Job Description

Overview

Responsible for the following Territories: Licences established in the Netherlands with supply and distribution into the EMEA region as well as import and export activities.

Youparticipate in the compliance with GDP/GDP-API & GMP requirements for the distribution of Medicinal Product (e.g., Drug Substance/Drug Product/Finished Product/QP Certified Finished Product) into the EMEA region as well as import and export activities.

Responsibilities

  • Ensure all aspect of Kyowa Kirin’s Quality Management Systems (QMS) are applied to medicinal product distribution activities:
  • Actively contributes to activities under the responsibility of the GDP Responsible Person, the Designated Person for API and the QP for distribution of Drug Substance(s)/Drug Product(s)/Finished Product(s)/QP Certified Finished Product(s).
  • Execute supplier and customer verification management (e.g., onboarding/offboard...

    • Ready to Apply?

    Take the next step in your AI career. Submit your application to Kyowa Kirin today.

    Submit Application