Quality Control Inspector

Endologix•Santa Rosa, CA

53d•$24 - $26

About The Position

Endologix LLC is seeking a temporary Quality Control Inspector for its Quality team in Santa Rosa, California. The role inspects components, subassemblies, and finished medical devices to ensure they meet quality standards and regulatory requirements. Work includes quality checks, performance testing, documentation review, and verification of Device History Records (DHR) for product release under the medical device Quality Management System (QMS). The inspector works in a cleanroom, documents results using Good Documentation Practices, and collaborates with Manufacturing, Engineering, and Quality teams to address discrepancies and support continuous improvement.

Requirements

High school diploma or equivalent.
1–5 years of Quality Control experience.
Ability to understand and follow technical procedures, work instructions, and basic product and component specifications.
Ability to identify relevant information in technical drawings and documents and report discrepancies to a supervisor.
Familiarity with applicable quality standards and willingness to learn specific regulations under supervision.
Mechanical aptitude and working knowledge of measurement instruments.
Strong written and verbal communication skills.
Mathematical proficiency in fractions, percentages, ratios, and proportions.
Problem-solving skills and ability to work cross-functionally while managing multiple priorities.

Nice To Haves

Quality Control experience in the medical device industry.

Responsibilities

Perform audits, inspections, configuration checks, and functional testing in accordance with established procedures.
Review lot history records for completeness, accuracy, and adherence to SOPs, and investigate records associated with customer experience reports.
Inspect subassemblies, finished products, purchased components, and tools using defined criteria and standard measurement techniques.
Rework subassemblies or finished goods as needed while preserving product integrity.
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 recommend corrective actions or process improvements.
Test products for conformance to quality standards and promptly escalate issues.
Work in a cleanroom while following applicable protocols and safety requirements.
Perform environmental monitoring and manage ERP (QAD) and MES transactions.
Prioritize work and collaborate with cross-functional teams to resolve discrepancies and maintain workflow.
Support continuous improvement with Manufacturing, Engineering, and Quality teams.
Take on additional responsibilities as needed and demonstrate punctuality, reliability, and a strong work ethic.