Leader in Global Regulatory Strategy

CMC Regulatory Strategy LeadAbout Our CompanyNovo Nordisk A/S is a leading global healthcare company with a 100-year legacy of driving change to defeat serious chronic diseases. Building on our strong legacy within diabetes, we are growing massively and expanding our commitment, reaching millions around the world and impacting more than 40 million patient...

About the TeamRA Obesity is a new and expanding area within Global Regulatory Affairs consisting of 20 dedicated and highly engaged Global Regulatory Leads, Regulatory Specialists, and Professionals, organised in two teams.We are responsible for developing and executing on global regulatory strategies, designed to advance projects across multiple...

We are looking for a talented and motivated individual to fill the role of Director of Regulatory Affairs for Biologics and Rare Diseases.About the responsibilitiesAs the Director for RA CMC Biologics & Rare Diseases, you will be responsible for leading and developing high-performing teams to achieve business objectives and deliver exceptional...

About the Department:The RA Business Development team is a team of 4 dedicated members. The team operates across all therapeutic areas, working closely with cross-functional groups, including deal teams, and providing direction in matrix teams across Regulatory Affairs.The department prioritises creating global regulatory strategies to advance projects from...

About UsWe are committed to securing process excellence and digital innovation to reach more patients faster by simplifying and standardizing ways of working with a focus on end users. Our Regulatory Affairs team manages submission, registration, and labelling to obtain authority approval for all Novo Nordisk products. We work across the value chain from...

Global Regulatory CMC Leadership RoleAbout Our CultureWe recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures.About the JobWe are seeking a highly...

The Regulatory Affairs Diabetes and Obesity therapeutic area is a key player in creating global regulatory strategies to advance projects from the early stages of development to worldwide submissions and approvals of initial Marketing Authorisation applications. As a senior member of this team, you will have the opportunity to collaborate with...

Director of Regulatory Affairs for CMC Biologics & Rare DiseasesAbout the PositionThe RA CMC organization is growing, and we are strengthening our leadership team with a new Director with strong experience and interest in Regulatory Life Cycle Management. As the Director for RA CMC Biologics & Rare Diseases, you will play a pivotal role in shaping the future...

Job Description">In this role, you will be responsible for evaluating external assets and companies for in-licensing, partnerships, or acquisitions across Novo Nordisk's therapeutic areas. You will also serve as a strategic business partner within global Regulatory Affairs in relation to Novo Nordisk's existing portfolio and lead portfolio-wide...

Job DescriptionThe position involves providing strategic regulatory input, assessing risks, and developing mitigation strategies. Key responsibilities may include:Representing Global Regulatory Affairs in various cross-functional teams.Planning, preparing, and leading Health Authority interactions.Developing regulatory documents, including briefing packages,...

Reckitt Benckiser is a global leader in hygiene, health, and nutrition products. Our purpose drives our actions: to protect, heal, and nurture people around the world.About the RoleWe are seeking a highly skilled Regulatory Affairs Associate to join our team in Hygiene. As a key member of our regulatory team, you will be responsible for ensuring compliance...

About UsNovo Nordisk A/S is a world-leading biopharmaceutical company with over 90 years of experience in delivering innovative medicines that improve the lives of people with diabetes and other serious chronic conditions. Our mission is to create value for patients, customers, and shareholders through sustained growth, customer satisfaction, and operational...

Category: Reg Affairs & Safety PharmacovigilanceLocation: Søborg, Capital Region of Denmark, DKAre you able to cut through complexity and drive regulatory strategies for high impact projects? Would you like to work together with experts across multiple functions in a global environment? Do you want to be part of an exciting area where engaged people are...

We are looking for a dynamic and visionary leader to spearhead our team as the Director of Regulatory Affairs for Biologics and Rare Diseases.About the positionThe RA CMC organization is growing, and we are strengthening our leadership team with a new Director with strong experience and interest in Regulatory Life Cycle Management.Be accountable for the...

Director of Regulatory Affairs for CMC Biologics & Rare DiseasesCategory: Project Management & AgileLocation: Søborg, Capital Region of Denmark, DKAre you an experienced purpose-driven and business-minded second line leader with extensive expertise in drug regulatory affairs? Do you excel in a dynamic environment and want to be part of a rapidly growing...

About the RoleWe are seeking a highly skilled Regulatory Affairs Specialist to develop and execute the late-stage regulatory strategy for a key project. This role requires strong scientific knowledge and regulatory expertise to evaluate strategies, manage multiple regulatory tasks with overlapping timelines, and collaborate closely with Global Regulatory...

Job Title: Global Regulatory Lead in CVD/CKD Area - Strategic ExpertWe are seeking a highly skilled and experienced professional to join our team as a Global Regulatory Lead. As a key member of our cross-functional project teams, you will be responsible for driving regulatory strategies and executing various regulatory tasks.The successful candidate will...

We are seeking a highly skilled and experienced professional to join our team as a Global Medical Manager for Alzheimer's disease.This role will be part of our Global Medical Affairs department, responsible for driving the worldwide strategic direction for Alzheimer's disease. As a Global Medical Manager, you will work closely with cross-functional...

As a Regulatory Affairs Business Development Director, you will play a crucial role in driving the integration process in RA when agreements are established, ensuring a smooth handover of asset/project to the global regulatory leads.

Company OverviewNovo Nordisk A/S is a leading global healthcare company focused on driving innovation and making a meaningful difference in people's lives.Our commitment to excellence drives us to push boundaries and strive for outstanding results.Job SummaryThis role is responsible for driving process excellence and digital transformation in regulatory...