Regulatory CMC Lead - Peptide & Oligo Therapeutics

A global biopharmaceutical client is seeking a Regulatory Affairs Senior/Consultant in Santa Fe, New Mexico to lead regulatory CMC strategy for peptide and oligonucleotide therapeutics. The ideal candidate will have 4-7 years of experience in peptide or oligonucleotide synthesis, mastery of regulatory submissions and compliance standards. This position requires excellent analytical skills, a solid educational background in chemistry or related fields, and the ability to work collaboratively with cross-functional teams. Candidates located in EST are preferred. #J-18808-Ljbffr