Supplier Quality Engineer Iii - Ce Electronics

Boston Scientific Foundation Inc

Arden Hills, MN, US
Base: $78,300 - $148,800; bonus/equity: annual bon...
On-site
Supplier performance improvement
Supplier corrective action plans
Global sourcing category teams
The Supplier Quality Engineer will play a key part in leading performance improvement of active pharmaceutical ingredients (API), excipient suppliers and increasing the supplier's capabilities to consistently meet Boston Scientific's requirements

Job Summary

  • The Supplier Quality Engineer will play a key part in leading performance improvement of active pharmaceutical ingredients (API), excipient suppliers and increasing the supplier's capabilities to consistently meet Boston Scientific's requirements.
  • Drives improvement and corrective action in the quality of components sourced from outside suppliers.
  • Plans and leads audits of suppliers to assess compliance with regulatory and Boston Scientific requirements, including audit scheduling, investigation, and evaluation of audit observations and findings, reporting, follow-up, and confirmation of follow-up actions.

Matching Summary

The Supplier Quality Engineer will play a key part in leading performance improvement of active pharmaceutical ingredients (API), excipient suppliers and increasing the supplier's capabilities to consistently meet Boston Scientific's requirements.

Salary

Base: $78300 - $148800; Bonus/Equity: Annual bonus target and long-term incentives; Benefits: See www.bscbenefitsconnect.com

Skills & Requirements

Must-have

  • Supplier performance improvement
  • Supplier corrective action plans
  • Global sourcing category teams
  • Quality Management System interpretation
  • Audits of suppliers

Nice-to-have

  • High-energy, driven, passionate people
  • Foster a work environment
  • Cultivate business relationships
  • Innovative approaches to solutions

Key Requirements

  • Bachelor's degree in Engineering
  • 3+ years of relevant experience
  • Experience with global supplier management
  • Experience with ISO 13485 and ISO 9001
  • Working knowledge of FDA 21 CFR 820

Work Rights

Not specified

Tailored Resume

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