Biologics Manufacturing Technician
| Job Type | Permanent |
| Area | Sligo, Ireland |
| Sector | Operations & Manufacturing |
| Start Date | |
| Advertiser | Ashling Guthrie |
| Job Ref | 3344 |
| Job Views | 150 |
- Description
Team Horizon is seeking a Biologics Manufacturing Technician for Clients pharmaceutical facility in Sligo.
Why you should apply:
- Join a leading-edge biotech supporting biologics operations
- Career Progression opportunities, competitive salary & benefits package
What you will be doing:
- You will be assigned to the daily production operations, operating different equipment.
- Efficiently operate all biologics processes minimizing material loss.
- Documentation of all activities in line with cGMP requirements.
- Operate Fill Line, Autoclave, Equipment Washer, Headspace Analyzer, Bioreactors, Chromatography Columns, Filtration Systems, Equipment Cleaning and Sterilization, Equipment Pressure Tests, Equipment/Filters Integrity Tests, Water Baths, Isolators and Lyophiliser, Headspace Analyser, as able.
- Perform final product visual inspection.
- Perform product intermediary packaging, as applicable.
- Perform all in process testing methods.
- Material receipt from warehouse, verifying all pertinent documentation.
- Transfer of final material to warehouse inventory.
- Perform process tests and participate in qualification and validation activities as required.
- Diagnose and resolve events or exceptions of production equipment and processes.
- Disposal of domestic, biomedical, and hazardous waste from their respective area as applicable, ensuring compliance with regulations, following the procedures and policies of the plant, division, and the corporation.
- Keep detailed records, manual or electronic, of the operations carried out during the work shift.
- Adhering to all relevant policies relating to Quality & Safety.
- Work with Engineering, Quality and other departments in the development and update of Standard Operating Procedures.
What you need to apply:
- Third level education in a relevant Science / Engineering course or 2 year's experience in GMP manufacturing is essential
- Knowledge of cGMP and regulatory requirements relating to the pharma/biologics industry
- Experience of operating in a highly automated environment and safe handling of dangerous chemicals is highly desirable.
- Possessing aseptic techniques and sterile fill experience is a distinct advantage for operators assigned to Fill Finish.
- Good I.T. skills are required
- Strong communication skills both verbal and written are required for the execution of this role.
- Demonstrates the highest levels of integrity and a strong work ethic at all Times
