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QA Specialist – Medical Device Manufacturing | 2nd Shift | $27+​/hr

Job in Mebane, Alamance County, North Carolina, 27302, USA
Listing for: Manpower
Full Time position
Listed on 2026-08-02
Job specializations:
  • Quality Assurance - QA/QC
    Production QC/QA, Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 27 USD Hourly USD 27.00 HOUR
Job Description & How to Apply Below
Position: QA Specialist – Medical Device Manufacturing | 2nd Shift | $27+/hr |

QA Specialist – Liquid Media (2nd Shift)

Our client, a leading medical device manufacturing organization, is seeking a QA Specialist – Liquid Media (2nd Shift) to join their team. As a QA Specialist, you will be part of the Quality Assurance department supporting Manufacturing, Quality Control, Engineering, and Maintenance teams. The ideal candidate will have strong attention to detail, critical thinking skills, and effective communication, which will align successfully in the organization.

Location:

Mebane, NC (Onsite)

Pay Range: $27.10 – $27.50 per hour

What's the Job?
  • Perform in-process quality checks and spot inspections on the production floor
  • Review production documentation in real time to ensure accuracy and GDP compliance
  • Verify line setup and line clearance activities prior to production
  • Identify nonconformances, initiate containment actions, and escalate issues as needed
  • Support investigations through documentation review and data collection
What's Needed?
  • Minimum 2 years of experience in manufacturing or quality within an FDA-regulated or ISO 13485 environment
  • Working knowledge of Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP)
  • Experience with inspection, documentation review, or production support activities
  • Ability to work on the production floor (standing/walking for extended periods)
  • Strong attention to detail and ability to identify errors and compliance risks
What's in it for me?
  • Competitive hourly pay within a regulated manufacturing environment
  • Consistent 2nd shift schedule (Monday–Friday)
  • Opportunity to gain hands-on experience in medical device quality operations
  • Exposure to cross-functional teams and quality systems
  • Valuable experience supporting FDA/ISO-compliant processes

If this is a role that interests you and you'd like to learn more, click apply now and a recruiter will be in touch with you to discuss this great opportunity. We look forward to speaking with you!

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