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Quality Control Engineer

Rhythmlink International LLC
Posted 2 months ago, valid for 13 days
Location

Columbia, SC, US

Salary

$75,000 - $90,000 per year

Contract type

Full Time

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Sonic Summary

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  • Rhythmlink is seeking a Quality Control Engineer who is eager to go beyond compliance checklists and engage in problem-solving and collaboration.
  • The role requires a Bachelor’s degree in Engineering and experience with medical device standards, particularly ISO 13485 and 21 CFR 820.
  • Candidates should have strong problem-solving skills and a passion for systems, data, and results, with additional certifications like CQE, CRE, PMP, or Lean Six Sigma being a plus.
  • The position offers a flexible work environment and the opportunity to work on meaningful projects that influence product quality and compliance.
  • While the salary is not specified, the role promises a supportive culture and the chance to be part of a company recognized as one of South Carolina’s Best Places to Work for 13 consecutive years.


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.




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By applying, a Sonicjobs account will be created for you. Sonicjobs's Privacy Policy and Terms & Conditions will apply.

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