Quality Engineer – Medical Device Manufacturing
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Engineering
Quality Engineering, Medical Device Industry, Biomedical Engineer, Regulatory Compliance Specialist
Job Description & How to Apply Below
UFP Technologies, Inc. in St. Charles, IL is seeking a Quality Engineer to support compliance, CAPA, and process validation across the supply chain.
The role collaborates with operations, supply chain, and new product development teams to ensure quality systems and regulatory requirements are met. The ideal candidate has 3–7 years in medical device manufacturing, strong QA knowledge, and hands-on experience with IQ/OQ/PQ/PPQ validation and risk management.
Our team is growing, and we are hiring a Quality Engineer – Medical Device Manufacturing in St. Charles, IL, United States.
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the Quality Engineer – Medical Device Manufacturing role in the description above.
We appreciate your interest in this position.
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