Quality Control Inspector- Temporary

Overview

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 training—supported by industry-leading clinical evidence.

At Endologix, we’re 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 you’re passionate about making a meaningful difference in healthcare, you’ll 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 what’s 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:

The Quality Control Inspector is responsible for performing inspections of components, subassemblies, and finished medical devices to ensure compliance with quality standards and regulatory requirements. This includes conducting quality checks, performance tests, reviewing documentation, and verifying Device History Records (DHR) for product release in accordance with the medical device Quality Management System (QMS).

What You’ll Do:

• Conduct detailed inspections of purchased components, tooling, subassemblies, and finished products using established measurement techniques, ensuring all evaluations support safe and effective patient outcomes.
• Identify nonconforming materials and take appropriate action, including rework or rejection, maintaining a strong commitment to quality and accountability.
• Adhere to established procedures and systems, demonstrating consistency, integrity, and respect for standardized processes.
• Accurately document inspection and testing results in compliance with Good Documentation Practices (GDP), ensuring transparency and traceability.
• Maintain controlled documentation and test records with a high level of accuracy and timeliness.
• Inspect and support the maintenance and calibration of test equipment and fixtures to ensure reliable and precise performance.
• Review Device History Records and related documentation to verify compliance with procedures and documentation standards.
• Assess quality issues and contribute thoughtful recommendations for corrective actions and continuous improvement.
• Partner cross-functionally with quality and production teams to enhance assembly accuracy, compliance, and overall product excellence.
• Operate effectively within a cleanroom environment, following all protocols to maintain product integrity.
• Perform product testing to verify conformance to established quality standards and performance expectations.
• Demonstrate reliability, accountability, and a proactive approach to work, contributing positively to team goals and shared success.

What You’ll Bring:

Education:

• AA degree or higher required.

Experience

• 3–6 years of Quality Control experience, in the medical device industry.

Skills/

Competencies:

• Mechanical aptitude and working knowledge of measurement instruments.
• Proficiency in Microsoft Excel and Word.
• Ability to read and interpret technical procedures, drawing, specifications, ASTM standards, and medical device regulatory requirements.
• Strong…