QA Engineer- Product Development for US Company
I am looking for bilingual, English/German speaking Quality Engineers for a US based Medical Device Manufacturer and client of mine who is urgently looking to gather a 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 and FDA knowledge on a global scale.
In return my client is offering a competitive and performance based salary with the chance to work for a globally successful company.
Further to this, joining now will enable you to progress quickly in your career towards a more senior managing position, leading a team of 10 Quality Engineers yourself.
Outrun your competition and add further value to your profile, by being amongst the first to gain working experience with the rewised FDA regulations in 2017.
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.
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