Description
The Validation Manager will manage validation activities for pharmaceutical or biotechnology manufacturing, developing validation strategy and overseeing teams responsible for equipment, utilities, facilities, computer systems, and manufacturing processes. The role ensures validated systems remain compliant with cGMP requirements while supporting new product introductions and technology transfers. It requires a bachelor's degree in a relevant technical discipline, 6–8 years of pharmaceutical or biotechnology manufacturing experience, validation and people-management experience, and expertise in cGMP, risk assessment, quality systems, and regulatory compliance.
