Job Description
We are seeking a highly skilled CQV Engineer to support the validation of equipment, systems, and facilities in accordance with cGMP standards. The role involves drafting and executing IQ/OQ/PQ protocols, coordinating equipment installation, and preparing comprehensive validation documentation.Project title: CQV EngineerType of employment: PayrollIndustry: BiotechSkills: commissioning and qualification, Validation (IQ/OQ/PQ)Project start: ASAPProject duration: 30.04.2026Location: 3930 Visp, Switzerland - 100% onsiteTasks:Coordinate commissioning and qualification activities for facilities, utilities, and equipmentDraft and execute IQ/OQ/PQ protocolsPrepare validation documentation including URS, DQ, FMEA, Risk Assessments, FAT, SATWrite detailed reports of completed validation activitiesIdentify efficiencies and improvements in validation processesStay updated on regulatory changes affecting equipment and facility validationSupport Quality Systems: Document Management, Change Control, Non-Conformities, CAPAsWrite and revise engineering proceduresAssist in developing validation, requalification, and maintenance programsPerform other duties as assignedQualifications:Bachelor’s degree in a scientific or technical fieldMinimum 5 years of experience in the pharmaceutical industryStrong technical writing and documentation skillsExcellent communication and organizational abilitiesFluent in German; English is a plus
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