Job Description
A leading company in medical technology in Mexicali is looking for an experienced professional to lead software quality engineering activities. You will ensure compliance with ISO 13485 and FDA regulations while developing software quality documentation. The ideal candidate has a Bachelor's degree in Engineering, over 5 years of experience in the medical device industry, and strong knowledge of global regulatory frameworks. This position is crucial for driving quality standards throughout the product lifecycle. #J-18808-Ljbffr
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