Supplier Quality Engineer (SQE)
The Supplier Quality Engineer (SQE) supports supplier quality activities across both New Product Introduction (NPI) and sustaining manufacturing operations within a regulated medical device environment. This role ensures supplier compliance to applicable requirements, including 21 CFR Part 820 and ISO 13485, and contributes to supplier qualification, development, monitoring, and performance management activities.
This role supports supplier qualification activities for NPI programs, including onboarding of new suppliers, documentation review, and participation in process validation and design transfer activities. The SQE also supports sustaining supplier quality activities for production materials and services, including monitoring supplier performance and supporting resolution of supplier-related quality issues.
How you will make an impact as a Supplier Quality Engineer:
Support supplier qualification activities for New Product Introduction (NPI) projects
Conduct supplier assessments in accordance with established risk-based procedures
Support supplier selection activities in collaboration with Engineering, Procurement, and Quality
Participate in supplier audits (remote and onsite) as part of qualification and surveillance activities
Review supplier documentation including certifications, quality records, and validation evidence
Support supplier readiness activities for production launch, including process and quality system evaluations
Participate in design transfer and process validation activities involving suppliers
Sustaining Supplier Quality Management
Support supplier quality oversight for assigned NPI projects and production suppliers
Monitor supplier performance using quality metrics (e.g., SCARs, defects, delivery performance)
Support supplier corrective action activities (SCAR/CAPA) and ensure timely closure
Conduct supplier performance reviews and drive continuous improvement initiatives
Support containment, root cause analysis, and resolution of supplier-related quality issues
Perform risk-based supplier re-evaluations and periodic assessments
Supplier Quality System & Compliance
Ensure supplier compliance with applicable regulatory and quality system requirements including ISO 13485
Maintain and improve Approved Supplier List (ASL) classification and risk-based controls
Support external and internal audits involving supplier quality systems
Skills you will need to be successful as a Supplier Quality Engineer:
Bachelors degree in Engineering, Life Sciences, or related technical field; or equivalent experience in regulated industry may be considered in lieu of degree.
1-3 years of experience in Supplier Quality, Quality Engineering, or related role in medical device or regulated industry
Strong knowledge of ISO 13485 and medical device regulatory requirements
Understanding of quality systems and regulatory expectations (21 CFR Part 820, ISO 13485)