CSV Specialist - 6 Month Contract - South West

England  ‐ Onsite
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Keywords

Description

A leading global Pharmaceutical company based in the South- West of England is currently seeking the services of a CSV (Computer Systems Validation) Specialist for their Global CSV team within their quality function with responsibility for all CSV validation deliverable.

The CSV lead will be responsible for assuring that the Computerised Systems are tested and validated to satisfy FDA regulations and addressing business and compliance needs.

The key responsibilities will include:
  • Working as a CSV Lead on projects.
  • To create and execute validation protocols.
  • Performing site and vendor audits.
  • You will lead the validation assessment which will include - GAP analysis, procedures, training, creating validation plans, reviewing deliverables, reviewing testing coverage, managing change controls and conducting risk analysis.
  • Work on the change control process and possible deviations.
  • Monitor and track compliance and computer validation trends, as well as corrective and preventive actions for the sites and corporate systems
  • Keep updated of the latest developments in computer validation and ensure that all technologies maintain a consistent, compliant, and cost-effective approach


The successful Validation specialist will need to have had 2- 3 years experience in CSV Validation - specifically within a Pharmaceutical or Biotech environment.

If this position is of interest and you would like to discuss it in more detail, please submit your CV or alternatively, contact myself directly on .
Start date
05/2014
Duration
6 Month
From
Real Staffing
Published at
03.06.2014
Project ID:
717443
Contract type
Freelance
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