CQ/RA Specialist: Quality & Regulatory Excellence

Johnson & Johnson Co.; Belgique; Presencial; EUR 63.000 - 98.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Annual bonus

Vacation days

Bereavement leave

Well-being programs

Insurance plans

Descripción de la vacante

Johnson & Johnson in Diegem, Belgium is recruiting a CQ/RA Specialist to support the Benelux Commercial Quality team. You will help maintain the Quality Management System for MedTech activities in Belgium and Luxembourg, collaborating with local partners and regional teams to ensure regulatory compliance.

The role requires Quality/Regulatory Affairs experience, strong communication, and the ability to train others.

Formación

• Previous Quality and/or Regulatory Affairs experience.
• Ability to collaborate across local and EMEA-based teams.
• Strong communication and influencing skills.
• Results-oriented with focus on quality and operational excellence.
• Knowledge of Good Documentation Practices and Data Integrity.
• Proficiency with Microsoft Office applications.
• Fluent English and Dutch or French.

Responsabilidades

• Support QMS and quality activities across Belgium and Luxembourg.
• Manage CAPAs, non-conformances, investigations, Field Safety Notices, recalls, document control, and training systems.
• Support implementation of corporate quality standards, procedures, and compliance activities.
• Plan and lead internal audits and supplier audits.
• Coach and train employees on quality topics.
• Lead change control activities and support quality system improvements.
• Maintain quality records and metrics.
• Collaborate with local and global Johnson & Johnson departments.

Conocimientos

Quality RA exp

Cross-functional collab

Strong communication

Analytical mindset

Training delivery

Microsoft Office

AI concepts awareness

Dutch or French

Educación

Bachelor's degree or equivalent

Herramientas

ISO 13485 knowledge

Descripción del empleo

Johnson & Johnson in Diegem, Belgium is recruiting a CQ/RA Specialist to support the Benelux Commercial Quality team. You will help maintain the Quality Management System for MedTech activities in Belgium and Luxembourg, collaborating with local partners and regional teams to ensure regulatory compliance.

The role requires Quality/Regulatory Affairs experience, strong communication, and the ability to train others.