Regulatory CMC Lead - Peptide & Oligo Therapeutics

A global biopharmaceutical company is seeking a Regulatory Affairs Senior/Consultant in Denver, Colorado. The role involves leading regulatory CMC strategy for peptide and oligonucleotide therapeutics, ensuring compliance with FDA/ICH regulations. Candidates should have a background in chemistry with 4-7 years of experience in synthesis and analytical testing. This opportunity emphasizes collaboration across functions and a solid understanding of regulatory requirements. Candidates from other US time zones may also be considered. #J-18808-Ljbffr