03 oct
|
Stryker
|
Madrid
Stryker is seeking a Regulatory Affairs professional to oversee post‑market surveillance and regulatory reporting across the EMEA region, ensuring medical devices remain safe, compliant, and effective throughout their lifecycle.
Asegúrese de leer detenidamente la información sobre esta posibilidad antes de presentar su candidatura.
You will collaborate with regulatory, quality, commercial, and operations teams to drive compliance and continuous improvement.The role requires a Life Sciences xqbhyrx or related degree and a minimum of four years in regulatory affairs or post‑market surveillance, with strong
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📌 EMEA Post-Market Surveillance Lead (Madrid)
🏢 Stryker
📍 Madrid