Director, Regulatory Affairs, Nordics

Revolution Medicines is a global, commercial-state oncology company dedicated to discovering, developing and delivering innovative medicines for patients with RAS-addicted cancers. Leveraging its differentiated RAS(ON) tri-complex inhibitor platform, the company is advancing a broad, integrated portfolio of oral RAS(ON) inhibitors designed to directly target the active, cancer-driving state of RAS. Founded on rigorous scientific inquiry and a willingness to challenge long-held assumptions, Revolution Medicines is committed to changing the trajectory of disease for patients with RAS-addicted cancers worldwide.

Our people are united by a shared way of working: follow the science, challenge assumptions, act with urgency and hold ourselves to a high standard of rigor—all in service of patients.

The Opportunity:

We are seeking a highly motivated and experienced professional to join our team as Director Regulatory Affairs, Nordics. Key aspects of this role will include leading and providing strategic input on all regulatory activities for assigned projects and territories in accordance with key requirements, regional/local regulations, and scientific and company policies and procedures, cross-functionally engaging in a team of regulatory professionals at global and European level supporting both early-stage and marketed products. This role will further ensure compliance with the applicant's and/or marketing authorization holder's responsibilities under legislation or regulatory guidelines for assigned products in the Nordic Countries.

The Director, Regulatory Affairs Nordics is an essential member of the local Management Team, while also acting as a contributor within the International Regulatory Team. The candidate will provide regulatory support for assigned products and therapeutic areas and work cross-functionally with medical affairs, clinical development, marketing and other teams to support the development and execution of medical strategies and tactics.

Further responsibilities include:

- In collaboration with regional and global RA as applicable supports with the preparation and follow-up for national scientific consultations and pre-submission meetings.

- Coordination of the creation of materials for risk mitigation activities and healthcare professional communication.

- Ensuring that product packaging and related information are updated and maintained in accordance with regulatory requirements.

- Review and approval of promotional materials.

- In collaboration with regional and/or global RA organization represents the regulatory function at internal and external meetings, as applicable.

- Close monitoring and analysis of all nationally relevant regulatory guidelines and communicates updates and implications to both regional and global teams.

- Maintains knowledge of complex regulatory requirements, contributes to the preparation of new regulatory guidelines wherever possible, comments on draft regulatory guidelines, and communicates changes to regulatory information to project teams and senior management locally and internationally.

- Ensure compliant and necessary inclusion at local MPAs and relevant platforms to ensure product availability.

- Initiates or contributes to local and/or global process improvements that have a significant impact on the business.

- Leading the creation, maintenance, continuous improvement, training, evaluation, and follow-up of all regulatory-related procedures, including policies, SOPs, manuals, and work instructions, to meet local regulatory requirements.

- Managing affiliate inspections and audits.

- Managing quality defects, counterfeit or imitation products, and batch recalls.

- Serving as the information officer.

- Responsible for any distribution and wholesale licenses.

- Managing local regulatory and regulatory compliance audits within the affiliate.

- Management and leadership responsibilities, as applicable.

- Providing