
Regulatory Affairs Associate (on-site Marburg)
Parexel seeks a Regulatory Affairs Associate to manage regulatory documentation (CPPs, GMP, CMC), coordinate legalisations/translations and vendor relationships, handle registration samples and fee payments, and maintain paper and physical archiving for inspection readiness. Role is full-time, office-based in Marburg and requires a bachelor's degree in a scientific discipline, knowledge of international pharmaceutical regulations and GMP, and strong English skills.












