Regulatory Affairs Associate — Benelux & Quality

Medtronic; Eindhoven; Híbrido; EUR 44.000 - 66.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Flexible Benefits Package

Hybrid work arrangement

Descripción de la vacante

Medtronic plc is seeking an Associate Regulatory Affairs Specialist in the Netherlands. The role supports regulatory and quality activities across the Benelux region with a flexible hybrid work model, based in Maastricht or Heerlen, and with occasional travel.

Fluency in English and Dutch is required, along with a Bachelor’s degree and strong organizational skills. You will coordinate field safety actions, respond to authorities, and assist in QMS processes, while collaborating with

Formación

• Bachelor's degree in a related field or equivalent experience.
• Fluency in English and Dutch, both written and spoken.
• Strong organizational and administrative capabilities in a regulated environment.

Responsabilidades

• Coordinate regulatory activities across Benelux (Netherlands, Belgium, Luxembourg).
• Support post-market surveillance and vigilance processes.
• Assist with quality management system activities and document control.
• Review promotional materials for regulatory compliance and liaise with authorities.
• Support inquiries from competent authorities and supplier/distributor management.

Conocimientos

English proficiency

Dutch proficiency

Attention to detail

Organizational skills

Educación

Bachelor's degree

Herramientas

Microsoft Office

Descripción del empleo

Medtronic plc is seeking an Associate Regulatory Affairs Specialist in the Netherlands. The role supports regulatory and quality activities across the Benelux region with a flexible hybrid work model, based in Maastricht or Heerlen, and with occasional travel.

Fluency in English and Dutch is required, along with a Bachelor’s degree and strong organizational skills. You will coordinate field safety actions, respond to authorities, and assist in QMS processes, while collaborating with