QP - Full Time Contract Outside IR35

4763097
  • Job type

    Contract
  • Location

    North England/Wales
  • Working Pattern

    Full-time
  • Specialism

    Quality Assurance And Validation
  • Industry

    Pharmaceuticals
  • Pay

    Outside IR35

QP CONTRACT | STERILE MANUFACTURING | OUTSIDE IR35 | BATCH RELEASE

Your Company
An established pharmaceutical manufacturing site is seeking an experienced Qualified Person (QP) to support batch certification and quality operations for commercial and clinical products.

This is a hands-on contracting role requiring a strong understanding of UK and EU GMP requirements, Annex 16, and quality leadership within a regulated manufacturing environment.

Key Responsibilities:

QP & Batch Certification
  • Act as a named QP on the site MIA and IMP licences.
  • Perform batch certification and release of commercial and clinical products in line with UK/EU GMP and Annex 16
  • Confirm compliance of manufacturing steps either directly or through agreed delegation.

Quality Operations & Oversight
  • Provide QP oversight of GMP activities across manufacturing, packaging, and testing
  • Support disposition of intermediates and finished products
  • Provide quality input into deviations, OOS, change controls, and CAPAs
  • Review and approve GMP documentation and operational procedures

Required Experience & Qualifications
  • Eligible to act as a QP under UK/EU regulations
  • Significant pharmaceutical manufacturing experience, ideally including sterile and/or biological products/ sterile manufacturing
  • Proven experience with Annex 16 batch certification

About the role:
  • On-site presence required for 5 days
  • Suitable for experienced QP contractors seeking a technically solid site with long-term potential

    Please click "apply now" to send an updated CV to Julia Bowden at Hays.

Apply for this job

Talk to Julia Bowden, the specialist consultant managing this position

Located in London-City, 5th Floor, 107 Cheapside, Telephone +443330106057
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