Bioprocessing Associate

https://www.teamhorizon.ie/job-search/1472-bioprocessing-associate/operations-manufacturing/sligo/job2024-12-18 16:46:582052-05-03Team Horizon
Job TypePermanent
AreaSligo, IrelandLeitrim, IrelandDonegal, IrelandSligoIreland
SectorOperations & Manufacturing
Start Date
AdvertiserAshling Guthrie
Job Ref3473
Job Views382
Description

Team Horizon is seeking a Bioprocessing Associate to join our client’s team in the Connaught region. This is a permanent role.


 


 


Why you should apply:



  • This is an excellent opportunity to join a state of the art manufacturing facility and support the launch of new high quality products.

  • Carrer progression opportunities

  • Competeive 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.

  • 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:



  • 3rd level qualification in a relevant Science discipline

  • 2 years’ experience in GMP manufacturing

  • Antibody drug, ADC and drug substance purification experience preferable


 


 

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