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Join our Quality team as the Supplier Quality Engineer at Endologix!

WHO WE ARE:

Endologix LLC is a California-based global medical device company dedicated to improving patients lives through innovative therapies for the interventional treatment of vascular disease. Our therapeutic portfolio addresses clinically relevant unmet needs, spanning from abdominal aortic aneurysms to lower limb peripheral vascular disease. We are committed to delivering excellent clinical outcomes through precision in product design, advanced manufacturing, and comprehensive physician trainingsupported by industry-leading clinical evidence. At Endologix, were driven by purpose, innovation, and the opportunity to make a lasting impact in vascular health.

What sets us apart is not just our technology, but our culture. At Endologix, we foster a forward-thinking, mission-driven environment where every team member plays a vital role in advancing patient care. Our core values guide how we operate. As for our people? We empower them with the tools, trust, and continuous learning they need to grow. If youre passionate about making a meaningful difference in healthcare, youll find purpose and belonging here.

Our Core Values are the guiding principles informing our choices and actions, because our customers and patients depend on us:

• Patient Outcomes Drive Us: We improve lives with every advancement we deliver.
• Integrity Defines Us: We do whats right, stay transparent, prioritize quality, and own our actions.
• Innovation Advances Us: We stay curious, adaptable, and push boundaries.
• Boldness Propels Us: We take smart risks and are unafraid in our pursuit of excellence.
• Collaboration Unites Us: We partner across teams and with physicians to drive exceptional results.

ABOUT THE ROLE:

We're looking for a Supplier Quality Engineer to join our Quality team. In this role, you'll be responsible for ensuring that purchased materials, components, and services meet defined quality, regulatory, and business requirements. This role partners closely with suppliers and internal cross-functional teams to manage supplier performance, drive continuous improvement, and support product quality throughout the product lifecycle. The SQE plays a critical role in supplier management and development, change management and issue resolution in a regulated medical device environment.

Please note, this is not an entry-level position and is designed for an experienced, hands-on professional who can operate with a high degree of independence while continuing to build depth and expertise within supplier quality and regulatory practices.

WHAT YOU'LL DO:

• Lead supplier identification, qualification, maintenance, and ongoing monitoring initiatives to ensure external partners consistently meet quality, regulatory, and performance expectations.
• Own and maintain the Approved Supplier List (ASL) and Approved Component List (ACL), ensuring records are accurate, complete, and aligned with quality system and regulatory requirements.
• Serve as the quality representative for supplier-related change orders, performing evaluations, impact assessments, and change order processing to safeguard product performance and patient safety.
• Review and approve supplier changes, deviations, and documentation to ensure transparency, regulatory compliance, and adherence to internal quality standards.
• Lead and manage supplier Corrective and Preventive Actions (CAPAs) and Supplier Corrective Action Requests (SCARs), facilitating root cause investigations, corrective action implementation, and effectiveness verification.
• Investigate supplier-related nonconformances and quality issues, coordinating containment actions, corrective measures, and risk assessments to prevent recurrence and protect product reliability.
• Support MRB activities, nonconforming material dispos tion, and failure investigations associated with outsourced products or services, ensuring timely and well-informed decisions.
• Develop, review, and maintain clear, high-quality technical documentation including procedures, reports, justifications, and quality records that support traceability, compliance, and operational excellence.
• Partner cross-functionally with Engineering, Manufacturing, Regulatory Affairs, Supply Chain, and Operations to maintain product quality and ensure uninterrupted supply of critical components.
• Support supplier audits through preparation, participation, and follow-up activities, working collaboratively with suppliers to address findings and strengthen quality systems.
• Apply structured project management practices to manage multiple initiatives, timelines, and deliverables while maintaining a high standard of execution.
• Drive continuous improvement of supplier quality processes, tools, and performance metrics to strengthen supplier partnerships and enhance overall product quality.
• Perform other duties as assigned by the supervisor in support of departmental and organizational objectives.