Regulatory CMC Lead - Peptide & Oligo Therapeutics

A leading global biopharmaceutical company is seeking an experienced Regulatory Affairs Senior/Consultant in Cheyenne, Wyoming. The successful candidate will lead regulatory CMC strategy for innovative peptide and oligonucleotide therapeutics, collaborating closely with R&D and compliance teams. Requirements include a relevant degree and 4-7 years’ experience in synthesis and regulatory processes. Competitive compensation and consideration for exceptional candidates in various US time zones offered. #J-18808-Ljbffr