Intern For Drug Product Manufactoring

Intern for Drug Product Manufacturing

Are you eager to gain hands-on experience within Drug Product manufacturing and contribute to a company with a strong purpose? We are looking for two Trainees to support our Aseptic Production and Finish Production departments. This is a great opportunity to develop your skills in a GMP-regulated environment while making a real impact.

Your new role As a Trainee, you will support daily operations across the Drug Product organisation, contributing to documentation, data analysis, and quality-related processes. Your key responsibilities will include:

• Supporting Specialists with daily follow-up, and assisting in preparation and handling of deviations and CAPAs (Actions)
• Collecting, structuring, and maintaining documentation in relevant systems (e.g., QMS - Quality Management System)
• Gathering and analysing data to support QMS meetings and decision-making
• Coordinating and following up on deadlines to ensure timely closure of cases
• Contributing to ongoing quality improvement initiatives and handling ad hoc tasks as needed

You will work approximately 15–20 hours per week, with flexibility during exam periods. Your new department You will join the EMTO team (External Manufacturing Technology and Optimization Team), a dedicated group of 39 colleagues based at our site in Taastrup. The team is part of a small but global and highly professional organisation, giving you the opportunity to work closely with international stakeholders and contribute to processes that support drug product manufacturing.

Your skills and qualifications You are currently pursuing a bachelor's or master's degree within engineering, pharmaceutical sciences, biotechnology, or a related field, and you have a strong interest in drug product manufacturing. To succeed, you bring:

• An analytical mindset, curiosity for processes, and a problem-solving approach
• Strong skills working with data and documentation
• A structured, proactive, and detail-oriented way of working
• Motivation to contribute to optimization, continuous improvement, and high-quality standards within GMP
• The ability to speak, read, and write English confidently and clearly
• You are eager to learn, adaptable, and take responsibility for your tasks—whether supporting daily operations, handling documentation, or collaborating with cross-functional colleagues.

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 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. The internship will be for 6 months and can potentially be extended and will be compensated.