Work ScheduleStandard (Mon-Fri)Environmental ConditionsAdherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Cold Room/Freezers -22degreesF/-6degrees C, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)Job DescriptionAbout Thermo Fisher ScientificAt Thermo Fisher Scientific, we develop solutions that help people live healthier, cleaner, and safer lives. This is more than our mission — it is the impact our colleagues make every day.At our Vilnius site, we develop and manufacture innovative life science and diagnostic technologies used by researchers, clinicians, and laboratories around the world. Our teams work with advanced manufacturing, laboratory, and quality systems that help ensure reliable operations and high-quality products.Join a collaborative environment where engineering, quality, technology, and continuous improvement come together to support products used globally.Job OverviewWe are looking for a Validation Engineer to join our team and support equipment, systems, facilities, and process qualification activities across manufacturing, laboratory, and technical environments.In this role, you will help ensure that equipment and processes are properly qualified, compliant, and ready to support reliable operations. You will work with modern production and laboratory equipment, prepare and execute validation documentation, investigate deviations, and support continuous improvement across regulated processes.This is a great opportunity for someone with an engineering, life sciences, chemistry, technical operations, quality, manufacturing, or laboratory background who wants to grow in validation and qualification.Previous job title does not need to be “Validation Engineer”. We welcome candidates from engineering, maintenance, manufacturing, laboratory, technical operations, quality, or regulated environments who want to develop in this field.You will collaborate closely with Manufacturing, Quality, Engineering, Technical Operations, Maintenance, Laboratory, and external contractor teams.Key ResponsibilitiesPlan, coordinate, and execute qualification and validation activities for equipment, systems, facilities, and processesMaintain validation schedules and help ensure equipment remains in a qualified statePrepare, review, and execute qualification documentation, including IQ/OQ/PQ protocols, procedures, and summary reportsSupport qualification activities for standard and customized equipment used in regulated environmentsIdentify, document, and investigate discrepancies, deviations, and validation-related issuesDefine and implement corrective actions in collaboration with cross-functional teamsAct as the main point of contact for qualification activities with internal stakeholdersCoordinate technicians, contractors, and external specialists during qualification activities when neededSupport process improvements related to validation documentation, execution quality, and complianceExperience and QualificationsAdvanced degree in Engineering, Life Sciences, Chemistry, Biotechnology, or another related technical fieldorBachelor’s degree with at least 2 years of relevant experience in validation, qualification, engineering, quality, manufacturing, laboratory operations, or another regulated environmentExperience in GMP, ISO, pharmaceutical, biotechnology, medical device, diagnostics, manufacturing, laboratory, or another regulated technical environment would be an advantageSkills and CompetenciesUnderstanding of equipment qualification, process validation, or regulated technical processesExperience with IQ/OQ/PQ protocols and validation documentation would be an advantageKnowledge of GMP, ISO, FDA regulations, GAMP5, or other industry standards would be beneficialStrong technical writing skills and ability to prepare clear, structured documentationAnalytical thinking and structured problem-solving skillsAbility to assess risks, identify gaps, and support evidence-based decisionsStrong organizational skills and ability to manage several priorities at onceGood communication skills and ability to collaborate with technical and non-technical teamsProficiency in Microsoft Office toolsGood written and spoken English and Lithuanian skillsAbility to work in cleanroom or regulated production/laboratory environments when requiredPreferred QualificationsExperience with equipment qualification or process validationExperience working with production, laboratory, utility, or facility systemsKnowledge of quality management systems and regulated documentation practicesExperience with risk assessments, gap analysis, deviation investigations, or CAPAExperience coordinating contractors or technical service providersKnowledge of calibration, metrology, statistical analysis, or process control methodsWhat We OfferAnnual performance bonus and additional financial benefitsComprehensive health package, including private health, life and accident insuranceWellbeing support for employees and their family members, including mental health consultations, health check-ups, vaccinations, and on-site health initiativesOpportunities for professional growth through internal training, access to Thermo Fisher e-University, and continuous developmentThe opportunity to work in a global, innovation-driven organization and collaborate with international teamsDaily benefits such as subsidized meals, gym access, and company transportationAn inclusive and supportive culture, with team events and community initiatives2 additional paid volunteering days per yearWe are an equal opportunity employer and value diversity. All qualified applicants will receive consideration regardless of race, religion, gender, age, disability, veteran status, sexual orientation, gender identity, or any other protected characteristic.How to ApplyIf you are interested in equipment qualification, validation, quality, technology, and continuous improvement — and want to grow your career in a global life sciences organization — we would love to hear from you.Even if your experience covers only part of the validation field, but you are motivated to learn and develop in this area, we encourage you to apply.CompensationThe monthly salary range estimated for this position based in Lithuania is €2 183,33–€3 270,83.