Validation / CQV Engineer (Commissioning, Qualification & Validation)

Validation / CQV Engineer (Commissioning, Qualification & Validation)Indianapolis, IN | Up to 40% TravelFind out more about the daily tasks, overall responsibilities, and required experience for this opportunity by scrolling down now.Help Bring Critical Manufacturing Systems OnlineWe are looking for a Validation /CQV Engineer to join our Indianapolis, IN team to support commissioning, qualification, and validation activities for pharmaceutical manufacturing facilities, equipment, utilities, and automation systems. This is an opportunity to work directly on major capital projects and play a hands-on role in taking systems from installation through production readiness.If you enjoy solving technical challenges, working in highly regulated environments, and seeing projects come to life in the field, we would like to talk with you.PACIV does not provide H-1B sponsorship, H-1B transfers, OPT sponsorship or CPT sponsorshipWhat You Will Work On Pharmaceutical Manufacturing Capital Projects

API Manufacturing Systems Filling & Packaging Equipment Device Assembly Operations Clean Utilities & Facility Systems Process Automation & Controls SystemsWhat You Will DoLead and execute commissioning and qualification activities for manufacturing systems and equipmentDevelop and review validation documentation, protocols, risk assessments, and summary reportsParticipate in FATs, SATs, startup activities, and system turnoverSupport requirements gathering, design reviews, traceability, and testing strategiesPartner with engineering, operations, quality, and project teams to ensure systems meet regulatory and operational requirementsSupport change controls, deviations, investigations, and project documentationDrive projects to completion while maintaining compliance with pharmaceutical industry standardsWhat Makes You a Strong CandidateEngineering degree in Chemical, Biomedical, Mechanical, Electrical, Industrial Engineering, or a related disciplineExperience supporting CQV, validation, commissioning, qualification, or manufacturing projectsUnderstanding of validation lifecycle principlesStrong technical writing and documentation skillsAbility to manage multiple priorities in a fast-paced project environmentWillingness to travel up to 40%PreferredPharmaceutical, biotech, medical device, or regulated manufacturing experienceFAT/SAT participation experienceGMP, GDP, FDA, or cGMP knowledgeUtilities, facilities, process equipment, packaging, or automation validation experienceExperience supporting capital projectsWhy Engineers Join PACIVAt PACIV, you are not confined to a single production line or facility. PACIV engineers gain exposure to multiple facilities, technologies, manufacturing processes, and capital projects. You will work alongside experienced CQV, automation, and engineering professionals. xhyhwjd Commissioning and startup activitiesPharmaceutical capital projectsManufacturing technologiesAutomation and controls systemsMultiple sites and engineering disciplinesExperienced CQV, automation, and validation professionalsCompensation & BenefitsCompetitive salary90% company-paid healthcare premiumsHSA with company contributions401(k) with company match up to 4% & Immediate vestingPaid vacation, sick time, and company holidaysImportant Hiring InformationFull-time, direct-hire positionNo Corp-to-Corp (C2C) or 1099 arrangementsPACIV does not partner with third-party recruiting agenciesPACIV does not provide H-1B sponsorship, H-1B transfers, OPT sponsorship, CPT sponsorship, or employment-based immigration support.PACIV is an Equal Opportunity Employer