Regulatory CMC Lead - Peptide & Oligo Therapeutics

A global biopharmaceutical company is seeking a highly experienced Regulatory Affairs Senior/Consultant to lead regulatory CMC strategy for innovative peptide and oligonucleotide therapeutics. In this role, you will drive global regulatory strategies and submission activities while collaborating closely with R&D, CMC, clinical, and quality teams to ensure compliance and accelerate product approvals. Ideal candidates will have at least 4-7 years of relevant experience and strong capabilities in analytical testing and regulatory processes. Preferably located in EST but open to exceptional candidates from other US time zones. #J-18808-Ljbffr