Validation Engineer
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Job Title: Validation Engineer II (Onsite)Location: Bothell, WADuration: 12 months (potential for extension)Overview:We are seeking a CQV / Validation Engineer with 5–8 years of experience to support validation and qualification activities within a GMP-regulated biotech environment. This is a hands-on role supporting equipment, process, and CQV execution.Key Responsibilities:Execute equipment qualification activities (IQ/OQ/PQ) for GMP systemsSupport commissioning and qualification (CQV) efforts across equipment and systemsAuthor and execute validation protocols and reportsSupport process validation (PPQ) activitiesCollaborate with engineering, manufacturing, and quality teamsAssist with deviations, CAPAs, and change controls related to validationEnsure all activities are performed in compliance with GMP requirementsRequired Experience:5–8 years of experience in CQV / Validation within pharma or biotechStrong hands-on experience with equipment qualification (IQ/OQ/PQ)Experience working in GMP-regulated environmentsExperience authoring and executing validation documentationAbility to work onsite and cross-functionally with multiple teamsPreferred (Nice to Have):Experience with cleaning validationExposure to process validation (PPQ)Experience with utilities or facility qualificationBackground in biologics or drug substance manufacturingAdditional Notes:Interview process includes resume review and team interviewsPotential for long-term engagement