Quality Assurance Associate

Key responsibilities:

  • Provide supporting day-to-day operation of the Quality Assurance department
    • Operate in accordance to GMP
    • Allocate unique identifier reference numbers to documents
    • Issue and publish documents
    • Archive documents
    • Maintain document spreadsheet
    • Track and trend compliance paperwork (deviations, change controls, both internal and external)
    • Author external deviations
    • Review Corrective and Preventative actions
    • Manage and store all Milton Park staff training records
    • Collate manufacturing and testing records
    • Provide support to all Replimune internal and external customers
  • Adhere to company documentation policies and maintaining documentation systems as required.

Preferred Educational requirements:

  • A minimum of a degree.

Experience and skill requirement:

  • A highly motivated individual, with excellent time management
  • A very organised and methodical approach to tasks
  • IT skills – competent in using Microsoft Office.
  • An interest in pharmaceutical Quality Assurance
  • A level of flexibility is essential to meet varying workloads.

Hours of work

  • 37.5 hours per week of five days Monday to Friday inclusive. The company operates a flexible working arrangement between the hours of 8am - 6pm.


  • £20K - £25K      + pension scheme, optional BUPA membership and other staff 

More informatio

Applicants should be highly organised and committed, have at least one year of experience within a GMP environment.  Quality Assurance experience is desirable, but enthusiasm and a willingness to learn are just as important.  Fluency in the French language is beneficial.  It is an expectation that the successful candidate will develop their Quality Assurance skills and experience to further support Replimune business as well as individual personal development.

Please send your CV to Chris.Kerley@Replimune.com