Quality & Regulatory Lead for Medical Devices

Qabird; Pijnacker; On-site; EUR 50,000 - 70,000; Full time

Job summary

Qabird is looking for a Quality Manager based in Pijnacker, Netherlands. In this role, you will be responsible for quality assurance and ensuring compliance with regulatory standards such as the EU Medical Device Regulation (MDR) and ISO 13485.

Your daily tasks will involve monitoring product quality and implementing necessary guidelines and improvements. Familiarity with Matrixreq and Odoo ERP is essential for success in this position.

Qualifications

• Experience in quality assurance and regulatory compliance.
• Familiarity with EU Medical Device Regulation (MDR) and ISO 13485.
• Previous experience with ERP systems is a plus.

Responsibilities

• Monitor quality of products on a day-to-day basis.
• Implement guidelines and improvements regularly.
• Ensure compliance with regulatory requirements.

Skills

Quality assurance

Regulatory compliance

ISO 13485 knowledge

Tools

Matrixreq

Odoo ERP

Job description

Qabird is looking for a Quality Manager based in Pijnacker, Netherlands. In this role, you will be responsible for quality assurance and ensuring compliance with regulatory standards such as the EU Medical Device Regulation (MDR) and ISO 13485.

Your daily tasks will involve monitoring product quality and implementing necessary guidelines and improvements. Familiarity with Matrixreq and Odoo ERP is essential for success in this position.