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:
Bachelors or Masters 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.
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