Key Responsibilities/Scope Of The Job
- Represent International region in Global Regulatory Team and other cross-functional forums, for assigned products
- Develop International regulatory strategies and filing plans, in partnership with the Global Regulatory Lead, and country leads, for assigned products in development
- Plan and create a core dossier for International, in partnership with cross-functional teams, for assigned products
- Develop regulatory strategies in assigned countries, in partnership with local Regulatory teams
- Manage, plan and direct all aspects for the successful preparation, submission and timely approval of marketing applications and post-approval management for assigned countries
- Provide strategic guidance on regulations and changes in assigned countries
- Support interactions with Health Authorities in assigned countries
Education/Learning Experience/Work Experience
- A University Degree in Life Sciences is required with 10 years of industry experience, of which at least 5 years of experience within Regulatory Affairs (registration, development, maintenance)
- Experience of regulatory requirements in countries outside the US and Europe
- Very good knowledge in written and oral English is required, knowledge of any other languages would be an asset
- Experience from leading projects and cross-functional teams
- A strong team player, with the ability to work effectively in a team setting and interact with people of different cultural, seniority and functional backgrounds
- Highly self-motivated and able to drive activities
- Excellent communication skills
- The suitable candidate should demonstrate the values; Care for our patients, for our colleagues and for our company, Ambition, Urgency, Ownership and Partnership
- Ensure exemplary behaviour, ethics and transparency within the Company and with regulatory agencies