Production Technician

Role overview

This position is responsible for carrying out sterile production activities from start to finish in a controlled manufacturing environment. The role involves aseptic processing, sterilizing equipment and materials, maintaining accurate records, and operating specialized machines while adhering to strict quality, safety, and compliance standards. The technician also supports daily output targets and contributes to ongoing improvements in the process.

Key responsibilities

• Carry out sterile manufacturing tasks, including preparation and sterilization of materials and tools used in aseptic filling.
• Perform aseptic filtration and assist with filter integrity checks.
• Support aseptic cleaning activities.
• Handle core production activities such as receiving materials, preparing disinfectants, and dispensing.
• Maintain process and cleaning logbooks accurately.
• Record manufacturing activities in the batch manufacturing record (BMR).
• Carry out reconciliation checks and yield calculations.
• Escalate any incidents that may affect safety, quality, or productivity.
• Assist the team leader with process improvement initiatives.
• Work with the wider team to meet daily and monthly supply plans.
• Operate sterilization and cleaning equipment, including autoclaves, ovens, and tunnels.
• Use CPM systems and other environmental monitoring equipment.
• Support sterilization qualification activities.
• Perform dry fog operations using the required equipment.
• Take part in aseptic process simulation activities according to local procedures.

Requirements

• Technical Diploma is required.
• At least 6 years of experience in aseptic processing.
• Strong understanding of GMP requirements.
• Knowledge of Class A aseptic behaviour.
• Familiarity with equipment qualification practices.
• Good grasp of ALCOA+ data integrity principles.
• Basic microbiology knowledge.
• Technically capable and comfortable working with specialized production equipment.
• Continuous improvement mindset.

Additional information

The role demands consistent attention to sterile manufacturing standards, documentation discipline, and teamwork in a regulated pharmaceutical environment. The incumbent is expected to help ensure safe operations, reliable supply, and compliance with quality requirements at all times.