Quality Control Inspector -SR Marquee Staffing Inc - 4.0 Santa Rosa, CA Job Details Temp-to-hire $24 - $26 an hour 15 hours ago Qualifications Inspection gauge Mechanical blueprint interpretation Regulatory compliance Good documentation practices (GDP) High school diploma or GED Manufacturing standard operating procedures Mechanical drawings Dimensional measurements Math Quality assurance standard operating procedures Quality control communication Cross-functional collaboration Standard operating procedures (SOPs) Mechanical knowledge Cross-functional communication

Full Job Description Location:

Santa Rosa, CA Pay Rate:

$24-$26/hr

DOE Schedule:

Monday-Thursday Position Summary Perform inspections of components, subassemblies, and finished medical devices to ensure compliance with quality standards, procedures, and regulatory requirements. Key Responsibilities Perform inspections, audits, configuration checks, functional testing, and product testing. Inspect components, subassemblies, finished products, purchased components, and tools. Review lot history records and Device History Records (DHR) for completeness, accuracy, SOP compliance, and Good Documentation Practices (GDP). Use mechanical and/or electrical measurement instruments. Accurately document inspection and testing results. Perform product rework as needed. Identify quality issues and report discrepancies or recommendations for corrective action. Work in a cleanroom environment and follow required protocols. Perform temperature and particle-count monitoring. Process transactions in QAD ERP and MES systems. Manage multiple priorities in a fast-paced manufacturing environment. Requirements High School Diploma or equivalent required. 1-5 years of Quality Control experience. Medical device industry experience preferred. Ability to follow technical procedures, work instructions, SOPs, and specifications. Ability to read technical drawings and identify discrepancies. Mechanical aptitude and working knowledge of measurement instruments. Familiarity with quality standards and regulated manufacturing. Strong documentation, communication, math, and problem-solving skills. Reliable, accountable, and able to work effectively across teams. Preferred Experience Medical device or regulated manufacturing. DHR review. GDP/QMS. Cleanroom environment. QAD, MES, or similar systems. #MS-OCMFG