Sterile Manufacturing Technician — cGMP & Compliance

Julphar; Ras Al Khaimah; Vor Ort; AED 60.000 - 90.000; Vollzeit

Zusammenfassung

Julphar in Ras al-Khaimah is seeking a Sterile Production Technician who operates and monitors sterile manufacturing equipment to produce pharmaceutical products safely and in compliance with cGMP, SOPs, and batch records. You will execute production schedules, operate equipment to SOPs, and maintain records while coordinating with Quality, Engineering, and Warehouse to prevent interruptions.

A Diploma with 2 years in sterile manufacturing is required, along with cGMP knowledge and a strong

Qualifikationen

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

Aufgaben

• 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.

Kenntnisse

Functional knowledge of pharmaceutical

Understand the operation process

cGMP principles

Ausbildung

Diploma, Secondary school with 2 year experience in sterile manufacturing

Jobbeschreibung

Julphar in Ras al-Khaimah is seeking a Sterile Production Technician who operates and monitors sterile manufacturing equipment to produce pharmaceutical products safely and in compliance with cGMP, SOPs, and batch records. You will execute production schedules, operate equipment to SOPs, and maintain records while coordinating with Quality, Engineering, and Warehouse to prevent interruptions.

A Diploma with 2 years in sterile manufacturing is required, along with cGMP knowledge and a strong