Technical Director Medical Devices - Regulatory Affairs

MICHAEL PAGE INTERNATIONAL; Bogotá ciudad; Presencial; COP 50.000.000 - 90.000.000; Jornada completa

Descripción de la vacante

MICHAEL PAGE INTERNATIONAL is seeking a Regulatory Affairs (RA) and QA Specialist to lead and supervise Technical Direction, Regulatory Affairs, Technovigilance, and Quality activities in Colombia, ensuring full compliance with sanitary requirements and aligning local operations with the regional strategy led by the Head of RA & QA in Mexico.

The role acts as the primary technical and regulatory contact before INVIMA and local health authorities, coordinating with manufacturers, clients, and the

Responsabilidades

• Lead and supervise Technical Direction, Regulatory Affairs, Technovigilance, and Quality activities in Colombia, ensuring full compliance with applicable sanitary requirements.
• Align local operations with the regional corporate strategy led by the Head of RA & QA in Mexico.
• Serve as primary technical and regulatory contact before INVIMA and local health authorities, coordinating with manufacturers, clients, and the regional quality team.

Descripción del empleo

We are looking for a RA and QA Especialist that will be Responsible for leading and supervising Technical Direction, Regulatory Affairs, Technovigilance, and Quality activities in Colombia, ensuring full compliance with applicable sanitary requirements while aligning local operations with regional corporate strategy led by the Head of RA & QA in Mexico.

Serves as the primary technical and regulatory point of contact before INVIMA and local health authorities, as well as coordinating directly with manufacturers, clients, and the regional quality team.