(Senior) Process Development Engineer

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. Key Responsibilities  • Applies technical knowledge to innovate, design, and develop processes, procedures, tooling and/or automation. • Develop and document processes, methods, tooling, and production controls for new programs. • Provide Design for Manufacturability (DFM) input to the engineering print package. • Executes the functional deliverables associated with the PDP/TDP, Project Management, and Quality Systems. • Plans, organizes, and conducts all aspects of technical reviews. • Ensures proper documentation is completed to meet quality systems requirements (e.g., BOM’s, Routers, FMEA’s, etc.). • Writes and reviews validation protocols and reports applicable to new processes. • Oversees development builds associated with the project using special work requests. • Contributes ideas to or generates Intellectual Property submissions. • Trains and/or provides work direction to technicians and engineers and may train manufacturing personnel when required as part of a validation. • May serve as a core team member or extended team member on new product projects. • Ensures that all aspects of the quality system are the first priority in all activities (e.g., validation protocols, quality plan development, FMEA’s and DCM’s). • Assesses process capabilities, prioritizes process improvement opportunities, and innovates and implements process improvements on platform or derivative projects. • Develop qualified production lines. • Design for manufacture, process optimization (ranging studies) and validation. Technology transfer into manufacturing. • Manage all phases of equipment qualifications and process validations (protocols, data analysis, reports). • Conduct test method validations (Gage R&R).   Requirements • Solid mechanical background, master or bachelor’s degree in Mechanical Engineering. • 5 - 10 years of experience in mechanical design for Senior position. Disposable medical product ，device development experience is preferred. • Good experience with Geometric Dimensioning and Tolerance (GD&T), Design for Manufacturing(DFM), Tolerance Stack Up Analysis. • Be familiar with SolidWorks. • Be familiar with different process for Process engineer.  • Familiar with common engineering materials and corresponding manufacturing technology (e.g. Plastic parts, metal-sheet parts, Die-casting and machining parts etc.) • Ability to work effectively in complex projects; With innovation skills and problem-solving skills. • Team player with good interpersonal/intercultural skills.     关于我们 波士顿科学（交易代码：BSX）承诺为生命创新，致力于创新医疗解决方案，改善全球患者生活。四十年来，波士顿科学始终引领全球医疗技术行业的发展，通过提供覆盖广泛疾病治疗领域的高性能医疗解决方案，满足广大患者亟待解决的医疗需求，提升医疗保健效率。为生命创新，是波士顿科学的使命，也是我们对全世界患者、医师以及医疗系统的承诺。每年约3000万名患者获益于波士顿科学创新医疗解决方案。 波士顿科学的职业不仅仅是一份工作，它对每个人都不同。如果你是天生的问题解决者，拥有想象力和勇气，愿意做出有意义的改变，我们鼓励你申请职位并期待与你联系！