Process Engineering Associate Co-op/New Grad

Additional Locations:   N/A Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we’ll help you in advancing your skills and career. Here, you’ll be supported in progressing – whatever your ambitions. This position is a 12-month co-op/new grad/PEY placement beginning January 2027. About the role As a Process Engineering Associate , you will join the Process Development Engineering team for a 12-month co-op/new graduate opportunity designed to provide meaningful, hands-on engineering experience. You will help translate product designs into robust manufacturing and assembly processes while gaining exposure to equipment development, process development and validation activities.   Work mode: At Boston Scientific, we value collaboration and synergy. This role follows a hybrid work model requiring employees to be in our local office at least three days per week. Sponsorship: Boston Scientific will not offer sponsorship or take over sponsorship of an employment visa for this position at this time. Relocation: Relocation assistance is not available for this position at this time. Your responsibilities will include: Support the development and optimization of innovative manufacturing processes and equipment including generating ideas, drafting 3D prototypes in SolidWorks, coordinating testing, and researching and providing input to the team as needed. Build and test prototype devices to ensure they meet requirements. Assist with the development of validation and test plans by supporting engineers with the execution of process characterization and testing of devices. Lead LEAN initiatives to make improvements to the manufacturing process. Aid in the development and provision of technical documentation by preparing drawings, writing work instructions, and providing training for new tools and equipment. Design test methods or follow standard protocols to ensure the device meets the patients’ needs. Monitoring safety practices and ensuring ISO 13485 and FDA compliance while collaborating with cross functional teams to meet product timelines. In all actions, demonstrates a primary commitment to patient safety and product quality by maintaining compliance with the Quality Policy and all other documented quality processes and procedures. Other duties as required. Required qualifications: Currently enrolled in an Engineering degree, or a recent graduate from a Mechanical Engineering, Process Engineering, Equipment Engineering, or Mechatronics. Experience with SolidWorks. Preferred qualifications: Six Sigma or LEAN knowledge  Minitab experience   Experience in a highly regulated…