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

Manpower Engineering

Mebane, NC

JOB DETAILS
SALARY
$27.10–$27.50 Per Hour
JOB TYPE
Temporary
SKILLS
Brand Positioning, Check Processing, Communication Skills, Cross-Functional, Data Collection, Detail Oriented, Diversity, Documentation, Documentation Review, FDA (Food and Drug Administration), GMP (Good Manufacturing Practices), Healthcare Quality, ISO (International Organization for Standardization), Maintain Compliance, Manufacturing, Medical Equipment, Medical Organizations, Process Quality, Production Support, Quality Assurance, Quality Control, Quality Engineering, Support Documentation, Talent Management
LOCATION
Mebane, NC
POSTED
12 days ago

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.

 

Job Title:

QA Specialist – Liquid Media (2nd Shift)

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!

 

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

ManpowerGroup® (NYSE: MAN), the leading global workforce solutions company, helps organizations transform in a fast-changing world of work by sourcing, assessing, developing, and managing the talent that enables them to win. We develop innovative solutions for hundreds of thousands of organizations every year, providing them with skilled talent while finding meaningful, sustainable employment for millions of people across a wide range of industries and skills. Our expert family of brands – Manpower, Experis, Talent Solutions, and Jefferson Wells – creates substantial value for candidates and clients across more than 75 countries and territories and has done so for over 70 years. We are recognized consistently for our diversity - as a best place to work for Women, Inclusion, Equality and Disability and in 2022 ManpowerGroup was named one of the World's Most Ethical Companies for the 13th year - all confirming our position as the brand of choice for in-demand talent.

About the Company

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Manpower Engineering