Regulatory Affairs Manager-Newly Created Role-Medical Devices
Regulatory Affairs Manager-Newly Created Role-Medical Devices-Zurich Area, Switzerland
Due to growth and continued success on the market our client have created an exciting new role within the regulatory department. The CTO has opened up this role to accommodate exciting expansion plans; providing you with the role where you can leave a legacy and build the department to your own skills and vision. A great role for someone looking to build up a department; with key influence over both strategy and the operational aspects of regulatory affairs.
As the regulatory affairs manager in this role you will:
- Manage 1 team member to start. Followed by the opportunity to hire and train your own team.
- Manage the strategic forecast and insight for all regulatory operations.
- Take a proactive approach to the operational aspects of regulatory affairs; where you will drive froward the full life cycle for successful registration of class III devices.
The ideal candidate for this role will have several years of experience within regulatory affairs from the medical device industry You will have good working knowledge of ISO 13485 and the European registration process. Any previous experience within cardiovascular or class III devices would be a bonus. You will be fluent in English. Fluency in German would be a bonus. French and German.
Be part of the growth of a medical device company in this leading regulatory affairs manager role.
Call me Tamanna Gandecha at NonStop Recruitment now for a confidential conversation. Contact me on email@example.com or +41 435 0808 16, please send your CV in word format OR if this does not sound like the opportunity for you, but you are a regulatory affairs professional within the medical device industry, please feel free to get in touch, to see other opportunities we may have within this field.
NonStop 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 Headhunter within regulatory affairs for the medical device 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 Switzerland.