ompany Description

Future Pharmaceutical Industries (FPi) is an established national Egyptian pharmaceutical company dedicated to advancing the healthcare industry since 2011. With a robust development pipeline of over 50 molecules, including 30 successfully launched products, FPi is recognized for its innovative approach and commitment to excellence. Under the leadership of CEO Dr. Gamal El-Leithy, the company is known for its dynamic management team and unique business culture grounded in core values. FPi maintains high compliance standards, validated by successful audits from leading organizations such as EMEA, Sanofi, and Sandoz. The company ensures consistent GMP compliance through regular inspections by the Egyptian Ministry of Health.

Role Summary

• The Microbiology Section Head is a full-time on-site role based in Badr City, Egypt. This position plays a key role in the start-up phase and establishment of a sterile microbiology laboratory, including designing laboratory layout, selecting equipment, and setting up operational systems in compliance with GMP and regulatory requirements.
• The role requires a proactive leader capable of building and developing a strong, high-performing microbiology team, while ensuring effective oversight of microbiological testing, environmental monitoring, method validation, and continuous improvement initiatives. The Section Head will collaborate closely with Quality Assurance and Production teams to maintain the highest standards of sterility, accuracy, and compliance.

• Experience Needed : 7–10 years
• Minimum 3 years in the same position within a sterile is preferred

Job Description

• Designs laboratory requirements with respect to facilities, equipment and instrumentation.
• Review and approve of documentation including SOP, logbook, validation protocols, reports and associated deviations.
• Report to lab management on the performance of the management system and any need for improvement ensuring the effectiveness of lab activities.
• Conducts internal audits on department test methods and activities to confirm compliance and to identify improvement.
• Participates in validation protocols of manufacturing sites and equipment.
• Ensures the development, implementation, and maintenance of quality control microbiology systems and activities.

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