Regulatory Affairs Coordinator

At Capgemini Engineering we value excellence, care, responsibility, dynamism and innovation. We offer a job with variation that leaves plenty of room for initiative and development. In fact, we are not just offering you a job, we’re inviting you to be part of our community where we will provide you trainings, tools & grounds for professional and personal growth. Each career experience is assorted by an attractive salary package.
If you are a team player, if you recognize yourself in this profile and are not afraid of taking on challenges… Apply today!

We will offer you

  • Insurances, a mobility plan of your choice and other benefits;
  • Integration in a solid and dynamic team;
  • Participation in exciting and motivating infrastructure projects;
  • Career evolution;
  • Training possibilities and official certification within our Capgemini Engineering Academy.

Your role
Regulatory affairs in the pharmaceutical sector is key to ensure product quality and patient safety in order to reach and maintain the Market Authorization agreement. ****

  • Establish a Project Coordination & Operational Services for Global Regulatory Affairs (GRA), allowing our clients RA department to focus on their Core Business
  • Bring together a range of business, administrative & analytic skills in one service to support GRA teams in delivering submissions and Q&A relating to regulatory filing of vaccines
  • Use Confidential Coordination & Administrative systems, processes, tools & templates
  • Have formal best practices adopted, published and used consistently across Global RA projects

Your profile

  • Master degree in Life Sciences (Engineering, Pharma, Chemicals etc)
  • Good knowledge of Regulatory Affairs
  • Minimum 1year of relavant RA experience
  • Fluent in English and French
  • Communication & coordination skills
  • Knowledge in Database Management



Posted on:

July 6, 2022

Experience level:

Mid level

Contract type: