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Quality Control Inspector (QC Inspector)

Endologix Inc

Santa Rosa, CATemporarySeen todaySeen in employer's feed today

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At a glance

Compensation
No compensation found
Location
Santa Rosa, CA
Schedule
Temporary
Work Authorization
Not specified

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Job overview

The Temporary Quality Control Inspector joins Endologix’s Quality team to inspect components, subassemblies, and finished medical devices for compliance with quality standards and regulatory requirements. The role performs quality checks and testing, reviews documentation and Device History Records for product release, and supports quality improvements in a medical-device manufacturing environment.

Skills & qualifications

RequiredNice to have

Skills

Quality InspectionFunctional TestingConfiguration ChecksLot History Record ReviewStandard Measurement TechniquesProduct ReworkGood Documentation PracticesDevice History Record ReviewCorrective Action RecommendationsEnvironmental MonitoringQADMESCross-Functional CollaborationPrioritizationAttention to Detail

Full job description

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 trainingsupported by industry-leading clinical evidence. At Endologix, were 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 youre passionate about making a meaningful difference in healthcare, youll find purpose and belonging here. Our Core Values are the guiding principles informing our choices and actions, 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 whats 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: Were looking for a temporary Quality Control Inspector to join our mission-driven Quality team. In this role, youll 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). 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, 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 clea room 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.

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