Quality Control Inspector

Endologix • Santa Rosa, CA

2d • $24 - $29

About The Position

We’re looking for a 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).

Requirements

• 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.

Responsibilities

• Perform audits, inspections, configuration checks, and functional testing to ensure product quality and compliance with established procedures.
• Review and verify lot history records for completeness, accuracy, and adherence to SOPs; investigate records related to customer experience reports.
• Inspect subassemblies, finished products, purchased components, and tools using defined criteria and standard mechanical, and/or electrical measurements.
• Conduct product rework on subassemblies or finished goods as required.
• Accurately document inspection and testing results in compliance with Good Documentation Practices (GDP).
• Review Device History Records (DHR) for compliance with established procedures and GDP requirements.
• Identify issues and provide initial recommendations for corrective actions or process improvements to supervisors.
• Perform product testing to ensure conformance to quality standards.
• Work within a cleanroom environment, following all applicable 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 the supervisor.
• Demonstrate punctuality, reliability, and a strong work ethic.

Benefits

• Hourly rate of $24.03/hr-$29.44/hr
• Discretionary bonus
• Equity participation as approved by Board of Directors (4-year vesting schedule)
• Comprehensive health, dental, and vision insurance plans
• Generous PTO and holiday schedule
• 401(k) retirement plan with company match
• Employee wellness initiatives and mental health support
• Collaborative and inclusive company culture focused on impact and innovation
• Opportunities for career growth and internal mobility

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: High school or GED
• Number of Employees: 501-1,000 employees