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Laboratory Equipment Validation Specialist
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Mostrado en español — traducción no disponibleThe Laboratory Equipment Validation Specialist is responsible for the validation and lifecycle management of laboratory equipment. This role ensures compliance with cGMP regulations through the planning, execution, and documentation of validation activities for analytical instruments, with a strong focus on UPLC systems and densitometer. The specialist will support laboratory operations by maintaining validated states and ensuring data integrity and regulatory compliance. Key Responsibilities Plan, execute, and document laboratory equipment validation activities. Develop, review, and approve validation protocols, reports, risk assessments, and traceability matrices. Perform validation of analytical laboratory instruments, including UPLC systems and densitometer, as well as other laboratory equipment as assigned. Ensure compliance with cGMP.
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QRC GROUP LLC
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