Job Description
Our Client:
My client is a Medical Devices manufacturer with main focus in improving critical health conditions by developing high- end products, currently hiring Regulatory Affairs Executive.
The Responsibilities :
* Conduct CE marking process for high risk medical devices.
* Prepare submission dossiers.
* Support internal and external audits when necessary.
* Involved in any other regulatory affairs related processes.
The Requirements:
* Bachelor Degree in Engineering or any Science related.
* Min. of 3 years of working experience within Regularity Affairs.
* Good knowledge of international regulations for medical devices.
* Experience with EU Notified body will be an added an advantage.
* Willing to travel in the region when necessary.