Quality Assurance Section Head

About the role

EVA Pharma, a leading pharmaceutical company based in Giza, is looking for a Quality Assurance Section Head to lead its QA activities on validation for sterile and non-sterile operations. The role ensures that validation processes meet regulatory and cGMP requirements and works closely with manufacturing, engineering and technical teams.

Key responsibilities

• Lead QA validation activities for sterile and non-sterile operations, ensuring compliance with regulatory and cGMP requirements.
• Plan, execute and monitor validation activities across manufacturing processes and systems.
• Collaborate with manufacturing, engineering and technical teams so validated processes are maintained and continuously improved.
• Conduct internal audits of validation activities, documentation and systems, and manage CAPA actions on validation findings and quality issues.
• Support technology transfer and new product introduction, ensuring validation requirements are met.
• Lead training on validation practices, sterile and non-sterile operations and cGMP requirements.

Required profile

• Bachelor's degree in Pharmacy, Chemistry or a related field.
• 7-8 years of QA experience in the pharmaceutical industry, with strong expertise in validation (process validation, cleaning validation, equipment qualification).
• Experience managing teams, leading audits, handling diverse customer requirements and technology transfer projects, and communicating clearly with customers.
• Proven ability to lead teams across multiple geographical regions.
• Solid background in new product project management, technology transfer and product launches under EU standards.

Required skills

• Good understanding of cGMP and quality systems.
• Excellent English, analytical, problem-solving and communication skills.