JobdescriptionOn behalf of our client, we are looking for a QAValidation Expert to support validation activities in a GMP-compliant pharmaceutical environment. The selected candidatewill play a key role in ensuring regulatory compliance and qualityoversight of processes and equipment, working in closecollaboration with technical departments to support ongoing andupcoming validationprojects. Location: Neuchâtel, SwitzerlandContract Duration: 07/04/2025 -31/05/2025 (Temporary contract via Randstad, with possibleextension)Work Mode: 100%OnsitePosition: QA Validation Expert On behalf of ourclient, we are looking for a QA Validation Expert tosupport validation activities in a GMP-compliant pharmaceuticalenvironment. The selected candidate will play a key role inensuring regulatory compliance and quality oversight of processesand equipment, working in close collaboration with technicaldepartments to support ongoing and upcoming validationprojects. Main Responsibilities:Review of Validation ProtocolsAssess protocols related toequipment, processes, CIP, SIP, computerized systems, and HVAC/UtilitiesEnsure alignment with GMPstandards, internal quality procedures, and internationalregulations (FDA, EMA, etc.)Validation Report ReviewEvaluate test results to confirm allprotocol requirements are metIdentifydeviations and propose appropriate correctiveactionsQuality SupportCollaborate with cross-functional teams(Production, Engineering, Validation) to ensure qualityintegrationProvide quality input duringprojectmeetings Required Profile:Education:Degreein Pharmacy, Biotechnology, Chemistry, or another scientificdisciplineExperience:Minimum2 years in a similar role within the pharmaceuticalindustryHands-on experience in validation ofprocess, equipment, CIP/SIP, computerizedsystemsExperience with filling lines andfreeze-dryers is a strong assetTechnical Skills:Solid knowledge of GMP and regulatoryguidelines (FDA, EMA, ICH)Familiarity with IQ/OQ/PQ protocols and risk assessmentmethodologiesSoft Skills:Excellent attention to detail andstrong analytical skillsEffectivecommunicator, able to interact with cross-functionalstakeholdersSolution-oriented mindset with theability to manage several priorities underpressureFluency in English and French is astrongadvantage What'sin it for you:Contribute tohigh-impact validation projects in a reputable pharmaceuticalcompanyGain valuable experience in GMP andregulatory-driven environments