Assistant Manager, Technical Writing

This role is responsible for managing and coordinating technical writing activities within a pharmaceutical manufacturing environment, ensuring that all standard operating procedures, batch records, work instructions, and other technical documents are developed, reviewed, and maintained in strict compliance with regulatory requirements and Good Manufacturing Practices. The incumbent applies specialized writing skills to translate complex manufacturing processes and technical information into clear, accurate, and compliant documentation. The position requires a thorough understanding of GMP documentation standards and regulatory requirements to ensure that all technical documents support product quality and regulatory compliance. The role involves developing and implementing documentation schedules and workflows to ensure the timely creation and revision of technical documents across manufacturing areas.