Global Regulatory Product Development Manager

About Novo Nordisk:">Novo Nordisk is a global healthcare company that is committed to creating an inclusive culture that celebrates the diversity of its employees, patients, and communities. We believe that our employees are the key to our success, and we strive to create a workplace where everyone can grow and develop their skills.">Job Description:">We are...

Job Overview">We are seeking a highly skilled and experienced Regulatory Affairs professional to join our team as a Regulatory Affairs Strategic Development Director. In this role, you will be responsible for leading the development and implementation of regulatory strategies to support the commercialization of medicinal products.The ideal candidate will...

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...

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...

About the Role">This position offers the chance to work on exciting projects and contribute to Business Development (BD) activities across Novo Nordisk's therapeutic areas, representing Global Regulatory Affairs within the Global Project BD Team.">You will be responsible for leading Regulatory BD activities and establishing a Matrix Team covering all...

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...

Select how often (in days) to receive an alert: Create AlertRegulatory Affairs Business Development DirectorCategory: Reg Affairs & Safety PharmacovigilanceLocation:Søborg, Capital Region of Denmark, DKDo you have experience developing medicinal products and identifying regulatory risks and opportunities? Are you knowledgeable about the drug development...

Select how often (in days) to receive an alert: Create Alert Regulatory Affairs Business Development Director Category: Reg Affairs & Safety Pharmacovigilance Location: Søborg, Capital Region of Denmark, DK Do you have experience developing medicinal products and identifying regulatory risks and opportunities? Are you knowledgeable about the drug...

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...

About the Department">The Regulatory Affairs Diabetes and Obesity therapeutic area is responsible for 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 key member of this team, you will collaborate with cross-functional...

Department Overview\The RA Rare Bleeding Disorders department at Novo Nordisk is a dynamic and innovative team that contributes to the development of different products and projects within Rare Bleeding Disorders.\Main Responsibilities:\\Contribute to the development of regulatory strategies and plans for rare bleeding disorders projects\Collaborate with...

At Novo Nordisk A/S, we are seeking a highly skilled Regulatory Affairs Professional to join our team. This role will play a key connection between scientists and Health Authority regulators, ensuring fast and successful regulatory submissions and approvals in all global markets.About the RoleThis is an exciting opportunity for a talented individual to join...

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...

Job OverviewWe are seeking a highly skilled Regulatory Affairs Specialist to join our team in innovative development within rare diseases.This is an exciting opportunity to become part of a fast-changing field where no two days are alike.The PositionAs a Regulatory Specialist, you will be responsible for setting the regulatory strategic direction in...

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...

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...

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,...

OverviewJob Title: Regulatory Affairs Specialist for Rare Disease DevelopmentThe Novo Nordisk A/S RA Rare Bleeding Disorders department is part of the company's Global Regulatory Affairs and situated in Søborg, Denmark. Our team contributes to the development of different products and projects within Rare Bleeding Disorders with a pipeline including various...

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...

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...