QUALITY PLANNING COORDINATOR

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.
Catalent Pharma Solutions is seeking a Quality Planning Coordinator to join our team. This role is pivotal in supporting our Quality objectives and ensuring timely and compliant execution of QA and QP processes across pharmaceutical and clinical trial packaging operations.

• Contribute to the achievement of Catalent’s GMP objectives and quality policies.
• Provide quality planning expertise to ensure processes meet standards and deadlines.
• Support QP and QA teams in batch review, S&D review, and certification processes.
• Attend site planning meetings to gather and align on project timelines.
• Collaborate with Project Managers and planning teams to schedule QA and QP tasks.
• Assess supply chain data for QP certifications.
• Review and validate Workfront timelines.
• Coordinate with internal departments and external Catalent sites to manage batch documentation.
• Monitor and manage the QP group mailbox.
• Compile internal and client metrics for business reviews.
• Conduct internal audits and walkthroughs.