Meet with contractors, perform pre-review of validation documents to support efficient review/approval by QA.
Lead the effort for protocol discrepancy related documentation and assist contractors in investigations related to protocol deviations.
Operations:
Collaborate with operations team to assess and update validation documents (VDAs, URS, Specifications, Trace documents) in support of user needs, process changes, and business improvements, and commercialization efforts.
Support validation/qualification efforts for facility expansion.
Quality Assurance:
Maintaining validated state of equipment. Ensure equipment parameters are maintained, especially after calibration/maintenance events.
Ensuring efficient and coordinated executions of validation events. Work with QA/Clinical team to minimize disruption to clinical operations.
iii. Execute validation protocols.
iv. Perform/support periodic review cycles for LBE equipment.
v. Assist with device related installation activities.
Act as a validation/equipment point of contact for Facility Managers and Quality Assurance.
Lead equipment/asset management process (for QA group) utilizing the Blue Mountain RAM system (electronic Asset/Equipment Manager).
Collaborate with on-site contractors/operations team to document calibration/PM work and electronically manage equipment assets.
Ensure RAM system, facility equipment, and equipment identification are aligned to support equipment control/management throughout the lifecycle.