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.br#J-*****-Ljbffr
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