Senior cmc regulatory specialist | global pharma

A multinational pharmaceutical company is seeking a CMC Senior Specialist in Bresso, Italy. The role involves managing regulatory submissions and ensuring compliance with c GMP and FDA standards. Candidates should have a degree in Life Sciences and over 5 years of Regulatory Affairs experience. Excellent English communication skills are essential. This full-time position offers a collaborative work environment focused on innovation and quality improvement. #J-18808-Ljbffr