Hello,

My job main objective is to make possible sales and comply with various countries regulations.

- Meet with the sales team to know in witch products we need to homologate to and in witch market.
- To convey to the development team all the necessarities.
- Exchange with other countries Ministry of Health.
- Draft and summit technical documentation.
- Make sure every certificate is up to date.
- Analyze and effectively communicate global regulatory requirements and medical device regulations within the company
- Assure the regulatory watch

I always wanted to work in the Medtech industry (Medical Devices).

I have a Master Degree in Material Science and Engineering with a specialty in Biomaterials.

I have started in R&D with various companies with my internships during my studies.
And to validate my degree, I did the Regulatory affairs internship to try the other side of the Medical Device.

At the end, I liked the job as the job proved to be challenging in the technical aspect and also in the human aspect. I liked the fact that I was the link between the R&D and the sales.

Feel free to contact me if you want to know more about my job
Johan