Position Overview: The Validation Specialist supports validation and maintenance activities essential to the development and manufacturing of medical devices. This role ensures compliance with regulatory standards through the qualification of equipment, software, and processes, contributing directly to product quality and patient safety. Key responsibilities include generating and executing validation protocols, maintaining calibrated equipment, and supporting equipment qualification activities for both manufacturing and quality control laboratory teams. The Validation Specialist also assists in developing and reviewing validation plans, user and functional requirements, protocols, final reports, and change control assessments. This cross-functional role collaborates closely with Engineering, Manufacturing, and Quality teams to maintain a compliant and efficient equipment maintenance and validation programs.