Regulatory CMC Lead - Peptide & Oligo Therapeutics

A global biopharmaceutical firm seeks a Regulatory Affairs Senior/Consultant to lead regulatory strategy and submission activities for peptide and oligonucleotide therapeutics. The ideal candidate will have 4+ years of experience in synthesis and regulatory requirements, a strong educational background in chemistry or related fields, and proficiency in analytical testing methods. This role involves close collaboration with various teams to ensure compliance with international standards for successful product approvals. Preference given to candidates in EST, but others in the US and Canada may apply. #J-18808-Ljbffr