Sterile Production Technician: Precision Pharma Operator

TALENTMATE

Ras Al Khaimah

Sur place

AED 67 000 - 100 000

Plein temps

Il y a 4 jours
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Résumé du poste

TALENTMATE in Ras Al Khaimah seeks a dedicated Sterile Production Technician to operate and monitor sterile manufacturing equipment, ensuring cGMP compliance and quality standards.

You will follow SOPs, document production records, and support cross-functional teams to prevent interruptions while maintaining HSE practices and PPE standards. On-the-job training will be provided; prior experience in sterile manufacturing and cGMP is preferred.

Qualifications

  • Diploma/secondary school with 2 years of experience in sterile manufacturing.
  • Functional knowledge of pharmaceutical industry and understanding of operation processes.
  • Knowledge of cGMP principles.

Responsabilités

  • Execute production schedules and monitor sterile manufacturing processes.
  • Operate production equipment in accordance with SOPs and batch manufacturing records.
  • Maintain compliance with cGMP, quality systems, safety procedures, EMS, HSE requirements, and PPE standards.
  • Identify and report process deviations, equipment issues, environmental risks, and safety hazards.
  • Coordinate with Quality, Engineering, Warehouse, and other cross-functional departments to prevent production interruptions.
  • Support investigations, audits, EHS activities, and continuous-improvement initiatives.
  • Train new employees on sterile production processes and equipment operation.
  • Maintain accurate production records and ensure documentation is completed correctly and on time.

Connaissances

Equipment operation
cGMP knowledge
Pharmaceutical industry knowledge

Formation

Diploma/secondary with 2 years sterile manufacturing experience

Description du poste

TALENTMATE in Ras Al Khaimah seeks a dedicated Sterile Production Technician to operate and monitor sterile manufacturing equipment, ensuring cGMP compliance and quality standards.

You will follow SOPs, document production records, and support cross-functional teams to prevent interruptions while maintaining HSE practices and PPE standards. On-the-job training will be provided; prior experience in sterile manufacturing and cGMP is preferred.

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