Job Summary

• The Investigations Supervisor provides oversight and leadership to the team responsible for conducting and authoring deviation and complaint investigations associated with the packaging, storage and distribution of clinical and commercial drug products.
• Maintains and enhances effectiveness of the Quality System, including developing and reporting metrics, identification and implementation of improvement opportunities for established Quality Systems, processes, procedures, and training to support Deviation, Out-of-Specification and CAPA processes.
• Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world.

Matching Summary

Skills & Requirements

Key Requirements

• Bachelor’s Degree required
• 2 - 5 years CAPA, investigations, or QA experience
• 5 years manufacturing/technical experience in regulated GMP environment

Work Rights