· Provide engineering support for new product and process introductions, ensuring that all activities are completed and documented in accordance with the Stryker new product development procedures. · ​Ensure quality of process and product as defined in the appropriate operation and material specifications. · ​Will assist in the selection of components and equipment based on analysis of specifications, reliability, and regulatory requirements. Work with quality engineers to develop component specific testing and inspection protocols. · ​Support capital acquisition activity from specifying equipment, contract negotiation, Installation and validation. · ​Will analyze equipment to establish operating data, conduct experimental test and result analysis. Lead and/or participate in process review meetings. · ​Participate in PFMEA, Control Plan, SOP and PPAP generation associated with product transfers and launches. · ​Complete capability studies for in process inspection and generate subsequent Inspection documentation. · ​Conduct MSA studies for new products and new processes. · ​Provide training for manufacturing team members. · ​Ensure adherence to GMP and safety procedures. · ​Review and approval of validation documentation. ​All other duties as assigned.​ Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually. Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer – M/F/Veteran/Disability.