Description
Quality Consulting Group is seeking a Quality Applications Specialist in Villalba, Puerto Rico to support product transfer, process validation, and compliant validation of quality IT systems in a medical device manufacturing environment. The role involves coordinating with clients and technical personnel, maintaining validation documentation and regulatory compliance, reporting validation status, and administering/configuring quality information systems. Candidates need a bachelor’s degree in engineering or science, at least 3 years of relevant experience, and knowledge of process validation, product transfer, process failure mode analysis, sterilization, and final pack.
