Jobs at Boston Scientific

Field-based clinical specialist supporting Watchman and FARAPULSE devices. Provide procedural support, hands-on training, clinical education, KOL engagement, territory development, cross-functional collaboration, trial support, regulatory compliance, and mentor new team members. Regular hospital travel and occasional on-call coverage required.

Field-based territory manager driving sales and adoption of WATCHMAN, FARAPULSE and EP products. Develop territory strategies, build physician and hospital relationships, support implant procedures clinically, lead product education, create pricing proposals, and expand hospital access to meet revenue and unit growth targets.

18-month entry-level sales trainee program for electrophysiology. Learn cardiac EP therapies, observe live procedures, develop clinical and customer-facing sales skills, and work with sales, clinical, and marketing mentors in hospitals.

Provide process and quality engineering support for manufacturing and product development: identify and control process defects, develop quality plans and risk analyses, create process monitoring systems, lead process improvement efforts, assist with quality tools and training, perform audits, and authorize final process releases.

Perform manufacturing operations including equipment setup, calibration, rework, and quality testing. Support process improvements, preventive maintenance, installations, validations, and investigations. Work with engineers on experiments, tooling, and documentation. Follow QSR/ISO and safety standards; may certify associates and train others.

Two-year rotational program with three eight-month rotations across demand planning, supply planning, and people leadership. Contribute to forecasting, inventory management, new product launches, SAP/RapidResponse planning execution, and SI&OP processes while developing leadership skills and preparing for a full-time supply chain role.

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.

The internship involves supporting the Financial Planning & Analysis team with budgeting, forecasting, financial modeling, and data analysis, while providing hands-on experience in finance operations.

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.

Plan and schedule production to meet service level and inventory objectives. Manage backorders, manufacturing priorities, net requirements, and schedule adherence. Provide inventory analysis, maintain master data, support PDP and COP processes, facilitate new product schedules, train associates, and use supply chain systems (SAP, MES, Rapid Response) to optimize production planning.

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.

Support manufacturing and product development by identifying and controlling process defects, developing quality plans and risk analyses, implementing process monitoring and improvements, creating quality tools and training, performing audits, and approving final process releases to ensure compliant, high-quality medical devices.