Quality & Regulatory Affairs Specialist (Benelux)

Johnson & Johnson Co.; Machelen; Hybrid; EUR 63,000 - 98,000; Full time

Benefits offered by this job

Annual bonus

Vacation days

Parental leave

Bereavement leave

Well-being reimbursement

Insurance plans

Job summary

DePuy Synthes is recruiting for a CQ/RA Specialist located in Diegem, Belgium. You will support and maintain the Quality Management System (QMS) for the MedTech businesses in Belgium and Luxembourg.

Working closely with the Commercial Quality Manager, Commercial Quality colleagues across the Benelux region, and local commercial teams, you will help ensure compliance with applicable quality requirements, company standards, and regulatory expectations.

Qualifications

• Bachelor’s degree or equivalent business experience.
• Knowledge of Quality Management Systems and/or the healthcare industry is preferred.

Responsibilities

• Support Quality Management System (QMS) activities across Belgium and Luxembourg.
• Plan and lead internal audits and support supplier audits.
• Coach and train employees on quality-related topics and requirements.
• Collaborate with local and global Johnson & Johnson departments to support quality and regulatory objectives.

Job description

DePuy Synthes is recruiting for a CQ/RA Specialist located in Diegem, Belgium. You will support and maintain the Quality Management System (QMS) for the MedTech businesses in Belgium and Luxembourg.

Working closely with the Commercial Quality Manager, Commercial Quality colleagues across the Benelux region, and local commercial teams, you will help ensure compliance with applicable quality requirements, company standards, and regulatory expectations.