QIAGEN is seeking a Senior Specialist Regulatory Affairs in Mexico City to ensure compliance and lifecycle management of IVD and medical device products. You will collaborate with teams like Quality, Operations, and Marketing while engaging with regulatory authorities.
Your tasks include managing regulatory submissions, ensuring accuracy and compliance, and acting as a key contact for COFEPRIS. The role requires a degree in life sciences and experience in regulatory affairs.
We offer bonuses, local benefits, and a hybrid work model.
#J-18808-Ljbffr
📌 Hybrid Senior Regulatory Affairs Specialist – IVD/Devices (Ciudad de México)
🏢 QIAGEN
📍 Ciudad de México
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.