Global Supplier Quality Engineer II

Boston Scientific; California (MO); Sur place; USD 52 000 - 99 000; Plein temps

Résumé du poste

Boston Scientific is seeking a Supplier Quality Engineer II to drive improvements in the quality of externally sourced components. You will support supplier selection, develop acceptance criteria, and monitor performance to enable corrective actions and improved yield.

The role requires an engineering degree and 3+ years in medical devices or regulated industries, with strong communication and project management skills. Collaboration across Quality, Operations, R&D, and Sourcing is essential.

Qualifications

• BS degree in engineering with 3+ years of related experience in medical devices or regulated industries.
• Experience in process validation, design controls, risk management, and CAPA.
• Ability to influence cross-functional global teams and communicate clearly.

Responsabilités

• Assess potential new suppliers for technical, quality and manufacturing capabilities.
• Generate and maintain incoming inspection procedures and train inspectors.
• Develop and/or source inspection tools and equipment.
• Assist in generating component specifications.
• Generate test protocols and approve components for use.
• Provide input to Design Engineering on component tech and reliability.
• Investigate field failures related to supplier materials and develop corrective action plans.
• Review new design specifications from quality/manufacturability perspective.
• Supervise inspectors as needed.
• Monitor supplier performance and support continuous improvement activities.

Connaissances

Quality engineering

Supplier management

Project management

Process validation

CAPA

Communication

Bilingual

Formation

BS degree in engineering

ASQ CQE (certification)

Outils

Inspection tools

Description du poste

Boston Scientific is seeking a Supplier Quality Engineer II to drive improvements in the quality of externally sourced components. You will support supplier selection, develop acceptance criteria, and monitor performance to enable corrective actions and improved yield.

The role requires an engineering degree and 3+ years in medical devices or regulated industries, with strong communication and project management skills. Collaboration across Quality, Operations, R&D, and Sourcing is essential.