Associate Director/Director Pharmaceutical Development

📋 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