
This senior leadership role within a well-funded clinical-stage biopharmaceutical organization focuses on driving small molecule drug substance development from late pre-clinical through commercialization. The position involves owning the technical strategy for process optimization, scale-up, and control, while managing external CDMO partnerships to ensure robust and compliant manufacturing. Key responsibilities include leading cross-functional teams to align CMC strategies with program timelines, authoring regulatory filings, and mitigating supply chain risks. The role offers the appeal of shaping an integrated CMC function in a lean, fast-moving environment with a mission to treat serious diseases. It is based in Boston, New Jersey, or remote with hybrid options, providing significant growth opportunities for experienced chemists to mentor teams and influence long-term pipeline success.



















