Overview:
Join our mission-driven Quality team as the Quality Control Inspector 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 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:
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Patient Outcomes Drive Us: We improve lives with every advancement we deliver.
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Integrity Defines Us: We do what’s right, stay transparent, prioritize quality, and own our actions.
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Innovation Advances Us: We stay curious, adaptable, and push boundaries.
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Boldness Propels Us: We take smart risks and are unafraid in our pursuit of excellence.
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Collaboration Unites Us: We partner across teams and with physicians to drive exceptional results.
ABOUT THE ROLE:
We’re looking for a Quality Control Inspector to join our mission-driven Quality team. In this role, you’ll be 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).
Responsibilities:
WHAT YOU'LL DO:
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Perform audits, inspections, configuration checks, and functional testing to ensure product quality and compliance with established procedures, recognizing the importance of precision and consistency in delivering safe and reliable outcomes.
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Review and verify lot history records for completeness, accuracy, and adherence to SOPs; investigate records tied to customer experience reports, maintaining clear, objective, and well-documented quality decisions.
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Inspect subassemblies, finished products, purchased components, and tools using defined criteria and standard measurement techniques to ensure products consistently meet performance and quality expectations.
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Conduct product rework on subassemblies or finished goods as needed, applying sound judgment and careful attention to detail to preserve product integrity.
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Accurately document inspection and testing results in accordance with Good Documentation Practices (GDP), ensuring records are clear, traceable, and audit-ready.
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Review Device History Records (DHR) for compliance with established procedures and GDP requirements, reinforcing traceability and confidence in the manufacturing process.
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Identify quality issues and provide well-reasoned recommendations for corrective actions or process improvements, contributing to stronger, more efficient systems over time.
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Perform product testing to confirm conformance to quality standards, raising concerns and escalating issues promptly when expectations are not met.
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Work within a cleanroom environment, strictly following protocols and safety requirements to maintain controlled conditions and protect product quality.
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Perform environmental monitoring and manage ERP (QAD) and MES transactions while effectively prioritizing responsibilities in a fast-paced setting, working closely with cross-functional teams to resolve discrepancies and maintain workflow continuity.
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Support continuous improvement efforts by partnering with Manufacturing, Engineering, and Quality teams to enhance processes and drive consistent, dependable results.
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Take on additional responsibilities as needed, demonstrating adaptability, accountability, and a proactive approach to supporting team and organizational goals.
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Demonstrate punctuality, reliability, and a strong work ethic, consistently following through on commitments and delivering work with care and consistency.
Qualifications:
WHAT YOU'LL BRING:
Education:
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High School Diploma or equivalent required.
Experience:
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1–5 years of Quality Control experience, preferably in the medical device industry.
Skills/Competencies:
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Ability to understand and accurately follow technical procedures, work instructions, and specifications related to the inspection of products and components, recognizing the critical connection between disciplined execution and patient safety.
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Skill in interpreting technical drawings and documentation, identifying relevant details, and proactively escalating discrepancies to ensure transparency, quality, and timely resolution.
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Familiarity with applicable quality standards and a demonstrated commitment to learning and applying regulatory requirements with curiosity and attention to detail.
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Strong mechanical aptitude and working knowledge of measurement instruments, applying precision and sound judgment to uphold product performance and reliability.
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Clear and professional written and verbal communication skills to prepare reports, correspond effectively, and collaborate across teams in support of shared objectives.
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Mathematical proficiency in fractions, percentages, ratios, and proportions to accurately perform measurements, calculations, and data interpretation.
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Effective problem-solving skills with the ability to manage multiple priorities in a fast-paced, cross-functional environment, partnering constructively with others to drive practical solutions and continuous improvement.
WHAT WE OFFER:
At Endologix, we know that great work starts with great people — and people do their best when they feel valued and supported. That’s why we offer competitive pay, solid benefits, career growth, a culture that genuinely cares, and the flexibility you need to thrive both at work and at home. But more than that, we offer purpose. You’ll be part of a team that’s making a real impact on patients’ lives. When you join us, you’re not just taking a job, you’re building a meaningful career with a team that’s invested in your success.
The compensation package includes:
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Hourly rate of $24.03/hr-$29.44/hr
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Discretionary bonus
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Equity participation as approved by Board of Directors (4-year vesting schedule)
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Comprehensive health, dental, and vision insurance plans
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Flexible Health Savings Accounts (HSAs) and/or Flexible Spending Accounts (FSAs)
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Generous paid time off (vacation, sick leave, holidays, and flexible time off that is available for Exempt employees)
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401(k) retirement plan with company match
Plus:
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Flexible work arrangements, such as hybrid or remote work for many of our positions
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Employee wellness initiatives, mental health resources, and Employee Assistance Program (EAP)
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Employee recognition programs and awards
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Commuter benefits or transportation stipends
OUR COMMITMENT TO EQUAL OPPORTUNITY & VETERAN INCLUSION:
Endologix LLC is an Equal Opportunity and Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status, or any other characteristic protected by applicable federal, state, or local law. As a federal contractor, Endologix LLC is committed to taking affirmative action to recruit, employ, and advance in employment qualified individuals with disabilities and protected veterans.
