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Quality Assurance Specialist

Job in Greenville, Pitt County, North Carolina, 27834, USA
Listing for: Manpower
Full Time position
Listed on 2026-08-29
Job specializations:
  • Quality Assurance - QA/QC
    Regulatory Compliance Specialist, Quality Control - QC Analysts/Managers, Production QC/QA, Quality Engineering
Salary/Wage Range or Industry Benchmark: 15 USD Hourly USD 15.00 HOUR
Job Description & How to Apply Below

Quality Assurance Specialist

Our client, a leading organization in the medical device manufacturing industry, is seeking a dedicated Quality Assurance Specialist to join their team. As a Quality Assurance Specialist, you will be an integral part of the quality assurance department supporting manufacturing and compliance efforts. The ideal candidate will demonstrate attention to detail, proactive problem-solving skills, and a strong commitment to quality standards, which will align successfully in the organization.

Job Title:

Quality Assurance Specialist

Location:

Greenville, NC

Pay Range: $15.00

Shift: Multiple Shifts

What's the Job?

  • Perform daily quality assessments of facility, personnel, manufacturing activities, and documentation to ensure compliance with site procedures, QMS, cGMPs, and regulatory requirements.
  • Interact with employees to troubleshoot issues, correct documentation, and provide guidance on manufacturing practices and contamination control.
  • Promote a quality-focused culture by helping personnel understand and apply quality policies, process controls, and regulatory standards.
  • Participate in quality event response, providing guidance on nonconformances, deviations, and manufacturing quality events.
  • Review and approve procedures, work instructions, training documents, and quality records of moderate to high complexity.

What's Needed?

  • Bachelor's degree in engineering, life sciences, technology, quality, or a related technical field.
  • Minimum of 4 years of experience in Quality Assurance, Quality Control, Engineering, or Manufacturing.
  • Experience in the medical device industry or regulated manufacturing environment preferred.
  • Familiarity with ISO 13485 and medical device regulatory requirements is advantageous.
  • Strong data analysis, troubleshooting, and documentation skills with a proactive approach.

What's in it for me?

  • Opportunity to work in a dynamic and innovative environment focused on quality and compliance.
  • Engage in meaningful work that impacts patient safety and product excellence.
  • Collaborate with a dedicated team of professionals committed to continuous improvement.
  • Gain valuable experience in a regulated industry with growth potential.
  • Be part of a company that values quality, integrity, and employee development.

Upon completion of waiting period associates are eligible for:

  • Medical and Prescription Drug Plans
  • Dental Plan
  • Supplemental Life Insurance
  • Short Term Disability Insurance
  • 401(k)
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