Key Responsibilities:

• Supervise Quality Control operations, including sampling, testing, and documentation.
• Ensure strict compliance with cGMP, GLP, and relevant regulatory requirements.
• Manage analytical testing for raw materials, in-process, and finished goods.
• Review and approve SOPs, test methods, and related QC documentation.
• Liaise with QA, Production, and R&D departments to maintain quality standards.
• Lead preparation and coordination for regulatory audits (e.g., DRAP, WHO).
• Drive continuous improvement in lab practices and quality systems.
• Must be able to design CTD dossiers.