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 process validation projects for pharmaceutical manufacturing at a CDMO, ensuring new therapeutics meet regulatory standards through design, execution, and analysis work. It suits engineers with biologics manufacturing experience who want to apply technical expertise to life-saving medicines in a regulated environment.
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 or Master's degree in engineering
- 2+ years of experience
- Experience leading process validation across all three stages in biologics or small/large molecule manufacturing
- Knowledge of global regulatory requirements and cGMP regulations
- Proficiency in technical writing, deviation investigations, root cause analysis, and risk assessments
Nice to have
- CDMO environment experience
- Sterile fill-finish process and equipment qualifications experience