QA/QC Technician

Contract: Pomona, California, US

Salary Range: 20.00 - 25.00 | Per Hour

Job Code: 360508

End Date: 2025-05-01

Days Left: 9 days, 8 hours left

Position Details:
Industry: Medical Devices
Job Title: QA/QC Technician - Onsite 
Location: Pomona, CA 91767
Duration: 09-12+ months [+ Possibilities of extension]
 
 
Pay Range: $20-$25/hr 
 
Summary: 
Perform a wide variety of activities to support the Quality Management System.
 
Responsibilities: 
 
  • Conduct product testing, including testing to support complaint investigations and stability verification
  • Generate product testing results reports
  • Review production batch records (DHR's) for accuracy and completeness in order to approve intermediate products for use in production. Review finished goods batch records. Report all deviations in these records and assures these have been addressed and resolved prior to issuing approval.
  • Conduct spot-check inspections/audits of production operations
  • Participate in the internal audit program
  • Write, review and approve Standard Operating Procedures (SOPs) as necessary
  • May assist in supporting the Document Control program, record retention areas, and sample retention areas
  • May support returned instrument processing: Log returned instruments from the field. Decontaminate returned instruments in a Biohazard level II environment following standard operating procedure and documenting decontamination as required. Inspect returned instruments for damage, and performing basic investigation and documenting results prior to second level processing. As necessary, process instrument documentation for return to repair facility, and pack instruments as required.
  • Other duties as assigned by supervisor
 
Qualifications: 
  • High School/AS/BS degree in a scientific or technical area or equivalent combination of experience and education. At least one year in quality assurance role in medical device industry is preferred.
  • Ability to follow Good Manufacturing/Laboratory Practices (GMP and GLP)
  • Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals.
  • Ability to write routine reports and correspondence. Ability to speak effectively before small groups of customers or employees of organization.
  • Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
 
Job Requirement
  • QA
  • Quality Assurance
  • inspection
  • inspect
  • batch record
  • DHR
  • device history file
  • MDR
  • medical devices
  • mdical devic
  • ISO 13485
  • GMP
  • GLP
  • Testing
  • troubleshooting
Reach Out to a Recruiter
  • Recruiter
  • Email
  • Phone
  • Niharika Shrivastava
  • niharika.shrivastava@collabera.com
Apply Now
Apply Now
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