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QA Associate Specialist Document Control
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- 2+ years of Document Control & Reporting Experience,
- Veeva experience preferred
- The Quality Assurance Document Control (QADC) Associate Specialist supports the cGMP Document Control operations for the Client Cell Therapy Above-site organization, including the document approvals, document change control process, periodic review and system reporting.
- Minimum of 1 year of relevant document control experience in a cGMP/FDA regulated environment.
- Some technical writing skill set including the ability to critically review documents while effectively inputting and expressing Quality principles.
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