Head of Manufacturing Science & Technology (MS&T)

Role Overview

Arcera is a global life sciences company headquartered in Abu Dhabi, United Arab Emirates, dedicated to enabling longer and healthier lives while creating sustainable growth. We are seeking a dynamic and experienced Head of Manufacturing Science & Technology (MS&T) to lead our technical operations, drive process innovation, and ensure robust manufacturing performance. This key leadership role will oversee the development, transfer, and optimization of manufacturing processes, bridging R&D and production to deliver high-quality biopharmaceutical products.

Key Responsibilities

• Lead and manage the MS&T team to support technology transfer, process validation, and continuous improvement initiatives.
• Develop and implement manufacturing strategies to enhance efficiency, scalability, and compliance with regulatory standards.
• Oversee process characterization, scale-up, and optimization across multiple production lines.
• Collaborate with R&D, Quality, and Supply Chain to ensure seamless integration of new products into commercial manufacturing.
• Drive root cause analysis and troubleshooting for manufacturing deviations, implementing corrective and preventive actions.
• Ensure all activities adhere to cGMP, safety, and environmental guidelines.
• Manage budgets, resources, and performance metrics for the MS&T department.
• Stay abreast of emerging manufacturing technologies and life sciences innovations to maintain competitive advantage.

Required Qualifications

• Bachelor's degree in Chemical Engineering, Biochemistry, Pharmaceutical Sciences, or a related technical field; advanced degree (MS/PhD) preferred.
• Minimum 10 years of experience in manufacturing science and technology within the pharmaceutical, biotechnology, or life sciences industry.
• Proven leadership experience managing cross-functional teams and complex manufacturing processes.
• Deep knowledge of process validation, tech transfer, and regulatory requirements (FDA, EMA, etc.).
• Strong analytical and problem-solving skills, with expertise in lean manufacturing and six sigma methodologies.

Preferred Qualifications

• Experience with biologics, sterile fill-finish, or advanced therapeutic modalities.
• Track record of successful regulatory inspections and quality audits.
• Excellent communication and stakeholder management abilities.