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Technical Manager, Clinical QA
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- Hybrid role - 3 days a week onsite
- Create, revise and approve the company's Phase Appropriate Quality Systems documentation.
- Review early-stage analytical testing in support of GLP and GMP clinical protocols and production activities.
- QA Issuance, Review and Approval of manufacturing production batch records in support of manufacturing operations.
- Perform walkthroughs and other support activities of Analytical Science and Process Development to ensure compliance with applicable GMPs/GLPs.
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