Junior CQV Engineer

Role: Junior CQV EngineerLocation: USA(Multiple)Job OverviewWe are seeking a Junior CQV Engineer to support commissioning, qualification, and validation activities for equipment, utilities, and facilities within a GMP-regulated pharmaceutical environment. This is an entry-level role ideal for recent graduates or early-career professionals looking to build experience in validation and compliance.Key ResponsibilitiesAssist in commissioning and qualification (IQ/OQ/PQ) of equipment, utilities, and systemsSupport preparation and execution of validation protocols and reportsParticipate in FAT (Factory Acceptance Testing) and SAT (Site Acceptance Testing) activitiesMaintain and review documentation in compliance with GMP and regulatory standardsAssist with deviation investigations, CAPA tracking, and change control documentationCollaborate with cross-functional teams (Engineering, QA, Manufacturing, Validation)Support risk assessments and impact analysis for validation activitiesEnsure proper data integrity and documentation practicesAssist in maintaining validation lifecycle and requalification activitiesRequired SkillsBasic understanding of CQV principles (IQ/OQ/PQ)Knowledge of GMP and regulatory requirements (FDA, cGMP)Strong attention to detail and documentation skillsGood analytical and problem-solving abilitiesEffective communication and teamwork skillsPreferred SkillsInternship or academic project experience in pharmaceutical, biotech, or regulated industriesFamiliarity with validation documentation and protocolsBasic knowledge of equipment qualification, utilities, or cleanroom validationExposure to quality systems such as CAPA, deviations, and change controlExperience0–2 years of experience in CQV, validation, or related engineering fieldRecent graduates with relevant coursework or internship experience are encouraged to applyApply / Refer:AbhiRecruiter | United Consulting HubPhone: +1 (469)429-8068Email: abhiram@unitedconsultinghub.com