Quality Control Inspector
$24 - $26 per hourEndologix
Overview Position: Quality Control Inspector Department: Quality Location: Santa Rosa, CA WHO WE ARE: Endologix LLC operates as 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.
- 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.
- High School Diploma or equivalent required.
- 1-5 years of Quality Control experience, preferably in the medical device industry.
- 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.
- Hourly range: $24.00/hr-$26.00/hr
Vacancy posted 4 days ago
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