Senior CMC Regulatory Lead for Global Submissions

A global pharmaceutical company seeks a Senior Regulatory Affairs CMC Specialist in Lombardy, Italy. The expert will manage submissions for regulatory authorities, requiring more than 7 years of CMC regulatory affairs experience. Responsibilities include writing technical sections, conducting gap analyses, and evaluating future regulatory impacts. Candidates must hold a degree in Chemistry, Pharmacy, or Biotechnology and have strong skills in regulatory guidelines and effective communication. Join a diverse environment committed to unlocking the potential of life and develop your career.
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