Project Engineer I

Catalent, 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. Catalent’s Greenville, N.C. facility specializes in end-to-end turn-key solutions for oral solid dosage forms, including integrated formulation development, analytical services, commercial manufacturing, and packaging. Position Summary The Project Engineer I will assure projects are executed in accordance with current site methodologies, policies, industry best practices, and cGMP requirements. The role will leverage the knowledge of GMPs and manufacturing processes to ensure that projects are executed with minimal disruption to operational schedules and must provide construction management oversight to ensure that projects are completed safely, efficiently, and in accordance with all applicable codes and requirements. This position is 100% on-site at the Greenville site. The Role Lead the planning and execution of all technical/engineering aspects of minor capital projects related to production and/or facility requirements. Directly responsible and accountable for delivering capital projects to scope, budget, and schedule. Assure capital projects have a clearly defined scope and are planned, executed, and documented to deliver best-in-class service, including a focus on aligning all internal and external stakeholders on the project details and objectives. Provide direct management, execution, and oversight of capital projects from concept/inception through implementation, commissioning, and qualification. Establish project team as well as develop project strategy, master schedule, and control utilization of financial resources. Provide construction management oversight to ensure that projects are executed safely, efficiently, and in accordance with all applicable codes and requirements. Coordinate the development of engineering and GMP documentation procurement, engineering services, construction, commission, qualification, and turnover to Operations. All other duties as assigned. The Candidate Bachelor’s degree in Mechanical, Chemical, Electrical, or Automation Engineering with 2 years of directly related Experience or; A Master's degree in Engineering with 1 year of directly related experience. Project Management Professional (PMP) certification Professional Engineer license or Six Sigma Black-Belt training is desired. Experience required in Capital Project Management, Facilities/Maintenance and/or Automation in the pharmaceutical, chemical process, semiconductor, or food industry, background in plant engineering desired. Knowledge of MS Project, AutoCAD or SolidWorks, document management, Teams or Zoom communications; strong knowledge of MS Excel and PowerPoint is required. Working knowledge of hazardous chemicals and their disposal, OSHA, EPA, FDA, and EU regulations. Experience with solid dose manufacturing preferred. Demonstrated technical capabilities in project management, critical path scheduling, resource planning, cost estimating. Some exposure to hazardous chemicals and other active chemical ingredients. Position requires the capacity to handle and manipulate objects using hands and arms. Why You Should Join Catalent Competitive medical benefits and 401K 152 hours of PTO + 8 Paid Holidays Dynamic, fast-paced work environment Opportunity to work on Continuous Improvement Processes Catalent is an Equal Opportunity Employer, including disability and veterans. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email to DisabilityAccommodations@catalent.com.

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