Its Belgian subsidiary is based in Ghent, offering a complete drug development package for new drug entities (biological and chemical) up to early clinical phases to third parties to help them in speeding up the development and manufacturing of their drugs. To support our ambitious growth plan, we are today looking for a QC Analyst for our site in Ghent, Belgium.
Role DescriptionThe Belgian subsidiary wishes to enforce its team with a QC Analyst. We are looking for a person that reports to the QC Manager.
ResponsibilitiesYou perform Quality Control activities according to instructions, procedures and protocols in compliance with the GMP principles and the Quality Management System. • You perform Quality Control analyses. • You perform ICH compliant stability studies. • You validate analytical methods to support the quality control and release of drug products for use in clinical trials. • You support preparation of the applicable protocols and reports. • You accurately report, document and review the analytical test results. • You support the maintenance, calibration and qualification of the analytical equipment.
RequirementsProfessional Bachelor degree in biomedical laboratory technology, chemistry or pharmaceutical sciences with a minimum of 5 years relevant professional experience.
• Experience in a regulated Quality Control laboratory and experience with core pharmaceutical analytical techniques (HPLC/UPLC, Dissolution) is a must. • Experience with Empower processing software is a must. • Experience with KF, Particle sizing, UV spectroscopy, etc. are real assets. • You are punctual and are able to work independently after a training in matters entrusted to you. • You are flexible, problem solving and quality minded. • You are fluent in Dutch and English (written and spoken).
Other informationWe offer you • A position with responsibility within a dynamic company • Personal development through learning on the job and additional external trainings • A market oriented compensation
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