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
Scientist – Process R&D Nanomedicines

YOUR ROLE

You will independently and in teams work on Process R&D of nanomedicines. This entails, in close collaboration with our clients, the development of scalable, robust, and GMP-compliant procedures for the preparation of nanomedicines for (pre)clinical use. You will work on the design and execution of process development experiments, possibly followed by (GMP) batch manufacturing, together with the Chemical Project Lead. Over time, you will be trained to adopt the full scientific leadership of your projects as Chemical Project Lead. The Chemical Project Lead forms the core project team together with the Project Manager, Analytical Lead and Quality Assurance.

YOUR KEY RESPONSIBILITIES

• You will design and coordinate lab experiments, for the development and scale up of processes towards (cGMP) manufacturing of nanomedicines
• You will write technical reports and maintain customer contact, written as well as verbally, to update on the status and progress of your projects
• You will be involved in the preparation and execution of (cGMP) manufacturing of nanomedicines, in close collaboration with colleagues from Production
• Working closely with colleagues from Process R&D, Production, Analytical Sciences and Quality Assurance
• Compliance to (company) regulations, procedures and (inter)national standards with regards to safety, product quality, order and tidiness
• You take up responsibility to run a smooth lab e.g. the management of your lab space, equipment and materials
• You will keep yourself up to date with the latest (nanomedicine) developments and insights
• You will report into a Senior/Principal Scientist - Group Lead Process R&D Nanomedicines

YOUR PROFILE 

• You have a MSc or PhD degree in chemistry, organic life sciences or equivalent
• (Extensive) knowledge of/experience with synthesis and formulation of nanoparticles
• In case of an MSc degree, you have experience in the pharmaceutical industry, specialized in process and scale-up development towards cGMP manufacturing
• You feel comfortable in a dynamic and changing environment
• You have a hands-on mentality
• You like to learn and develop yourself
• You are flexible, a problem solver, pro-active, and a team player
• You have an analytical mindset and you are stress resistant
• You have excellent communication skills and are fluent in both Dutch & English (written as well as spoken)                                                                                                                                                         

 WHAT WE OFFER

At Ardena, we recognize that our people drive our success. We offer:

✔ A competitive salary with a tailor-made benefits package, including: bonus plan, option for extra leave, great pension plan
✔ Flexible working hours and 30 days of paid holiday per year
✔ A dynamic, international work environment with career growth opportunities
✔ Access to Ardena Academy, our internal learning platform for professional development
✔ A chance to contribute to groundbreaking drug development projects that make a real impact

HOW TO APPLY

Want to know more? Contact Roy van de Camp at hr.oss@ardena.com.

Ready to start your career path with Ardena? Click the application button and join us in shaping the future of drug development!