Jobs at Boston Scientific

Drives capital equipment, service contract, and disposable revenue within the Urology division. Partners with field sales, marketing, finance, contracting, and training teams; coaches territory managers and business partners; develops sales strategies; presents to customers; monitors performance; supports product launches and pricing models; and manages administrative activities. Requires medical device and capital equipment sales experience, strong leadership, strategic problem-solving, communication, and business skills.

Provides field-based clinical, technical, and educational support for electrophysiology and atrial fibrillation medical devices during cardiac procedures. Trains physicians and EP lab staff, demonstrates mapping and ablation technologies, develops hospital relationships, supports sales and market development, responds to technical inquiries, and manages clinical trial activities including site initiation and investigator education.

Develops manufacturing processes, technologies, and test systems for medical devices. Connects research and design with manufacturing, scales processes for high-volume production, reduces variation, improves quality, partners with technology leaders, and maintains process plans, manufacturing instructions, and material implementation throughout product development.

IT Analyst Interns apply business analysis, data analysis, visualization, user experience, project management, and product management skills to real IT challenges. They deliver a project outcome during a 12-week program, collaborate with cross-functional teams, complete a group project, and participate in professional development activities. Successful interns may be considered for Boston Scientific’s two-year technology leadership rotational program.

IT Analyst Interns apply business analysis, data analytics, visualization, user experience, project management, and product management skills to real IT challenges. They complete individual and group projects, such as developing chatbots, dashboards, workflow automation tools, and cybersecurity solutions. Interns collaborate with Supply Chain, Finance, HR, R&D, Sales, Operations, and Quality teams during a 12-week program and may be considered for a future IT leadership rotation program.

Supports quality engineering in a medical device manufacturing environment through yield and process improvements, tooling and equipment development, inspection system creation, systematic problem solving, and quality issue resolution. The intern collaborates cross-functionally to improve manufacturing processes, apply design-for-manufacturing principles, and support quality initiatives that meet regulatory and patient-safety requirements.

Process Development Engineering Interns develop and improve manufacturing processes, test systems, fixtures, tooling, and equipment for medical devices. Responsibilities include hands-on design, testing, troubleshooting, process validation, statistical analysis, manufacturing documentation, and cross-functional collaboration. Interns support scalable, high-quality production processes across areas including electrophysiology, cardiac rhythm management, diagnostics, endoscopy, and urology while ensuring compliance with quality procedures.

Supports development of scalable manufacturing processes, automated equipment, controls, test systems, and data acquisition solutions for medical devices. The intern connects R&D with manufacturing, troubleshoots process and automation issues, maintains process plans and manufacturing instructions, ensures quality and procedural compliance, and collaborates with cross-functional engineering teams. Assignments may support electrophysiology, cardiac rhythm management, diagnostics, endoscopy, or urology products.

Manufacturing Engineer Intern supporting medical device production through engineering investigations, troubleshooting, process improvement, validation data generation, and project execution. The role focuses on reducing scrap, increasing output, developing products and processes, and meeting safety, quality, delivery, and cost goals. The intern collaborates with cross-functional teams, applies academic engineering knowledge, reviews production reports, and participates in hands-on manufacturing problem solving.

Process Development Engineering Interns develop scalable manufacturing processes and test systems for medical devices. They apply chemistry, materials science, and engineering principles to process development, material selection, characterization, quality improvement, and manufacturing implementation. Interns collaborate with R&D, manufacturing, and technology teams; maintain process plans and manufacturing instructions; and ensure compliance with process development and quality requirements.

Develop and refine manufacturing processes for next-generation medical devices. Responsibilities include maintaining process plans, collaborating cross-functionally, designing and testing prototypes, conducting process characterization and validation experiments, and evaluating new manufacturing technologies.

Develop and refine manufacturing processes for next-generation medical devices. Responsibilities include maintaining process plans, collaborating cross-functionally, designing and testing prototypes, conducting process characterization and validation experiments, and evaluating new manufacturing technologies.

Develops and improves the site’s environmental, health, and safety programs, ensuring compliance with regulations, corporate policies, and ISO 14001 requirements. Maintains EH&S metrics, supports workers’ compensation and emergency response programs, manages waste and pollution prevention initiatives, conducts audits, inspections, risk assessments, and incident investigations, and delivers compliance and safety training. The role also coordinates with waste vendors, cross-functional teams, and employees while promoting injury reduction and safe workplace conditions.

Lead analysis, design, and implementation of manufacturing and business process improvements to increase capacity, reduce lead-time and WIP, and improve fill rates. Perform capacity analyses, develop metrics, support layout and workflow optimization using AutoCAD, facilitate Kaizen/Gemba, conduct time studies and ergonomic projects, train teams on Lean principles, and collaborate with cross-functional/internal and supplier stakeholders to resolve supply issues and improve manufacturability.

Develop, implement, and monitor EHS policies and procedures to ensure regulatory compliance. Conduct inspections, industrial hygiene assessments, incident investigations, training, ergonomics evaluations, waste minimization, ISO 14001 activities, and serve as site liaison with regulators and emergency responders.

Develop and maintain quality systems and methodologies, support manufacturing activities, analyze quality issues, and ensure compliance with regulations.

Drive supplier quality improvements for medical device components: assess suppliers, develop incoming inspection procedures and test protocols, support component qualification, analyze defects, manage supplier corrective actions and CAPA, liaise with Design Engineering, and may supervise inspectors.

Lead financial planning, forecasting, reporting and analysis for manufacturing operations. Prepare budgets, variance analysis, journal entries, and sensitivity/NPV modeling. Partner with production, engineering and quality to evaluate cost improvements, product integrations and business opportunities. Support month-end close, annual planning, and continuous improvement of reporting and analytics.