Regulatory CMC Lead - Peptide & Oligo Therapeutics

A global biopharmaceutical client seeks a highly experienced Regulatory Affairs Senior/Consultant in Indianapolis, Indiana. The role involves leading regulatory CMC strategy and submission activities for peptide and oligonucleotide therapeutics. Candidates should have a strong background in analytical chemistry (HPLC, LC-MS, NMR) and 4-7 years of relevant experience. A Bachelor's or Master's degree in a related field is required, while a Ph.D. is preferred. Competitive consideration will also be given to candidates across US time zones. #J-18808-Ljbffr