RA Manager - Medical Devices
- Employer
- NonStop Consulting
- Location
- Germany
- Salary
- Negotiable
- Closing date
- Mar 20, 2018
View more
- Sector
- Pharmaceutical, Regulatory Affairs
- Contract Type
- Employee
- Hours
- Full Time
- Organization Type
- Clinical Practice
Job Details
NonStop is currently working with a well-established international company specializing in development, production and sales high-quality medical devices. They are looking for a Regulatory Affairs Manager to join their dynamic team. You will support three new product launches in diagnostics and will be responsible for China and US submissions.
The company offers flexible working hours so you will be responsible for your time management. Moreover, you will also have the opportunity for sports compensation (gym, badminton, etc). This suggests work and life balance what is a primary goal of the client.
Main responsibilities:
* Processing national and international product approvals and certifications
* Participation in the preparation and release of technical documentation
* Conception and participation in validations and studies
Your profile:
* Experience with the US (510 (k) procedure) submissions
* Experience in quality management desirable
* Fluent in English
* Proficient in German
Location: Germany, Bavaria
Please let me know if you are interested in a new challenge.
If interested, please send your CV in MS Word format (I am unable to accept PDF copies!) or contact me for a further confidential discussion
Kate Keller
Tel: +49 8921093363 | Ext: 3255
E-mail: K.Keller@nonstop-recruitment.com
Not what you are looking for? Feel free to pass this information on to friends or colleagues that might be interested. NonStop has an excellent referral policy in place.
NonStop Recruitment is one of the largest and fastest growing specialised life sciences 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 across Europe. Please visit our website for a full list of the niche markets we cover.
What I offer: As a specialist Consultant within Regulatory Affairs for the pharmaceutical industry, I can offer: market knowledge and a personal service, therefore not just finding you suitable roles but in addition to this offering accurate and honest advice about salaries, work conditions and department reputations for positions across Germany and the EU.
medical devices, diagnostics, ISO, IVD, Germany, Deutschland, Regulatory Affairs, RA, Zulassung, FDA, China, 510k, 510(k), US, USA, submissions, dossier
Company
Our Consultants are trained to deliver an exceptional standard of recruitment services to clients across the life sciences, chemical, care, educations, technical, digital and finance industries.
Our clients – and bottom line profits - tell us that we do a great many things very well. Complacency, however, is the last word you would associate with us. We work incredibly hard to deliver better and better results, based on stronger and stronger service delivery. Which is why we believe the best is yet to come – for us, our clients and for the people who have what it takes to join us on the journey.
The result? We’re expanding (in the UK and across Europe and even to Boston, US) and continue to post impressive performances in all our niche sectors.
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