Production Technician - Sterile

Julphar; Abu Dhabi; On-site; AED 72,000 - 110,000; Full time

Job summary

Julphar in Abu Dhabi, United Arab Emirates, seeks a Sterile Production Technician to operate and monitor sterile manufacturing equipment, ensuring safe, efficient production in line with cGMP, SOPs and batch records.

The role requires a Diploma with 2 years of sterile manufacturing experience and knowledge of cGMP. You will collaborate with Quality, Engineering and Warehouse teams to maintain production schedules and documentation.

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.

Responsibilities

• Operate and monitor sterile manufacturing equipment following SOPs and batch records.
• Maintain compliance with cGMP, quality systems, safety procedures, EMS, HSE and PPE standards.
• Identify and report process deviations, equipment issues, and safety hazards; coordinate with Quality, Engineering, Warehouse and other departments to prevent interruptions.
• Support investigations, audits, EHS activities, and continuous improvement initiatives.
• Train new employees on sterile production processes and equipment operation; maintain accurate production records.

Skills

Sterile manufacturing

SOP adherence

Education

Diploma, Secondary school with 2 year experience in sterile manufacturing

cGMP knowledge

Job description

Job description

Job Role:

The Sterile Production Technician operates and monitors sterile manufacturing equipment to produce pharmaceutical products safely, efficiently, and in compliance with cGMP, SOPs, batch manufacturing records, quality systems, and HSE requirements.

Responsibilities:

• Execute production schedules and monitor sterile manufacturing processes.
• Operate production equipment in accordance with approved 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.

Education & Experience:

• Diploma, Secondary school with 2 year experience in sterile manufacturing.
• Functional knowledge of pharmaceutical industry, understand the operation process.
• Knowledge with cGMP principles.