Submission Strategist

We are seeking an experienced Regulatory Affairs Specialist to join our Device and Digital Health team at Novo Nordisk A/S. In this role, you will be responsible for driving submission activities related to primary packaging and collaborating with colleagues across the organization.

The main responsibilities of this role include:

• Driving submission activities related to primary packaging in cross-functional RA matrix teams and device project teams
• Collaborating closely with colleagues across the organization, leading key activities from early development through to clinical trials and up to marketing applications
• Ensuring alignment of planning and strategy across areas for primary packaging, representing Novo Nordisk internally and externally
• Celebrating the diversity of our employees, patients, and communities, and contributing to creating an inclusive culture

• An academic degree such as a Master's degree within engineering, pharmacy, or a relevant field
• Strong project management skills and outstanding communication abilities
• A proactive, solution-oriented mindset and fluency in written and spoken English
• Experience in the pharmaceutical industry and knowledge of international legislation and standards

We offer a dynamic and inclusive work environment, with opportunities for career growth and development. Our employees are passionate about making a difference in patient care, and we encourage collaboration and innovation.