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Quality Control Inspector -SR

Job in Santa Rosa, Sonoma County, California, 95402, USA
Listing for: Marquee Staffing
Full Time position
Listed on 2026-10-14
Job specializations:
  • Quality Assurance - QA/QC
    Quality Control - QC Analysts/Managers
  • Manufacturing / Production
Salary/Wage Range or Industry Benchmark: 24 - 26 USD Hourly USD 24.00 26.00 HOUR
Job Description & How to Apply Below

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.

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