Thermo Fisher Scientific·9 days ago
9 days ago
Staff Validation Engineer, Process and Cleaning
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What you'll do
- Lead process and cleaning validation activities
- Ensure manufacturing processes and cleaning procedures meet cGMP and regulatory standards
What they're looking for
- Significant experience in sterile/aseptic manufacturing
- Expertise in validation strategies
Summarised by NextRaise from the employer’s description, which follows in full below.
Full description from employer
We are looking for a Staff Validation Engineer, Process and Cleaning to lead process and cleaning validation activities, ensuring manufacturing processes and cleaning procedures meet cGMP and regulatory standards. The ideal candidate brings significant experience in sterile/aseptic manufacturing and expertise in validation strategies.
Skills
- process validation
- cgmp compliance
- data analysis
- validation protocols
- validation reporting
- change control
- capa support
- lifecycle validation
- residue limits
- risk-based validation
- technical writing
- audit support
- internal audit
- external audit
- project management
Company
Thermo Fisher Scientific
Greenville, United States of America
Company facts come from this company's own listings. We only show what the postings themselves carry.