INTRODUCTION TO ARDENA

As a leading Contract Development and Manufacturing Organization (CDMO), Ardena partners with pharmaceutical companies of all sizes—from emerging biotech to global industry leaders—united by the mission to help biopharma innovators navigate drug development with precision, quality, and speed, bringing their molecules from discovery to the clinic and market. Our fully integrated services span drug substance and drug product development, manufacturing, nanomedicine, clinical logistics, bioanalytical services, state research, fill & finish, and CMC regulatory support.
With a rapidly growing international footprint, Ardena is home to over 750 professionals across six strategic locations—Belgium (Ghent), the Netherlands (Oss and Assen), Sweden (Södertälje), Spain (Pamplona), and Somerset, New Jersey (the US). Our open and transparent culture is built on collaboration, ownership, and innovation, guided by our We CARE values. We foster a communicative environment where mutual respect, accountability, and excellence empower our team.
We are looking for skilled and motivated professionals eager to grow their careers in an exciting and fast-paced environment. Whether you’re an experienced expert or just starting out, Ardena provides a dynamic workplace where you can contribute to meaningful drug development projects, expand your knowledge, and be part of a global team committed to making a difference. As an international organization, we help you navigate a career path that expands your possibilities beyond borders, opening doors to personal and professional growth without limits. Your potential to grow is limitless with us.
If you are ready to take on new opportunities, work alongside industry experts, and contribute to the future of medicine, Ardena is the place for you.
For the Ardena Business Unit based in Oss, we are looking for a

YOUR ROLE

We are looking far a a proactive and flexible (Associate) Scientist to join our Analytical Department of the Nanomedicines Business Unit, supporting the development and quality control of pharmaceutical products in a Good Manufacturing Practice (GMP) environment.
The successful candidate will perform routine and standard analyses to ensure the quality and compliance of products, contributing to our mission of delivering safe and effective therapies to patients.
Next, you will implement, develop and qualify chromatographic methods to support development of new pharmaceuticals in different stages of development.

YOUR KEY RESPONSIBILITIES

• You implement, develop, and validate chromatographic methods for analysis of starting materials, intermediates, drug substances and drug products.
• Conduct routine analytical testing including complex sample pre-treatments on pharmaceutical products, raw materials, and stability samples following GMP standards
• Utilize and maintain analytical equipment such as LC, GC, UV-Vis, AAS, DLS and other laboratory instruments
• You prepare reports containing analytical results.
• Collaborate with cross-functional teams to ensure timely completion of testing and reporting.
• You take up responsibility to run a smooth lab e.g., the management of lab spaces, equipment, or materials.
  You will report into one of the group leads in the Department of Analytical Sciences Nanomedicines.