eBay Classifieds » All ads » Jobs » Biotech, R&D, & science » 

document control in Boston

(1-14 of 14 ads)
View as:
Categories
  1. Senior C/C++ Software Developer at ProTom International

    Support, maintain and document software functionality. Experience with designing, documenting, implementing and testing control systems....

  2. Senior CFD development engineer at ADINA R & D

    ADINA R & D is seeking a Senior CFD Development Engineer. If you are interested in working with us at ADINA R & D, please respond to this ad to the attention of...

  3. Cook at Brightview Senior Living, LLC

    At Brightview Senior Living, we believe in creating Vibrant Living experiences for our residents by embracing a genuine commitment to STARS – our core values of...

  4. Senior Network Security Engineer at Federal Home Loan Bank of Boston

    Ability to document technical designs and concepts. Bachelor’s degree in Computer Science or related field, or comparable professional experience....

  5. Director, Integrated Program Management-Global Medicines Development at Vertex Pharmaceuticals

    For four years in a row, Science magazine has named Vertex one of its Top Employers in the life sciences. Bachelor’s degree in Life Sciences or a relevant field...

    Ads
    1. Senior Manager, GLP QA

      The Senior Quality Manager of Quality Assurance is responsible for conducting and monitoring internal and external GLP activities in support of the audit program. This role is responsible for assisting with the strategic alignment of projects and activities and refining those projects and/or activities proactively. RESPONSIBILITIES:· Demonstrates strong expertise related to understanding the ...

    1. Senior Director, Regulatory Labeling at Vertex Pharmaceuticals

      For four years in a row, Science magazine has named Vertex one of its Top Employers in the life sciences....

    1. Quality Manager 223.16CM

      :: If you meet the qualifications listed below and would like more information contact Crystal at 815-756-1221 Attach resume when responding to this posting :: This Quality Manager will have overall responsibility for the quality management system at their facility. Will maintain oversight for the industry required certifications for the site, as well as supplier quality and customer ...

      No PartTime
      No Contract
      No Internship
      No Freelance
      No Telecommute

    1. Medical Director, Oncology at Vertex Pharmaceuticals

      For four years in a row, Science magazine has named Vertex one of its Top Employers in the life sciences. Medical Director, Oncology....

    1. Automation Validation Engineer

      PSC Biotech is one of the world’s largest consulting firms in the Biotechnology/Pharmaceutical and Life Science industry. We have been around for more than 19 years and continue to grow worldwide.Presently, we are looking for a Validation Engineer with a strong background on the Computer Systems Validation of the Process Control System (PCS) and Building Management System (BMS) in the ...

    1. Senior Lab Instrument Engineer at Vertex Pharmaceuticals

      For four years in a row, Science magazine has named Vertex one of its Top Employers in the life sciences. The Senior Instrument Engineer will report to the...

    1. Change Control (Document) Analyst

      Responsible for overall coordination of controlled documentation (electronic and hard copies) for one of our clients. Performs the Document Control function within the company’s electronic and manual control processes. Coordinates Change Control Board meetings.  Responsible for coordinating document and engineering change orders (DCOs and ECOs), facilitates review, approval, and retention 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. Clinical Data Manager

      Summary of Position:  The Clinical Data Manager is responsible for the hands-on oversight of data management activities for all Corrona clinical, non-interventional registries and is part of the Quality and Regulatory Compliance (QRC) team. This position manages end-to-end delivery of data management services for all registries and collaborates with internal clinical leads, pharmacovigilance, ...

    1. Program Manager (Pharma or Biotech) at Solid GT

      Pharma and Biotech PROGRAM MANAGER. Experience Managing Projects and working with Scientific teams in Pharma and Biotech fields....

    1. IT Quality Analyst

      Description:Drive process improvements related to:• Changes to IT applications and related processes, particularly in the areas change control records, segregation of duties (SOD) between development and production environments, utilization of system change logs to track such changes to ensure they are authorized and properly reflected in the change management system.• IT SOX Program ...

