Responsibilities

• Supervise daily pharmaceutical production activities to ensure efficiency and compliance with GMP standards.
• Ensure quality control and assurance by working closely with QA/QC teams and monitoring product standards.
• Maintain accurate batch manufacturing records and ensure proper documentation for regulatory compliance.
• Monitor and maintain production equipment, ensuring proper cleaning, calibration, and functionality.
• Coordinate with cross-functional teams and support training of production staff to maintain workflow and safety standards.

Requirements

• Knowledge of GMP and pharmaceutical regulations
• Attention to detail and strong documentation skills
• Familiarity with production equipment and processes
• Team coordination and leadership abilities
• Problem-solving and decision-making under pressure.