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Specialist II, Quality Systems
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- We're building a sustainable network of high-tech, end-to-end manufacturing solutions to better withstand disruptive events, serve scientific discovery, and reach those in need.
- Coordinate and support GxP Documentation Control Systems to include the issuance of controlled documents and maintenance of site GxP records.
- Coordinate document and record archival with representatives from other departments
- Review completed documentation for quality, completeness, and cGMP (Good Manufacturing Practices) compliance
- Proficiency in MS Office applications and data management applications such as EDMS, LIMS, and SAP
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