Job Description
📋 Description Provide strategic pharmaceutical development guidance as the CMC lead to cross functional project Develop robust formulations and manufacturing processes for QED products. Review development and manufacturing programs at CROs/external vendors for compliance and timelines. Manage drug forecasts and related transactions. Integrate with CMC team; provide regulatory submission support (IB, IND, NDA). 🎯 Requirements PhD or advanced degree in Chemistry or Pharmacy with 7+ years in formulation development and Expertise in formulation; strong PK/PD, ADME concepts; regulatory docs/authorship. Experience in managing Clinical Supply, Formulation development and CRO/CMO manufacturing. Thorough knowledge of US/EU CMC regulatory requirements. 🎁 Benefits Market-leading compensation; $223,000 – $239,000 USD 100% employer-paid medical, dental, and vision premiums; plus ESPP 401(k) with employer match; comprehensive commuter benefits Flexible PTO; in-office benefits; paid holidays; hybrid work options
