You are working for a leading contract development organization for the pharmaceutical industry. Assisting 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 services.
The company is operating from six sites in Europe. For the branch based in Ghent, Belgium, we are looking for an expert/group leader in analytical development.
The main functions of the role
The company 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:
The key responsibilities of the role
You have a PhD with scientific orientation (Pharmaceutical Sciences, Bioscience- Engineering, Science or Chemical Engineering, Industrial Engineering, Chemistry ...) or equivalent by experience.
Required experience, competences and skills