Pharmaceutical Production Supervisor — GMP Leader (UAE)

TalentOne; Dubai; On-site; AED 90,000 - 130,000; Full time

Job summary

TalentOne is seeking an experienced Production Supervisor in the UAE to lead daily pharmaceutical manufacturing operations and ensure GMP-compliant production of solid dosage forms. The role requires at least 5 years of supervisory experience and strong knowledge of cGMP, SOPs, and quality systems.

You will oversee dispensing, manufacturing and packaging, drive continuous improvement, and coordinate with QA, maintenance and supply chain to meet daily targets while maintaining safety and

Qualifications

• Bachelor’s degree in Pharmacy required.
• Minimum 5 years supervisory experience in pharmaceutical manufacturing.
• Solid dosage form manufacturing experience preferred.

Responsibilities

• Supervise dispensing, manufacturing and packaging activities to achieve daily production targets.
• Ensure all production activities comply with cGMP, SOPs, EHS standards, hygiene and PPE requirements.
• Monitor production output, efficiency, yield, wastage and adherence to planned timelines.
• Ensure readiness, qualification, calibration and preventive maintenance of production equipment.
• Review batch records, SOPs, protocols, reports and other manufacturing documents.
• Initiate and support deviation investigations, CAPA, change controls and timely quality-document closure.
• Coordinate material availability with Warehouse and Supply Chain teams.
• Support internal audits, customer audits and regulatory inspections.
• Lead, train and develop production personnel to build a high-performing team.
• Identify and implement continuous-improvement initiatives to improve productivity, quality and cost control.

Skills

Leadership

Problem solving

Communication

GMP compliance

cGMP

SOP knowledge

Quality systems

Education

Bachelor’s degree in Pharmacy

Job description

TalentOne is seeking an experienced Production Supervisor in the UAE to lead daily pharmaceutical manufacturing operations and ensure GMP-compliant production of solid dosage forms. The role requires at least 5 years of supervisory experience and strong knowledge of cGMP, SOPs, and quality systems.

You will oversee dispensing, manufacturing and packaging, drive continuous improvement, and coordinate with QA, maintenance and supply chain to meet daily targets while maintaining safety and