Tech Transfer Head

Job Scope

The Tech Transfer Head will lead, oversee, and optimize manufacturing processes related to sterile biologic drug production. This includes designing and implementing technology transfer programs, improving routine manufacturing processes, solving technical issues, and providing scientific input for regulatory submissions.

The role ensures alignment with GMP and international regulatory standards while supporting commercial manufacturing activities.

Job Requirements

Education: Master’s degree in Chemical Engineering, Biotechnology, Biochemical Engineering, or a related field.

Experience

1. 10+ years of experience in process engineering or Tech transfer within the pharmaceutical/biotechnology industry.
2. Strong preference for experience in sterile biologics manufacturing.

Language: Strong written and spoken English, French & Arabic

Professional Knowledge

1. International & EU Health Authority Regulations
2. GMP & GDP
3. Ministry of Health Regulations
4. General Safety Regulations
5. Aseptic Processing & Gowning Procedures
6. Process Validation & Equipment Qualification
7. Single-Use Technologies
8. Technology Transfer
9. Continuous Improvement
10. Statistical Analysis
11. Project Management
12. MS Office Suite

Main Competencies

1. Technical Excellence: Strong analytical and problem-solving skills; ability to plan and execute projects with high quality.
2. People & Collaboration: Strong team player; excellent communication skills.
3. Self-Management: Proactive, adaptable, able to work in a dynamic environment.
4. Leadership: Ability to inspire and motivate teams; strong supervisory and coaching skills.
5. Communication: Clear and effective communicator with strong feedback and conflict-resolution skills.

Duties & Responsibilities

1. Lead the MSAT Team and optimize manufacturing processes.
2. Design and implement process improvements to enhance quality, yield, and efficiency.
3. Perform process risk assessments and support commercial manufacturing operations.
4. Lead and coordinate technology transfer activities to ensure seamless transition from development to production.
5. Provide technical support and training to manufacturing personnel during PPQs and commercial batches.
6. Contribute to equipment design and qualification, including Single-Use Systems.
7. Support troubleshooting of equipment and processes to minimize downtime.
8. Analyze process data for continuous improvement initiatives.
9. Ensure compliance with FDA, ISO, and cGMP requirements.
10. Support regulatory submissions and inspections.
11. Investigate deviations, propose and implement CAPAs, and manage change controls.
12. Assess technical risks related to new equipment and participate in continuous improvement projects.
13. Ensure compliance with national and international HSE laws and maintain relevant documentation.
14. Perform any other tasks assigned by the direct manager.