About 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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