Regulatory CMC Lead - Peptide & Oligo Therapeutics

A global biopharmaceutical company seeks a highly experienced Regulatory Affairs Senior/Consultant to lead regulatory CMC strategies for innovative peptide and oligonucleotide therapeutics. Candidates should have a Bachelor’s or Master’s in relevant fields, with 4-7 years in peptide/oligonucleotide synthesis and regulatory submission activities. Strong analytical skills and understanding of FDA/ICH/USP standards are required. This role is located in Carson City, Nevada, with a preference for candidates in the EST time zone. #J-18808-Ljbffr