Our client is looking for a pharmaceutical manufacturing professional to join their greenfield manufacturing setup and play a key role in establishing their world-class tablet and liquid production processes.

Roles & Responsibilities:

• Oversee tablet and liquid manufacturing operations, ensuring compliance with cGMP and regulatory guidelines.
• Optimize production processes for efficiency, quality, and cost-effectiveness.
• Ensure compliance with UAE Ministry of Health, WHO, US FDA, and EMA standards.
• Monitor production metrics, troubleshoot bottlenecks, and implement process
• Collaborate with QA, QC, supply chain, and engineering teams for smooth operations.
• Supervise equipment validation, maintenance, and troubleshooting.
• Train and mentor production staff on best practices and safety protocols.

Qualifications & Experience:

• Bachelor’s or Master’s degree in Pharmacy, Chemical Engineering, or related fields.
• 5-7 years in tablet and liquid manufacturing (greenfield setup experience preferred).

Technical Skills & Behavioral Skills:

• Strong understanding of cGMP, production planning, process optimization, and regulatory compliance.
• Problem-solving, analytical, and documentation skills.
• Ability to work in a dynamic, cross-functional environment.

Skills

Technical Skills & Behavioral Skills:

• Strong understanding of cGMP, production planning, process optimization, and regulatory compliance.
• Problem-solving, analytical, and documentation skills.
• Ability to work in a dynamic, cross-functional environment.