Regulatory Affairs Specialist-World Leader-Warsaw, Poland
A world leading medical device company are currently searching for a regulatory affairs specialist to join their growing global team. Be the next regulatory affairs specialist and develop your career in a world leader, globally.
This is a great opportunity for an experienced regulatory affairs professional to take the next step in their career with a globally leading medical device company. Through their global network, you will gain the opportunity to work closely with some of the top regulatory and quality experts in Europe. You will also develop your career internationally, working closely with professionals from all over the world.
As the regulatory affairs specialist in this role, your responsibilities will include but not be limited to:
- Work on the polish market registration process.
- Play an integral role in the MDR and MDD process.
- Handle the technical documentation for medical devices in EU.
The ideal candidate for this role will have:
- Several years of experience within regulatory affairs for medical devices.
- Good working knowledge of the polish market registration process.
- Fluency in English.
Ensure you apply now to develop your regulatory affairs career with a global leader in medical devices.
Call me Tamanna Gandecha at NonStop Recruitment now for a confidential conversation. Contact me on or +, 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.
- ISO 13485
- medical devices
- quality assurance
- regulatory affairs
- regulatory affairs specialist
- regulatory affairs manager
- regualtory affairs manager
- regulatory affairs consultant
Bank or payment details should not be provided when applying for a job. reed.co.uk is not responsible for any external website content. All applications should be made via the 'Apply now' button.Report this job