• Handle sterile manufacturing operations including injectables and IV fluids
• Ensure adherence to GMP guidelines (WHO, EU GMP, PIC/S, FDA)
• Monitor and execute production processes as per approved SOPs
• Maintain batch manufacturing records (BMRs) and related documentation
• Ensure compliance with quality, safety, and regulatory requirements
• Coordinate with QA, QC, and Engineering teams for smooth operations
• Participate in deviation handling, investigations, and CAPA implementation
• Support continuous improvement and process optimization activities
• Bachelor’s Degree in Pharmacy (B.Pharm) or M.Pharm
• Minimum 3 years of experience in sterile manufacturing
• Hands-on exposure to injectables, IV fluids, or sterile dosage forms
• Experience in GMP-regulated pharmaceutical manufacturing environments
• Strong knowledge of sterile manufacturing processes
• Sound understanding of GMP and regulatory compliance
• Good documentation and reporting skills
• Attention to detail and problem-solving ability
• Ability to work independently and in cross-functional teams
• Effective communication and coordination skills
Wellpharma Medical Solutions LLC, a Mubadala Bio company, is a UAE-based pharmaceutical manufacturer committed to delivering high-quality sterile pharmaceutical products. The organization operates under stringent global regulatory standards and focuses on innovation, compliance, and excellence in pharmaceutical manufacturing.
• Email CV to: hr@wellpharmams.ae
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