Regulatory CMC Lead - Peptide & Oligo Therapeutics

A global biopharmaceutical organization is seeking a Regulatory Affairs Senior/Consultant to lead the regulatory CMC strategy for innovative peptide and oligonucleotide therapeutics. The ideal candidate will have 4-7 years of experience in peptide synthesis and a strong understanding of regulatory requirements for these products. This role involves close collaboration with R&D and quality teams to ensure compliance and accelerate product approvals. Preference for candidates in EST, consideration for others in the US and Canada. #J-18808-Ljbffr