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: Minimum NITEC / Higher NITEC in Engineering, Manufacturing or any discipline related to pharmaceutical manufacturing.
Experience: Between 1-3 years of experience in a manufacturing environment, preferably in pharmaceutical manufacturing or partially qualified internally.
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