Quality/Regulatory Specialist - ISO 13485 (Permanent)

Quality/Regulatory Specialist - Medical Devices

This company is a leading distribution company based in Antwerp, Belgium and specialises in the distribution of a wide variety of medical devices from well-known companies. This unique positioning provides professionals with the opportunity to work with a diverse portfolio of medical devices, each subject to different regulatory requirements. This dynamic environment ensures that every working day is engaging and presents continuous learning opportunities in the field of medical devices.

The team in Antwerp consists of a small, close-knit group, providing an environment where clear communication and direct guidance from the manager are readily available. This setup allows professionals to develop their skills efficiently and progress in their careers. If you are assertive, independent, and looking to explore the intersection of QA and RA in the medical devices industry, this role offers an excellent opportunity for personal and professional growth.

Benefits:
- Exposure to a diverse range of medical devices, enhancing your knowledge and expertise in the field
- Training provided at the start to equip you with essential skills for handling new devices effectively
- Combined role of Quality Assurance (QA) and Regulatory Affairs (RA), offering a comprehensive skill development experience

Responsibilities:
- Manage quality and regulatory aspects of medical devices, ensuring compliance with relevant standards and regulations
- Collaborate with suppliers, including those from China, to facilitate smooth distribution processes
- Support the development and implementation of quality systems, contributing to the overall success of the organisation

Requirements:
- Minimum of 1 year of experience in QA
- Proficiency in English, French, and Dutch; knowledge of Chinese is a plus
- Ideally, experience in the medical devices field, with knowledge of MDR and ISO 13485

If this role suits your personal and professional profile, send your CV to myself, Christian Finnegan (C.finnegan@nonstopconsulting.com), on the NonStop consulting website or to my LinkedIn. If you yourself are not interested in this opportunity however you know someone whom might be interested in a new role, please forward this job posting to them and help them expand their network.

NonStop is one of the largest and fastest growing specialised life-sciences & Med-tech recruitment companies in Europe. We are proud members of the APSCo life sciences group who ensure we meet the highest quality standards within the recruitment industry. Our offices are located in the UK, Switzerland, Romania, Luxembourg, France, US and the Czech Republic and we hold labour leasing licences for all EU8 countries. Please visit our website for a full list of the niche markets we cover.