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Validation Consultant

2 months ago

South East, United Kingdom PM Group Full time

PM Group requires a site-based Validation Consultant in the South East to oversee a pharmaceutical project.

We understand that the scope associated with this assignment will be as follows:

* Work closing with Capital Project, Production, QA, and R&D departments to get the validation scopes and agreements to release the desired production status in the agreed timelines.

* Weekly update to report the progress status of the validation works.

* Perform General Validation works for the impacted GMP and non-GMP systems as part of the Capital investment project.

* Update and draft the required validation documentation, including but not limited to CSV/CQV validation protocols, VP, C&QP, SIA, URS, DRR/VRA, IOQ, OCD, C&QR, RTM, and VR.

* Execution and approval of the corresponding protocols to release the required equipment for GMP production.

We understand that the deliverables associated with this assignment will be as follows:

* Weekly validation report.

* Draft, execution, and approval CSV/CQV validation protocols