Quality Review Specialist

Quality Review SpecialistBioTalent is supporting a 6 month contract, short notice start (max 4 weeks notice). The role is hands on, 5 days per week onsite, German speaking required. Your main task will be reviewing electronic batch records to GMP standards (see more detail below) Experience required: Professional experience in a GMP production environment (2+ years) Bachelor’s/Master’s in Pharmaceutical Technology, Biotechnology, Chemistry or similarStrong attention to detail & ability to work independentlyFluent in German (additional English language)Experience with systems TrackWise, SAP or MES Responsibilities: Review electronic batch records to GMP standardsMonitor release metrics and report deviationsSupport investigations and CAPA definitionParticipate in EBR documentation & change requestsReach out to dominic.pritchard@biotalent.ch +41415625046