- Establish and maintain a comprehensive document control system for all manufacturing processes, including batch records, standard operating procedures (SOPs), and quality control documentation
- Ensure that all documentation complies with relevant regulatory requirements, industry standards, and Positive Manufacturing Practices (GMP) for Ayurvedic products
- Stay informed about changes in regulations and update documentation accordingly
- To compile and review batch records and conduct regular audits of documentation for accuracy and completeness
- Maintain a systematic filing system for batch records and related documentation