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Pharmaceutical industry





  • Start date

    From the 06 April 2020

Ideal profile

  • Educational background

    Master degree in Quality & Regulatory Affairs

  • Experience

    • 2 years minimum acquired in the pharmaceutical industry.2 years minimum acquired in the pharmaceutical industry.
    • You know and master all or some of the GMP and Common Technical Document standards.

Proposed project

  • Reporting to the Quality & Regulatory Affairs Manager, you are actively involved in the regulatory policy.
  • To these functions, you create the homologation files, make the AMM filing as well as the monitoring of registrations at the national and / or international level.
  • Guarantor of the registration procedures, you deal with the answers to the authorities questions.
  • In liaison with the regulatory authorities and / or the certification bodies, you ensure the regulatory and normative watch and are responsible for the documents traceability and archiving.
  • Finally, in a demanding context, you intervene in the management and the follow-up of the complaints and nonconformities and put in place the CAPA.

The different steps to integrate the tribe

  • First interview with the HR team
  • Technical interview with a Business Engineer
  • Physical meeting in our office and constitution of the skills file
  • Last exchange with one of our leaders

Apply for this position

Join the tribe !