Regulatory Affairs Manager, Power-to-X

Does it motivate you to be on the very frontline of the renewable energy business? Would you like to put your extensive experience within the biogas sector and your strong commercial and project management profile to work at European Energy in our Power-to-X division? Then we look forward to welcoming you as our new colleague.Your new team You will be part...

Does it motivate you to be on the very frontline of the renewable energy business? Would you like to put your extensive experience within the biogas sector and your strong commercial and project management profile to work at European Energy in our Power-to-X division? Then we look forward to welcoming you as our new colleague.Your new team You will be part...

Do you want to work with policies and regulation on advanced data science capabilities and methodologies ? Do you enjoy working in a fast-changing environment where engaged people have a unique combination of scientific and technical insight and ability to navigate political agendas and external stakeholders? If yes, you might be the new Data Science...

Join a fast-changing environment where people do their best to get Novo Nordisk products approved across the globe. In Global Regulatory Affairs, o ur people have a unique combination of scientific insight and ability to navigate many external requirements and stakeholders. Are you our new colleague? About the Department You will be part of...

Are you passionate about shaping future regulatory frameworks and policies? Do you thrive in solving unique and complex problems that have a significant impact on the development of future medicines and devices? If so, we have an exciting opportunity for you to join our Global Regulatory Affairs Policy & Intelligence department at Novo Nordisk. Apply...

The position As Regulatory Integration Lead, you will drive activities that enable us to manage regulatory activities across the product portfolio, with a primary focus on securing a smooth and effective integration of acquisitions into our regulatory IT platform Vault RIMYour main responsibilities include: Leading the migration of regulatory documents into...

The job is a unique opportunity to demonstrate your capacity for analysing, responding to, and influencing new regulatory requirements. As an RA Policy Professional, you will conduct impact assessments around new and draft requirements that impact Novo Nordisk regulatory procedures, and you will drive the development of Novo Nordisk responses to these...

Are you ready to play a crucial role in driving and coordinating multiple tasks with challenging timelines? Do you have experience in regulatory affairs or clinical trials? We are looking for a motivated EU Submission Lead for Clinical Trials to join our newly established virtual team in Novo Nordisk. If you are passionate about making a difference in the...

Are you ready to take on impactful projects and drive the implementation of complex regulatory requirements? Do you have a passion for improving processes and setting the direction for labelling coordination? If so, we have an exciting opportunity for you to join our Labelling Coordination department at Novo Nordisk in Søborg, Denmark.  Apply today...

The position As our new Project Manager for labelling at Novo Nordisk, you will be responsible for implementing complex regulatory requirements for packaging material updates. Your primary responsibilities will include:• Lead impactful projects across organizational boundaries• Ensure assessment of labelling impact for integrating new...

The position As an EU Submission Lead for Clinical Trials, you will play a crucial role in driving, coordinating, and actively following up on multiple tasks with challenging timelines. Your responsibilities will include: Working closely with various submission teams across the organization and all countries in Europe Managing initial clinical trial...

The position As our new Project Manager for labelling at Novo Nordisk, you will be responsible for implementing complex regulatory requirements for packaging material updates.Your primary responsibilities will include: Lead impactful projects across organizational boundaries Ensure assessment of labelling impact for integrating new assets/engagements driven...

The position includes some traveling activities. The workplace is our office buildings in Søborg but we can also offer flexible working. We do as well support you with a mobility package when moving from your home country. Qualifications To be successful in this role you will need to have: A university degree as a Medical Doctor and scientific...

The position You will be responsible for leading a team consisting of dedicated safety surveillance advisers with medical and life science background. It will be your job to: Set direction for your team and contribute to quality improvement projects Lead and develop the people in your team Ensure safety contribution to the clinical and regulatory...

Do you want to play a key role in driving the ongoing safety surveillance activities for early development projects in Novo Nordisk? And would you like to be part of one of the most skilled and advanced pharmacovigilance functions in Denmark, setting direction and inspiring a team of highly engaged professionals?  If so, you may be our new Department...

Would it motivate you to work directly with renewable energy assets, ensuring that they operate to the best of their ability, thereby accelerating the green transition? As a Renewable Asset Management Specialist with European Energy, you have a chance to work with the Solar PV Systems in our international portfolio of assets, including improvement and...

Would it motivate you to work directly with renewable energy assets, ensuring that they operate to the best of their ability, thereby accelerating the green transition? As a Renewable Asset Management Specialist with European Energy, you have a chance to work with the Solar PV Systems in our international portfolio of assets, including improvement and...

The position includes some traveling activity. Qualifications We're looking for candidates who have a university degree as a Medical Doctor and scientific training at PhD level or similar. Experience with clinical development of pharmaceutical drugs, medical devices, or Software as Medical Device development (SaMD) is an advantage, but not a...

Are you a Medical Doctor with an interest in clinical development of pharmaceutical drugs, medical devices and digital health? Would you like to be part of our medical and scientific team supporting our portfolio of medical device projects across diverse therapeutic areas? Is continuous personal and professional development important for you? If so, this...

Do you aspire to accelerate your leadership career within a global pharmaceutical company built on life-changing innovations? Does leading a department of incredibly talented and engaged colleagues from diverse cultural and professional backgrounds inspire you? In Novo Nordisk, we are embarking on a journey to reach 5D ambitions moving towards being a...