Senior Supplier Quality Engineer - Global Impact

Boston Scientific; United States; On-site; USD 52,300 - 99,400; Full time

Job summary

Boston Scientific is seeking a Supplier QA Engineer II to drive supplier quality improvements and provide technical support for external components. You will establish acceptance criteria, monitor supplier performance and guide corrective actions across Quality, Operations, R&D and Sourcing.

The role requires a BS in engineering with 3+ years in a regulated medical devices environment, strong project management, and the ability to communicate effectively with global teams.

Qualifications

• BS degree in engineering or equivalent with 3+ years of related experience.
• Experience in medical devices or regulated environments.
• Strong project management capabilities spanning cross-functional teams.
• Knowledge of design controls, risk management, and CAPA processes.
• Excellent communication, packaging and presenting information clearly.

Responsibilities

• Assess potential suppliers for technical, quality and manufacturing capabilities.
• Provide technical support for supplier introductions and qualifications.
• Generate and maintain inspection procedures and train staff.
• Develop inspection tools and equipment as needed.
• Create component specifications and qualification test reports.
• Advise Design Engineering on component technology and selection.
• Analyze incoming defects and drive corrective actions with suppliers.
• Review design specs from a quality and manufacturability perspective.
• Investigate field failures and implement corrective actions; may supervise inspectors.

Skills

Project management

Communication

Problem solving

Cross-functional collaboration

Bilingual

Education

BS degree in engineering

ASQ Certification (CQE/CBA/SSGB/SSBB)

Job description

Boston Scientific is seeking a Supplier QA Engineer II to drive supplier quality improvements and provide technical support for external components. You will establish acceptance criteria, monitor supplier performance and guide corrective actions across Quality, Operations, R&D and Sourcing.

The role requires a BS in engineering with 3+ years in a regulated medical devices environment, strong project management, and the ability to communicate effectively with global teams.