Regulatory CMC Lead - Peptide & Oligo Therapeutics

A leading global biopharmaceutical company is seeking a Regulatory Affairs Senior/Consultant in Juneau, Alaska. This role will focus on leading regulatory CMC strategy for peptide and oligonucleotide therapeutics. The ideal candidate will have 4-7 years of experience in regulatory submissions, expertise in HPLC and LC-MS, and a strong understanding of FDA and ICH regulations. This position is preferred for candidates in EST, but exceptional candidates from other U.S. time zones will be considered. #J-18808-Ljbffr