Regulatory Data Expert

As a Data Steward at Novo Nordisk, you will be part of the growth of our processes in digital transformation and bring our new products to our patients faster. You will be responsible for implementing and supporting our data strategy in the Regulatory organisation, ensuring alignment with digital transformation efforts.The ideal candidate will have a strong...

Select how often (in days) to receive an alert: Create Alert Expert in Regulatory Affairs - Primary Packaging Category: Reg Affairs & Safety Pharmacovigilance Location: Søborg, Capital Region of Denmark, DK Are you ready to take on new challenges in primary packaging development across emerging therapeutic areas and innovative products? Would you like to...

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...

We are seeking an experienced Regulatory Affairs expert to join our team and lead the development of regulatory CMC strategies for biologics products.The ideal candidate will have a strong background in drug regulatory affairs, with experience working in a dynamic environment and collaborating closely with stakeholders at senior management level.The position...

Novo Nordisk A/S is a global leader in diabetes care and a leading manufacturer of human insulin and analogs. Our mission is to improve the lives of people affected by diabetes and other serious chronic conditions.We are seeking a highly motivated and experienced Quality & Compliance Partner to join our R&D Data Governance Office. In this role, you will play...

About the Role\This exciting opportunity is part of Novo Nordisk's Global Regulatory Affairs team. As a Regulatory Specialist, you will play a key role in shaping the company's regulatory strategies and ensuring compliance with regulatory requirements.\Key Responsibilities:\\Develop and implement effective regulatory strategies to support the development and...

Global Regulatory Affairs CMC SpecialistWe are seeking a highly skilled Regulatory Affairs Chemistry, Manufacturing and Control (RA CMC) Specialist to join our team in a fast-paced, dynamic environment.As a CMC Regulatory Specialist, you will provide strategic, tactical, and operational regulatory input to projects. You will lead activities for synthetic...

Senior Medical Expert in Clinical DevelopmentAbout the PositionWe are seeking a highly experienced Senior Medical Expert to join our Clinical Development team. As a key member of our team, you will be responsible for interpreting data, assessing benefit-risk, and supporting regulatory submissions and interactions.Your Key ResponsibilitiesInterpret data,...

Regulatory Chemistry and Manufacturing ExpertWe are looking for a Regulatory Affairs Chemistry, Manufacturing and Control (RA CMC) Specialist with expertise in synthetic small molecules to join our team.The position involves leading activities for synthetic small molecule projects in late development and driving scientific and regulatory discussions across...

Take on the role of Regulatory Document Preparation Specialist at Novo Nordisk A/S and play a crucial part in driving the preparation of complex clinical documents that meet regulatory requirements.About UsNovo Nordisk A/S is a leading healthcare company focused on defeating diabetes and other serious chronic conditions. We value continuous learning, being...