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Quality Control Inspector

Job in Santa Rosa, Sonoma County, California, 95402, USA
Listing for: Endologix LLC
Full Time position
Listed on 2025-12-28
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering
Salary/Wage Range or Industry Benchmark: 80000 - 100000 USD Yearly USD 80000.00 100000.00 YEAR
Job Description & How to Apply Below

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 values guide how we operate: we prioritize patient outcomes, act with integrity, stay curious and innovative, move boldly in pursuit of excellence, and collaborate across teams and with physicians to achieve exceptional results.

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.

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
  • Perform audits, inspections, configuration checks, and functional testing to ensure product quality and compliance with established procedures.
  • Review and verify lot history records for completeness, accuracy, and adherence to SOPs; investigate records related to customer experience reports.
  • Inspect subassemblies, finished products, purchased components, and tools using defined criteria and standard mechanical, and/or electrical measurements.
  • Conduct product rework on subassemblies or finished goods as required.
  • Accurately document inspection and testing results in compliance with Good Documentation Practices (GDP).
  • Review Device History Records (DHR) for compliance with established procedures and GDP requirements.
  • Identify issues and provide initial recommendations for corrective actions or process improvements to supervisors.
  • Perform product testing to ensure conformance to quality standards.
  • Work within a cleanroom environment, following all applicable protocols and safety requirements.
  • Perform temperature and particle count monitoring; manage ERP (QAD) and MES application transactions; handle multiple tasks efficiently in a fast-paced manufacturing environment.
  • Demonstrate punctuality, reliability, and a strong work ethic.
Qualifications Education
  • High School Diploma or equivalent required.
Experience
  • 1–5 years of Quality Control experience, preferably in the medical device industry.
Skills/Competencies
  • Ability to understand and follow technical procedures, work instructions, and basic specifications related to the inspection of products and components.
  • Skill in identifying relevant information in technical drawings and documents and reporting any discrepancies to the supervisor.
  • Familiarity with applicable quality standards and willingness to learn about specific regulations under supervision
  • Mechanical aptitude and working knowledge of measurement instruments.
  • Strong written and verbal communication skills for reports, correspondence, and presentations.
  • Mathematical proficiency in fractions, percentages, ratios, and proportions.
  • Problem-solving skills with the ability to work in a cross-functional environment and manage multiple priorities.
What We Offer

At Endologix, we know that great work starts…

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