Senior Medical Device Software Quality Engineer

hace 5 días


Mexicali, México Ivemsa A tiempo completo

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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    A leading medical device company located in Mexicali, Baja California, is seeking a Software Quality Engineer to lead engineering activities ensuring compliance with regulatory standards. The role requires developing quality documentation, managing risk activities, and collaborating with global teams. Candidates should have a Bachelor's degree in a related...


  • Mexicali, México Ivemsa A tiempo completo

    A leading medical device company located in Mexicali, Baja California, is seeking a Software Quality Engineer to lead engineering activities ensuring compliance with regulatory standards. The role requires developing quality documentation, managing risk activities, and collaborating with global teams. Candidates should have a Bachelor's degree in a related...


  • Mexicali, México Ivemsa A tiempo completo

    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...

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  • Mexicali, México Ivemsa A tiempo completo

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  • Mexicali, México Ivemsa A tiempo completo

    · Leadsoftware quality engineering activities across the full product lifecycle,ensuring compliance with ISO 13485, FDA QSRs, IEC 62304, ISO 14971, andrelevant cybersecurity and data-protection requirements.· Develop,review, and approve software quality documentation, including validation plans,protocols, reports, requirements traceability,...


  • Mexicali, México Ivemsa A tiempo completo

    · Leadsoftware quality engineering activities across the full product lifecycle,ensuring compliance with ISO 13485, FDA QSRs, IEC 62304, ISO 14971, andrelevant cybersecurity and data-protection requirements. · Develop,review, and approve software quality documentation, including validation plans,protocols, reports, requirements traceability,...


  • Mexicali, México Ivemsa A tiempo completo

    · Leadsoftware quality engineering activities across the full product lifecycle,ensuring compliance with ISO 13485, FDA QSRs, IEC 62304, ISO 14971, andrelevant cybersecurity and data-protection requirements.· Develop,review, and approve software quality documentation, including validation plans,protocols, reports, requirements traceability,...