Supplier Quality Engineer (Fixed Term)

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Job Reference:

540f2a443bea

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2

Posted:

26.04.2025

Expiry Date:

10.06.2025

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Job Description:

About Zimmer Biomet

Zimmer Biomet is a global leader in medical technology with nearly 100 years of innovation. Our mission is to improve mobility and quality of life through our products and technologies, impacting patients worldwide.

We are committed to fostering an inclusive environment that promotes development, employee resource groups, flexible working, competitive rewards, wellness incentives, and recognition programs.

Position Overview

This is a fixed-term, full-time role supporting a global project ending September 2026. The Supplier Quality Engineer (SQE) ensures the delivery of high-quality products to our customers by managing supplier quality processes.

1. Support overall Supplier Quality Management activities.
2. Evaluate new and existing suppliers, resolve supplier issues promptly.
3. Conduct supplier qualifications, material assessments, and maintain approved supplier lists.
4. Perform audits to ensure compliance with regulatory and corporate standards.
5. Participate in new product development and process improvement teams, establishing quality policies for suppliers.

Key Responsibilities

1. Conduct external system and process audits at suppliers.
2. Follow-up on supplier corrective actions and report metrics.
3. Assist project teams with quality issues.
4. Monitor corrective action effectiveness, assist in developing strategies.
5. Identify risks related to quality systems and compliance.
6. Analyze quality metrics, develop reports, and recommend improvements.
7. Collaborate with sourcing to track supplier performance and quality issues.
8. Approve supplier selection through qualification processes.
9. Support qualification of new parts and supplier change management.
10. Build strong relationships with global supplier management and project teams.

Desired Qualifications

1. Ability to interpret drawings and technical documentation.
2. Knowledge of regulatory standards (FDA, ISO 13485, GMP).
3. Experience in auditing and applying standards.
4. Proficiency in MS Office, SAP, and MS Project.
5. Strong report writing and communication skills.
6. Technical background with a degree or equivalent.
7. Auditor certification preferred.
8. Experience in medical devices or pharmaceutical manufacturing.
9. Analytical and problem-solving skills, attention to detail.
10. Fluent in English, both written and spoken.

Travel Requirements

Up to 10% travel expected.

EOE/M/F/Vet/Disability