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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
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