(Senior) Regulatory Professional - Veeva RIM - Maternity Cover

Research & Development 

Søborg, Denmark 

This opportunity is unordinary because it allows you to directly influence how Regulatory Affairs operates in a globally impactful organization. You’ll not only contribute to meaningful improvements but also drive transformative change in a dynamic environment that values innovation and forward thinking.  

Your new role  

As our (Senior) Regulatory Professional working with Veeva RIM, you will play a key role in driving the continuous optimisation of the submission and registration processes in the Veeva RIM system, triggered by evolving business needs and the three yearly releases from the vendor Veeva. The main purpose of the role is to impact processes and solutions while ensuring business value through smooth adoption across the organisation. 

Your main responsibilities will be: 

• Ensure evaluation, prioritisation, implementation, communication, and training in new Veeva RIM features across Regulatory Affairs.  

• Support and drive Veeva RIM process development and optimisation.  

• Engage with stakeholders and external vendors, providing technical guidance and regulatory input to ensure fit-for-purpose processes and solutions.  

• Guarantee alignment with external regulatory requirements.  

Your new department  

Regulatory Affairs is an exciting area involved across the full value chain. We are responsible for global regulatory strategies to obtain and maintain regulatory licenses for current and future products, responsive to the worldwide business needs of Novo Nordisk. In this role, you will have the unique opportunity to be part of a strategically crucial business transformation programme across multiple processes and geographies and take an active part in shaping the way Regulatory Affairs will work in the future.  

 You will join RQ&C Business Platforms. The department consists of 19 Professionals and Specialists located in Denmark and India. In this position, you will get the opportunity to join our team in Denmark. Our aspiration is to ensure that Veeva RIM is used in an optimal manner, identifying business needs in the Submission and Registration process and leveraging digital solutions and automations to the benefit of our regulatory purposes. The atmosphere in the department is informal, and our commitment to innovation also applies to the way we work. We embrace a flexible workplace, with a blend of in-office and remote work.  

Your skills and qualifications  

To be a competitive candidate, you:  

Need to have:  

• A Master’s degree in a relevant field, such as science, pharmacy, or equivalent.  

•  3+ years of experience in the pharmaceutical or other similar industry, preferably within Regulatory Affairs. We are open to different levels of seniority.  

• Strong understanding of overall business processes, an analytical and quality mindset, and a flair for IT.  

• Fluency in English, both written and spoken.  

Nice to have:  

• Experience working with Veeva RIM or a similar Registration Information Management system.  

On a personal level, you are curious and eager to learn, well-organised, able to multitask, and proactive in solving challenges. You enjoy collaborating in a diverse, global team and can communicate complex ideas clearly and convincingly to support sound business decisions. You thrive in a dynamic environment, maintain a can-do attitude, and bring a healthy sense of humour to your work.  

Working at Novo Nordisk  

At Novo Nordisk, we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development to manufacturing, marketing and sales – we’re all working to move the needle on patient care. 

More information 

For further information, please contact Associate Director, RQ&C Business Platforms, Anette Schøndorff Enggaard at ascc@novonordisk.com  

Deadline