CMC Regulatory Affairs Lead — Global Submissions
Job in
4800, Breda, North Brabant, Netherlands
Listed on 2026-08-04
Listing for:
Amgen SA
Full Time
position Listed on 2026-08-04
Job specializations:
-
Pharmaceutical
Job Description & How to Apply Below
Amgen Breda seeks a Regulatory Affairs Manager to translate CMC regulatory requirements into practical plans. You will manage site changes, coordinate with global authorities, and lead regulatory submissions for new marketing applications and post-market changes.
The role requires strong leadership, English and Dutch communication, and experience in QA/RA within pharma/biotech. Enjoy a dynamic, global team environment with extensive collaboration across sites.
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