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Sr QA Associate I / II - Sterile Ops
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Full-time
- Job Description: This function is responsible for supporting the daily manufacturing and facility operations along with project support.
- Interact with manufacturing and facility operations and support personnel to ensure cGMP compliance and provide general guidance and support.
- Act as the QA Contact and QA Approver for deviation investigations, executed CAPA, and effectiveness checks.
- Minimum Education & Experience Requirements: Sr. QA Associate I- Requires a Bachelor’s degree in a scientific discipline or equivalent with a minimum of 5 - 8 years’ experience in a Quality Assurance role in the pharmaceutical industry.
- Sr. QA Associate II- In addition to above, w ould have experience in complex critical investigations, quality control or lab investigation experience required versus preferred, audit or other professional quality certification or equivalent experience preferred.
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