• Work with Supervisor and in a team to maintain sterile or clean condition of rooms and equipment associated with aseptic filling, and to perform aseptic filling of ophthalmic products that meet quality and output requirements

• Prepare, operate and monitor all equipment associated with filling of ophthalmic products, in accordance to current Good Manufacturing Practices (cGMP).

• Perform routine cleaning and sanitization on all equipment and rooms associated with aseptic filling, and steam sterilization of the necessary production/cleaning equipment/components, including the operation and routine cleaning of steam sterilizer.

• Perform routine microbiological sampling; for environmental and personnel monitoring in a clean room environment.

• Prepare, verify and transfer materials/components used in aseptic filling. Execute activities in support of validations associated with cleaning and aseptic filling.

• Assist in investigation of process deviations and work in a team to identify and work on opportunities  for productivity/process improvements.

• Perform any other responsibility as assigned by supervisor.

Education:

NITEC/ Higher NITEC in Engineering, Manufacturing or any discipline related to pharmaceutical manufacturing.   

Experience:      

Between 1-3 years of relevant working experience in a manufacturing environment, preferably in pharmaceutical manufacturing.