Work ScheduleStandard (Mon-Fri)Environmental ConditionsAdherence to all Good Manufacturing Practices (GMP) Safety Standards, OfficeJob DescriptionDiscover Impactful Work:As part of the Thermo Fisher Scientific team, you’ll do meaningful work that makes a positive impact on a global scale. Join colleagues who bring our Mission to life every day—enabling customers to make the world healthier, cleaner, and safer.Join our growing validation team supporting Automatic Visual Inspection (AVI) operations, a critical and expanding function within sterile pharmaceutical manufacturing. With new lines being added—including auto-injector technology—this role offers hands-on experience in one of the most in-demand areas of the industry.This is an entry-level opportunity designed for growth, where you’ll gain valuable, highly marketable experience in sterile manufacturing validation.A Day in the Life:This role offers a balance of technical documentation and hands-on execution:~60% desk-based: writing validation protocols, data analysis, reporting, and documentation~40% on the production floor: executing validation activities alongside team membersPartner with experienced engineers for hands-on training and executionParticipate in data calculations, evaluations, and summary reportsGradually interface with clients and become a point of contactWork directly with commercial manufacturing equipment in sterile/inspection environmentsWhat to Expect:Structured onboarding with SOP training and hands-on mentorshipDirect exposure to AVI and sterile pharmaceutical processesCareer growth within a rapidly expanding function (AVI + auto-injector lines)Collaborative team environment (team of ~4 engineers)Keys to Success:Education & Experience:Bachelor’s degree in Engineering, Life Sciences, Chemistry, or related field0–2+ years of experience in validation or regulated/GMP environment preferredRequired Skills & Experience:Strong technical writing and documentation skillsHigh attention to detail and quality-focused mindsetComfort working around large-scale manufacturing equipmentAbility to learn quickly in a hands-on environmentExposure to pharmaceutical manufacturing—especially sterile/aseptic environments—is strongly preferred and highly valuedAdditional Requirements:Knowledge of cGMP and regulated environments preferredFamiliarity with IQ/OQ/PQ concepts a plusAbility to work onsite in Greenville, NC (Monday–Friday, standard hours)Strong communication and teamwork skillsWhy Join Us:Entry point into high-demand sterile validation engineeringHands-on learning with experienced mentorsExposure to cutting-edge pharmaceutical technologies (AVI & auto-injectors)Clear career progression into advanced validation roles