    1. Downstream Process Manager at Solid GT

      Knowledge of quality control systems and CMC regulatory filings is highly desirable. The DSP Manager will support the downstream process development and...

    1. Systems Engineer Manager - Medical Devices

      Target salary is $128k with a 20% bonus targetPosition Summary:The Systems Engineering Manager will be hands-on and responsible for leading a small group of engineers with the key focus of guiding the systems engineering effort of complex systems throughout the complete product development process.The individual will apply knowledge of multidisciplinary processes and systems engineering ...

    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,...

    1. Project Operations Coordinator (Medical Publications Ops)

      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: Project Operations CoordinatorJob ID: 7989Industry: Biotech/PharmaceuticalLocation: Cambridge, MADuration: 7 Month ContractPay Rate Range: Depends on Experience (W2, no ...

    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 Director - Oncology Drug Clinical Development - Medford, MA

      Seeking Medical Doctor with pharmaceutical or biotech industry experience progressing drugs from early Phase I through Phase III resulting in successful NDA submission. *** Lead the Clinical Development team during Phase I-III studies leading creation of clinical study development plans. *** Oversee Adverse Event and Serious Adverse Event reporting to safety monitoring and regulatory ...

      No PartTime
      No Contract
      No Internship
      No Freelance
      No Telecommute

    1. Head, Strategy & Planning, Global Clinical Operations at EMD

      Global Strategic Plan, Target Product Profile, Target Product Plan, and other portfolio development documents)....

    1. Director - Clinical Development - Oncology Therapeutics - Waltham, MA

      Seeking Medical Doctor or Doctor of Osteopathic Medicine with expertise in Oncology who can lead a Clinical Development team focused on cancer therapeutics. Exciting growth opportunity within a large pharmaceutical company with a strong pipeline of successful drug projects. Leadership opportunity with plenty of interactions with upper executive board and chance to advance higher in ...

      No PartTime
      No Contract
      No Internship
      No Freelance
      No Telecommute

    1. Associate Director, Outsourcing Programming & Analytics at EMD

      Design, develop, document and provide quality assurance of new systems. Supports the maintenance and further evolution of electronic document management and...

    1. 99838 - R&D Process Document Management

      Job Description:This position supports the Research and Development (R&D) organization and is responsible for assisting in the maintenance, management and retirement of controlled process documents, including the tracking of deviations related to such processes. ESSENTIAL JOB FUNCTIONS • Ability to navigate and work within an electronic document management system (EDMS). • Maintain and ...

    2. 99838 - Process Control Document Management

      6+ Month contractPharmaceutical - Cambridge, MA This position supports the Research and Development (R&D) organization and is responsible for assisting in the maintenance, management and retirement of controlled process documents, including the tracking of deviations related to such processes. ESSENTIAL JOB FUNCTIONS • Ability to navigate and work within an electronic document management ...

    3. CAD Drafter/Designer III

      Job Code: CAD Drafter/Designer IIIReq# 4563049Job Title: CAD Drafter/Designer IIIDuties: Provides CAD drafting support operations to support facilities documentation, engineering design, and/or project planning functions. Operates CAD drafting equipment to produce and print process and instrumentation diagrams, floor plans, and electrical, mechanical, equipment and piping drawings. Data ...

    4. Documentation Associate - Training and Compliance

      Hello, My name is Domenic and I represent The Fountain Group.  We are a national staffing firm and are currently seeking a Document Control Associate/Training & Compliance Specialist I for a prominent client of ours.  This position is located in Lexington, MA. Details for the position are as follows: Job Description: Manager Notes:Documentation training and compliance in Pharmaceutical ...

      1. Senior Manager/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...

      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. Account Manager - Recruiting Services at Commonwealth Sciences

        Commonwealth Sciences, Inc. Is a Boston area recruiting firm currently specializing in life sciences, engineering and green technologies....

      5. New England Account Manager at Proteintech Group Inc.

        Must have a Life Sciences qualification (minimum B.Sc). As a rapidly expanding biotech company, you will participate in our worldwide growth and be responsible...