Senior Engineer - Engineering, EquipmentPosition SummaryShift: Monday – Friday 8:00am – 5:00pm100% on-siteCatalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually.The Senior Engineer, Equipment supports process, equipment, or automation engineering activities by troubleshooting complex issues, leading technical projects, and driving continuous improvement in a GMP biologics manufacturing environment.
The role partners cross-functionally and provides on-the-floor technical support while leading projects, managing data analysis, and interacting with clients.The role:Support engineering activities including troubleshooting mechanical/process issues and identifying improvements to minimize downtime and reduce costProvide on-call and on-the-floor technical support to manufacturing operationsDevelop and execute technical work plans and ensure projects meet scope, schedule, and performance metricsWork cross-functionally with Operations, MS&T, Quality, Supply Chain, and other departments to support manufacturing processesLead or support deviation investigations, change controls, CAPAs, and risk assessmentsCompile and analyze process data, identify trends, and communicate project status to internal and client stakeholdersAuthor and review technical documentation (batch records, protocols, reports, specifications)Participate in client meetings and provide technical leadership across projects and disciplinesThe candidate:Bachelor's degree in Engineering or related scientific field with 6–9 years of experience, ORMaster's degree with 4–6 years of experience, ORPhD with 0–2 years of experienceStrong technical knowledge and hands-on experience in GMP biologics manufacturing and validationExperience with deviations, CAPAs, change control, and risk assessmentsAbility to analyze data, troubleshoot issues, and drive corrective actionsExperience authoring technical documentation such as SOPs, batch records, and reportsStrong communication skills and ability to work cross-functionally and with clientsWhy you should join Catalent:Competitive medical benefits and 401K152 hours PTO + 8 Paid HolidaysDynamic, fast-paced work environmentOpportunity to work on Continuous Improvement ProcessesCatalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.Personal initiative. Dynamic pace. Meaningful work.Visit Catalent Careers to explore career opportunities.Catalent is an Equal Opportunity Employer, including disability and veterans.