Validation Engineer II

Job Title: Validation Engineer IILocation: 2251 Faraday Ave, Carlsbad, CA 92008Duration: 10 MonthsWork Arrangement: 100% OnsitePosition SummaryWe are seeking a Validation Engineer II to support validation activities for systems, processes, and equipment within a regulated quality environment. This role is responsible for developing, executing, and maintaining validation documentation while ensuring compliance with internal quality standards and regulatory requirements.The ideal candidate will have experience working in validation, quality systems, or regulated manufacturing environments and possess strong technical, analytical, and communication skills.Key ResponsibilitiesCreate, maintain, and execute validation documentation for new and existing systems and processesSupport implementation of validation programs in compliance with internal and external regulatory requirementsWrite and review validation protocols, reports, and related documentationManage execution of validation protocols to ensure timely and cost-effective completionEvaluate validation results and summarize findings in final reportsSupport Validation Master Plans (VMPs) for new product development and existing manufacturing processesPerform validation assessments related to change management activities, including document, system, and process changesTrack and report validation project progress using departmental tracking toolsRepresent the division during internal and external audits related to validation projects and documentationCollaborate with cross-functional teams to support validation and compliance activitiesProvide guidance and mentorship to junior team members when neededQualificationsEducationBachelor’s Degree in Engineering, Life Sciences, or a related field requiredMaster’s Degree preferredExperienceMinimum 2–3 years of related experience in validation, quality engineering, or regulated manufacturing environmentsWorking knowledge of validation concepts, quality systems, and regulatory compliance requirementsExperience creating and executing validation documentation and protocolsUnderstanding of change management processes and validation assessmentsAbility to analyze data, troubleshoot issues, and make sound technical decisionsPreferred SkillsStrong technical writing and documentation skillsExcellent organizational and project coordination abilitiesStrong communication and collaboration skillsAbility to work independently and manage multiple prioritiesExperience working in FDA-regulated or quality system environments preferredConsultants Eligible Benefits Upon Waiting PeriodMedical and Prescription Drug PlansDental PlanVision PlanHealth Savings Account (for High Deductible Health Plans)Flexible Spending Accounts (Health, Limited Purpose, Dependent Care, Commuter Parking and Commuter Transit)Supplemental Life InsuranceShort Term Disability (coverage varies by state)Long Term DisabilityCritical Illness, Hospital coverage, Accident InsuranceMetLife Legal, MetLife ID Fraud, and MetLife Pet Insurance401(k)Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritional and branded generic medicines.Working together, Abbott and Talent Solutions partner to deliver top talent for contingent roles at Abbott, building better and healthier lives. Abbott believes all employees are essential to creating life-changing breakthroughs, performing key duties to create life-changing breakthroughs.