Job Description

Overview

Position: Quality Control Inspector (Temporary)

Department: Quality

Location: Santa Rosa, CA

WHO WE ARE:

Endologix LLC operates as a is a subsidiary of Rhevera Medical Holdings, LLC, a global medical device company focused on preserving and restoring the blood flow patients depend on. Our innovative vascular portfolio spans aortic repair, peripheral arterial disease, and thrombectomy, including the ALTO® Abdominal Stent Graft System, AFX®2 Endovascular AAA System, DETOUR™ System, and Pounce™ Thrombectomy System.

At Rhevera Medical, innovation is more than what we create. It’s how we think, collaborate, and move patient care forward. We’re building a mission-driven culture where your ideas matter, your growth is supported, and your work can make a meaningful difference.

Our Core Values guide the choices we make and the way we work, 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.

Ready to bring your ideas, experience, and passion to work that matters? Join us and help shape what’s next in vascular care.

Employment with Endologix LLC: Candidates applying for this position are applying for employment with Endologix LLC, which operates as is a Rhevera Medical company. Candidates for this role will not be employed, or jointly employed, by Rhevera Medical Holdings, LLC.

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

WHAT YOU'LL DO:

• 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.
• Inspect subassemblies, finished products, purchased components, and tools using defined criteria and standard measurement techniques.
• Conduct product rework on subassemblies or finished goods as required.
• Accurately document inspection and testing results in accordance with Good Documentation Practices (GDP).
• Review Device History Records (DHR) for compliance with established procedures and GDP requirements.
• Identify quality issues and provide well-reasoned recommendations for corrective actions or process improvements.
• Perform product testing to confirm conformance to quality standards.
• Work within a cleanroom environment, strictly following 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.
• Perform other duties as assigned by supervisor.
• Demonstrate punctuality, reliability, and a strong work ethic.

Qualifications

WHAT YOU'LL BRING:

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:

The compensation package includes:

• Target hourly range: $24.00/hr-$26.00/hr depending on experience

OUR COMMITMENT TO EQUAL OPPORTUNITY & VETERAN INCLUSION:

Endologix LLC, which operates as a Rhevera Medical company, 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.