Our client is a global leader in healthcare and pharmaceutical products, with base in Leiden. The company focuses on the discovery, development, manufacture, and marketing of vaccines to protect people worldwide from infectious diseases.
The Sr Technical Integrator is responsible, with some managerial guidance, for developing the technical eCTD sections to support Regulatory CMC dossier applications (module 3).
- PhD + 3 years of relevant experience // University degree + 6 years of relevant experience.
- Experience with module 2.3 and module 3 writing.
- Very good communication skills in English
For more information please contact Carla Garcia at firstname.lastname@example.org or +31 (0) 20 658 98 01.