Chief Regulatory Affairs Officer for Biologics

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...

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...

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...

We are seeking an experienced purpose-driven and business-minded second line leader with extensive expertise in drug regulatory affairs to join our team as the Director of Regulatory Affairs for Biologics and Rare Diseases.About the roleAs the Director for RA CMC Biologics & Rare Diseases, you will play a pivotal role in shaping the future of RA CMC. We are...

Select how often (in days) to receive an alert: Create AlertExpert in Regulatory Affairs - Primary PackagingCategory: Reg Affairs & Safety PharmacovigilanceLocation:Søborg, Capital Region of Denmark, DKAre you ready to take on new challenges in primary packaging development across emerging therapeutic areas and innovative products? Would you like to use...

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...

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...

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...

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...

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 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...

Navigating Complex Regulations to Drive Business SuccessIn this dynamic role, you will leverage your expertise in regulatory affairs to drive business growth and expansion while ensuring compliance with product safety standards and regulatory requirements in Nordic markets. As a Regulatory Affairs Associate in our Hygiene division, you will develop and...

We are recruiting for a Regulatory Affairs and Clinical Trials professional to join our team at Novo Nordisk A/S. As a Global Trial Manager, you will play a critical role in ensuring the quality and integrity of our clinical trials.Key responsibilities include:Ensuring compliance with regulatory requirements, good clinical practices, and internal...

About the RoleWe are seeking an experienced Analytical Project Manager - Biologics to join our team. As an Analytical Project Manager - Biologics, you will be responsible for coordinating and overall timeliness of analytic method validations in collaboration with QC Subject Matter Experts.You will maintain knowledge and overview of QC Project milestones and...

We are committed to finding the best candidate for this exciting opportunity as the Director of Regulatory Affairs for Biologics and Rare Diseases.About the departmentThe newly established RA CMC BRD Development Projects & LCM is one of three areas in RA CMC Biologics & Rare Diseases, which is a VP area organized in the RA CMC & Device organization with 270...

About UsWe are a global pharmaceutical company committed to creating innovative solutions for better lives.Our Regulatory Affairs team plays a crucial role in ensuring the safe and effective use of our products.Job DescriptionKey Responsibilities:Develop and implement process strategies to drive excellence in regulatory affairsManage cross-functional...

Job Description\Novo Nordisk A/S is seeking an experienced Regulatory Affairs Specialist to join our team. The ideal candidate will have a strong background in regulatory affairs and be able to drive the strategic direction of innovative development projects.\Main Responsibilities:\\Execute and drive the regulatory strategy to obtain approvals\Provide...

Select how often (in days) to receive an alert: Create AlertCategory: Reg Affairs & Safety PharmacovigilanceLocation:Søborg, Capital Region of Denmark, DKDo you want to be part of a growing organization, contributing to the success of Novo Nordisk's expanding product portfolio? Are you passionate about regulatory guidelines and committed to ensuring...

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 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...