Quality Engineer I
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, and 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. As a Quality Engineer II, you will provide quality engineering support for manufacturing operations and New Product Introduction (NPI), ensuring delivery of the high-quality products to our customers while driving continuous improvement initiatives. In this role, you will partner closely with production and manufacturing engineering teams to provide operational support for the TDX, EKOS and Iron Heart production lines. This position is part of the Sensors and Micro-Interconnects (SMX) business unit and offers the opportunity to make a direct impact on manufacturing excellence, product quality and patient outcomes.
Requirements
- Bachelor's degree in a STEM discipline.
- Knowledge of quality systems and good documentation practices.
Nice To Haves
- Bachelor's degree in engineering, biomedical engineering or a related technical discipline.
- Experience supporting manufacturing operations within the medical device industry.
- Experience providing quality engineering support, including process validation, equipment qualification, CAPA and production line support.
- Knowledge of analytical techniques, statistical analysis and structured problem-solving methodologies.
- Experience collaborating with cross-functional teams, including manufacturing engineering, process engineering, supplier quality and risk management, to drive projects to successful completion.
- Familiarity with Manufacturing Execution Systems (MES), product and component documentation, inspection and testing.
- Strong written and verbal communication skills, with the ability to work independently and identify continuous improvement opportunities.
- Proficiency with Microsoft Office applications, including Word, Excel, PowerPoint and Outlook.
Responsibilities
- Identify and implement effective process control systems to support the development, qualification and ongoing manufacturing of products that meet or exceed internal and external requirements.
- Lead the implementation of quality assurance systems, process controls and corrective and preventive action (CAPA) activities designed to meet or exceed internal and external requirements.
- Serve as an effective leader and collaborative team member in supporting quality systems, decisions and best practices.
- Apply structured problem-solving methodologies to identify, prioritize, communicate and resolve quality issues.
- Support the development and execution of streamlined business systems that effectively identify and resolve quality issues.
- Provide production floor support and serve as the quality owner for assigned manufacturing lines.
- Perform or support process validation and verification activities and prepare or review associated documentation.
- Lead corrective and preventive action (CAPA) projects and drive timely implementation of effective solutions.
Benefits
- www.bscbenefitsconnect.com
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
