More jobs:
Quality Assurance Specialist
Job in
Greenville, Pitt County, North Carolina, 27834, USA
Listed on 2026-08-29
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
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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