Senior Operator – Manufacturing / Manufacturing Officer
Posted:
Company Details
Job Details
Job Description
Position: Senior Operator – Manufacturing / Manufacturing Officer
Date Posted: July 21, 2026
Industry: Pharmaceutical Manufacturing | Healthcare | Production
Employment Type: Full Time
Experience: Relevant Experience in Pharmaceutical Manufacturing and GMP-Regulated Environments
Qualification: Bachelor’s Degree or Diploma in Pharmacy, Chemistry, Biotechnology, Pharmaceutical Sciences, or a Related Field
Salary: AED 5000 to 10000 (estimated)
Location: Jebel Ali, Dubai, United Arab Emirates
Company: LIFEPharma FZE
Description:
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
CV Job Description Matcher See how well your CV matches this job and get tips to improve your chances AI Tool
This tool helps you see how closely your CV matches a job description. It also gives you simple suggestions on what to improve so you have a better chance of getting shortlisted.
Never pay anyone for job applications, interview tests, or job interviews. A genuine employer will never ask you for payment under any circumstances.