Manufacturing Engineer III
About The Position
Boston Scientific was recognized by Forbes as one of the Best Workplaces for Engineers in 2026, reflecting a culture where engineers do meaningful work. Boston Scientific was recognized as a Glassdoor Best Place to Work in 2026, ranking No. 15 on the Top 100 list, reflecting the culture our employees experience every day. The engineer in this role will support manufacturing operations, improve existing processes and contribute to the successful introduction of new products into production. This position serves as a key liaison between production and engineering, helping resolve issues on the manufacturing floor while driving efficiency, quality and performance improvements.
Requirements
- Bachelor’s degree in engineering or a related technical field
- Minimum of 4 years' experience in engineering, manufacturing or a related discipline
- Solid knowledge of engineering principles, manufacturing processes and validation methodologies
- Experience with process validation, including IQ, OQ and PPQ
- Working knowledge of risk management and FMEA
- Ability to analyze data, perform root cause analysis and implement effective solutions
- Strong communication and cross-functional collaboration skills
Nice To Haves
- Experience in medical device or regulated manufacturing environment
- Experience supporting new product introduction (NPI) into manufacturing
- Experience with equipment, tooling or fixture design and validation
- Knowledge of continuous improvement methodologies such as Lean or Six Sigma
- Experience working with external suppliers or contract manufacturers
Responsibilities
- Evaluate, select and apply standard engineering techniques, procedures and criteria, using judgment to make minor adaptations and modifications.
- Improve existing manufacturing processes and act as a liaison between production and engineering to resolve issues encountered on the production floor.
- Assist with the introduction of new products into the operations production area.
- Participate in project teams to identify and implement process and product improvements that increase yield, efficiency, throughput and performance.
- Design, perform and document engineering experiments to evaluate product and process performance.
- Participate in quality improvement initiatives and support continuous improvement efforts.
- Design, develop, test and validate equipment, tools and fixtures.
- Analyze and interpret process data and models, recommending improvements based on findings.
- Participate in equipment and process validation activities, including writing and executing Installation Qualification (IQ), Operational Qualification (OQ) and Process Performance Qualification (PPQ) protocols and reports.
- Apply working knowledge of risk management and Failure Mode and Effects Analysis (FMEA) requirements.
- Interface with assemblers, production supervisors and engineers to troubleshoot production issues.
- Coordinate with suppliers and external partners to support process and product improvements.
- Perform root cause analysis on nonconforming or failed products and implement corrective actions.
- Support project planning and scheduling activities.
- Optimize processes to improve yield, reduce cycle time and minimize scrap.
- Participate in product core team meetings and contribute to cross-functional initiatives.
- Demonstrate a primary commitment to patient safety and product quality by maintaining compliance with the Quality Policy and all documented quality processes and procedures.
- Support a work environment that promotes adherence to the Boston Scientific Quality Policy and Quality System requirements, when applicable.
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Number of Employees
5,001-10,000 employees
