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The Operations Zone Manager at Catalent is responsible for overseeing the production process in the pharmaceutical manufacturing sector, ensuring compliance with cGMP standards, managing staff, and maintaining quality control. This role includes resolving technical issues, optimizing performance, and maintaining communication across departments.

The Senior QC Scientist will oversee the administration of the LabVantage LIMS, providing end-user support, ensuring compliance with global policies, managing accounts, roles, and system functions, and assisting in the development of data tracking processes. The role requires knowledge of pharmaceutical laboratory requirements and regulatory standards.

The Room Lead, Form Fill at Catalent is responsible for overseeing the filling lines and equipment operations. This includes troubleshooting issues, ensuring compliance with regulations, training staff, and coordinating tasks among team members. The role emphasizes leadership in investigations of procedural deviations and communication of production activities.

The Senior Manager, Form/Fill leads a team ensuring compliance with regulations and operational efficiency in the production process. They develop departmental plans, manage staff, and support continuous improvement projects while maintaining safety and quality standards.

The Quality Systems Specialist (Training) manages training documentation and LMS, develops training curriculums, supports audit preparations, reports training metrics, and conducts training sessions. This role ensures compliance with regulatory requirements and promotes effective training practices across departments.

The Senior Manager, Procurement is responsible for managing indirect and capital spend, establishing supplier relationship management programs, leading cross-functional initiatives to cut costs and enhance quality, negotiating contracts, processing requisitions, and handling supplier quality issues to support product launches.

The Specialist, Quality Assurance is responsible for quality support functions related to product packaging for clinical and commercial batches. Key duties include batch record review, product release, compliance with FDA guidelines, participation in QA programs, and interaction with clients. The role demands adherence to Good Documentation Practices and support for efficiency improvement projects.