- University degree in Pharmacy, Chemical Engineering or Chemistry - Minimum 2 years of Analytical Laboratory experience with equipments e.g. HPLC, GC, UV/Vis and Wet Chemistry preferably at a pharmaceutical company - Knowledge of cGMP& cGLP and basic SAP - Ability to work in a fast-paced changing environment - Team working and customer oriented mindset - Good analytical thinking skills - Strong interpersonal written and verbal communication skills - Good knowledge of MS Office applications - Good command of English is required - No military obligation for male candidates Job Description - Executing the main activities according to prepared SOPs and laboratory rules - Fulfill the responsibilities, which are given by Team Coordinator and Unit Manager, at the right time and correctly in conformance with methods, procedures and work flow - Following the global analytical method development studies, current guidelines and pharmacopeia - Routinely assess testing monographs and proactively sustain compliance of all activities with current official regulations, pharmacopeias, QM, QD, GOP and SOP - Preparing the analytical method validation protocols and reports according to related SOPs and publishing after QA approval - Execute analytical method development, pre-validation and validation studies as well as planning and testing of all Drug Substance and Drug Product batches in accordance to global priorities - Ensure right first time in all analysis and documentation |