Quality Engineer - Medical Devices | ISO/QMS Compliance
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Quality Assurance - QA/QC
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Engineering
Job Description & How to Apply Below
Keystone Manufacturing Llc in Kalamazoo, MI is seeking a Quality Engineer to develop, maintain and improve quality standards for medical device manufacturing. The role involves root cause analysis, investigations into external complaints and internal non-conformances, and driving continuous QMS improvements.
Candidates should have a Bachelor’s in Engineering and at least two years in a regulated environment, with ISO 13485/QSR/GMP experience and proficiency in measurement tools.
Step into the Quality Engineer
- Medical Devices | ISO/QMS Compliance role at Keystone Manufacturing Llc in Kalamazoo, MI, United States and grow with us.
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 Devices | ISO/QMS Compliance role in the description above.
We appreciate your interest in this position.
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