Computer Systems Validation Consultant

England  ‐ Onsite
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Keywords

Description

A Pharmaceutical company based in the South- West of England is currently seeking the services of a CSV (Computer Systems Validation) for a 12 Month contract.

The Computer Systems Validation consultant 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 Computer Systems Validation Lead on projects.
  • To create and execute Validation protocols.
  • 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 and experience in Computer Systems 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
09/2014
Duration
12 Months
From
Real Staffing
Published at
10.08.2014
Project ID:
756200
Contract type
Freelance
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