16 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.
Las cualificaciones, habilidades y toda la experiencia relevante necesaria para este puesto se pueden encontrar en la descripción completa a continuación.
You will collaborate with regulatory, quality, commercial, and operations teams to drive compliance and continuous improvement.
The role requires a Life Sciences xhfqzwm or related degree and a minimum of four years in regulatory affairs or post‑market surveillance, with strong
📌 Emea Post-Market Surveillance Lead (Madrid)
🏢 Stryker
📍 Madrid