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. You will collaborate with regulatory, quality, commercial, and operations teams to drive compliance and continuous improvement. The role requires a Life Sciences 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
Postulate a este anuncio
Muestra tus habilidades a la empresa, rellenar el formulario y deja un toque personal en la carta, ayudará el reclutador en la elección del candidato.