$100,000 – $130,000
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 validation projects for pharmaceutical and biotechnology manufacturing, designing and executing strategies to ensure new medicines meet regulatory standards before commercialization. It suits experienced engineers who want to combine technical expertise with mentorship in a mission-driven environment focused on life-saving therapies.
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
- 5+ years of experience in process validation
- Experience leading process development and validation across all three stages in biologics or small/large molecule manufacturing
- Knowledge of global regulatory requirements and cGMP regulations
- Proficiency in technical writing including deviation investigations, root cause analysis, and risk assessments
- 15% travel to sites for validation projects, inspections, audits, and client visits
Nice to have
- Experience with packaging and shipping validation of final product container closure configurations
- Prior experience in a CDMO environment or client-facing roles