Industriepark-Zwijnaarde 7B, Gent, Belgium
You follow up on the quality of a variety of Drug Products during Release and ICH stability studies (capsules, tablets, solutions, suspensions, injectables, biologics).
You perform Quality Control analyses using validated methods and pharmacopoeial procedures, in compliance with the GMP principles and the Quality Management System.
You accurately calculate, report, and review the analytical test results.
You support the preparation of the applicable protocols and reports.
You support the set-up of deviations and investigations
You support the maintenance, calibration and qualification of the analytical equipment.
You support the validation of analytical methods needed for the quality control and release of Drug Products.
You hold a professional Bachelor's degree in biomedical laboratory technology, chemistry or pharmaceutical sciences.
You have 2 years of relevant professional experience with core analytical techniques such as chromatography (HPLC/UPLC - Empower CDS), dissolution and Karl Fischer.
You have experience in a regulated quality control environment (GMP).
You are punctual, well organized and able to work independently after training in matters entrusted to you.
You have a proactive analytical, problem-solving mindset.
You are fluent in Dutch and English (written and spoken).
Work in a fast-growing organization.
A position with responsibility within a dynamic company.
Personal development through learning on the job and additional external training.
A market-oriented compensation.
Please send us your CV and motivation: https://smrtr.io/9NjKH