Regulatory CMC Lead - Peptide & Oligo Therapeutics

A global biopharmaceutical company is seeking a Regulatory Affairs Senior/Consultant to lead regulatory CMC strategy for peptide and oligonucleotide therapeutics. The role requires a Bachelor's or Master’s degree in a scientific field, with 4-7 years of experience in peptide synthesis and strong regulatory understanding. You will collaborate across functions to ensure compliance and accelerate product approvals. Preferred candidates are located in EST but exceptional applicants from other US time zones will be considered.
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