QA Administrator
About this role
Purpose of the Position / Role Summary
Responsible for effectively maintaining site QA / QMS documentation systems. Responsibility for site Documentation review and QC testing activity for materials and finished product.
Key Role Specific Requirements
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Maintenance of all Site QMS systems, including retains and documentation archive.
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Maintain documentation control processes and issuing for all QMS systems.
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Review of Bimeda and third-party product release documentation and maintain MRP inventory status.
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Maintenance of finished product retains and the retain room including annual inspections.
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Complete incoming inspection and verification checks for receipt of human pharmaceutical product. Complete QA review documentation for QP batch release.
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