Hiring: Product Development Operations Supervisor Company: Catalent Location: Greenville, NC Job Posted Time: 2026-09-15 11:32:21 Employment Type: On-site Target Skills & Keywords : Project Management About the job Experience: •5 years of relevant pharmaceutical development, clinical manufacturing, oral solid dose, or pharmaceutical production experience •6 years of relevant experience •7 years of relevant experience •At least 5 years of relevant pharmaceutical development, clinical manufacturing, oral solid dose, or pharmaceutical production experience •At least 6 years of relevant experience Required Skills: •Plan, coordinate, and supervise Pharmaceutical Development and Clinical Manufacturing activities, including development, clinical, engineering, registration-support, and scale-up batches •Lead daily production execution to ensure batch records, protocols, logbooks, forms, procedures, and other controlled documents are completed accurately, contemporaneously, and in accordance with cGMP and Catalent data integrity expectations •Provide direct supervision, coaching, training, and performance support for production team members to promote safe, compliant, and consistent execution •Coordinate daily priorities with cross-functional site teams to support project timelines, client commitments, production readiness, and effective communication •Ensure manufacturing suites, equipment, materials, and documentation are maintained in a state of readiness and compliance with site procedures, safety standards, quality expectations, and regulatory requirements •Supervise equipment set-up, changeover, cleaning verification, material staging, line clearance, area readiness, batch execution, in-process sampling, and post-run documentation •Actively facilitate and support site’s oral solid dose operations, including blending, milling, granulation, fluid bed processing, compression, encapsulation, coating, potent compound handling, controlled substance handling, and related development or clinical manufacturing processes, as applicable •Provide input on equipment needs, set-up strategies, containment controls, facility readiness, and production workflows to support safe and effective development, clinical, and scale-up manufacturing Qualifications: •Bachelor’s degree in Pharmaceutical Sciences, Engineering, Industrial Technology, Business Administration, Operations, or related discipline with at least 5 years of relevant pharmaceutical development, clinical manufacturing, oral solid dose, or pharmaceutical production experience •Associate degree in a related discipline with at least 6 years of relevant experience •High school diploma or equivalent with at least 7 years of relevant experience •Demonstrated success leading teams in a regulated environment, including employee development, performance management, cross-functional collaboration, investigation support, and execution of business objectives in compliance with quality and regulatory requirements •Demonstrated capacity to lift in excess of 40 lbs. unassisted •Majority of work day is performed while standing, walking, lifting, pulling, pushing •Demonstrated capacity to communicate effectively using speech, vision and hearing •Requires the use of hands for simple grasping and fine manipulations •Requires bending, squatting, reaching, pushing, climbing •Requires the ability to stand for extended periods of time Compensation: •Competitive Paid Time Off plus 8 paid holidays Interested candidates, please apply directly through the job posting on company's career page or try via AI auto apply on this platform. Don't miss this opportunity to join a forward-thinking team!