Associate Director in RA CMC Semaglutide

Are you passionate about leading teams and supporting regulatory strategies? Do you excel in working with a wide range of stakeholders to ensure compliance and quality? We are looking for an Associate Director in RA CMC Semaglutide to join our team and make a difference in the lives of millions of people around the globe. If this sounds like you, read on and apply today!

The position

As an Associate Director in RA CMC Semaglutide, your main responsibilities will include:

• Leading the team in line with Novo Nordisk Way to ensure optimal employee development, planning, and resource utilization
• Coordinating and prioritising tasks for all team members while ensuring effective performance follow-up to meet targets within deadlines
• Clarifying direction and strategy for the team to align with organisational goals
• Being responsible for Occupational Health & Safety in the team, recruitment, and terminations
• Ensuring the quality of work processes in the department/team and compliance with internal and external requirements

Qualifications

We are looking for a candidate who possesses the following qualifications:

• A master’s degree or PhD in life science or similar and professional proficiency in English
• +8 years drug development experience in similar position, from the pharmaceutical industry or Health Authority, of which at least 3 years should be spent in leadership position
• Experience of working on projects in late-stage development or LCM phase and submission experience combined with experience with leading effective teams
• Proven track record of leadership, project management, stakeholder management and planning
• Out-of-box thinking complemented with hands-on experience in navigating within an environment of tight timelines, high complexity, and diverse tasks

About the department

The RA CMC Semaglutide department is responsible for defining and driving regulatory strategies for our marketed Semaglutide products, which are transforming and improving the lives of millions of people worldwide. The team focuses on CMC activities, including health authority interactions and providing regulatory expertise and tactics to product development plans. The position can be based in either Soborg, Denmark or Bangalore, India, offering you the opportunity to work in a vibrant and collaborative atmosphere with a global impact.Working at Novo Nordisk

Working at Novo Nordisk 

Every day we seek the solutions that defeat serious chronic diseases. To do this, we approach our work with an unconventional spirit, a rare determination and a constant curiosity. For over 100 years this unordinary mindset has seen us build a company unlike any other. One where a collective passion for our purpose, mutual respect and a willingness to go beyond what we know delivers extraordinary results.Contact and Deadline

Contact 

For further information please contact Milos Marinkovic at mmvc@novonordisk.com or +45 30 79 41 55 or get to know us better by visiting www.novonordisk.com/careers.

Deadline 

12th Apr 2026.

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.