related to implementation (SOPs, URS, Risk Assessment, Validation protocols/reports) Own change controls, ...

    1. Software Engineer at Rudolph Technologies, Inc

      Design, document, implement, test and maintain equipment control software for Rudolph Technologies' semiconductor equipment front end modules (EFEM)....

    1. Multiplex Assay Development Scientist - Preclinical Research

      Growing company in the largest biotech hub on the East Coast seeks experienced Scientist with several years of direct immunoassay development and validation experience who can: *** Design, develop, test, and validate assays. *** Analyze, interpret and document results. *** Provide technical and theoretical support. *** Identify, research, and promote new methods and technologies. ** ...

      No PartTime
      No Contract
      No Internship
      No Freelance
      No Telecommute

    1. STARLIMS SME/Developer and Configuration Specialist at LabAnswer

      Opportunities to work across a variety of laboratory environments (analytical testing, biotech, clinical trials, forensics, medical device, pharmaceutical,...

    1. Electrical Engineer with Medical Device Experience

      Biotech company seeks a principal level Electrical Engineer to design and develop complex electro-mechanical medical devices. The Electrical Engineer will work in a project leadership role.Responsibilities include:Using requirements document: design, develop, model and analyze system architecture including circuit boards, embedded micro controllers, motion control, mixed signal circuit ...

    1. Stability Coordinator at Grafton Engineering Services

      Bachelor's Degree in chemistry or closely related physical science is required. Utilize all elements of the quality system to identify, classify and control the...

    1. Quality Control Analyst II

      We're hiring!Azzur Group is a GxP compliance and consulting organization dedicated to providing high quality, expertly backed, assistance that drives life science companies to success. We are seeking highly motivated and talented individuals to join our incredible team of skilled problem solvers. Qualified candidates must have a desire to learn, apply, engage, and adapt in the ever- changing ...

    1. In Mkt OTE Proj Coord, AL/FL at FL

      Lea rn in g an d development solution sets based on a broad spectrum of potential interventions. M easu re s pe r formance trends and develops new programs or...

    1. Senior Network Engineer

      Job Title:Senior Network Engineer - Pharmaceuticals 4557186Location :Cambridge - MADuration:12+ Months with possible extensionDuties:The ideal Engineer with have experience with the following: - 8 Years IT Experience and Minimum 5 years direct Network Experience in a Fast Paced Environment- The Candidate must have Expertise with Routing and Switching in Global Enterprise environment- Expert ...

    2. CMC Manager

       Hello, My name is Carlane and I represent The Fountain Group. We are a national staffing firm and are currently seeking a CMC Manager position  for a prominent client of ours.  This position is located in Allston, MA Details for he position are as follows: Job DescriptionPerform general Regulatory Affairs Chemistry Manufacturing and Controls (CMC) work including dossier and document ...

    3. Quality Control Analyst

      Hello, My name is Mark and I represent The Fountain Group.  We are a national staffing firm and are currently seeking a Quality Control Analyst for a prominent client of ours.  This position is located in Northborough, MA. Details for the positions are as follows:Job Description·        Support validation of analytical methods and lab equipment·        Author validation protocols / reports, ...

    4. Quality Control Analyst III

      We're hiring!Azzur Group is a GxP compliance and consulting organization dedicated to providing high quality, expertly backed, assistance that drives life science companies to success. We are seeking highly motivated and talented individuals to join our incredible team of skilled problem solvers. Qualified candidates must have a desire to learn, apply, engage, and adapt in the ever- changing ...

    5. Senior Project Document Control Coordinator (SharePoint)

      Project Documentation / Knowledge Management Expert (40% of time)Responsible for developing and implementing of business processes (Procedures / Training Guidelines / Tools / Systems)  to support the Project Engineering & Management organization efficiently manage and delivery projects for project candidate stage to closeout and business benefits realization, working both internally and ...

    6. Research Associate II - Immunofluorescence

      The primary responsibility for this position will be performing and documenting western blot and immunohistochemistry quality control experiments on antibody products and detection reagents according to established SOP's and relevant regulations. The candidate will support the evaluation and development of new products in the pipeline, especially in support of the release of various ...

    7. Documentation Specialist II

      We're hiring!Azzur Group is a GxP compliance and consulting organization dedicated to providing high quality, expertly backed, assistance that drives life science companies to success. We are seeking highly motivated and talented individuals to join our incredible team of skilled problem solvers. Qualified candidates must have a desire to learn, apply, engage, and adapt in the ever- changing ...

    8. Analytical Coordinator/Senior Analytic Coordinator

      This is a position that requires self-motivation, strong organization and flexibility to meet the needs of the company. This opportunity requires robust information technology skills, fluency in Microsoft Office (Word, Access, PowerPoint, and Excel), SharePoint and MS Project. The position requires careful and thoughtful problem solving skills, as well as diplomacy.Description:As a key member ...

    9. 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• ...

    10. 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. Sr Proposal Specialist- Contract at weinberg and associates, Inc.

        Manage R & D efforts from initial Quad Chart, BAA, White Paper and RFP analysis through final submission. Strong Technical Writing capabilities in support of...

      2. Manufacturing Operations Specialist at B&A

        Experience in the biotech or pharmaceutical industry:. Bachelor’s Degree (Life Science, Quality, Engineering, Business Administration or a related field)....

      3. Salesforce Administrator at EXPERIAN

        Support change control and testing processes for modifications to data delivery system changes. Design, code, test, and document all new or modified CRM systems...

      4. Sr. Program Consultant at Agfa-Gevaert Group

        Bachelor’s Degree in Engineering, MIS, Computer Science, Healthcare or related field. Insure all Agfa Healthcare quality documents required for the project’s...

      5. Director/Sr. Director, Clinical Research, TTR Amyloidosis Program at Alnylam

        Science of RNAi. Alnylam is a medium-size biotech dedicated to the. RNAi is a powerful technology enabling the targeting of....