Senior Principal Medical Writer — Global Regulatory Submissions Lead
milliporeBillerica, MA
Senior Principal Medical Writer — Global Regulatory Submissions Lead
milliporeBillerica, MA
yesterday
Occupations
Regulatory Affairs ManagersRegulatory Affairs SpecialistsMedical Scientists, Except EpidemiologistsIndustries
Biological Product (except Diagnostic) ManufacturingResearch and Development in Biotechnology (except Nanobiotechnology)Electromedical and Electrotherapeutic Apparatus ManufacturingAbout the role
Millipore Corporation in Billerica, MA is seeking a Senior Principal Medical Writer to lead end-to-end regulatory documentation development, ensuring scientific rigor, regulatory compliance, and timely delivery across global markets.
You will mentor writers, define document strategy, oversee clinical sections of regulatory dossiers, collaborate with clinical, regulatory affairs, pharmacovigilance, and statistics, and drive consistency and quality across programs.
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JOB OVERVIEW
Experience level
Lead
Location
Billerica, MA
Occupation
Regulatory Affairs Managers
Industry
Biological Product (except Diagnostic) Manufacturing
Posted
yesterday
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