Quality Control Inspector

Endologix LLC; Santa Rosa (CA); On-site; USD 33,000 - 36,000; Full time

Benefits offered by this job

Competitive pay

Career growth

Work-life flexibility

Job summary

Endologix LLC is seeking a Temporary Quality Control Inspector to perform inspections of components, subassemblies, and finished medical devices per QMS and GDP. You will review DHRs, conduct tests, and document results in a regulated, audit-ready format.

The role requires 1–5 years in quality control within medical devices, strong procedural skills, and meticulous attention to detail in a fast-paced manufacturing environment.

Qualifications

• High school diploma or equivalent required.
• 1–5 years of quality control experience, preferably in medical devices.
• Ability to follow procedures and interpret technical documentation.

Responsibilities

• Perform audits, inspections, and functional testing to ensure product quality and compliance.
• Review lot history records for completeness and accuracy according to SOPs.
• Inspect subassemblies, finished products, and purchased components using defined criteria.
• Document inspection and testing results in GDP-compliant records.
• Identify quality issues and recommend corrective actions or process improvements.

Skills

Procedural understanding

Reading drawings

Quality standards

Measuring tools

Written & verbal communication

Problem solving

Education

High School Diploma or equivalent

Tools

QAD ERP

MES system

Measurement instruments

Job description

Overview

Join our mission-driven Quality team as the Temporary 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.

• 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

We’re looking for a temporary 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, recognizing the importance of precision and consistency in delivering safe and reliable outcomes.
• 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.
• Inspect subassemblies, finished products, purchased components, and tools using defined criteria and standard measurement techniques to ensure products consistently meet performance and quality expectations.
• Conduct product rework on subassemblies or finished goods as needed, applying sound judgment and careful attention to detail to preserve product integrity.
• Accurately document inspection and testing results in accordance with Good Documentation Practices (GDP), ensuring records are clear, traceable, and audit-ready.
• Review Device History Records (DHR) for compliance with established procedures and GDP requirements, reinforcing traceability and confidence in the manufacturing process.
• Identify quality issues and provide well-reasoned recommendations for corrective actions or process improvements, contributing to stronger, more efficient systems over time.
• Perform product testing to confirm conformance to quality standards, raising concerns and escalating issues promptly when expectations are not met.
• Work within a cleanroom environment, strictly following protocols and safety requirements to maintain controlled conditions and protect product quality.
• 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.
• Support continuous improvement efforts by partnering with Manufacturing, Engineering, and Quality teams to enhance processes and drive consistent, dependable results.
• Take on additional responsibilities as needed, demonstrating adaptability, accountability, and a proactive approach to supporting team and organizational goals.
• Demonstrate punctuality, reliability, and a strong work ethic, consistently following through on commitments and delivering work with care and consistency.

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 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

• Target hourly range: $24.00/hr-$26.00/hr

Our Commitment To Equal Opportunity & Veteran Inclusion

Endologix LLC is an Equal Opportunity and Affimative 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.