CMC Regulatory Leader – Global Submissions (Biotech)

A pioneering biotechnology organisation in Italy is seeking a strategic leader to drive CMC regulatory activities and guide product development. The ideal candidate will have 8 to 10 years of experience in CMC regulatory affairs, proven skills in managing regulatory submissions, and strong leadership capabilities. Responsibilities include producing robust regulatory strategies, overseeing submissions, and collaborating with EMA and FDA. This position requires a Bachelor’s in a relevant scientific discipline, with a PhD being desirable.
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