Quality Control Engineer
Quick Summary
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,
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.
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.
- 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.
- 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
Responsibilities
~1 min read- →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
What We Offer
~1 min readLocation & Eligibility
Listing Details
- Posted
- July 15, 2026
- First seen
- July 15, 2026
- Last seen
- July 16, 2026
Posting Health
- Days active
- 0
- Repost count
- 0
- Trust Level
- 52%
- Scored at
- July 15, 2026
Signal breakdown
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