Assistant Manager, QA Validation

About the role

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.

What you'll do

• Define and specify quality activities, processes, and standards for validation programs in compliance with regulatory requirements
• Build and maintain quality infrastructure and systems to ensure timely delivery of validated and compliant pharmaceutical products
• Lead and manage a team of quality professionals to deliver validation quality assurance objectives
• Conduct audits and monitoring of validation activities and manufacturing processes against internal and regulatory standards including 21 CFR Part 210 & 211 and GMP…
• Ensure efficient workflow, procedures, policies, and validation inspection programs are implemented and maintained across manufacturing operations

What you need

• 8–10 yrs of experience
• GMP
• B.Sc or BA or M.Sc