Regulatory Affairs Specialist Medical Devices
A medical devices company is looking for a Regulatory Specialist to strengthen the multicultural team. It is an enriching environment where you can learn from the opinions and views of your colleagues who come from a different background and culture. Therefore, they are also open to welcome people that are willing to relocate to Belgium.
You will be responsible for all product-related information that is legally required and ensure that all CE-marking and registration documents are up-to-date. To complete this, you will fulfil a more cross-functional role where you have contact with other departments in the office and international teams. This will be good to expand your network and to enjoy your daily activities.
- Master Degree in Science or Engineering or equivalent by experience
- Some years experience in Regulatory Affairs or Quality for the Medical Devices industry
- Strong knowledge of ISO 13485
- Knowledge of new MDR is preferred
- Fluent level of English is required
This medical device company is a leader in a specific product line so they have a good exposure on the market which will give you extensive knowledge in this field and a more unique experience for your future career.
If this job appeals to you please apply here or send your CV to me, Annelies De Baere, on the NonStop Recruitment website. If you are not available but you know someone that would be interested, please forward this to them and help the people in your 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 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.
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