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Job description
Kennedy Bond, a clinical-stage biotechnology company, seeks an experienced CMC professional to lead oral drug-product formulation and development across its peptide portfolio. This role hands-on ownership of external programs and will manage CDMO partners through formulation, scale-up, tech transfer, and GMP manufacturing.
Ideal candidates have 12+ years in pharma/biotech, strong oral solid-dose expertise, peptide formulation experience, and history of CDMO oversight.
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Worksite address
san francisco, CA, 94199, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.