Adv. Professional

Novo Nordisk; Måløv; On-site; DKK 570,000 - 838,000; Full time

Job summary

Novo Nordisk is seeking a GMP Supporter to maintain cGMP standards within tablet production and act as a quality partner to manufacturing. You will contribute to continuous improvement and support new product introductions to ensure safe, compliant, and timely delivery of medicines worldwide.

The role requires a structured, quality-driven professional with 2–3 years in pharma GMP, strong ownership of quality and compliance, and excellent English; we offer integration into a global, regulated

Qualifications

• Bachelor's or master's degree in Natural Sciences
• 2–3 years of pharmaceutical industry experience in a GMP-regulated environment
• Solid understanding of daily GMP operations and ownership of quality & compliance
• Experience with deviations, change control, SOPs, and inspection readiness (advantage)
• Strong collaboration skills and fluency in English

Responsibilities

• Being present and handling issues on the shopfloor
• Ensuring manufacturing processes are executed in a GMP-compliant manner
• Handling deviations and change controls to timely and robust resolution
• Supporting new product launches through input on process, production, qualification, and facility readiness
• Preparing, reviewing, and approving SOPs, job instructions, protocols, and reports
• Participating in cross-functional projects focused on optimisation, digitalisation, and implementation of new systems
• Represent the site during internal and external audits and inspections

Skills

GMP experience

Fluency in English

Collaboration skills

Quality ownership

Education

Bachelor's or Master's in Natural Sciences

Job description

GMP Supporter (Adv. Professional)

Turn quality and compliance into a daily driver of patient impact. Join us where your GMP expertise helps ensure that life-changing medicines reach millions of people – safely, consistently and on time.

Your new role

As a GMP Supporter, you will play a key role in maintaining high cGMP standards within tablet production. You will act as a quality and process partner to manufacturing, ensuring that operations run smoothly, efficiently, and in full compliance. At the same time, you will contribute to continuous improvement and support the introduction of new products that bring tangible value to patients worldwide.

Day-to-day, Your Responsibilities Will Include

• Being present and handling issues on the shopfloor
• Ensuring manufacturing processes are executed in a standardised, cGMP-compliant manner
• Handling deviations and change controls related to processes and equipment, driving them to timely and robust resolution
• Supporting new product launches through input on process, production, qualification, and facility readiness
• Preparing, reviewing, and approving SOPs, job instructions, protocols, and reports
• Participating in cross-functional projects focused on optimisation, digitalisation, and implementation of new systems

You will also represent the site during internal and external audits and inspections, helping to ensure ongoing inspection readiness and a strong quality culture across the organisation.

Your new department

In Global Manufacturing & 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.

You will join our Tablet Production Site – a fast-paced and highly regulated GMP environment where quality, compliance, and continuous improvement are at the heart of everything we do. Collaboration is key, and you will work closely with colleagues across production, quality, and project teams to strengthen current ways of working while preparing for the technologies and products of tomorrow.

Your Skills & Qualifications

We are looking for a structured and quality-driven professional who thrives in a dynamic environment where priorities can shift and learning is continuous.

To Succeed In The Role, You Likely Bring

• A bachelor's or master's degree within Natural Sciences
• 2–3 years of experience from the pharmaceutical industry, ideally within a GMP-regulated environment
• A solid understanding of daily operations in a GMP setting and a strong sense of ownership for quality and compliance
• Experience with deviations, change control, SOPs, and inspection readiness (considered an advantage)
• Strong collaboration skills and the ability to work effectively across teams, combined with fluency in English

You are detail-oriented, proactive, and motivated by improving processes and ensuring high standards in everything you do.

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

Salary: For this role, the Annual Base Salary ranges from 570,200 DKK - 838,100 DKK (DK), 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

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.

Contact

For further information about the position, please contact Hiring Manager Lars Skovgaard at [e-mail].

Deadline

4 October 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.