CSV Technologist

Wiltshire  ‐ Onsite
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Description

An exciting opportunity has arisen for a Validation Specialist to join a successful and growing Pharmaceutical team in the South East. You will work to manage and execute validation activities associated with the cGMP compliance of computerised and software systems, ensuring that they are appropriately qualified and fit for operational use.

The organisation are very pro-active with employee career development and there are endless opportunities to expand your skill set in the future, within the Quality team should you wish.

Salary: Up to £33,000 plus benefits

Main responsibilities will be to:
  • Lead and execute CSV validation activities of computerised systems and associated equipment in accordance with current regulatory requirements.
  • Minimise business risk associated with the processing and storage of electronic documentation ensuring continuity over the equipment and product's life cycle.
  • Take the lead in computer system validation and compliance projects, manage and deliver specific Validation Projects according to the business priorities, including work scheduling and supervision of junior members of staff.
  • Write, review and approve validation documentation including protocols and reports and manage the timely closure of any discrepancies or non-conformities.
  • Providing a reliable service to our internal customers to ensure that timescales are met and work is carried out to meet expectations.
  • Maintaining the ongoing compliant status of computer systems associated with equipment, facilities and utilities by involvement of the scheduling of activities.
  • Communicating validation activities with our internal and external customers and working with them to resolve problems and conflicts.
  • In line with overall responsibilities, perform additional tasks assigned by the line manager.


This role is a hands-on position and requires the post holder to be able balance multiple project based activities, coordinating the generation, review and execution of validation protocols with the relevant stake-holders.

To apply for this role please email me your CV
Start date
08/2015
From
Real Staffing
Published at
01.07.2015
Project ID:
935151
Contract type
Permanent
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