×
Register Here to Apply for Jobs or Post Jobs. X

Quality Control Engineer

Job in Columbia, Richland County, South Carolina, 29204, USA
Listing for: Rhythmlink International, LLC
Full Time position
Listed on 2026-08-05
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering
Job Description & How to Apply Below

Quality Control Engineer

Calling Quality Control Engineers Who Crave More Than Just Compliance Checklists! Are you ready to elevate your career beyond audits and standard procedures? Do you thrive in environments where problem-solving, collaboration, and technical challenges are part of the daily rhythm? If you're nodding "yes," Rhythmlink might be your next great move.

As a Quality Control Engineer at Rhythmlink, you won't just be maintaining the status quo—you'll be driving it forward. You'll tackle meaningful projects that support global product portfolios, help shape quality systems, and directly influence how we meet and exceed medical device standards.

Why Rhythmlink?

  • Impact:
    This isn't just a box-checking role. You'll be a key player in risk management, product development, supplier quality, and regulatory compliance—all while helping to support life-changing technologies.
  • Challenge:
    From participating in global audits to managing sterilization validations and software qualifications, your technical expertise will be tested and sharpened.
  • Visibility:
    You'll work cross-functionally with teams across the company—and even directly with customers and suppliers—to solve tough problems and improve product quality.
  • Innovation:
    We embrace continuous improvement. You'll have the chance to shape our QMS processes, develop new testing methods, and push documentation to the next level.
  • Culture:
    We've been one of South Carolina's Best Places to Work for 13 straight years—and for good reason. We believe that great people do their best work in a supportive, flexible, and fun environment.

What You Bring:

A Bachelor's degree (Engineering preferred) Experience with medical device standards (ISO 13485 & 21 CFR 820) Strong problem-solving skills, with a passion for systems, data, and results Bonus points for certifications like CQE, CRE, PMP, or Lean Six Sigma What You'll Do:
Own risk management processes per ISO 14971 Oversee supplier quality performance and validation activities Lead technical investigations for CAPAs and non-conformances Review labeling, design controls, and sterilization documentation Participate in audits and ensure compliance across global markets Perks:
Flexible work environment Work with proven products in a purpose-driven industry Join a company with a proven track record of quality and employee satisfaction If you're ready to make a bigger impact while doing work that matters—let's talk. Apply now and join a company where quality isn't just a department. It's our mindset.

To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)
0
200
Filters
Education Level
Experience Level (years)
Posted in last:
Salary