Senior Operator – Manufacturing / Manufacturing Officer

Job Overview

  • Date Posted
    21 July 2026
  • Expiration date
    31 July 2026
  • Experience
    Relevant Experience
  • Gender
    Both
  • Qualification
    Degree
  • Career Level
    Advanced - Level

Job Description

Job Title: Senior Operator – Manufacturing / Manufacturing Officer

Company: LIFEPharma FZE

Location: Jebel Ali, Dubai, United Arab Emirates

Employment Type: Full‑time

Salary: AED 5,000 to 10,000 per month (Estimated)

Experience Required: Relevant hands-on experience in pharmaceutical manufacturing within GMP-regulated environments

Position Profile

LIFEPharma FZE is recruiting an experienced Senior Operator / Manufacturing Officer to support its expanding production facilities in Jebel Ali. This role manages daily pharmaceutical manufacturing operations, monitors batch processing compliance, performs in-process quality audits, and upholds strict regulatory standards to ensure high-grade pharmaceutical production.

Main Duties

  • Execute daily production schedules in compliance with approved Batch Production Records (BPRs) and Standard Operating Procedures (SOPs).

  • Perform batch reconciliations, track yield metrics, and carry out routine in-process quality checks against product specifications.

  • Log precise entries across BPRs, equipment utilization logbooks, and internal Quality Management System (QMS) records.

  • Track cleanroom environmental metrics, including temperature parameters, humidity, and room pressure differentials.

  • Investigate process deviations, formulate Corrective and Preventive Actions (CAPA), and assist with root-cause analysis during internal audits.

  • Collaborate with QA, QC, Engineering, and Warehouse units to ensure streamlined material handling and equipment calibration.

Ideal Candidate Profile

  • Education: Bachelor’s Degree or Diploma in Pharmacy, Chemistry, Biotechnology, Pharmaceutical Sciences, or a related field.

  • Professional Background: Direct, proven background operating inside a GMP-regulated pharmaceutical production facility.

  • Domain Mastery: Deep familiarity with Good Manufacturing Practices (GMP), BPR logging, QMS workflows, and CAPA protocols.

  • Core Aptitudes: High precision in documentation, strong leadership capabilities for onboarding junior technicians, and acute attention to cleanroom safety standards.

  • Availability: Candidates who can join immediately will be given priority consideration.

Value Proposition

  • Placement within a major, state-of-the-art pharmaceutical manufacturing hub in Dubai

  • Dynamic exposure across multi-departmental pharmaceutical operations, QA audits, and QMS management

  • Long-term career progression pathways within an expanding healthcare manufacturing enterprise

How to Apply

Forward your updated CV and professional background directly to the corporate recruitment team: [email protected]