Celestica is seeking a Quality QMS Manager in Monterrey, Mexico.
You will lead global QMS harmonization, drive CAPA processes, and oversee audits and regulatory inspections (FDA/Notified Bodies).
The role requires travel and strong collaboration with general teams to ensure compliance across sites.
The ideal candidate has 7–10 years in medical device QA/QMS, ISO ***** knowledge, and experience with regulatory inspections, with a Bachelor's in engineering or life sciences and an advanced degree
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📌 Global Quality & Qms Lead — Medical Devices (Monterrey)
🏢 Celestica
📍 Monterrey
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