Stryker Senior Engineer, Process DevelopmentWe are excited to be named one of the World's Best Workplaces by Fortune Magazine! We are proud to offer you 12 paid holidays annually. For an overview of our benefits and time off, please follow this link to learn more: US Stryker employee benefits.Stryker is one of the world's leading medical technology companies and is dedicated to helping healthcare professionals perform their jobs more efficiently while enhancing patient care. We are currently seeking a Senior Engineer, Process Development to join our Instruments Division to be based in Portage, MI.Who we want:Analytical problem solvers: People who go beyond just fixing to identify root causes, evaluate optimal solutions, and recommend comprehensive upgrades to prevent future issues.Dedicated achievers: Relentless about quality, people who thrive in a fast-paced environment and will stop at nothing to ensure a project is complete and meets regulations and expectations.Collaborative partners: People who build and leverage cross-functional relationships to bring together ideas, information, use cases, and industry analyses to develop best practices.What you will do:Provide hands-on 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.Select components and equipment based on analysis of specifications, reliability and regulatory requirements.Work with quality engineers to develop component specific testing and inspection protocols.May lead or support capital acquisition activity from specifying equipment, contract negotiation, installation and validation.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.Use the latest engineering techniques to reduce product time to market whilst adhering to regulatory requirements, project deadlines and product costs.Build productive internal and external working relationships and may periodically provide guidance and train other team members.Provide training for manufacturing team members.Ensure adherence to GMP and safety procedures.Review and approval of validation documentation.What You Need:Bachelor's Degree in Engineering.2+ years of relevant post-grad work experience.Preferred Skills:Knowledge of manufacturing processes, materials, product and process design.Ability to read and interpret complex engineering drawings.Electrical/Mechanical Engineering degree.Experience in a FDA regulated or highly regulated industry.Understanding of Design for Manufacturing (DFM), related statistical tools and validation/verification techniques.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.
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