Biologics Manufacturing Technician

https://www.teamhorizon.ie/job-search/1381-biologics-manufacturing-technician/operations-manufacturing/sligo/job2024-07-18 13:54:182051-12-02Team Horizon
Job TypePermanent
AreaSligo, IrelandSligoIreland
SectorOperations & Manufacturing
Start Date
AdvertiserAshling Guthrie
Job Ref3344
Job Views173
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

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