Process Scientist in Specialized QC Utility

Novo Nordisk A/S; Kalundborg; Remote; DKK 570,000 - 838,000; Full time

Job summary

Novo Nordisk A/S in Kalundborg seeks a Process Scientist to support Specialized QC Utility, focusing on qualification of analytical equipment and method development across production control. You will collaborate with development teams to ensure reliable, compliant QC processes and contribute to technology implementations.

Applicants should hold a relevant degree and have hands-on GMP QC experience, with strong IT skills and proficiency in English and Danish.

Qualifications

• Relevant academic degree in chemistry, pharmaceutical sciences, chemical engineering or related scientific discipline.
• Experience with GMP environment and analytical equipment in QC lab.

Responsibilities

• Qualify and implement new analytical equipment (NIR, PSD, Karl Fischer, pH meters, balances, pipettes).
• Collaborate with process and manufacturing development to develop and validate methods from study design to data reporting.
• Troubleshoot equipment issues and provide hands-on support to keep QC analyses on track.
• Conduct annual lifecycle management, assess performance trends and recommend actions.
• Manage change requests, deviations and SOP updates to meet GMP requirements.
• Contribute to implementing new technologies across production areas as the team scales.

Skills

English proficiency

Danish proficiency

GMP equipment experience

Method development

Change control / deviations

IT and LIMS familiarity

Team collaboration / communication

Education

Chemistry / Pharmaceutical Sciences / Chemical Engineering degree

Tools

LIMS

TIMS

Job description

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Process Scientist in Specialized QC Utility

Location: Kalundborg, Region Zealand, DK

This is an exciting opportunity for you to join our team Specialized QC Utility as a Process Scientist in Kalundborg.

Your new role

As Process Scientist, you will work across two connected areas — analytical equipment management and analytical technology — ensuring the tools and methods behind our quality control and production processes are qualified, reliable and advancing. Your work will directly support the quality and release of medicines for people living with serious chronic diseases. You will join a rapidly growing team where technical curiosity and hands‑on expertise drive real progress every day.

Moreover, you will have the responsibility to

• Qualify and implement new analytical equipment — including NIR, PSD, Karl Fischer, pH meters, balances and pipettes — expanding the laboratory's capabilities to meet growing demand.
• Collaborate with process development and manufacturing development colleagues to develop and validate methods, from study design through hands‑on work, data evaluation and reporting.
• Troubleshoot equipment-related issues and provide hands‑on support to laboratory colleagues, minimizing downtime and keeping QC analysis on track.
• Conduct annual life‑cycle management activities, assessing equipment performance trends and recommending actions to maintain reliability and compliance.
• Manage change requests, deviations and SOP updates, ensuring all documentation meets GMP requirements.
• Contribute to the implementation of new technologies across production areas as the team scales its capabilities.

Your new department

The team you will join is named Specialized QC Utility and consists of 16 colleagues. Specialized QC Utility is part of Global QC, supporting site KA. The department consists of 3 teams with approx. 70 lab technicians and chemists. Specialized QC Utility is responsible for equipment in the lab and NIR instruments placed in the PS-API production.

Your skills & qualifications

To succeed in this role, you have a relevant academic degree in chemistry, pharmaceutical sciences, chemical engineering or a related scientific discipline. Moreover

• Experience in working with equipment in a GMP environment and Experience with analytical equipment at work in a quality control laboratory
• Preferably experience with systems like LIMS, TIMS, and a natural flair for IT
• Experience with method development, validation and data evaluation, including preparation of study protocols and reports.
• Familiarity with change control, deviation handling and SOP management within GMP.
• A proactive mindset with a can‑do attitude, combined with technical skills and a strong interest in technology
• Professional proficiency in English and Danish

Useful, but not essential:

• Familiarity with IT systems used for equipment management or laboratory documentation.

As a person, you are a team player who is solution‑orientated and has a positive attitude. You have excellent communication skills and can establish and nurture relationships across teams and departments. You enjoy working with people from different professional backgrounds who are dedicated to meeting our common goals and working in an informal atmosphere where flexibility and responsibility go hand in hand and are eager to see things progress. Lastly, you are good at communicating complex content to people with different backgrounds.

Working at Novo

At Novo we use our skills, dedication, and ambition to help people with diabetes and obesity and change their lives. By working with us you will have the opportunity to do the same in a global business environment.

Working at Novo we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing and sales – we’re all working to move the needle on patient care.

What we offer

At Novo, 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 570,200.00 to 838,100.00 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 .

More information

If you want to learn more about the position, please contact Manager, Global QC Specialised

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.