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)

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!

About ManpowerGroup, Parent Company of: Manpower, Experis and Talent Solutions.

Manpower® is a global leader in contingent staffing and permanent resourcing, providing companies with strategic and operational flexibility and creating talent at scale. Our specialized recruiting teams assess and guide talent into meaningful, sustainable employment, while our PowerSuite technology enables deeper insight and smarter matching, helping candidates find opportunities that align with their strengths, experience, and career goals.

In this constantly shifting world, our flexible workforce solutions provide companies with the business agility needed to succeed. Manpower is part of the ManpowerGroup® (NYSE: MAN) family of brands, which also includes Experis and Talent Solutions. For more information about Manpower, follow us on LinkedIn, Facebook, X and Instagram.

ManpowerGroup is committed to providing equal employment opportunities in a professional, high quality work environment. It is the policy of ManpowerGroup and all of its subsidiaries to recruit, train, promote, transfer, pay and take all employment actions without regard to an employee's race, color, national origin, ancestry, sex, sexual orientation, gender identity, genetic information, religion, age, disability, protected veteran status, or any other basis protected by applicable law.