Regulatory Affairs Executive (Clinical)
Carrot Pharma Recruitment
11d ago

The Company

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

The Role

  • As the Regulatory Affairs Executive (Medical Devices) - Clinical you will be responsible for;
  • 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

    Create PSURs

    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

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