Senior Principal Medical Writer — Global Regulatory Submissions Lead

L6

milliporeBillerica, MAyesterday
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.
Apply now
Apply now

Level

LeadL6

Location

Billerica, MA

Occupation

Regulatory Affairs Managers

Industry

Biological Product (except Diagnostic) Manufacturing

Posted

yesterday

To get sharper similar jobs, create your profile using the link below.

Create profile