Do you want to transform the lives of patients by taking a vital role in a company that follows science and turns ideas into life changing medicines? Then AstraZeneca has an exciting opportunity for you!
As part of AstraZeneca, the Nordic Marketing Company employs over 550 people across 5 countries and has offices located in Copenhagen, Oslo, Stockholm, and Helsinki. By 2025 AstraZeneca Nordic aims to become a recognized leader in its core therapy areas and improve the lives of millions of people. This will be achieved by driving innovative science, preparing launches, building close teamwork and partnerships within health care systems, and developing hard-working teams. In other words, this is the place to make an impact. Here we ensure everyone can reach their full potential, perform at their best, and make a valued contribution to the enterprise.
Join our team in Espoo, Helsinki, as a Regulatory Affairs Manager and play a key role in ensuring patients’ access to great medicines in the Nordics. Our dedicated teams seek efficient regulatory processes and facilitate successful launches and lifecycle management of our medicines. We provide an inspiring innovative workspace where you can influence the ways of working and always have support to manage your tasks.
You will become a regulatory expert for all Nordic countries, ensuring that our products meet regulatory requirements. Your responsibilities span across functions and therapy areas where you provide your regulatory insights and framework-understanding to support business decisions, and externally to influence the regulatory environment.
We partner in a multinational environment and interact with Global Regulatory Affairs, Therapeutic Areas Teams, Labelling, Logistics and Operations as well as with Translation CRO’s and Health Authorities.

TYPICAL ACCOUNTABILITIES

• Providing operational regulatory input and guidance to partners and in cross-functional teams
• Applying EU regulatory procedures in your daily work and provide long-term strategy
• Ensuring texts and other materials meet external requirements and AZ policies (e.g. labelling including product information and compendium texts)
• Monitoring and shaping the regulatory environment

WHAT WE NEED FROM YOU

In combination with your regulatory interest, successful candidates will have worked in one or more areas in Regulatory Affairs in the pharmaceutical or other relevant industry or at a Health Authority. Candidates with curiosity, relevant studies / internships, and a strong interest in regulatory affairs will be considered with great interest.

• Master’s degree in Life Sciences, such as Pharmacy, Chemistry, Biology
• Communicate and write with strong purpose
• Excellent knowledge of English and proficient in at least one of the Nordic languages
• Good knowledge of legislation requirements and procedures

I&D
We are proud to have a unique workplace culture that inspires innovation and collaboration. Here, employees are empowered to express diverse perspectives - and are made to feel valued, energized and rewarded for their ideas and creativity.

Please refer the Job description for details