POSITION SUMMARY:

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. 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 Research Triangle Park (RTP) facility is home to Catalent’s Inhalation franchise including product development, clinical and commercial manufacturing for inhalers and Nasal Sprays.
Catalent Pharma Solutions in Morrisville, NC is hiring a Laboratory Scheduler. The Laboratory Scheduler is responsible for scheduling laboratory testing activities, managing day-to-day laboratory operations, optimizing workflow for maximum efficiency and compliance, coordinating testing activities, and ensuring smooth workflow and compliance with regulatory standards. This individual will work closely with project managers, project directors, laboratory staff, and other departments to support ongoing client projects and continuous improvement initiatives.
This is a full-time salaried position on 1st shift with core hours Monday-Friday, 8:00AM – 5:00PM.
This position is 100% on-site at the Morrisville site.
Catalent is committed to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer, and Catalent employee.

• Develop, maintain, and communicate laboratory schedules to ensure optimal workflow and resource utilization.
• Support oversight to tracking of real time status of laboratory projects to identify and address scheduling conflicts or delays.
• Maintain laboratory equipment and ensure compliance with safety, quality, and regulatory standards (e.g., GMP, GLP, ICH guidelines).
• Coordinate with cross-functional teams (quality assurance, manufacturing ops, product development) to align schedules and support project timelines.
• Lead the development and improvement of scheduling processes to enhance laboratory efficiency.
• Communicate proactively with stakeholders about scheduling changes, delays, and potential impacts.
• Responsible for managing laboratory orders and ensuring laboratory supplies are maintained at the required stock levels.
• All other duties as assigned