GMP Document Administrator – CPI – Darlington


Why this role is important for CPI’s


As the GMP Document Administrator, you will be responsible for establishing and maintaining the document management processes including the issuing and reconciliation of GMP documentation. You will be joining the established, growing Quality team. Reporting to the Quality Manager – Biologics, you will be working in CPI’s National Manufacturing Biologics Centre and supporting the new, state-of-the-art , also based at the site in Darlington.

You will perform a variety of tasks in support of Document Control Systems’ and ​‘Writing, Reviewing, Version Control, Issuing & Archiving of BMR’s and Logbooks to ensure compliance to the CPI Biologics quality management system to meet GMP requirements.

Key tasks will include (but are not limited to) the below:

  • Document controller activities for all GMP controlled documentation including policies, SOPs and protocols.
  • Control, issue, reconciliation, and archive of GMP manufacturing documentation including batch manufacturing records and logbooks. 
  • Printing, issuing and reconciliation of labels.
  • Supporting the Quality team with any other requirements as required.
  • The person we are seeking

    You will be educated to a minimum of 5 GCSE’s (or equivalent) including Mathematics and English Language.

    You will have great attention to detail. 

    It would be great if you had:

  • Document management expertise and experience of operating within a quality management system.
  • Use and implementation of paper and electronic Document Management systems.
  • What does CPI offer you?

    At CPI, we offer a wide range of benefits to our employees, this includes:

  • Up to 36 days holiday, including bank holidays – Plus a holiday purchasing scheme
  • Generous pension scheme
  • Life assurance and accident insurance schemes
  • Flexible working
  • Learning and Development Opportunities
  • Free parking
  • Read more…

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