Key Accountabilities:
- 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.
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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:
Experience:
Between 1-3 years of experience in a manufacturing environment, preferably in pharmaceutical manufacturing or partially qualified internally.
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