Job DescriptionMy client is a global Medical Technology Company that is advancing the world of Life Science by improving Med discovery, diagnostics and the delivery of care. Due to their ever continous growth my client is looking for a ´Clinical Evaluation Specialist EU/MDR´ to join theri worldwide Regulatory Affairs Team.
The contract length for this position is 18 months, allows you to be home based and has an immediate start date.
This is a great opportunity for someone whis experienced in Regulatory Affairs to be involved in the evaluation of cutting edge innovation and state of the art technologies. The Regulatory affairs activities for this client are taking place in the UK & US so you will benefit from the international exposure and procedures of different markets.
- 7+ years experience in Clinical Evaluation
- Fluent in English
- Batchelors degree in a discipline with relevance to medical device manufacture and use e.g. engineering, medical, nursing etc.