This is an exciting time to join an expanding, highly successful medical devices company based at their Gloucestershire site.
They offer excellent training and development opportunities as well as great career progression opportunities.
Highly successful medical devices company with a range of devices in the market
Great benefits with bonus, pension, healthcare etc
Great career progression opportunities
Preparation of clinical assessment / evaluations as well as post market clinical follow up studies
Upgrade the company's clinical evaluation reports to comply with MEDDEV 2.7.1 Rev 4 and MDR 2017 / 745
Assist the Regulatory Affairs Manager in creating and maintaining documents ensuring compliance to the MDR.
As the Regulatory Affairs Executive (Medical Devices) - Clinical you will have the following experience :
Knowledge of regulatory and legal requirements regarding Medical Devices
1-2 years' experience in medical devices
Knowledge and experience of writing clinical evaluation reports is preferable
Relevant life sciences degree or equivalent