Join Stanford University as a Process Development Specialist, leading clinical materials biomanufacturing under cGMP guidelines. Your expertise will directly impact the development of innovative therapies for patients with incurable diseases.
Key Responsibilities
Lead human clinical materials biomanufacturing campaigns
Coordinate campaign activities with all functional teams
Train on biomanufacturing procedures
Plan and perform complex components of process development
Identify strategies for innovation in production systems
Develop manufacturing budget and ensure qualified raw materials
Prepare and submit abstracts for publication
Required Qualifications
Bachelor's degree in related scientific field
Two years of related experience or Master's degree
Strong biological scientific background
Working experience with aseptic cell culture
cGMP clean room experience
Strong computer skills
Ability to work under deadlines with minimal supervision
Excellent organizational skills
Benefits & Perks
Health insurancePTO401kComprehensive rewards package