by Julphar in Pharmaceuticals

The Lead MSAT (Validation) role is responsible for leading Manufacturing Science & Technology validation activities across pharmaceutical GMP-regulated manufacturing environments, supporting commercial production, technology transfer, and site readiness activities. The role acts as a technical bridge between R&D, Technology Transfer, Production, Quality Assurance, Engineering, and Procurement teams, ensuring seamless coordination across the product lifecycle.

A core responsibility includes owning the end-to-end validation lifecycle using the V-Model approach, covering URS development, FAT, SAT, IQ, OQ, PQ, and re-qualification activities. The role ensures that all validation documentation is prepared, reviewed, approved, archived, retrieved, and distributed in compliance with GMP documentation standards and data integrity requirements including ALCOA+ principles.

It is accountable for maintaining va...