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Category:
Manufacturing

GMP Coordinator

CMC & Product Supply

Hillerød, Denmark

This is a rare opportunity to shape Godd Manufacturing Practice (GMP) excellence at the heart of Novo Nordisk’s aseptic manufacturing in Hillerød—where your expertise will directly influence the production of life-changing injectable treatments. You’ll lead strategic compliance initiatives, collaborate across departments, and drive continuous improvement in a high-impact, cross-functional role.

Your new role

As a GMP Coordinator at Novo Nordisk site in Hillerød, you will be at the center of a dynamic environment where no two days are alike. In this role, you will be the driving force behind our commitment to excellence in the production of life-changing injectables products within diabetes and obesity. You will juggle coordination, follow-up, and strategic direction-setting, while pushing key actions. Your ability to stay flexible, prioritize effectively, and manage your time efficiently will be crucial as you balance a wide range of responsibilities alongside your own tasks.

Your main responsibilities in this role will include:

  • Driving the preparation and overseeing the follow-up on authority inspections and internal audits.
  • Collaborating with stakeholders to ensure implementation of requirements from authorities.
  • Coaching and assisting your colleagues in GMP-related tasks such as deviations, validations, changes etc.
  • Preparing trend reports, Quality Oversight Tools, Quality Management Reviews (QMR) and Quality Monitoring Trends (QMT).
  • Maintaining a high-level GMP overview and reporting on GMP and quality trends to management.
  • Collaborate with relevant stakeholders, such as IT, QA and AMSAT.

But that is not all – you will also be an essential member of the GMP network within the CVP area. You will have the opportunity to foster collaboration, align goals, and share best practices. If you are energized by the prospect of making a broad impact while driving both team and individual success, this is the perfect role for you.


Your new department

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.

Aseptic Manufacturing (AM) in Hillerød consists of three departments: AM Operations & Support, Filling Operations & Support, and AM Operations & Support. The role covers activities across all three departments in collaboration with another GMP coordinator. You will be part of a team that includes the GMP coordinator, Local Training Coordinator, and six supporters.

Your skills and qualifications

To excel as our GMP Coordinator we expect you to have:

  • An academic degree in pharmacy, biology, engineering, or a related field.
  • +3years of experience in process support or QA in the pharmaceutical, medical device or similar regulated industry.
  • Strong experience and skills in GMP-regulated environments and complex production processes, preferably from aseptic production and filling lines
  • A mindset which is rooted in LEAN principles, and experience in systematic problem-solving, always looking for ways to improve efficiency and effectiveness.
  • Fluency in both Danish and English, allowing you to communicate seamlessly across our organization.


On a personal level, you are positive, action-oriented, and thrive in a cooperative environment. You approach challenges with a solution-focused attitude, working systematically and proactively. You possess the ability to see the big picture while never losing sight of the critical details that make all the difference.

Your communication skills enable you to connect with everyone from operators to management as well as other departments. You are proud of your ability to tackle hands-on tasks, ensuring that the key stakeholders are engaged and involved throughout the process.




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

You are welcome to contact Associate Manager Maria Lysgaard on +45 30792987 if you have questions about the role. Be advised Maria will not support queries about your recruitment status.

Deadline

30 October, 2025.

Novo Nordisk is 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.

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