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The Senior Manager, QC oversees microbiological and environmental monitoring activities, ensuring routine testing of drug products and substances align with quality standards. Responsibilities include managing a team, collaborating with stakeholders, executing analytical testing, and revenue reporting.

The Master Scheduler oversees the development and maintenance of the Master Schedule and short-term production schedules for Catalent's Commercial and Development products. They partner with various teams to translate requirements into schedule, monitor daily operations, and facilitate production capacity reviews, ensuring alignment across departments and timely delivery of products.

The Senior Associate Scientist will conduct experiments, perform analytical product testing, and ensure compliance with regulatory standards. Responsibilities include testing stability samples, conducting laboratory investigations, and data analysis, all while adhering to SOPs and cGMPs.

The Buyer/Planner at Catalent Pharma Solutions is responsible for indirect and direct material procurement, delivery, and confirmation to support the Master Production Schedule. Duties include supply chain management, vendor management, inventory control, and problem resolution. Candidates must have experience in the pharmaceutical industry and working with MRP systems.

The Manager, Human Resources at Catalent Gene Therapy in Harmans, MD is responsible for developing and implementing HR policies and programs, supporting staffing, employee relations, compensation, benefits, training, and organizational development. They oversee compliance with company policies and regulations, provide HR counsel and training, and work on talent management and cultural change initiatives.

The Quality Assurance Specialist II oversees production activities in a GMP Manufacturing Facility, reviews batch records, manages discrepancies, supports environmental monitoring, and assists in compliance inspections while ensuring adherence to quality standards.