Commissioning & Qualification (C&Q) Engineer
Occupations:
Validation EngineersQuality Control AnalystsQuality Control Systems ManagersRegulatory Affairs SpecialistsEngineers, All OtherIndustries:
Pharmaceutical and Medicine ManufacturingProfessional and Commercial Equipment and Supplies Merchant WholesalersEducational Support ServicesConsumer Goods RentalGrantmaking and Giving ServicesJob Title: Commissioning & Qualification (C&Q) EngineerLocation: Lehigh Acres ,FL(Onsite)Duration: 1+ Year Contract Only: w2Job SummaryWe are seeking a motivated Junior C&Q Engineer with 1–2 years of experience to support commissioning, qualification, and validation activities within a pharmaceutical manufacturing environment. The ideal candidate will assist with IQ/OQ/PQ execution, documentation, and compliance activities in support of GMP-regulated systems and equipment.Key ResponsibilitiesSupport commissioning and qualification activities for equipment, utilities, and systemsAssist in executing IQ, OQ, and PQ protocolsMaintain validation documentation in compliance with GMP/FDA standardsSupport equipment startup, troubleshooting, and qualification activitiesCoordinate with engineering, quality, and manufacturing teamsEnsure accurate documentation and timely project completionRequired QualificationsBachelor’s degree in Engineering, Life Sciences, or related field1–2 years of experience in commissioning, qualification, validation, or pharmaceutical manufacturingBasic understanding of GMP/cGMP and FDA regulationsFamiliarity with validation lifecycle and documentation practicesStrong communication and technical writing skillsAbility to work in a team-oriented environmentPreferred SkillsExposure to aseptic manufacturing environmentsExperience with Kneat, ValGenesis, or similar validation systemsKnowledge of utilities such as WFI, clean steam, or process equipmentExperience Required1–2 years relevant experience in pharma/biotech industryRecruiter | united Consulting HubPhone: +1 (469)-429-8065