Analytical R&D

This role manages and executes analytical R&D documentation activities to ensure accuracy, consistency, and compliance with regulatory and data integrity requirements across drug substance and product development. The position supports the preparation, review, and lifecycle management of analytical documents, protocols, and validation records while adhering to ALCOA+ and GLP/GMP standards. It involves driving documentation workflows, supporting change control processes, and collaborating with cross-functional teams to maintain audit readiness and enable reliable data reporting.