Experis is a global leader in IT professional resourcing, permanent recruitmSpecialist, Pharmaceutical Products, Quality AssuranceExperis is a global leader in IT professional resourcing, permanent recruitment, project solutions, and managed services. With over 25 years of experience in Switzerland and offices in Zürich, Basel, and Geneva, we connect top IT talent with leading companies. Our mission is to help professionals unlock their potential and thrive in dynamic, future-ready careers.Specialist, Pharmaceutical Products, Quality AssuranceExperis is a global leader in IT professional resourcing, permanent recruitment, project solutions, and managed services. With over 25 years of experience in Switzerland and offices in Zürich, Basel, and Geneva, we connect top IT talent with leading companies. Our mission is to help professionals unlock their potential and thrive in dynamic, future-ready careers.Specialist, Pharmaceutical Products - Quality Assurance (Interim)About the role: We're recruiting for an experienced pharmaceutical QA specialist to join our Clients Supply Operations team on an interim basis. You will help ensure that pharmaceutical products procured through global health programmes meet quality, safety and efficacy standards, working across policy, risk management, partner engagement and grant implementation support.Key responsibilitiesLead investigations of quality complaints, safety events and out-of-specification findings, advising on risk mitigationProvide QA guidance and support to internal teams on pharmaceutical product eligibility and complianceManage the Expert Review Panel (ERP) secretariat process in collaboration with WHOMaintain and update product master data and eligibility listsContribute to QA policy development, tools and guidanceEngage with WHO, regulatory authorities and international procurement agencies on QA harmonisationSupport cross-functional collaboration across supply operations, grant management and technical teamsEssential requirementsAdvanced degree in pharmacy, laboratory science, or biomedical/chemical engineeringMinimum 5 years' experience in pharmaceutical products QA, risk management and regulatory affairsExperience working with UN agencies, international NGOs or donors on QA mattersTrack record managing complex QA issues at country, regional or international levelExperience developing QA policies, tools and guidanceFluent English7+ years in pharmaceutical design and manufacturingExperience with a major multilateral organisationProject management or process improvement qualificationsWorking knowledge of FrenchFor this position we can only consider applicants with a Swiss work permit or a Swiss/EU passport. jid8026997afr jit0521afr jpiy26afr