Laboratory Equipment Validation Specialist

The Laboratory Equipment Validation Specialist is responsible for the validation and lifecycle management of laboratory equipment used in a regulated pharmaceutical environment. 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.