Staff Validation Engineer, Process and Cleaning
Thermo Fisher Scientific · Greenville, NC
The apply link worked recently (not employer-confirmed).
Role summary
Staff Validation Engineer supporting process and cleaning validation activities for sterile manufacturing at Thermo Fisher Scientific. Ensures manufacturing processes and cleaning procedures meet regulatory compliance and quality standards in aseptic environments.
Where this listing comes from
This listing was compiled by RoleLantern from the employer's publicly available posting on Phenom, captured and rephrased by RoleLantern using automated (AI) tools on 2026-10-02 (originally posted 2026-09-18). It was not submitted or confirmed by the employer through RoleLantern. Details may be inaccurate, incomplete, outdated, or no longer available; please confirm with the employer's official posting before applying.
What they're looking for
- Bachelor's degree in Engineering, Chemistry, Life Sciences, or related field
- 8+ years process and/or cleaning validation experience
- Sterile/aseptic manufacturing environment experience required
- Knowledge of cleaning validation, residue limits, and risk-based approaches
- Strong cGMP and regulatory requirements understanding
- Data analysis, problem-solving, and technical writing expertise
What you'll be doing
- Lead process validation and cleaning validation activities for manufacturing
- Develop validation strategies for new and existing products and processes
- Author and execute validation protocols and generate reports
- Support change controls, deviations, and corrective action requests
- Collaborate with Manufacturing, Quality, and Materials Science teams
Privacy & handoff
This role links to Thermo Fisher Scientific's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.