Quality Control Technician

Intellectt INC

  • Pomona, CA
  • 5 days ago
  • $24–$25
Want to know if you’re a fit?
Upload your resume and let our AI show you.

Skills

  • Auditingunmatched
  • Detail Orientedunmatched
  • Document Controlunmatched
  • Documentationunmatched
  • GLP (Good Laboratory Practices)unmatched
  • GMP (Good Manufacturing Practices)unmatched
  • Internal Auditunmatched
  • Maintain Complianceunmatched
  • Manufacturingunmatched
  • Medical Equipmentunmatched
  • Procedure Developmentunmatched
  • Product Reviewsunmatched
  • Product Supportunmatched
  • Product Testingunmatched
  • Quality Assuranceunmatched
  • Quality Controlunmatched
  • Quality Managementunmatched
  • Quality Metricsunmatched
  • Returns Processingunmatched
  • Standard Operating Procedures (SOP)unmatched
  • Support Documentationunmatched
  • Testingunmatched

Description

Job Title: Quality Control Technician

Location:Pomona, CA
Duration:6 months
Shift:8:00 AM 5:00 PM

Job Summary

We are seeking a Quality Control Technician to support the Quality Management System in a medical device manufacturing environment. The ideal candidate will perform product testing, review batch records, conduct inspections and audits, maintain quality documentation, and ensure compliance with GMP, GLP, and company quality standards.

Key Responsibilities

  • Perform product testing and support complaint investigations.
  • Generate and maintain testing reports.
  • Review production batch records (DHRs) for accuracy and compliance.
  • Conduct production inspections and quality audits.
  • Participate in internal audit activities.
  • Write, review, and update SOPs.
  • Support document control and record retention.
  • Process returned instruments, including decontamination, inspection, and documentation.
  • Ensure compliance with GMP, GLP, and quality procedures.

Required Qualifications

  • Bachelor's degree in a scientific or technical field or equivalent experience.
  • 1+ year of Quality Assurance/Quality Control experience in the medical device industry preferred.
  • Knowledge of GMP, GLP, and quality systems.
  • Experience reviewing batch records and quality documentation.
  • Strong attention to detail and documentation skills.
  • Proficient in Microsoft Office and database/spreadsheet applications.
  • Ability to work independently and follow established procedures

Numbers & Facts

LocationPomona, CA
Salary$24–$25

Similar Jobs

See more jobs