(Senior) Analytical Project Manager

Category:  Project Management & Agile
Location: 

Bagsværd, Capital Region of Denmark, DK

   

Are you looking for an exciting opportunity to lead the implementation of analytical methods for drug products?

 

If you have a foundation in analytical chemistry/QC and are eager to enhance your project management skills, read on! We are seeking an engaged and passionate individual who can drive our projects to success. 

 

Your new role
As Analytical Project Manager you will be the one point of contact for one or more development projects or lifecycle management (LCM) projects in the Analytical Projects and Innovation department. You will play a key role in leading analytical development activities across different products in the AMSAT (Aseptic Manufacturing Science and Technology) area.

 

Activities include coordination of analytical validations and transfers, coordination of writing of regulatory documents, submissions and questions from authorities across the globe. You will be a member of the core project teams along with other technical project managers.  

 

Your main responsibilities will include:

  • Ensuring progress, planning, and execution of analytical activities in development or LCM projects. 
  • Managing the department’s project portfolio and providing professional guidance and sparring to the projects regarding analytical methods incl. validation.
  • Interact with a wide variety of stakeholders such as technical project managers (for e.g., drug product and drug substance), CMC, Quality Assurance, Regulatory Affairs, and representatives from Quality Control departments.
  • Collaborate and coordinate with analytical professionals who are working hands-on with method validation and optimization, transfers and regulatory writing.
  • Be responsible for aligning the needs of the project organization with those in line of business.

 

You will work closely with stakeholders across the organization regarding both planning and execution and facilitating resolving concrete scientific challenges. All of this requires clear and timely communication of project requirements to team and department members.

 

Finally, you will join a harmonious team and department with competent, caring, and positive colleagues. We have a strong foundation of employees with high seniority mixed with more recent newcomers.

 

The job is ideal for a dedicated and result-oriented project manager who enjoys working in a flexible, collaborative, international, and open-minded environment. A few yearly travel days might be expected.

 

Your new department

You will be joining a team with 13 Analytical Project Managers, who combine many years of experience in coordinating analytical tasks both during Phase 3 and marketed phases. The rest of the department includes technical project managers who coordinate analytical automation projects, so project management is our core expertise.

 

In CMC & Product Supply, we cover the full value chain from drug and device development to marketed Novo Nordisk products. We are more than 30,000 colleagues across the globe with the shared responsibility of scaling molecules, processes, devices, and products, dedicated to supplying life-saving medicines to the patients who need them most.

 

Your skills and qualifications
This position is the natural next step for an experienced project manager but can also be a learning path for someone with less project management experience and a strong background in analytical chemistry.

 

To succeed in this role, we imagine that you have:

  • A relevant academic degree within Pharmacy, Biology, Chemistry, Engineering or a similar field.
  • Experience within analytical chemistry combined with knowledge of GMP requirements. 
  • Experience in managing/coordinating and executing smaller and larger projects within CMC analytical development and/or QC
  •  Experience in leading analytical activities in either early phase and/or late phase clinical development.
  • Scientific experience within analytical development and/or validation and preferably experience with regulatory submissions.
  • Experience in transfer of analytical methods and CMO collaboration is an advantage.
  • Strong communication skills both in spoken and written English.

 

In addition, you easily collaborate between departments, you are proactively reaching out to your stakeholders and are accustomed to presenting project status overviews.

 

You are motivated by the opportunity of getting a large network in and across our area. You see opportunities in new ideas and thrive in a changing environment with ambitious deadlines.

 

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.

 

What we offer

There is, of course, more on offer here than the uniqueness of our culture and the extraordinary results we produce. Being part of a global healthcare company means opportunities to learn and develop are all around us, while our benefits are designed with your career and life stage in mind.

 

More information
For further information, please contact Manager; Lina Ilia on +45 34482752  

 

Deadline 
19th of  January 2026

 

You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying in your resume or CV. To ensure an efficient and fair recruitment process, please refrain from adding a photo in your CV.

 

We will be reviewing application on an ongoing basis, so please submit your application at your earliest convenience.

 

Novo Nordisk is currently in the process of adjusting job titles globally. Please note that the job title listed in this advertisement may be subject to change. More detailed information will be provided during the recruitment process.

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

 

We’re not your typical healthcare company. In a modern world of quick fixes, we focus on solutions to defeat serious chronic diseases and promote long-term health. Our unordinary mindset is at the heart of everything we do. We seek out new ideas and put people first as we push the boundaries of science, make healthcare more accessible, and treat, prevent, and even cure diseases that affect millions of lives. Because it takes an unordinary approach to drive real, lasting change in health.