Regulatory CMC Lead - Peptide & Oligo Therapeutics

A global biopharmaceutical firm is seeking a Regulatory Affairs Senior/Consultant in Providence, RI, to lead regulatory strategy and submission activities for peptide and oligonucleotide therapeutics. The ideal candidate has a Bachelor's or Master's in chemistry or related fields and 4-7 years of relevant experience. Proficiency in analytical testing (HPLC, LC-MS, NMR) and a strong understanding of regulatory requirements are essential. Candidates located in EST are preferred but exceptional candidates in other US time zones will be considered. #J-18808-Ljbffr