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 drives documentation workflows, supports change control processes, and ensures timely availability of compliant documentation for development and regulatory submissions.