QC Sample Management Analyst

A fantastic career opportunity for an eager Science graduate with GMP lab experience from an internship or someone working within a QC Sample Management role that wants to gain exposure to sample management in a large biopharmaceutical company. Reporting to the QC Material Management Supervisor, they will be responsible for supporting site activities related to Sample Management Laboratory, in-process samples, and laboratory duties in accordance with cGMP regulations.

12 month contract.

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• Liaise with manufacturing to ensure all Drug Substance samples are processed and delivered to the appropriate destination in an appropriate timeframe.
  
• Liaise with Engineering Stores to ensure all Drug Product samples are processed and delivered to the appropriate destination in an appropriate timeframe.
  
• Liaise with Warehouse Cryogenics Logistics (WCL) to ensure all Raw Material samples are processed and delivered to the appropriate destination in an appropriate timeframe.
  
• Manage TempTales and shipping documents when receiving samples from external sites.
  
• Log in of samples to LIMS/CIMS or logbooks, and label accordingly.
  
• Release samples for QC testing.
  
• Storage of backups and reserve samples.
  
• Perform monthly reconciliation and report deviations to Sample Management Lead, if any.
  
• Aliquot samples for the QC activities for Global Biologics Laboratory and Multi Product Cell Culture (MPCC) Facility.
  
• Generate and update SOPs and other relevant documents as required.
  
• Maintain a high standard of GMP compliance including the completion and provision of training as required.
  
• Keeps abreast of current corporate and industry requirements and compliance trends as they pertain to laboratory operations and aseptic manufacturing.
  
• Performing any other activities as indicated by the Lab Supervisor.
  
• The successful candidate must demonstrate excellent written and verbal communication skills and the ability to work in a team based collaborative environment.
  

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• Hold a minimum of a third level qualification (Degree) in Chemistry/Biology or related discipline.
  
• 1 - 2 years' work experience/internship/placement in a pharmaceutical / healthcare laboratory or related technical function.
  
• Knowledge of GMP regulations. xcfaprz
  
• Previous experience in a sample management role required.