$115,000 – $145,000
Listed on Beckman Coulter’s own careers site. You apply with them directly — we never stand between you and the employer.
What this role is
This role leads manufacturing process improvement projects for diagnostic consumables at a major medical device company, requiring deep expertise in design controls, GMP compliance, and cross-functional project execution in a medical device environment. It suits experienced scientists or engineers who have navigated regulated product development and enjoy driving operational excellence across complex manufacturing systems.
Our summary, not Beckman Coulter’s wording. The full posting is on their site.
Skills this role names
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What they ask for
Required
- Bachelor's degree in Biology or related technical field with 9+ years experience, or Master's degree with 7+ years, or PhD with 4+ years
- Design control processes expertise including design change and risk management
- Project management experience
- GMP environment experience
Nice to have
- Working knowledge of statistics
- Cell culture techniques