Validation Specialist to support validation activities within a regulated Medical Devices manufacturing environment. The ideal candidate will have strong knowledge of the Validation Life Cycle and hands-on experience executing validation deliverables in compliance with FDA and global regulatory requirements.
Key Responsibilities:
Execute and support validation protocols and reports including IQ, OQ, PQ for equipment, utilities, processes, and/or computer systems.
Ensure all validation activities comply with applicable regulations and site quality standards.
Lead and/or support the full Validation Life Cycle (planning, risk assessment, execution, and closure).
Develop and review validation documentation including Validation Plans, URS, FRS, RTM, protocols, and summary reports.