Fresenius Medical Care Reynosa plant in Mexico seeks a Regulatory Affairs Expert to manage general documentation, registrations, and regulatory compliance across product lifecycles. You will lead regulatory aspects of changes and provide guidance on standards and testing requirements.
The role requires 3–5 years in Regulatory Affairs or QA in medical devices/pharma, knowledge of MDR/MDD, ISO 13485/14971, and fluent English/Spanish. Visa required for the US, reflecting global collaboration.
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📌 Global Regulatory Affairs Expert – Medical Devices (Tamaulipas IV)
🏢 Ch01 Che Fresenius Medical Care (Schweiz
📍 Tamaulipas IV
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