Manufacturing Engineer – Aseptic Filling

This position offers the chance to take ownership of process performance within a complex and highly regulated manufacturing setting. Your main focus will be on process implementation, process optimisation and continuous improvements in aseptic vial filling.

You will be joining a team that values development and collaboration, while also recognising the importance of experience in a period of change. For that reason, we are looking for someone who can bring a strong foundation, sound judgment and the ability to support both the process and the people around it.

Lead and support process improvements within aseptic filling, helping the organisation improve efficiency, consistency and operational performance.

Drive implementation of our new or updated manufacturing processes, including support for equipment, process changes and new fill line introduction.

Act as a process owner for part of the manufacturing operation, using your knowledge of aseptic vial filling to identify, analyse and address process inefficiencies.

Work closely on the production floor, observing how processes perform in practice and translating those insights into targeted improvements.

Review batch-related documentation and manufacturing records, ensuring a strong operational foundation and smooth execution.

Collaborate with cross-functional stakeholders including Manufacturing, Quality, MS&T and Supply Chain to deliver practical and sustainable solutions.

Coach and support colleagues during process improvements and implementation activities, helping to strengthen capability across the wider team.

This is a varied role in a dynamic manufacturing environment. While there is structure in the week, flexibility is essential. Priorities can shift, unexpected issues can arise and no two weeks are the same. Around 60-70% of the role is focused on implementation, optimisation and improvement activities. The remaining part covers the core GMP responsibilities that keep the operation running effectively, such as documentation, batch record review, deviations and change controls. Those elements are important, but the real emphasis is on bringing the right experience to improve the process itself.

What we are looking for We are looking for a candidate who brings relevant experience from a pharmaceutical manufacturing environment and is ready to apply that experience in a hands-on, improvement-focused role.

Experience in pharmaceutical manufacturing

Strong knowledge of aseptic processing, ideally within aseptic vial filling

Experience in process implementation, optimisation and continuous improvement

A solid understanding of GMP and the quality expectations of a regulated environment

The ability to assess issues, prioritise effectively and respond well in a changing operational setting

Strong communication skills and the confidence to work across teams and disciplines

An analytical mindset, with the ability to translate observations into practical improvements

Good written and spoken English; Dutch is preferred, but we are open to candidates with strong English and the right experience

In addition, you are:

Calm and resilient in a fast-paced environment

Comfortable managing multiple priorities at the same time

A strong communicator with excellent stakeholder management skills

Analytical and solution-oriented

Practical and visible on the workfloor

Additional information Your working days are Monday - Friday with no regular shift work. The role does include participation in an on-call rotation, currently approximately one week in every four, during which you are available between 07:00 and 22:00. An allowance is provided, with additional compensation if you are called in outside of office hours.

At AstraZeneca we support continuous learning and provide room to grow, both professionally and personally. In addition, we offer: 27 vacation days + option to buy 10 additional days, 1 paid volunteering day, €230 annual sports allowance 8% holiday allowance, 12.5% target bonus.

AstraZeneca works to improve quality of life for patients with serious diseases. We develop medicines in oncology, cardiovascular, renal and metabolic diseases, respiratory and immune disorders, and vaccines.

Globally, 75,000 colleagues work across six continents. In Nijmegen, around 100 colleagues produce, test, and package biologics for early clinical development. Our site plays a crucial role in bringing new medicines into first-in-human and early-phase studies.

We follow the science, put patients first, and strive to do the right thing. We value curiosity, collaboration, and continuous improvement - creating an environment where people can grow and thrive.

A great opportunity to help shape the future of our site and contribute to meaningful work.

Apply today by clicking on the apply button at the bottom of this page.

Questions? Our Recruitment Team, Karin Raadschelders or Caroline van Oppen, is available at [email protected] or +31 (0)85 - 047 0244.

We don’t work with a fixed closing date; we will commence our screening process immediately - the vacancy will close as soon as we’ve found the right candidate.

Date Posted01-Jul-2026

Closing Date11-Aug-2026

AstraZeneca embraces diversity and equality of opportunity.  We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills.  We believe that the more inclusive we are, the better our work will be.  We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics.  We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.