Hybrid Pharmacovigilance & Regulatory Affairs Officer (Benelux)

A pharmaceutical company in Almere, Netherlands is seeking a Pharmacovigilance Regulatory Affairs Officer to support key safety and registration processes within a regulated environment. The ideal candidate must be fluent in Dutch and English and have 1-3 years of experience in pharmacovigilance or regulatory affairs. Responsibilities include recording safety information, regulatory submissions, and translation of product information. This role offers a chance to contribute to the safe availability of medicines with a possible work-from-home option.br#J-18808-Ljbffr