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naukri

Production Engineer - (Caps & Pharmaceutical Packaging)

AURAFEST MANAGEMENT SERVICES PRIVATE LIMITED
Dubai, UAE
Senior
1 weeks ago
engineeringdesignproject managementmaintenancequality controltechnical
Free

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Overview

The Production Engineer oversees daily cleanroom manufacturing operations for the Caps and Pharmaceutical Packaging division.

This hands-on, highly technical role focuses on maximizing the efficiency of all-electric and highspeed injection molding lines while ensuring absolute compliance with GMP/cGMP and BRCGS standards to prevent contamination.

Key Performance Indicators (Kpis)

  • OEE & Cycle Times: Drive daily production lines to meet target Overall Equipment Effectiveness (OEE).
  • Scrap Rate: Keep material and cleanroom waste strictly below target percentages.
  • Audit Compliance: Maintain zero major non-conformities under ISO 15378, BRCGS, and cGMP standards.
  • Changeovers: Optimize line clearances and mold changes to minimize transition downtime.
  • Safety (HSE): Maintain a zero-incident record on all supervised shifts.

A. Operational & GMP Compliance

  • Production Scheduling: Direct shift operations to ensure on-time delivery of pharmaceutical and foodgrade orders.
  • Cleanroom & cGMP Adherence: Enforce Good Manufacturing Practices (GMP/cGMP) and positive-pressure cleanroom protocols to prevent contamination.
  • Line Clearance & Traceability: Execute strict line clearance protocols between runs and maintain 100% material lot traceability.

B. Technical Process Control & Machinery

  • All-Electric Molding: Setup, optimize, and troubleshoot state-of-the-art all-electric injection molding machines, with a direct focus on JSW and Fanuc
  • High-Speed Systems: Address process and mechanical issues on high-speed machines (e.g., Netstal, Engel, Husky).
  • Auxiliary Coordination: Monitor and coordinate the maintenance of critical cleanroom auxiliaries (desiccant dryers, water chillers, HVAC filtration).

C. BRCGS & Quality Assurance

  • BRCGS Standards: Ensure all floor operations and material handling adhere strictly to BRCGS Global Standards.
  • CAPA & RCA: Partner with Quality Control to resolve Non-Conformity Reports (NCRs), lead Root Cause Analysis (RCA), and implement Corrective Action (CAPA) plans.
  • Documentation: Complete and audit batch records, parameter logs, and shift reports following Good Documentation Practices (GDP).

D. Shift Leadership & Safety

  • Team Supervision: Train and manage a multicultural crew of operators and technicians in machine operation and hygiene safety.
  • EHS Enforcer: Maintain safety compliance, including lock-out/tag-out (LOTO) and active machine guarding.
  • Handovers: Conduct structured shift handovers to communicate priorities, quality notes, and machine status.

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