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Johan
Regulatory Affairs Associate – International Homologation
Air Liquide Medical Systems

Mon parcours

  • 2021 Master Sciences et Génie du Matériaux – Biomatériaux Université Paris 13

Formation conseillée

  • Bac +5
  • Compétences recommandées

    • Teamwork
    • Positive attitude
    • critical thinker
    • Crisis management
    • Alaise à l'oral
    • Organization skills

    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

    Contacter