Group Leader Analytical Sciences
Il y a 2 mois
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.
Ardena is a rapidly growing international orientated organization with a dedicated team of about 550 professionals operating from 5 sites in Belgium, The Netherlands, Sweden and Spain. Ardena has an open and transparent culture: team-spirit, an open mindset and ownership are important values in our company.
We are a dynamic drug developer offering exciting career opportunities to skilled and motivated people who want to work in a fast-growing market within the global pharmaceutical industry. Do you want to work in a challenging contract research and development environment, where experts come together to develop innovative drugs for unmet medical needs? Do you want to further develop Ardena and grow with us by becoming our next colleague? Then we might have the right opportunity for you.
For the Ardena Business Unit Drug Product Development and Manufacturing (DDM) based in Ghent (Belgium), we are looking for a
GROUP LEADER ANALYTICAL SCIENCES
YOUR KEY ROLE
Ardena Gent guides a worldwide portfolio of customers through the processes of formulation and analytical development, preparation of regulatory dossiers and the manufacturing and labeling of early-phase clinical materials according to GMP appropriate standards.
The analytical laboratory plays a key role in the development and validation of analytical methods to characterize drugs and to perform quality control testing on incoming raw materials and on the finished clinical materials.
You act as technical expert with respect to analytical method development and GMP QC analysis. You are the first point of contact for all analytical challenges within the company.
YOUR KEY RESPONSIBILITIES
YOUR PROFILE
You have a PhD with scientific orientation (Chemistry, Pharmaceutical Sciences, Bioscience-Engineering, Science or Chemical Engineering, Industrial Engineering) or equivalent by experience. You have profound experience in development of chromatographic analytical methods such as HPLC, UPLC, GC (and MS detection systems) and spectroscopic techniques such as UV-Vis, FTIR Experience in CMC method development is a plus Experience in a GMP environment is a plus You are able to run development projects independently and to keep an eye on budget and timelines You are able to motivate the analysts of the project team You have a strong interest in drug research and development and the associated analytical development. You are familiar with MS Office (knowledge of Empower is an asset) You have strong analytical and reporting skills (oral, written, presentations) You are a team player You show flexibility and you are open-minded and change oriented (always looking for ways to improve).WE OFFER
A true learning environment where you will have the ability to grow your skills A rapidly developing and growing international company with an attractive services, product and customer portfolio A dynamic working environment with nice colleagues Open straightforward but also caring culture We are true to our values An attractive remuneration package including 32 holidays Flexible working hours-
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