More jobs:
Quality Control Technician | GMP Manufacturing | 1st Shift
Job in
El Paso, El Paso County, Texas, 88568, USA
Listed on 2026-07-27
Listing for:
ManpowerGroup
Full Time
position Listed on 2026-07-27
Job specializations:
-
Quality Assurance - QA/QC
Quality Control - QC Analysts/Managers, Production QC/QA, Quality Engineering, Regulatory Compliance Specialist -
Manufacturing / Production
Production QC/QA, Quality Engineering, Regulatory Compliance Specialist
Job Description & How to Apply Below
Our client, a global leader in Medical Device Manufacturing, is seeking a Quality Control Inspector / QC Technician to join their team. As a Quality Control Inspector / QC Technician, you will be part of the Quality Control Department supporting the Incoming Inspection, Quality Assurance, and Manufacturing Operations teams. The ideal candidate will have strong attention to detail, excellent documentation skills, and the ability to follow regulated procedures, which will align successfully within the organization.
Job Title:Quality Control Inspector / QC Technician – Medical Device Manufacturing
Location:El Paso, TX
Pay Range:$16.50 - $17.50 per hour (DOE)
Shift:1st Shift: 6:00 AM – 2:30 PM or 8:30 AM – 5:00 PM
Contract Type:Long-Term Contract (12 Months+)
What's the Job?- Perform raw material sampling and incoming inspections to ensure compliance with quality standards and specifications.
- Follow documented inspection procedures, SOPs, and quality processes while maintaining accuracy and consistency.
- Maintain quality reports, inspection records, notebooks, and related documentation.
- Support calibration, preventive maintenance, and quality system compliance activities.
- Assist with FDA, GMP, safety, audit readiness, and continuous improvement initiatives within the facility.
- High School Diploma or GED required.
- Experience in Quality Control, Quality Assurance, Inspection, Manufacturing, Laboratory, or a related environment preferred.
- Ability to follow detailed written procedures, SOPs, and multi-step work instructions.
- Strong attention to detail with experience maintaining accurate records and documentation.
- Comfortable working in a regulated manufacturing environment focused on quality, safety, and compliance.
- Opportunity to work for a globally recognized medical device manufacturing company.
- Stable first-shift schedule with multiple shift options available.
- Gain experience in FDA-regulated and GMP-compliant manufacturing environments.
- Develop valuable quality inspection, documentation, and compliance skills.
- Long-term assignment with potential for professional growth and future opportunities.
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