A very reputable Medical Device consultancy is looking for a Regulatory and Quality Manager to consult several medical device companies. These projects will require some specific skills such as biocompatibility, sterilization or EMC. Accordingly, you will get even more knowledge in these fields and have a valuable experience to help different clients and have a rewarding feeling because you could see them improve.
The company consists of talented people with a long outstanding experience in the medical device industry. You will be able to learn from the best, but also get a lot of autonomy. This will enable you to organize the projects independently so you can combine it with your private life.
This will get you an interview:
- Scientific or Technical degree
- Some years experience in Regulatory Affairs for the medical device industry
- Strong knowledge of ISO 13485 and the medical device directive
- Experience with biocompatibility, sterilization, and/or electronic safety/EMC
- Fluent in Dutch and English required
Do you like what you read? Do not hesitate to contact me, Annelies De Baere, your most recent CV in Word format to – Klik op de solliciteer-button om te solliciteren – or call me on +32 2 891 98 99. If you are not interested and you know someone else, do not hesitate to pass on their contact details.
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.
What I offer: As a specialist Headhunter within Regulatory Affairs for the pharmaceutical industry in Belgium I have a strong market knowledge and good relationships within companies. Therefore I will not just find you suitable roles but also offer you accurate, honest advice and provide you with inside information on the team/company culture.
Key words: Regulatory Affairs/RA/Quality/Belgium/Belgique/Belgie/Consultant/Manager/Senior Manager/Expert/Specialist /Brussel/Brussels/Bruxelles/Sterilization/Sterilisatie/EMC/Safety/Biocompatibility/Biocompatible/Medical Devices/ISO13485/Medical Device