Regulatory Professional

.

We are looking for a Regulatory Affairs Professional to join RA CMC & Device in the area handling life-cycle management and late-stage development for the semaglutide pipeline. The role offers the opportunity to become a subject matter expert in our leading international organisation and to take the lead in setting the strategic direction for products of great importance to Novo Nordisk’s growth on a global level.

Your new role

The role will both involve working with late-stage development and life-cycle management submissions worldwide where you will be at the centre of project planning and execution, responsible for planning, coordinating, and reviewing regulatory documentation related to the drug, including preparing applicable sections of submission packages, responses to agency questions for global markets, and agency meeting packages.

You will be accountable for:

• Planning, executing and driving strategic regulatory CMC activities and submissions
• Applying CMC regulatory intelligence to develop robust regulatory strategies
• Identifying and improving regulatory CMC practices, processes, and approaches related to regulatory CMC documentation and strategies.

Your new department

Novo Nordisk Regulatory Affairs CMC & Device makes medicine available to patients around the world by ensuring fast regulatory submissions and approvals in all our global markets. The role in question will be anchored in an area handling life-cycle management for the semaglutide pipeline for regulatory CMC activities, an area consisting of approximately 40 employees in Denmark and India, where you would be working closely with colleagues across both locations as will collaborating with colleagues around the world in our affiliates.

Your skills and qualifications

To succeed in the role, we expect you to have:

• An academic degree in science, pharmacy, biology, or a similar field
• Preferably 1–2 years of relevant experience in the pharmaceutical industry, particularly within a CMC-related area.

• A strong scientific and technical mindset, along with a thorough understanding of related pharmaceutical operations, such as manufacturing, process development, analytics, and quality assurance

• Excellent communication skills, both written and spoken, with fluency in English.

• Strong collaboration skills, as all work takes place in multidisciplinary project groups across location

In this role, your collaborative skills will be well-trained and further developed, allowing you to build an extensive internal network.

On a personal level, you are a curious, well-organized, and proactive problem solver who thrives in dynamic environments. With a can-do attitude and strong teamwork skills, you adapt to change effectively while bringing innovation and independence to overcoming challenges.

Working at Novo Nordisk

Every day we seek the solutions that defeat serious chronic diseases. To do this, we approach our work with determination, constant curiosity and a commitment to finding better ways forward. For over 100 years, this dedication has driven us to build a company focused on lasting change for long-term health. One where diverse thinking, shared purpose and mutual respect come together to create extraordinary results. When you join us, you're not just starting a job, you're becoming part of a story that spans generations.

What we offer

At Novo Nordisk, you'll join a global healthcare company with a unique culture and strong results. We offer continuous learning, career development, and benefits tailored to your life and career stage.  

Salary: For this role, the Annual Base Salary ranges from 570,200 to 838,100 DKK corresponding to the level of the position.

The placement within the salary range will be assessed during the recruitment process based on the candidate’s skills, competencies, knowledge, and relevant experience.

Incentives and Benefits: The salary package may include short-term and/or long-term incentives as well as other employee benefits based on position level, location, functional area and relevant market benchmarks.

Learn more about our Reward Philosophy here

Deadline

7 September 2026. Applications are reviewed on an ongoing basis.

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.

At Novo Nordisk, we're not chasing quick fixes, we're creating lasting change for long-term health. For over 100 years, we've been driven by a single purpose: to defeat serious chronic diseases and help millions of people live healthier lives. This dedication fuels our constant curiosity and inspires us to push the boundaries of what's possible in healthcare. We embrace diverse perspectives, seek out bold ideas, and build partnerships rooted in shared purpose. Together, we're making healthcare more accessible, treating and preventing diseases, and pioneering solutions that create change spanning generations. When you join us, you become part of something bigger, a legacy of impact that reaches far beyond today.