Regulatory Affairs Specialist

About the RoleWe are seeking a skilled Regulatory Affairs Specialist to support our team in ensuring compliance with regulatory requirements for new products, license renewals, and variations. The successful candidate will have a strong background in regulatory planning and experience with regional regulatory affairs. Key responsibilities include:Develop and...

Unlock a World of Possibilities in Regulatory AffairsAre you a high-potential master's student with a passion for regulatory landscapes and processes? Do you want to be part of a dynamic team that drives change in the pharmaceutical industry? At Novo Nordisk, we invite you to embark on a life-changing journey as a Regulatory Affairs Graduate.About the...

About the Regulatory Affairs PositionNovo Nordisk's Regulatory Affairs Graduate ProgrammeAre you a master's student with an interest in the regulatory landscape and processes? Be part of our growth journey and accelerate your own. Turn your degree into a global career at a leading pharmaceutical company.About the RoleThe Regulatory Affairs Graduate Programme...

   Regulatory Affairs Graduate: Kick-start your life-changing career! Are you a master’s student with an interest in the regulatory landscape and processes? Be a part of Novo Nordisk’s growth journey and accelerate your own. Turn your degree into a global career at one of the world's leading pharmaceutical companies!  About the Regulatory Affairs...

About the PositionAs a Regulatory Affairs Supervisor at Novo Nordisk, you will play a key role in ensuring compliance with regulatory requirements for new products, license renewals, and variations. Your expertise will guide our regional regulatory affairs team, ensuring seamless submissions and approvals.Key ResponsibilitiesLead Regulatory Planning...

The position Regulatory Planning Submissions and Approvals for new products, license renewal, variation, eregistration, etc Regional Regulatory Affairs Regulatory Compliance & System Cross Functions/Departments Supporting Regulatory Influence Qualifications Relevant graduate level degree, e.g. Pharmacy, Pharmacology, Biology. Fluency in both written &...

Are you passionate about crafting high-quality regulatory content that drives meaningful impact in pharmaceutical operations? Do you bring experience in API manufacturing processes or the regulatory field, with a keen eye for detail and a knack for collaboration?As a Regulatory Content Specialist, you will play a crucial role in shaping the way we write our...

Are you passionate about finding solutions that benefit society, private businesses, and citizens? Do you have a keen interest in gaining practical experience in how the collision of policy and politics comes together for patients? If yes, this internship in the International Government Affairs & Policy team at Novo Nordisk is a unique opportunity to support...

About the RoleWe are seeking a skilled Regulatory Writer to join our team in the Product Supply API MSAT Project Office department. As a Regulatory Writer, you will play a critical role in shaping the way we write our regulatory documents based on continuous learnings and feedback.Key ResponsibilitiesDefine the regulatory storyline in collaboration with...

   Are you passionate about writing and ready to make a meaningful impact in regulatory submissions? Do you bring experience within API manufacturing processes or the regulatory field, excelling in a role with a clear purpose and direct impact on Novo Nordisk’s ability to deliver to patients? If you share our drive to make a difference in the production...

   Are you a passionate expert within cold chain and logistics? Do you have experience within shipping validation or qualification and ready for the next challenge? We are driving change in our global supply chain networks by delivering innovative and robust transport solutions for temperature-sensitive products. If so, we invite you to join our team as a...

About the RoleWe are seeking a highly skilled Regulatory Writer to join our Product Supply API MSAT Project Office team. As a Regulatory Writer, you will play a critical role in shaping the way we write our regulatory documents, working closely with colleagues across our department and partner teams from other parts of Novo Nordisk.Your key responsibilities...

Project Manager for API Manufacturing Science and TechnologyWe are looking for a skilled Project Manager to join our team in the Project Office department within Product Supply (PS) API Manufacturing Science and Technology (MSAT). As a Project Manager, you will oversee projects with high impact on the supply of API, drive and follow-up on optimization...

Are you interested in a challenging role with significant responsibility in the development of new injectable drug products to treat serious chronic diseases?About the RoleAs an Advanced Product Professional in the New Product Introduction (NPI) team at Novo Nordisk, you will be responsible for ensuring the stability and control strategy of our late-stage...

About the RoleWe are seeking a highly skilled Senior Counsel to join our Global Legal and Compliance Operations team as a Senior Counsel for Competition Law and Regulatory Compliance. The ideal candidate will have a strong background in competition law and regulatory affairs, with experience in developing and implementing compliance programs, handling...

About the RoleWe are seeking a highly skilled and experienced Corporate Counsel to join our Pharma Law Development team at Novo Nordisk A/S. As a key member of our team, you will play a critical role in advising on legal matters related to clinical trials, scientific exchange, and regulatory affairs.Key ResponsibilitiesProvide legal advice and guidance to...

The Role As Director of Quality and Compliance for Inspection Office at Novo Nordisk, you will have a unique opportunity to set direction and provide consultation for line of business in all matters related to interpretations and implementation of cGMP. In this senior expert role, you will have a key role in managing and hosting inspections from...

About the RoleWe are seeking a highly skilled Quality Assurance Specialist to join our team at Novo Nordisk. As a Quality Assurance Specialist, you will be responsible for leading strategic quality projects and initiatives across our business area, driving reporting, and conducting quality management reviews. You will also liaise with and advise senior...

About the Role:We are seeking a Quality Assurance Specialist to join our Corporate Facilities team at Novo Nordisk.Key Responsibilities:Lead strategic quality projects and initiatives across CVP areaDrive reporting and conduct quality management reviewsLiaise with and advise senior stakeholders on quality mattersReview, optimize, and strengthen quality...

Internship Opportunities in Life SciencesWe are seeking highly motivated and dedicated students to join our Life Sciences – Pharma & Biotechnology Talent Pipeline. This program offers internships in various areas of our business, including Clinical Development, Medical, Regulatory, Rare Diseases, and Research.As an intern, you will have the opportunity to...