The role
0301Operate, maintain, and troubleshoot analytical laboratory equipment and electronic laboratory systems.
02Support qualification of analytical equipment and computerized system validation activities for QC laboratory systems.
03Generate, review, and maintain GxP documentation throughout the lifecycle of QC systems, equipment, and applications.
04Evaluate analytical data, document results accurately, and ensure compliance with applicable quality standards.
05Support investigations related to out-of-specification, out-of-expectation, deviations, change controls, and corrective and preventive actions.
06Provide timely technical support to QC laboratory units to ensure reliable laboratory operations.
07Support inspection and audit readiness activities, including gap assessments, remediation actions, and participation in customer or health authority inspections as needed.
08Contribute to the implementation of automated data flows, laboratory process improvements, and Practical Process Improvement initiatives.
09Support data integrity expectations by ensuring reliable, complete, accurate, and compliant laboratory records.
10Collaborate with Quality, Manufacturing, Manufacturing Science and Technology, Supply Chain, Maintenance and Facilities, Procurement, IT, and global laboratory systems teams.
11Adhere to cGMP, quality, EHSS, and site procedures.
12Actively contribute to continuous quality improvement, safety initiatives, deviation reporting, and near-miss follow-up.
13Demonstrate Thermo Fisher Scientific values through accountability, ethical behavior, customer focus, intellectual curiosity, and collaboration.
