Regulatory toxicology job offers

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  • (U971) Claims quality assurance officer

    PI Health Sciences Hyderabad, Andhra Pradesh

    ...comply with OECD GLP, ISO 9001:2015, and ISO 17025:2017 guidelines. Oversee quality systems and documentation associated with pharmacology, toxicology...
    4 days ago in Kitjob_in

    Report
  • [J-144] | Quality assurance manager

    PI Health Sciences Hyderabad, Andhra Pradesh

    ...comply with OECD GLP, ISO 9001:2015, and ISO 17025:2017 guidelines. Oversee quality systems and documentation associated with pharmacology, toxicology...
    2 days ago in Kitjob_in

    Report
  • PGO-653 - Qa lead (electrical)

    PI Health Sciences Hyderabad, Andhra Pradesh

    ...comply with OECD GLP, ISO 9001:2015, and ISO 17025:2017 guidelines. Oversee quality systems and documentation associated with pharmacology, toxicology...
    4 days ago in Kitjob_in

    Report
  • Qa electrical lead - [P064]

    PI Health Sciences Hyderabad, Andhra Pradesh

    ...comply with OECD GLP, ISO 9001:2015, and ISO 17025:2017 guidelines. Oversee quality systems and documentation associated with pharmacology, toxicology...
    4 days ago in Kitjob_in

    Report
  • [YX-98] | Senior Hazard Communication Specialist

    Dow Chemical Mumbai, Maharashtra

    ...Toxicology or related fields Experience 3-5 years of experience in product safety hazard communication including GHS classification requirements Your Skills...
    3 days ago in Kitjob_in

    Report
  • Specialist Medical Review Physician - YHO748

    ClinChoice Bangalore, Karnataka

    ...medical device, and consumer care innovators in the world. Established in 1995, we provide expertise in clinical operations, biometrics, regulatory...
    4 days ago in Kitjob_in

    Report
  • Global Hazard Communication Specialist | [E914]

    Exxon Mobil Bangalore, Karnataka

    ...Regulatory Advisors What you will do. Plan and execute SDS and related projects in coordination with business teams and stakeholders. Work within...
    3 days ago in Kitjob_in

    Report
  • JE34 Testreq - Italy Walkthrough

    new Charles River India, India

    ...helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory...
    1 day ago in Kitjob_in

    Report
  • BBRC - Deputy Research Director - Veterinary Science - JD897

    Syngene International Bangalore, Karnataka

    ...quality assurance, facilities, safety, and security teams. Provide veterinary input to study design, protocol development, and regulatory submissions.
    4 days ago in Kitjob_in

    Report
  • [HD108] - Bbrc - deputy research director - veterinary scien

    Syngene International Bangalore, Karnataka

    ...with research, quality assurance, facilities, safety, and security teams. Provide veterinary input to study design, protocol development, and regulatory
    4 days ago in Kitjob_in

    Report
  • Testreq - Italy Walkthrough E-674

    new Charles River India, India

    ...helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory...
    1 day ago in Kitjob_in

    Report
  • C621 - BBRC - Deputy Research Director - Veterinary Science

    Syngene International Bangalore, Karnataka

    ...quality assurance, facilities, safety, and security teams. Provide veterinary input to study design, protocol development, and regulatory submissions.
    2 days ago in Kitjob_in

    Report
  • [QJM-857] | BBRC - Deputy Research Director - Veterinary Sci

    Syngene International Bangalore, Karnataka

    ...quality assurance, facilities, safety, and security teams. Provide veterinary input to study design, protocol development, and regulatory submissions.
    5 days ago in Kitjob_in

    Report
  • BBRC - Deputy Research Director - Veterinary Science - (QY54

    Syngene International Bangalore, Karnataka

    ...quality assurance, facilities, safety, and security teams. Provide veterinary input to study design, protocol development, and regulatory submissions.
    2 days ago in Kitjob_in

    Report
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