Supplier Quality Engineer 3

Position Summary

The Supplier Quality Engineer III (SQE III) leads supplier quality activities to ensure consistent delivery of high-quality materials, components, and services. This role is responsible for driving supplier performance through qualification, risk management, audits, and continuous improvement.
The SQE III partners with cross-functional teams to assess supplier risks, resolve complex quality issues, and support new product introductions, design transfers, and supplier changes. Acting as a subject matter expert, the role drives compliance, mentors junior team members as needed, and uses data-driven insights to proactively manage supplier performance and risk.

Principal Responsibilities

•    Drive supplier quality performance across commodities, PFGs, and critical services, ensuring alignment with business and quality objectives
•    Lead supplier qualification and approval activities for new and existing suppliers, including risk assessment and compliance evaluation
•    Advance supplier capability through targeted development initiatives focused on quality, performance, and risk reduction
•    Lead resolution of supplier quality issues, including oversight of SCARs, root cause effectiveness, and escalation as needed
•    Support new product introductions, design transfers, and supplier changes to ensure robust supplier quality and process readiness
•    Drive continuous improvement by analyzing supplier performance data, identifying trends, and implementing proactive actions
•    Oversee supplier-related quality activities including audits, quality planning, and performance reviews
•    Lead cross-functional supplier quality initiatives and represent Supplier Quality in business and project teams
•    Support integration of acquired suppliers into the Teleflex quality system and standards
•    Ensure compliance with applicable regulatory requirements, quality standards, and company policies

Education / Experience Requirements

•    Bachelor’s degree in engineering, science, or related technical discipline preferred
•    5–10 years of experience in a regulated industry, preferably medical devices
•    Strong knowledge of applicable regulations and standards (e.g., 21 CFR 820, ISO 13485, ISO 9001), with emphasis on supplier controls
•    Demonstrated expertise in problem-solving and root cause analysis methodologies
•    Experience applying statistical techniques to support quality and process improvement

•    Proven experience in supplier or quality auditing (third-party certification preferred)
•    Professional certification (e.g., ASQ CQE) or equivalent technical qualification preferred

Specialized Skills / Other Requirements

•    Experience supporting manufacturing environments and supplier quality activities
•    Strong analytical and data-driven decision-making skills
•    Effective communication and technical writing skills
•    Ability to present information clearly and influence cross-functional teams
•    Experience facilitating problem-solving and improvement initiatives
•    Proficiency in standard business and quality tools (e.g., Excel, PowerPoint, SharePoint, statistical software such as Minitab)

TRAVEL REQUIRED: 30 %

WORKING ENVIRONMENT:
☒ Office/Professional    

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