Utility Engineer

Utility Engineer

Måløv, Denmark, Onsite

Clinical Supply Packaging & Shipping

Are you looking for a new challenge where you can apply your extensive knowledge within facilities, equipment, and qualifications? Do you have a strong passion for managing and validating GxP equipment/systems in a setup that supports the growth of the business and ensures patient safety? And do you want to be part of a growing Clinical Supply Packaging & Shipping (CSPS) where we secure all Novo Nordisk products for clinical trials that are packed and delivered to patients all over the world?

If so, read on to find out more about our Utility Engineer opportunity in Clinical Supply Packaging & Shipping (CSPS) at Site Måløv.

Your new role

In this position you will:

• Be responsible for the current and future equipment/facilities including HVAC, BMS and FMS.
• Handle upgrades / rebuild and problem solving, maintain equipment in a validated state, and improve their performance.
• Do project management and drive LEAN processes to execute systematic problem solving.
• Potentially implement new equipment/facilities to support the growth in clinical trials.
• Collaborate closely with internal and external stakeholders and often be a part of the project team in a department in constant development with many exciting opportunities ahead of us.
• Deliver right-first-time solutions with an eye for small details and high quality.
• Support validation activities, change requests, deviations and overall documentation of our activities.

Your new department

The CMC Clinical Supplies Packaging & Shipping (CSPS) department is in Måløv and currently consists of 110 employees divided into six teams. Our overall goal in CMC Clinical Supplies is to ensure timely supply of our clinical studies to patients.

We are responsible for packaging and distributing products for clinical studies, and we work closely with the rest of the Clinical Supply Chain at CMC to achieve our ambitious goal of delivering high quality products on time to patients worldwide. We continuously work to optimize our processes, reduce lead time, and efficient use of resources using various LEAN tools.

Your skills and qualifications

Strict must-haves:

• Minimum of 3 years' hands-on experience within facilities and utilities.
• Master in etc. Engineering, Biotechnology, or other relevant education.

The following experiences will be a plus:

• Background within GxP regulated environment in the pharmaceutical industry. But other regulated industries like aero/space, electronics, plastic production and similar are also durable.
• GMP-knowhow / change control / deviation handling.
• Management of GxP facilities including troubleshooting, optimization and handling of critical alarms.
• Validation of GxP facilities including HVAC, BMS and FMS.
• Project management with technical knowledge.
• Stakeholder management cross functionally and with external suppliers.

As a professional, you are self-motivated, thrive working independently and enjoy driving projects, improvements, and initiatives across an organization. You have a structured approach towards challenges and utilize your problem-solving skills to create a standardized way of working. Furthermore, you have a visionary and innovative outlook to drive process optimization and digitalization.

What we offer

A unique opportunity to take rare, end-to-end ownership of the GxP-critical utilities and facility systems that directly enable clinical trial supply to patients worldwide. In CSPS at Site Måløv, you won’t be “just maintaining” HVAC, BMS and FMS. You’ll be the engineer who keeps them inspection-ready, solves complex issues at the root, drives upgrades/rebuilds, and helps shape what we build next as the clinical pipeline grows.

You’ll work in a high-trust environment with real influence and visibility, partnering closely across operations, QA, projects and suppliers to deliver right-first-time solutions through strong validation, change control and documentation. If you’re looking for a role that combines hands-on technical depth with genuine project leadership, LEAN-driven improvements and digitalisation, and where your decisions protect patient safety and accelerate trials, this is a standout step in your career.

Working at Novo Nordisk

Every day we seek the solutions that defeat serious chronic diseases. We approach our work with an unconventional spirit, rare determination and constant curiosity. For over 100 years, this mindset has built a company where purpose, mutual respect and a willingness to go beyond deliver extraordinary results. You’ll join colleagues who care deeply about users, quality and doing the right thing. Especially when the technology is new, powerful and fast‑moving.

Deadline

March 31st - 2026

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.