Bilingual Quality Engineer -Product Development
I am looking for bilingual, English/German speaking Quality Engineers for a global client who is looking to gather an international QA team for a new manufacturing site opening in North Germany.
This is an excellent opportunity for those of you having 4 years of experience focusing on FDA Regulations and Risk Management, to join a globally successful US based Med Device Manufacturer and Distributer.
Joining the company at this point in time will allow you to develop your pre-market regulatory knowledge on a global scale, adding further value to your profile.
And the opportunities do not stop there - as the department will continues to expand, there will be more room for promotions in the future regarding Management and team leadership.
You will be focusing on global regulatory submissions, dealing with the relevant authorities and notified bodies as well as maintaining current approvals, reporting directly to the US based Director of the company.
In return my client is offering a competitive and performance based salary with the chance to work for a internationally successful medical devices firm.
Successful candidates for this position will have:
- 4+ years experience in Risk Management with in the Medical Devices industry
- Good ISO Standards knowledge
- EU CE Mark approval + FDA 510 (k) forms experience is necessary
- Fluent in German and English
If you are a Quality Assurance professional with 4+ years experience, speak fluent English and German then please contact me, Hanna Gallos of NonStop Recruitment , contact details listed below, or add me on LinkedIn.
I am a Headhunter and Recruiter specialised in the Medical Device Market Europe, and looking forward to assist you trough your entire application and interview process
Hanna Gallos - Headhunter, Medical Devices