The Medical Device Combination Product Manager is a member of the Global Quality Organisation who is a quality liason between Global Product Development, Regulatory, Manufacturing Operations, Quality Control, and Quality Assurance to ensure regulatory compliance with design control activities and documentation, technology transfer to manufacturing and QC testing processes. Provide Quality oversight for the development, review, and approval of key Design History File deliverables including Verification and Validation Protocols and Reports, Risk Management deliverables, Transfer Plans, Design Reviews, Design History File management and supporting operational procedures.