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Cleaning Validation Engineer
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Full-time
- The Cleaning Validation Engineer will be focused on various tasks and responsibilities including generating protocols, equipment swab diagrams, product risk assessments and general technical reports related to cleaning validation.
- The consultant will execute validations as needed, including assisting in product sampling, auditing and technical review functions as defined in study protocols.
- The consultant will also review and approve change control documentation to assure all validation requirements are detailed in the Action Items.
- 5+ years of cleaning validation experience within the pharmaceutical industry
- Strong knowledge of cGMP regulations and 21CFR Part 11 standards
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