Process Engineer III
Listed on 2026-01-13
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Engineering
Manufacturing Engineer, Process Engineer, Quality Engineering
Process Engineer III
• Boston Scientific
Boston Scientific is looking for a highly motivated Process Engineer III to join our fast‑growing team. In this role you will support clinical builds of a unique product, develop manufacturing technology for a commercial solution, and validate processes to support rapid growth in demand. You will use your technical skills and passion for innovation to drive the commercialization of new products and improvements, working hands‑on to solve complex problems in a fast‑paced, global environment.
The role focuses on developing processes from concept to production and involves cross‑functional collaboration across our global plant network.
- Assess process capabilities, prioritize process improvement opportunities, and innovate and implement process improvements on multiple and moderately complex processes.
- Apply technical knowledge to innovate, design, and develop processes, procedures, tooling, and/or automation.
- Execute the functional deliverables associated with the PDP/TDP processes, Project Management, and Quality Systems.
- Write clean and concise work instructions that can be understood by product builders.
- Own/contribute to technical reports, validations, and qualifications by capturing experimental results.
- Complete proper documentation to meet quality systems requirements (e.g., BOMs, routers, FMEAs, etc.).
- Write validation protocols and reports applicable to new processes.
- Prepare and present technical data and recommendations at technical and business reviews.
- Oversee development builds associated with the project using special work requests.
- Provide Design for Manufacturability (DFM) input to the engineering print package.
- Partner cross‑functionally to develop design specifications, test methods, and material selection.
- Contribute ideas to or generate intellectual property submissions.
- Train manufacturing personnel, when required, as part of early prototype line development and validation.
- May serve as core team member or extended team member on new product development projects.
- Bachelor’s degree in Engineering or a related technical field.
- Minimum of 3 years of professional engineering experience in an ISO 13485 quality environment.
- Experience validating medical device manufacturing processes.
- Hands‑on mechanical aptitude.
- Demonstrated engineering fundamentals (Lean, DFM, etc.) and problem‑solving skills.
- Demonstrated cross‑functional teamwork in a technically demanding environment.
- Strong written and verbal communication skills.
- Demonstrated use of Design for Six Sigma tools (Design of Experiments, problem‑solving).
- Experience in New Product Development.
- Experience developing and characterizing various types of processes.
- Demonstrated understanding and usage of statistics to drive improvements; proficiency in Minitab.
- Demonstrated ability to develop equipment, fixtures, or tooling from concept to production.
- Troubleshooting in combination with product yield and performance.
- Experience with mechanical design.
- Ability to schedule timelines with specific milestones to achieve and demonstrated success.
- Open to travel (domestic or international) up to 10% of time.
Requisition : 619180
Minimum Salary: $76,000
Maximum Salary: $144,400
Boston Scientific Corporation has been and will continue to be an equal opportunity employer. To ensure full implementation of its equal employment policy, the Company will continue to take steps to assure that recruitment, hiring, assignment, promotion, compensation, and all other personnel decisions are made and administered without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, gender expression, veteran status, age, mental or physical disability, genetic information or any other protected class.
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