Regulatory CMC Lead - Peptide & Oligo Therapeutics

A global biopharmaceutical firm is seeking a Regulatory Affairs Senior/Consultant to lead the regulatory CMC strategy for peptide and oligonucleotide therapeutics. You will be responsible for driving global regulatory strategy, partnering with R&D and quality teams, and ensuring compliance with international standards. The ideal candidate should have a strong background in analytical chemistry with 4-7 years of experience in peptide or oligonucleotide synthesis and familiarity with regulatory requirements.

This role is based in Jackson, Mississippi, with preference for candidates in EST.
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