Job Description
- Prepare, operate and monitor all equipment associated with compounding of ophthalmic products in accordance to current Good Manufacturing Practices (cGMP).
- Perform routine cleaning and sanitisation on all equipment and rooms associated with compounding processe
- Prepare, verify and transfer materials/components used in Compounding
- Execute activities in support of validations associated with Compounding
- Perform and review all necessary documentation as required and in accordance to Good Documentation Practice (GDP)
- Assist in investigation of process deviations and work in a team to identify and work on opportunities for productivity/process improvements.
- Adhere with Alcon Values and Behaviors and HSE guidelines & 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.
