Description
A global Pharmaceutical company based in West London is currently seeking the services of a CSV Consultant on an initial 3 month contract.The ideal CSV Consultant will be required to carry out the following tasks:
- Planning and managing validation of high cost, complex, strategic systems using risk based approaches to ensure systems are fit for purpose.
- Preparation and approval of validation documentation or management of the process (fulfilling the Quality Assurance role) in accordance with the relevant processes (e.g. Quality Management System)
- Validation planning for projects including project interaction with IT, software suppliers, and outsource companies.
- Project problem resolution/avoidance - this typically involves ongoing interaction with IT Managers/Directors, site Validation Managers and senior management of suppliers.
- Managing the collection of data for the assigned KPIs and Service Level Agreements
- Providing Compliance oversight and training to internal and external suppliers, e.g., IT teams outside GMS and globally sourced providers, as applicable
The successful CSV Consultant will need to have had 2- 3 years Computer Systems Validation experience within a Pharmaceutical or GMP environment.
This is an excellent opportunity with an attractive hourly rate. If this role is of interest to you please contact Reshma Patel on or alternatively email immediately.