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Quality Document Coordinator

Merseyside   •  Negotiable  •  Permanent, Full time

Quality Document Coordinator
140 a day
Outside IR35
Liverpool based
6 Month Contract

CPL are recruiting for a Quality Document Coordinator to join a pharmaceutical company at their site based in Liverpool on a contract basis for 6 months.

Quality Document Coordinator Role:

  • Monitor and review in-process and completed Batch Production Records, expedite correction of any errors, maintain a tracking system to ensure all documentation is completed
  • Generate Certificates of Analysis (and any other Quality documents required for shipping) and ensure they are approved and provided to shipping via the appropriate channels
  • Provide a channel of communication between manufacturing functions (technical and planning), appropriate Quality Assurance Representative/QPs and other customers to prioritise workload to ensure expected service levels are met

Your Background:

  • Background working with controlled documents or within a Quality function would be a distinct advantage
  • Experience within a GMP environment
  • Good eye for detail and organised

If you're interested please apply or send your CV to luke.sandilands@cpl.com

  • Agency: Cpl Life Sciences
  • Contact: Luke Sandilands
  • Reference: JO-2201-483627
  • Posted: 14th January 2022
  • Expires: 11th February 2022

Cpl Life Sciences

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