Validation Specialist

5 days ago


London, Greater London, United Kingdom PM Group Full time

**Job Summary**

PM Group is seeking a highly skilled Validation Consultant to join our team in the South East region. As a key member of our team, you will be responsible for overseeing a pharmaceutical project and ensuring that all validation activities are completed to the highest standards.

Key Responsibilities:

  • Collaborate with Capital Project, Production, QA, and R&D departments to obtain validation scopes and agreements to release production status in agreed timelines.
  • Provide weekly updates on the progress status of validation works.
  • Perform general validation works for impacted GMP and non-GMP systems as part of the Capital investment project.
  • Develop and draft required validation documentation, including CSV/CQV validation protocols, VP, C&QP, SIA, URS, DRR/VRA, IOQ, OCD, C&QR, RTM, and VR.
  • Execute and approve corresponding protocols to release required equipment for GMP production.

Deliverables:

  • Weekly validation report.
  • Draft, execution, and approval of CSV/CQV validation protocols.


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