QA Engineer ensuring software quality at LCCC, collaborating with development teams and implementing effective testing strategies. Reporting to Software Engineering Manager for continuous improvement in testing processes.
About the role
- Supplier Quality Engineer responsible for managing supplier quality performance across Asia and EMEA. Collaborating with internal and external partners to ensure compliance and continuous improvement.
Responsibilities
- Manage and monitor quality performance of suppliers across Asia and EMEA.
- Build strong supplier relationships to ensure alignment on quality and operational goals.
- Review quality audits to ensure compliance with ISO 13485, ISO 9001, MDR 2017/745 and customer requirements.
- Implement and maintain supplier quality processes and control plans with QA.
- Lead SCAR investigations and ensure effective CAPA implementation.
- Ensure supplier compliance with all relevant international standards and regulations.
- Partner with Procurement, Quality & Regulatory, Operations and Supply Chain to align supplier quality with business needs.
- Serve as primary quality contact for suppliers and resolve issues efficiently.
- Support qualification of new suppliers and collaborate closely with Medline Shanghai.
- Maintain accurate records of supplier audits, metrics and corrective actions.
- Provide regular supplier quality performance reports and risk insights.
- Use data analysis to identify root causes and drive strategic improvements.
- Identify and lead quality and process improvement initiatives internally and with suppliers.
- Apply best practices to strengthen the QMS and reduce non‑conformances.
- Monitor and improve key KPIs such as PPM, on‑time delivery, audit outcomes, complaints, and inspection results.
Requirements
- Bachelor’s degree in engineering, Supply Chain Management or a related field.
- Minimum five years of experience in Supplier Quality Management, ideally in global manufacturing or medical devices.
- In‑depth knowledge and formal training in ISO 9001, ISO 13485, and MDR 2017/745.
- Certified Quality Engineer (CQE), Six Sigma Green/Black Belt or equivalent certification.
- ISO 13485 Lead Auditor certification.
- Proficiency in Excel, Power BI and data analysis/reporting tools.
- Strong understanding of supplier quality processes and quality standards.
Benefits
- An opportunity to make a significant impact during a pivotal phase in Medline’s growth and transformation.
- A dynamic, international work environment.
- Direct exposure to senior leadership and involvement in high-visibility projects.
- One-year contract, with the expectation of a permanent contract following successful completion.
- Market based base salary and a bonus plan.
- Employee Assistance Program and wellness allowance.
- 26 vacation days with the option to purchase 5 additional days.
Job title
Job type
Experience level
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Not specified
Degree requirement
Location requirements
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