Laboratory Manager – IV fluids manufacturing - Libya

Job Title: Laboratory ManagerLocation: LibyaJob Type: Full-timeRole ObjectiveTo oversee and manage the laboratory operations within an IV fluids manufacturing plant, ensuring full compliance with GMP standards, pharmaceutical regulations, and quality systems. The role is responsible for maintaining product quality, operational efficiency, and regulatory compliance throughout all production stages. Key ResponsibilitiesManage daily operations of the pharmaceutical manufacturing laboratory.Ensure strict compliance with GMP, ISO standards, and relevant health authority regulations.Supervise all stages of IV fluid production (preparation, mixing, sterilization, filling, and quality testing).Monitor and enforce quality control procedures to ensure product safety and consistency.Lead and manage laboratory staff including chemists, technicians, and quality control personnel.Prepare and review technical, production, and quality reports.Develop, implement, and continuously improve Standard Operating Procedures (SOPs).Investigate production deviations and implement corrective and preventive actions (CAPA).Coordinate with production, quality assurance, and maintenance departments to ensure smooth operations.Oversee calibration and maintenance of laboratory and production equipment.Ensure raw materials meet required specifications before use in production.Participate in internal and external audits and ensure compliance readiness. Bachelor’s or Master’s degree in Pharmacy, Chemistry, Biochemistry, or Chemical Engineering.Minimum 5–10 years of experience in pharmaceutical or IV fluids manufacturing environments.Strong background in laboratory management within sterile pharmaceutical production.Solid knowledge of GMP, ISO 13485, and pharmaceutical quality systems.Proven experience in team leadership and operational supervision.Prior experience in the GCC or North Africa region is an advantage. Bachelor’s or Master’s degree in Pharmacy, Chemistry, Biochemistry, or Chemical Engineering.Minimum 5–10 years of experience in pharmaceutical or IV fluids manufacturing environments.Strong background in laboratory management within sterile pharmaceutical production.Solid knowledge of GMP, ISO 13485, and pharmaceutical quality systems.Proven experience in team leadership and operational supervision.Prior experience in the GCC or North Africa region is an advantage.