Established in 2003, Angiocare is a leading distributor of interventional cardiology, radiology, oncology, neuroradiology, venous diseases and gastro-enterology within the Benelux region. Angiocare has developed strong relationships with both the medical and industry communities over the past 20 years, which has gained them loyalty and trust within the market. Angiocare is part of the Uniphar Plc group based in Dublin which comprises of several Medical Device distribution businesses across 14 European markets with direct operations in Ireland, Northern Ireland, U.K., The Netherlands, Belgium, Luxemburg, Germany, Austria, Switzerland and the Nordics, and is the medical device arm of the Uniphar Medtech Group.

ETHICAL COMPLIANCE & EDUCATION

• Track mandatory compliance training with HR
• Manage requests for educational support and submit Eucomed CVS documentation
• Support documentation related to labour standards for audit preparation

They should have the following skills and qualifications:

• Fluency in Dutch and English
• Bachelor’s degree in quality, Science, Business, or a related field preferred
• 2+ years of experience in Quality or Regulatory Affairs within medical devices or pharma distribution would be a pre.
• Familiarity with EU MDR and ISO 9001:2015 standards
• Strong interpersonal and communication skills
• High attention to detail, organizational abilities, and proactive time management
• A collaborative spirit and a hands-on, problem-solving mindset
• Passion for continuous improvement and patient safet

PURPOSE OF THE ROLE

As Quality Coordinator at Angiocare, you will work closely with the QCRA Manager and collaborate across the Uniphar network to support Quality, Compliance, and Regulatory Affairs. You will ensure ongoing compliance with relevant medical device regulations, manage our Quality Management System, and contribute to a high-performance culture rooted in safety, precision, and innovation.
Products: Angiocare offers a wide portfolio of diagnostic and interventional devices, primarily in the fields of Interventional Cardiology, (Neuro)Radiology, Vascular Surgery, Interventional Oncology, Gastro-enterology, Venous Diseases and Diagnostic Imaging.

ROLE REQUIREMENTS:

The successful candidate will be hard working and enthusiastic with an interest in quality, compliance and regulatory affairs possibly pursuing further training in this area.

They should have the following skills and qualifications:

• Fluency in Dutch and English
• Bachelor’s degree in quality, Science, Business, or a related field preferred
• 2+ years of experience in Quality or Regulatory Affairs within medical devices or pharma distribution would be a pre.
• Familiarity with EU MDR and ISO 9001:2015 standards
• Strong interpersonal and communication skills
• High attention to detail, organizational abilities, and proactive time management
• A collaborative spirit and a hands-on, problem-solving mindset
• Passion for continuous improvement and patient safety