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Job description
Role: Oversee technical transfer, qualification, and lifecycle management for commercial drug products, focusing on specialized solid-dose operations including spray-dried dispersions, granulation, and coating.
Responsibilities
manage CMO site performance, assess manufacturing capability, execute process transfers, qualification, validation, and ongoing process verification. Support post-approval changes, process improvements, deviations, investigations, and compliance readiness through cross-functional collaboration with Quality, Supply Chain, and Regulatory teams.
Requirements
Bachelor’s or Master’s in Pharmaceutical Sciences, Chemical or Biochemical Engineering, with 6–8 years of pharma/biotech industry experience. Proven expertise in commercial drug manufacturing, process validation, equipment qualification, and cGMP compliance. Preferred skills include experience managing external CMOs, strong technical oversight, and risk assessment capabilities.
HighValue
focus on solid oral dose manufacturing, particle-engineering (SDD), process validation, lifecycle management, cGMP compliance, and cross-functional collaboration.
WorkSetup
on-site at Redwood City, CA with willingness to travel.
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Worksite address
california, MO, 65018, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.