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The Principal Representative, QA will implement and maintain the Data Integrity program, manage System and Validation Lifecycle Documentation, and ensure compliance with GxP standards. Responsibilities include reviewing validation documents and SOPs, performing data integrity assessments, and participating in audit trail reviews.

The Master Scheduler at Catalent is responsible for creating and managing the Master Production Schedule (MPS) as well as the short-term production schedule for the Greendale site. The role involves collaborating with various departments to ensure efficient production planning and schedule execution. The candidate should have a Bachelor's degree with 3+ years of Manufacturing scheduling experience and knowledge of Finite Planning techniques.

The Associate Scientist engages in pharmaceutical development and clinical manufacturing projects, overseeing tasks like formulation, data interpretation, and documentation while ensuring timely execution of responsibilities and ongoing communication with internal teams and clients.