• Manager, Global Pharmacovigilance Quality

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …collaborate with other GxP quality representatives and act as QA point person for US and EU Medical Affairs programs, eg interact with stakeholders for prompt ... end proactive quality support across programs ensuring GCP, GPV, GDP , and adherence to safety requirements are adequately considered...representatives and act as the QA point person for US and EU Medical Affairs programs, eg… more
    Daiichi Sankyo Inc. (06/02/24)
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  • Senior Director, Head of PV Quality ( US

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …the CSPV and key business function and collaborate with RD and Medical Affairs Quality to provide clinical safety QA advise wherever necessary. Ensure requirements ... with internal QA stakeholders such as GMP QA, specifically for GDP requirements, risk-based assessment for Distributors, co-partners, and affiliates. Liaise with… more
    Daiichi Sankyo Inc. (06/02/24)
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  • Senior Staff Biocompatibility Specialist - Hybrid

    Stryker (Mahwah, NJ)
    …Here are 10 reasons to join our Regulatory Affairs /Quality Assurance team: https://www.strykercareersblog.com/post/10-reasons-to-join-strykers- regulatory ... to align to best practices, benchmarking against industry leads and regulatory requirements. + Lead root cause analysis, problem solving, out-of-specification… more
    Stryker (05/23/24)
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  • Senior Biocompatibility Specialist - Hybrid

    Stryker (Mahwah, NJ)
    …Here are 10 reasons to join our Regulatory Affairs /Quality Assurance team: https://www.strykercareersblog.com/post/10-reasons-to-join-strykers- regulatory ... Preferred: + MS in Chemistry/Biochemistry/Toxicology or related discipline + Knowledge of GDP , ANSI, AAMI, ISO, FDA, and USP guidelines related to biocompatibility… more
    Stryker (05/23/24)
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