Production Supervisors at Kairuki Pharmaceuticals Industry

Key Responsibilities The Production Supervisors will oversee day-to-day manufacturing activities and ensure that production targets are achieved in accordance with approved procedures, GMP requirements, quality standards, and safety requirements. Key responsibilities will include: Supervising daily production activities and production personnel. Ensuring production schedules and targets are achieved. Ensuring manufacturing processes are performed according to approved SOPs and batch manufacturing records. Supervising sterile IV pharmaceutical manufacturing activities. Ensuring compliance with Good Manufacturing Practices (GMP). Monitoring production processes and identifying deviations. Working closely with QA and QC to resolve quality and production issues. Ensuring proper documentation of production activities. Monitoring production equipment and reporting breakdowns promptly. Coordinating with Engineering for equipment maintenance. Managing production personnel and allocating duties effectively. Monitoring production performance and productivity. Ensuring proper housekeeping and workplace safety. Participating in investigations of deviations, non-conformances, and corrective actions. Supporting continuous improvement initiatives. Qualifications and Experience Bachelor’s Degree or Diploma in Pharmaceutical Manufacturing, Pharmaceutical Sciences, Chemical Engineering, Industrial Production, or a related field. Minimum 5 years of relevant experience in a manufacturing industry. Demonstrated experience supervising production teams. Experience in pharmaceutical manufacturing will be a significant advantage. Knowledge of GMP, production documentation, quality systems, and occupational safety. Strong leadership and people-management skills. Ability to work under pressure and meet production targets.