Quality Control Inspector

Us-Ca-Santa Rosamid
OtherQuality Control Inspector
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Quick Summary

Overview

Overview Join our mission-driven Quality team as the Quality Control Inspector at Endologix!

Key Responsibilities

Conduct detailed inspections of purchased components, tooling, subassemblies, and finished products using established measurement techniques, ensuring all evaluations support safe and effective patient outcomes.

Requirements Summary

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.

Technical Tools
excel

 

 

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.

About the Role

~1 min read

 

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

~1 min read

Responsibilities

~1 min read

 

  • 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.

Requirements

~1 min read

 

  • AA degree or higher required. 
  • 3–6 years of Quality Control experience, in the medical device industry.
  • 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 written and verbal communication skills for reports, correspondence, and presentations.
  • Mathematical proficiency in probability, statistical inference, fractions, percentages, ratios, and proportions.
  • Problem-solving skills with the ability to work in a cross-functional environment and manage multiple priorities.
  • Experienced in using measuring equipment such as Microscope, CMM, Instron tester, calipers, pin gauge, micrometer, snap gauge etc.

What We Offer

~1 min read
Hourly pay of $24.03-$29.44/hr

 

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.

Location & Eligibility

Where is the job
Us-Ca-Santa Rosa
On-site at the office
Who can apply
Same as job location

Listing Details

Posted
April 24, 2026
First seen
May 6, 2026
Last seen
May 6, 2026

Posting Health

Days active
0
Repost count
0
Trust Level
19%
Scored at
May 6, 2026

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careersus-endologixQuality Control Inspector