Ardena

General company profile

An international and fast growing contract development and manufacturing organization (CDMO). We strongly believe that our multidisciplinary approach accelerates the drug development and approval process. By seamlessly integrating our services, we’re able to better mitigate development risks and ultimately reduce time-to-clinic. We have currently over 550 professionals working at 6 sites in Belgium, The Netherlands, Sweden and Spain.

We are a group of professionals and have a lot of opportunities to grow further. We are constantly looking for qualified employees to join our team of experts. Interested? See what opportunities there are for you.

Company activities:

As a CDMO Ardena provides comprehensive Drug Substance Development services. We support the entire work flow required to make your drug substance available for clinical studies and market authorization.

We support any type of CMC writing activity at all stages of the drug development process.

Drug Product Development and Manufacturing. We provide expert drug product services, whether you are looking for the development of a fit-for-purpose preclinical formulation or the manufacture of clinical trial material.

The control of materials in the nanometer size range requires scientifically demanding chemistry, analysis and manufacturing techniques. Our nanomedicine expertise encompasses formulation, process and analytical development, GMP manufacturing and dossier development.

Ardena offers comprehensive bioanalytical laboratory services for a wide range of pharmaceutical and biopharmaceutical products.

We provide both primary and secondary packaging services for a wide range of container types. We also assemble patient kits and provide comprehensive kit labelling printing services.

Clinal logistics services. Our clinical logistics team provides trial supply randomisation, blinding & un-blinding services and rescue medication packaging and labeling. They also provide a full comparator sourcing service, release testing, re-packing and labelling for clinical trial use.

We are looking for

We are rapidly growing and welcoming new enthusiastic skilled colleagues, we have many different job opportunities, amongst which:

Scientific writers:
With a Master’s degree in a scientific discipline e.g., pharmacy, biotechnology, biomedical sciences, chemistry or similar.
Passion for scientific and/or technical writing for chemical and/or biopharmaceutical products and a strong interest in regulatory guidelines

Analytical Scientists
• Who develop, validate and implement innovative and cost-effective analytical methods (HPLC, dissolution, etc.)
• You have a Bachelor or Master in Life Sciences, with a minimum of two years of relevant experience in an industrial setting

Project Managers / Scientific Project Officers
• You are in contact with our customers and you will translate their needs into a scientific project and lead this project through our different business units and you will write scientific reports.
• You have a Master or PhD in Life Sciences

What we have to offer

An international and highly innovative and challenging environment where people are proud of what they are doing. We are flexible and we encourage personal development and teamwork.

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