Regulatory CMC Lead - Peptide & Oligo Therapeutics

A leading biopharmaceutical consultancy 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 synthesis, purification, and analytical testing of these products. Responsibilities include driving global regulatory strategy and submission activities while collaborating with R&D teams. Candidates located in EST or exceptional candidates from other US time zones are preferred. #J-18808-Ljbffr