Regulatory CMC Lead - Peptide & Oligo Therapeutics

A global biopharmaceutical client seeks a highly experienced Regulatory Affairs Senior/Consultant in Tallahassee, Florida. The role focuses on driving global regulatory strategy and submission activities for peptide and oligonucleotide therapeutics. The ideal candidate holds a Bachelor's or Master's degree in a scientific discipline, has 4-7 years of relevant experience, and is proficient in analytical testing methods. Strong regulatory document preparation skills and a solid understanding of FDA/ICH regulations are essential. Remote work is possible for exceptional candidates. #J-18808-Ljbffr