ABOUT US
Ardena is a leading contract development organization for the pharmaceutical industry. We assist pharmaceutical companies, from virtual biotech to big pharma, in bringing their valued molecule(s) to the clinic and market. We provide a comprehensive and integrated portfolio of drug substance and drug product development, manufacturing, logistics and bioanalytical services.
The Ardena Group is operating from five sites in Europe and one in US.
For the Ardena Business Unit Drug Product Development and Manufacturing (DDM) based in Ghent (Belgium), we are looking for an Associate Scientist - Aseptic Manufacturing .
YOUR KEY ROLE
The main role as Associate Scientist – Aseptic Manufacturing is to actively take part in small-scale GMP manufacturing for new chemical entities and new treatments under the guidance of the Group Leader - Aseptic Manufacturing.
As an Associate Scientist – Aseptic Manufacturing, you will be working in Ardena Gent’s brand new Fill & Finish facility on e.g. sterile solutions intended for injectables. Activities mainly involve executing manual operations, such as manufacturing of parenteral solutions (containing small molecules or protein-based drugs), filling and capping of vials using high-end equipment in an isolator.
In order to perform these GMP activities in line with the authority guidelines, you will follow a detailed Batch Record Documentation (BRD) to execute this protocol step by step. Furthermore, you will always work in team of at least 2 other technician and/or scientists.
YOUR PROFILE
WE OFFER
An attractive and tailor-made remuneration package including extra-legal benefits such as:

We are a global provider of drug development and discovery services, encompassing drug substance, drug product, bioanalysis, and CMC regulatory services across small molecules, large molecules, and nanomedicines. Our six international locations offer comprehensive CDMO and BioAnalytical CRO services to a wide range of clients worldwide.
We recognize the intricate challenges associated with advancing a promising molecule from the laboratory to the patient. Our multidisciplinary team is eager to collaborate with you throughout your development process, utilizing specialized technologies to optimize formulation and manufacturing. We possess extensive expertise in spray drying, hot melt extrusion, and lipid-based formulations that enhance bioavailability and solubility. Additionally, our capabilities include polymeric, metal, and lipid nanoparticles for advanced drug delivery applications, as well as high-potency and controlled substance handling for highly specialized therapeutics.
At Ardena, all work adheres to the appropriate regulatory standards as you progress through the clinical development pathway. Please contact us to further discuss your clinical and scientific objectives and explore how we can work together.