Regulatory Affairs Specialist, Nordics
T
Takeda Pharmaceutical
📍 asker, asker, Norway
Job Description
Our team is growing and for this we need bright minds with creativity and flexibility - **what talent do you have?**
For our Nordic Regulatory Affairs team, we are looking for a **Regulatory Affairs Specialist, Nordics**who will cover RA responsibility across all four countries.
This is fixed term contract from March 2025 until April 2026 for our Norwegian office in Asker, and it is an exciting early career opportunity to explore RA.
OBJECTIVES/PURPOSE
- Nordic product responsible (NPR) for regulatory lifecycle management of a product portfolio with the purpose to successfully deliver the EUCAN regulatory plans in alignment with agreed business priorities.
- Contribute to a strong collaboration and strong working relationship in Lifecycle Team and regulatory TA community, respectively.
- Subject matter expert (SME) within the department in defined area(s).
ACCOUNTABILITIES
- Nordic point of contact for a portfolio of inline products for EUCAN RA and in the MCO a...
For our Nordic Regulatory Affairs team, we are looking for a **Regulatory Affairs Specialist, Nordics**who will cover RA responsibility across all four countries.
This is fixed term contract from March 2025 until April 2026 for our Norwegian office in Asker, and it is an exciting early career opportunity to explore RA.
OBJECTIVES/PURPOSE
- Nordic product responsible (NPR) for regulatory lifecycle management of a product portfolio with the purpose to successfully deliver the EUCAN regulatory plans in alignment with agreed business priorities.
- Contribute to a strong collaboration and strong working relationship in Lifecycle Team and regulatory TA community, respectively.
- Subject matter expert (SME) within the department in defined area(s).
ACCOUNTABILITIES
- Nordic point of contact for a portfolio of inline products for EUCAN RA and in the MCO a...