Description
Computer Systems Validation Specialist - West Sussex - Contract
My client a leading pharmaceutical company is currently looking to recruit a Computer Systems Validation Specialist to join its team in West Sussex.
Key Skills for the Computer Systems Validation Specialist:
- Experience writing, reviewing and approve validation documents relating to projects and plans to comply with good manufacturing practice and meet both FDA and MHRA requirements
- To ensure computer systems and End User Applications are inspection ready and to provide support for audit plans and corporate, customer and regulatory audits.
- To liaise with IT support groups to ensure all equipment is maintained and updated as required and ensure visiting engineers are supervised and comply with GMP and EHS requirements.
- To interface with the laboratory service providers over the provision of IT service and maintenance, facility servicing/maintenance and equipment servicing provision
- To own the Site Equipment and System Register.
- To be the validation lead for CSV and IT issues and equipment computer systems administration when required
- To participate in the change control process with regard to new equipment installation, changes and decommissioning. Ensuring change controls are raised and plans are created, and tasks completed on time.
- To investigate, trouble-shoots, root-cause and solve laboratory equipment issues (including IT) when these arise, in a timely manner to ensure the downtime of systems is kept to a minimum and all remediation is carried out in compliance with departmental and company procedures.
- To perform Periodic Validation Reviews of IT systems, facilities and equipment. Experience of working within a lab environment
This is a contract role for a Computer Systems Validation Specialist working for a top company. To apply to the Computer Systems Validation Specialist please send a CV or call to discuss options.