Assistant Manager, QA Validation

This role is responsible for defining and specifying the activities, processes, and standards required to fulfill quality requirements for manufactured materials, components, and products within a global pharmaceutical environment. The position builds and maintains the infrastructure and systems necessary to consistently ensure the timely delivery of quality-compliant products. It leads and manages validation quality assurance activities to ensure manufacturing processes and equipment meet defined regulatory and internal standards. The role ensures efficient and effective workflows, procedures, policies, and validation programs are in place and adhered to across manufacturing operations. It manages in-process product quality in coordination with vendors and contract manufacturers. The position facilitates communication with customers and vendors to resolve quality-related issues in a timely and compliant manner. It reports and troubleshoots manufacturing process deviations and defects identified in finished goods and validation studies. The role leads a team of quality professionals and contributes to continuous improvement initiatives aimed at reducing defects, errors, and rework across manufacturing operations. It also supports the development and maintece of validation master plans and related documentation.

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