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QA Associate Specialist - Document Control
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- Job Title : Quality Assurance Document Control (QADC) Associate Specialist
- Leading Pharmaceutical company looking for an experienced QA Document Control Specialist.
- Ideal candidates should have 2+ years of Document Control and report experience with at least 1 year being in cGMP/FDA regulated environment.
- Managing an electronic document system for the Cell Therapy Above-Site which includes reviewing and approving document change requests, troubleshooting and releasing documents to an effective state.
- May write and revise document control procedures including participating in the development and roll-out of document control tools.
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