Ireland Job Openings
LEO Pharma A/S
Process Operator
Cork
FULL TIME
December 2, 2024
Location: Cork T45 RP82, Ireland, Ireland
Contract type: Permanent
Job ID: 2734
- Maintain Production of Heparin Intermediates and API’s according to established Standard Operating Procedures.
- Knowledge of and work in compliance with c GMP in accordance with Irish, European Union and FDA regulations, including compliance with hygiene, garbing, and procedures for controlled areas.
- Work in compliance with LEO Code of Conduct and Site HR policies.
- Completing all stock transactions on the Stock Control System.
- Compliance with Health, Safety, Security and Environmental procedures such as security regulations, safety procedures, fire procedures, protective clothing, local ventilation, and Ex proof installations.
- Compliance with safe operating procedures for handling chemicals e.g. Heparin, Ethanol, Celkate, Glacial Acetic Acid.
- Control of starting materials, intermediates and API’s, including weighing, measuring, labelling and reconciliation of production materials.
- Completion and maintenance of batch manufacturing records, log sheets, in-process control sheets.
- Fulfilling all sampling requirements specified on Batch Manufacturing Records.
- Operation of all Production Equipment including associated valves, pumps, services and utilities.
- Preparing fittings for Autoclaves: Filter Housing, Container Closure, Pipe Fitting, Sampling equipment.
- Cleaning and disinfection of production area. Maintaining production areas free from dust and dirt and in a general state of cleanliness and upkeep.
- Participation in performance improvement initiatives.
- Receipt of raw materials to the warehouse.
- Receipt and labelling of raw materials in the warehouse.
- Receipt of pure ethanol to the tank farm.
- Back-loading of regenerated ethanol to a tanker.
- Start-up, shutdown and running of the ethanol distillation column.
- Control and calibration of effluent p H and relevant logbooks.
- Active participation in Lean Manufacturing Initiatives e.g. 5S, Continuous Improvement, Waste Elimination, Visual Management.
- A Level 5 Certificate (or higher) in a technical field such as science, chemical or industrial engineering, material science or equivalent scientific field is required. Equivalent experience may also be considered.
- Experience of working in API manufacturing, biotechnology or bioprocessing.
- Experience of working in a GMP regulated environment.
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