Job Description
📋 Description Design, execute experiments to develop scalable chemical synthesis processes Lead CDMO oversight and tech transfer for drug substances Plan DoE, QbD, and scale-up activities; impurity control Prepare plans, protocols, reports, and data summaries Collaborate with chemistry, analytical, QA, regulatory, and PM teams Travel up to 25% for CDMO oversight and project activities 🎯 Requirements PhD in organic chemistry with 7+ years in small-molecule work MS with 10+ years in synthetic organic chemistry Hands-on experience in synthetic organic chemistry and process development Experience scaling chemical processes at CDMOs or external sites Experience in synthesis, isolation, and crystallization of chiral molecules Knowledge of solid-form development; polymorph screening Strong knowledge of cGMP and ICH guidelines Experience applying DOE, QbD, and risk-based PD principles Ability to manage technical workstreams and deliver in fast-paced env 🎁 Benefits Medical, dental and vision plans Paid time off, holidays, and sick leave 401(k) with Erasca contributions and stock purchase option Annual bonus and equity grants at hire and ongoing Employee assistance program FSA/HSA and commuter benefits Pet insurance, life and disability coverage
