Senior IT Process Engineer (POMS MES)

Novo Nordisk A/S; Måløv; On-site; DKK 651,000 - 957,000; Full time

Job summary

Novo Nordisk A/S in Denmark is seeking a Senior IT Process Engineer to drive development, optimization, and support of POMS MES for Clinical Supplies packaging and shipping.

You will design and implement .NET/C# applications, APIs, and data integrations, collaborate with stakeholders, ensure GMP/GxP compliance, and coordinate external suppliers to deliver reliable digital solutions.

Qualifications

• Bachelor's or Master's degree in Computer Science, Software Engineering, IT, Engineering, or a related discipline.
• At least 5 years of professional .NET/C# development experience.
• 5-10 years of hands-on SQL development experience, including database design, complex queries, and performance optimisation.
• Experience working in GMP- or GxP-regulated environments.
• Strong understanding of computer system validation, data integrity, and quality processes.
• Experience developing enterprise-level applications, interfaces, integrations, APIs, schedulers, or similar technical solutions.
• Hands-on experience with Manufacturing Execution Systems (MES) is required. Experience with POMS, PAS-X, or comparable MES platforms is considered essential for success in this role.
• Fluent in English, written and spoken.

Responsibilities

• Designing, building, testing, and supporting .NET/C# applications, APIs, interfaces, background services, and custom MES functionality.
• Developing and maintaining SQL databases, data models, stored procedures, and integrations that support business-critical processes.
• Driving optimisation and continuous improvement of POMS and related Clinical Supplies processes.
• Translating business requirements into robust, scalable, and compliant technical solutions.
• Collaborating with stakeholders across Clinical Supplies, Quality, Validation, and IT to ensure alignment between business needs and system capabilities.
• Coordinating development activities delivered by external suppliers and ensuring successful implementation of new functionality.
• Supporting testing, validation, releases, change management, and system improvements in accordance with GMP/GxP requirements.
• Acting as a technical problem solver and driving resolution of complex incidents and operational challenges.

Skills

NET/C#

SQL

GxP

Validation

MES POMS/PAS-X

APIs & schedulers

English fluency

Education

Bachelor's or Master's in CS/IT/Engineering

Tools

Databricks

POMS MES

Job description

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Are you passionate about developing digital solutions that enable the delivery of clinical supplies to patients around the world? Do you thrive in a role where software development, manufacturing systems and business processes come together? If so, you could be our new Senior IT Process Engineer in Clinical Supplies Digital Solution.

Your new role

As Senior IT Process Engineer, you will play a key role in the development, optimisation, and support of POMS, a business-critical Manufacturing Execution System (MES) supporting Clinical Supplies packaging and shipping processes.

Working closely with business stakeholders, IT colleagues, and external partners, you will drive the continuous improvement of POMS and related business processes, ensuring the solution remains reliable, compliant, and fit for future growth. Over time, you may also contribute to the wider digital landscape, including technologies such as Databricks, helping to strengthen the digital capabilities that support the global Clinical Supplies supply chain.

Your key responsibilities will include:

• Designing, building, testing, and supporting .NET/C# applications, APIs, interfaces, background services, and custom MES functionality.
• Developing and maintaining SQL databases, data models, stored procedures, and integrations that support business-critical processes.
• Driving optimisation and continuous improvement of POMS and related Clinical Supplies processes.
• Translating business requirements into robust, scalable, and compliant technical solutions.
• Collaborating with stakeholders across Clinical Supplies, Quality, Validation, and IT to ensure alignment between business needs and system capabilities.
• Coordinating development activities delivered by external suppliers and ensuring successful implementation of new functionality.
• Supporting testing, validation, releases, change management, and system improvements in accordance with GMP/GxP requirements.
• Acting as a technical problem solver and driving resolution of complex incidents and operational challenges.

You will have significant ownership of your area and the opportunity to influence the future digital landscape supporting Clinical Supplies.

Your new department

You will join CS Digital Solution, a team responsible for developing, maintaining, and supporting digital solutions used throughout Clinical Supplies.

We work closely with colleagues across Line of Business, Quality, Validation, and IT to deliver reliable, compliant, and innovative solutions that support the supply of clinical products globally. The team combines strong technical expertise with deep business understanding and has a clear focus on continuous improvement, collaboration, and delivering value to patients through digital innovation.

You will become part of an ambitious and supportive environment where knowledge sharing, professional development, and teamwork are key elements of how we work together.

Your skills and qualifications

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

• A Bachelor's or Master's degree in Computer Science, Software Engineering, IT, Engineering, or a related discipline.
• At least 5 years of professional .NET/C# development experience.
• 5-10 years of hands-on SQL development experience, including database design, complex queries, and performance optimisation.
• Experience working in GMP- or GxP-regulated environments.
• Strong understanding of computer system validation, data integrity, and quality processes.
• Experience developing enterprise-level applications, interfaces, integrations, APIs, schedulers, or similar technical solutions.
• Hands-on experience with Manufacturing Execution Systems (MES) is required. Experience with POMS, PAS-X, or comparable MES platforms is considered essential for success in this role.

In addition, we are looking for someone who:

• Has strong analytical and problem-solving skills.
• Can work independently while navigating a complex stakeholder landscape.
• Communicates effectively with both technical and non-technical audiences.
• Enjoys collaborating across functions and building strong working relationships.
• Is fluent in English, written and spoken.

Experience from the pharmaceutical industry and familiarity with Clinical Supplies processes would be considered an advantage.

Working at Novo Nordisk

At Novo Nordisk, we don't wait for change. We drive it. Every day, our employees work to improve the lives of millions of people living with serious chronic diseases.

We believe that success comes from diverse perspectives, curiosity, and a willingness to challenge the status quo. That's why we create an environment where talented people can grow, collaborate, and make a meaningful difference.

When you join Novo Nordisk, you become part of a company with a strong purpose, ambitious goals, and opportunities for both professional and personal development.

What we offer

Salary: For this role, the Annual Base Salary ranges from 651,000 to 956,900 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

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.

Deadline

27 September 2026.