As a GxP Consultant at MFT Consult, you will play a vital role in ensuring pharmaceutical organizations meet Good Practice (GxP) standards across manufacturing, distribution, and clinical processes.

As a Regulatory Affairs Expert, you will help clients navigate complex regulatory pathways to bring products to market efficiently and compliantly in Africa, the Middle East, and global markets.

As a CQV Specialist, you will be responsible for ensuring that pharmaceutical facilities, equipment, and systems are properly commissioned, qualified, and validated in accordance with GMP guidelines.

As a Biopharma Project Manager, you will oversee the planning, coordination, and delivery of complex pharmaceutical and biotech projects, ensuring high standards and on-time execution.