Regulatory CMC Lead - Peptide & Oligo Therapeutics

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