Senior CMC Regulatory Specialist | Global Pharma

14 ott - Milano
Zambon

A multinational pharmaceutical company is seeking a CMC Senior Specialist in Bresso, Italy. The role involves managing regulatory submissions and ensuring compliance with cGMP 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.

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