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Head of Regulatory Affairs - Innovative Class III Devices

Employer
NonStop Consulting
Location
Frankfurt am Main
Salary
€80000 - €100000 per annum + Bonus
Closing date
Oct 23, 2016

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Sector
Pharmaceutical, Regulatory Affairs
Contract Type
Employee
Hours
Full Time
Organization Type
Clinical Practice
Jobseeker Type
Professional

Job Details

A great client of mine based in Frankfurt, is looking for a Regulatory Affairs Leader to lead their regulatory team of 2 members of staff. This role would be covering day to day operations within the regulatory function with their product portfolio on a global scale. For those of you with 6+ years of experience who are looking to develop their career in regulatory affairs - THIS IS THE PERFECT OPPORTUNITY. By continuing to develop such global experience on high risk devices, you are guaranteeing success in your future. Furthermore this is a leading role so this would also be a great step up. My client is open to aspiring managers who would like to take the next step into a leading position.

As a growing company, the opportunities are endless - as the department continues to expand, there would be more room for improvement and promotions in the future. You would also be developing pre-market regulatory work on a global scale, adding further value to your profile as well as having the chance to work in the niche area of combination products.

In this position You will be focusing on global regulatory submissions, dealing with the relevant authorities and notified bodies as well as maintaining current approvals and leading the team on daily basis. In return my client is offering a fantastic performance based salary package and if you are relocating then they can assist you with this as well.

Successful candidates for this position will have:

  • 6+ years experience in Regulatory Affairs in the Medical Devices industry
  • Good ISO Standards knowledge
  • Supervisory experience would be of advantage
  • EU CE Mark approval + FDA 510 (k) forms experience
  • Class III devices experience is a must
  • APAC submissions would be an advantage
  • Fluent in German and English

So if you are a Regulatory Affairs professional and you think you are ready for the next step then please contact me, Mahdi Chab of NonStop Recruitment to find out more! Alternatively you can send me a WORD copy of your CV to apply. If you are a Regulatory Affairs professional but this does not seem like a suitable opportunity then feel free to get in touch as I have many other positions in Germany.

Mahdi Chab - Headhunter - Regulatory Affairs - Medical Devices - Germany

Tel No: +49 8921 0933 64

Email: m.chab@nonstop-recruitment.com

Keywords: Regulatory Affairs, medical devices, Germany, Zulassungen, Medizinprodukte, Medizintechnik, Deutschland, Stellanangebote, jobs, Germany, Deutsch, Englisch, Stellen, Positionen, Regulatory, Quality assurance, Quality management, ISO 13485, Regulatory Affairs, medical devices, submissions, documentation, auditors, auditor, Zulassungs, FDA, Medizinische Produkte, Dental, Zahnarzt, Dentaleprodukten.

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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