Description
The role prepares, develops, maintains, audits, and controls technical documents for manufacturing, quality, regulatory, and engineering activities in compliance with cGMP and applicable regulatory requirements. Responsibilities include translating technical information into compliant documentation, identifying gaps, supporting document-control and change-control processes, maintaining revision histories, participating in process-improvement initiatives, and supporting cGMP-related training. A B. Pharm is required, while an M. Pharm is preferred; the posting specifies 5–8 years of experience.
