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.