Jobs at Boston Scientific

Provides clinical and technical support for spinal cord stimulation procedures, including programming, troubleshooting, intraoperative guidance, patient follow-up, and healthcare professional education. Partners with sales teams, physicians, and hospital staff to promote therapy adoption, support patient outcomes, identify referral opportunities, and develop customer relationships. The role includes frequent regional travel, surgical case participation, training sessions, administrative compliance, and community awareness initiatives.

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 medical device production through engineering investigations, process improvement, troubleshooting, validation reporting, and project execution. The intern helps reduce scrap, increase output, develop products and processes, and achieve safety, quality, delivery, and cost goals while collaborating with cross-functional teams.

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.

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.

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.

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 Boston Scientific’s Endoscopy commercial teams through sales and marketing exposure, product market assessments, customer insight research, hospital visits, sales training evaluations, and cross-functional projects. The intern develops clinical selling skills, learns the sales process, and gains experience in product marketing, professional education, field sales, and product lifecycle management.

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.

Develop deep learning and AI/ML models to predict cardiac events from ECG and physiological signals. Apply signal processing, analyze implantable-device datasets, build Python tools, validate algorithms, and support feasibility studies for diagnostic features. Collaborate with clinical, software, and hardware teams to improve implantable-device performance and patient outcomes.

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.

Coordinates employee engagement events, site visits, leadership meetings, and administrative projects from planning through completion. Manages schedules, budgets, vendors, procurement, logistics, stakeholder communications, visitor access, catering, and action tracking. Supports office administration and improves event, meeting, visitor, and operational processes while working cross-functionally with employees, leaders, contractors, and business partners.

Supervises third-shift production employees, ensuring quality, productivity, staffing, scheduling, policy compliance, and performance management. Develops staff through training, task assignments, reviews, and disciplinary actions. Analyzes operational issues, allocates resources, maintains personnel records, and communicates team achievements and requirements to management and internal or external customers. The role supports regulated medical device manufacturing and requires English-Spanish bilingual communication.

Supervises second-shift production employees, ensuring quality, productivity, staffing, training, scheduling, policy compliance, and operational performance. Develops team members, manages personnel records, addresses performance issues, coordinates hiring with Human Resources, interacts with customers, and reports accomplishments to management. The role supports regulated medical-device manufacturing and requires bilingual English-Spanish communication, analytical decision-making, and availability for second shift.

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 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.

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.