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IPQA Associate I
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Full-time
- IPQA Associate I The IPQA Associate I is responsible for identifying deviations in the processes and ensure that all activities are cGMP compliant, identifying corrective actions, establishing path forward activities, and appropriate documentation.
- Job Description: Focuses on initial deviation investigative phases related to manufacturing process deviation.
- Perform acceptance sample analysis for validation and investigation support.
- Responsible for the review and approval of controlled documents including manufacturing and packaging batch records.
- May complete specific project work such as process improvement/remediation, maintain ownership and responsibility for specific QA processes.
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