Regulatory CMC Lead - Peptide & Oligo Therapeutics

A leading biopharmaceutical company is looking for a highly experienced Regulatory Affairs Senior/Consultant in Salt Lake City, Utah. In this role, you will lead global regulatory strategy for peptide and oligonucleotide therapeutics, ensuring compliance and driving successful product approvals. Ideal candidates will have 4-7 years of experience in regulatory affairs, a strong educational background in chemistry, and expertise in analytical methods. This position offers opportunities to work across teams in a dynamic environment. #J-18808-Ljbffr