Quality Control Engineer

Rhythmlink International, LLC; Columbia (SC); On-site; USD 85,000 - 115,000; Full time

Benefits offered by this job

Flexible work environment

Job summary

Rhythmlink International, LLC invites a Quality Control Engineer to elevate our medical device quality efforts in a fast‑paced environment. You’ll influence risk management, supplier quality, and regulatory compliance while working with global portfolios and customers.

The role emphasizes problem solving, data‑driven decisions, and collaboration across teams. A flexible work environment and opportunities to advance QA processes are offered.

Qualifications

• Experience with medical device quality standards is required.
• Strong problem‑solving skills with a systems and data focus.
• Certifications such as CQE, CRE, PMP, or Lean Six Sigma are a plus.

Responsibilities

• 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 global compliance.
• Flexible work environment and cross‑functional collaboration.
• Support ongoing QA improvements and documentation.

Skills

Quality control

Risk management

Regulatory compliance

Data analysis

Tools

CAPA investigations

Job description

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:

• 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
• 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.