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p>On behalf of our client, we are looking for a QA Validation Expert to support validation activities in a GMP-compliant pharmaceutical environment. The selected candidate will play a key role in ensuring regulatory compliance and quality oversight of processes and equipment, working in close collaboration with technical departments to support ongoing and upcoming validation projects.
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p>Location: Neuchâtel, Switzerland
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p>Contract Duration:Â 07/04/2025 â 31/05/2025 (Temporary contract via Randstad, with possible extension)
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p>Work Mode:Â 100% Onsite
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p>Position:Â QA Validation Expert
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p>On behalf of our client, we are looking for a QA Validation Expert to support validation activities in a GMP-compliant pharmaceutical environment. The selected candidate will play a key role in ensuring regulatory compliance and quality oversight of processes and equipment, working in close collaboration with technical departments to support ongoing and upcoming validation projects.
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p>Main Responsibilities:
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Review of Validation ProtocolsAssess protocols related to equipment, processes, CIP, SIP, computerized systems, and HVAC/UtilitiesEnsure alignment with GMP standards, internal quality procedures, and international regulations (FDA, EMA, etc.)Validation Report ReviewEvaluate test results to confirm all protocol requirements are metIdentify deviations and propose appropriate corrective actionsQuality SupportCollaborate with cross-functional teams (Production, Engineering, Validation) to ensure quality integrationProvide quality input during project meetings
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p>Required Profile:
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Education:Degree in Pharmacy, Biotechnology, Chemistry, or another scientific disciplineExperience:Minimum 2 years in a similar role within the pharmaceutical industryHands-on experience in validation of process, equipment, CIP/SIP, computerized systemsExperience with filling lines and freeze-dryers is a strong assetTechnical Skills:Solid knowledge of GMP and regulatory guidelines (FDA, EMA, ICH)Familiarity with IQ/OQ/PQ protocols and risk assessment methodologiesSoft Skills:Excellent attention to detail and strong analytical skillsEffective communicator, able to interact with cross-functional stakeholdersSolution-oriented mindset with the ability to manage several priorities under pressureFluency in English and French is a strong advantage
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p>Whatâs in it for you:
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Contribute to high-impact validation projects in a reputable pharmaceutical companyGain valuable experience in GMP and regulatory-driven environments