NEW JOB OPENING
QUALITY CONTROL INSPECTOR - MEDICAL DEVICE MANUFACTURING
IN SUMTER, SC, USA!

 

Date Posted: 10/05/2026
Hiring Organization: Rose International
Position Number: 508655
Industry: Medical Equipment & Supplies
Job Title: Quality Control Inspector - Medical Device Manufacturing
Job Location: Sumter, SC, USA, 29153
Work Model: Onsite
Shift: 8 pm - 8 am and 3 days on-2 days off-2 days on-3 days off schedule, and weekends included
Employment Type: Temporary
FT/PT: Full-Time
Estimated Duration (In months): 7
Min Hourly Rate($): 18.00
Max Hourly Rate($): 18.00
Must Have Skills/Attributes: Manufacturing, Quality Control (QC)
Experience Desired:
Quality inspection, product testing, defect identification, or manufacturing inspection experience (1 yrs),
Strong attention to detail with the ability to identify product defects and quality issues (1 yrs),
Ability to perform basic statistical analysis, sampling, and defect trending (1 yrs),
Experience accurately documenting inspection, testing, audit, or quality results (1 yrs),
Proficiency with Microsoft Office and general computer systems (1 yrs)
Required Minimum Education: High School Diploma or equivalent

**C2C is not available**

 

Job Description
Required Education:
• High School Diploma or equivalent

Required Skills and Experience:
• Strong attention to detail
• Ability to think independently
• Strong problem-solving skills
• Computer literate
• Proficiency with Microsoft Office Suite
• Ability to perform various testing procedures
• Ability to perform basic statistical analysis
• Knowledge of Quality System Regulations (QSR)
• Knowledge of quality control and defect trending
• Ability to accurately document inspection and audit results
• Ability to follow safety, environmental, and quality standards

Responsibilities:
• Perform various product testing procedures and simple statistical analysis
• Complete inspections of products prior to release according to applicable specifications
• Review raw materials and finished goods prior to warehouse or shipment transfer
• Sign release documentation when applicable
• Compile and review release documentation for lot Device History Records (DHRs)
• Submit completed documentation to supervision for final approval
• Perform statistical sampling of hold products according to applicable specifications
• Record inspection and audit findings on appropriate forms and/or in the SAP Quality Module
• Identify and report product nonconformances to the appropriate Quality and Production leadership
• Monitor product quality and control chart defect trends
• Maintain compliance with Quality System Regulations
• Maintain adherence to all safety, environmental, and quality system standards


  • **Only those lawfully authorized to work in the designated country associated with the position will be considered.**

  • **Please note that all Position start dates and duration are estimates and may be reduced or lengthened based upon a client’s business needs and requirements.**

 

Benefits:
For information and details on employment benefits offered with this position, please visit here. Should you have any questions/concerns, please contact our HR Department via our secure website.

California Pay Equity:
For information and details on pay equity laws in California, please visit the State of California Department of Industrial Relations' website here.

Rose International is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender (expression or identity), national origin, arrest and conviction records, disability, veteran status or any other characteristic protected by law. Positions located in San Francisco and Los Angeles, California will be administered in accordance with their respective Fair Chance Ordinances.

If you need assistance in completing this application, or during any phase of the application, interview, hiring, or employment process, whether due to a disability or otherwise, please contact our HR Department.

Rose International has an official agreement (ID #132522), effective June 30, 2008, with the U.S. Department of Homeland Security, U.S. Citizenship and Immigration Services, Employment Verification Program (E-Verify). (Posting required by OCGA 13/10-91.).

 

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About Rose

  • Founded in 1993
  • Office Locations Across the U.S.
  • 150+ Clients: Corporations and Government Agencies
  • Employee Oriented Company
  • Challenging Assignments Across the U.S.
  • Continuous Professional Development

As a contractor, I have to say that Rose International was by far the best agency I have worked for.

Q'testdalir, Consultant

It was great working for Rose International. Everyone was extremely helpful.

Rosann, Consultant

The interactions that I have had with your representatives have always been prompt and very professional. I am very pleased and impressed with your company and services.

Sioe, Consultant

I am very happy with the Rose International, and the professionalism of the employees.

Robin, Consultant

My on-boarding with Rose was outstanding. The packets of information, the process, and great attention to detail each person gave me allowed me to get started quickly.I appreciated each person's friendly and helpful attitude.

Diana, Consultant

EMPLOYEE COMMENTS

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