As a Sterilization & Validation Engineer you will perform a critical role in the design, development, and maintenance of TJO’s orthopedic implant packaging systems. Focusing primarily on cleaning, packaging, sterilization, and process validation activities, you will help to facilitate conformance to regulatory standards while enabling manufacturing, design, and supplier changes to be successfully implemented and commercialized. As a member of the Quality and Regulatory team, you will interface primarily between Product Development and with each of our packaging/sterilization suppliers. Your work will be a voice to translate the application of technical regulatory packaging and sterilization requirements to the Product Development team to ensure design and development projects reach the market successfully. You will also help to ensure all sterilization validation maintenance activities at each of our critical packaging/sterilization suppliers continue to meet all stakeholder needs.