Posted:
LIFEPharma FZE is expanding its Manufacturing Department and is seeking experienced professionals for the positions of Senior Operator – Manufacturing and Manufacturing Officer. This opportunity is ideal for candidates with hands-on experience in pharmaceutical manufacturing and a strong understanding of GMP-regulated production environments.
The selected candidates will support daily manufacturing operations, ensure compliance with approved procedures, maintain accurate production records, and collaborate with cross-functional teams to achieve efficient and high-quality manufacturing processes. Immediate joiners will be given preference.
Key Responsibilities:
• Plan and execute daily manufacturing activities in line with the monthly production schedule.
• Perform manufacturing processes according to approved Batch Production Records (BPRs) and Standard Operating Procedures (SOPs).
• Carry out batch reconciliation and ensure production yields remain within approved limits.
• Conduct in-process quality checks based on product specifications and approved procedures.
• Complete accurate entries in BPRs, machine logbooks, and manufacturing records.
• Ensure compliance with GMP standards, SOPs, safety regulations, and personal hygiene requirements.
• Monitor and record environmental conditions, including temperature, humidity, and pressure differentials.
• Ensure proper machine operation, calibration, and preventive maintenance compliance.
• Coordinate with QA, QC, Engineering, Warehouse, HR, and other departments to support smooth production activities.
• Train and guide team members on SOPs, GMP requirements, workplace discipline, hygiene, and safety practices.
• Manage process deviations, change controls, incident reports, and other Quality Management System (QMS) activities.
• Support internal audits, self-inspections, investigations, root cause analysis, CAPA implementation, and manufacturing documentation updates.
Requirements:
• Relevant experience in pharmaceutical manufacturing within a GMP-regulated environment.
• Strong understanding of pharmaceutical manufacturing processes and production operations.
• Knowledge of GMP, SOPs, batch documentation, and quality compliance.
• Ability to work effectively with cross-functional teams.
• Strong attention to detail and commitment to quality standards.
• Immediate joiners will be preferred.
Strong knowledge of:
• Good Manufacturing Practices (GMP)
• Standard Operating Procedures (SOPs)
• Batch Production Records (BPRs)
• Quality Management Systems (QMS)
• CAPA & Root Cause Analysis
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