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We are seeking a highly motivated and results-driven Senior Associate to join our Regional Regulatory Affairs team at Amgen SA. As a key member of this team, you will provide European regional regulatory leadership and expertise for the development, registration, and lifecycle management of Amgen molecules.
This exciting opportunity will see you working closely with cross-functional teams to execute regional regulatory strategies and plans, prepare supportive documentation for regulatory deliverables, and ensure regulatory product compliance.
You will work in a dynamic environment where no two days are the same, and your ability to think critically and strategically will be essential in driving business success.
To succeed in this role, you will need to have:
- A Master's degree in a scientific area or a Bachelor's degree in a scientific area and 2 years of directly related experience.
- In-depth knowledge of regional countries legislation and regulations relating to medicinal products.
- Excellent communication and relationship-building skills.
