Regulatory CMC Lead - Peptide & Oligo Therapeutics

A global biopharmaceutical client is seeking a Regulatory Affairs Senior/Consultant to lead regulatory CMC strategy for peptide and oligonucleotide therapeutics. The ideal candidate will have 4-7 years of experience in peptide synthesis, a strong understanding of regulatory requirements, and expertise in analytical testing. This role focuses on ensuring compliance and accelerating product approvals while collaborating across various teams. Candidates in EST are preferred, with flexibility for exceptional candidates in other US time zones.
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