Regulatory CMC Lead - Peptide & Oligo Therapeutics

A leading global biopharmaceutical company is seeking a Regulatory Affairs Senior/Consultant to drive regulatory CMC strategy for peptide and oligonucleotide therapeutics. The ideal candidate has 4-7 years of experience in synthesis and analytical testing, along with a strong understanding of regulatory requirements. This role requires collaboration with cross-functional teams to ensure compliance and accelerate product approvals. Candidates in EST are preferred, but exceptional candidates from other US time zones will be considered. #J-18808-Ljbffr