Quality Engineer II — Medical Device PLM & Compliance
Listed on 2026-10-19
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Engineering
Quality Engineering, Biomedical Engineer, Medical Device Industry
KARL STORZ North America is seeking a collaborative Quality Engineer to support product development teams through the medical device lifecycle. You will ensure DHF/DMR readiness, audit preparation, and GPDP compliance while focusing on patient safety and product quality.
Based in Charlton, MA, the role may require occasional travel up to 10% and involves partnering with Regulatory Affairs, Engineering, and Quality to drive continuous improvement and efficient documentation.
This is a strong role to take on the Quality Engineer II — Medical Device PLM & Compliance role at KARL STORZ.
Consider building your career as a Quality Engineer II — Medical Device PLM & Compliance at KARL STORZ.
The Quality Engineer II — Medical Device PLM & Compliance position in the Engineering field is open for applications.
We have an opening for a Quality Engineer II — Medical Device PLM & Compliance in Folkston, GA, United States within Engineering.
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