
Computer System Validation Engineer
- Waterford
- €70,000-80,000 per year
- Temporary
- Full-time
- Integrally involved in the validation of all new computerised equipment, and control systems.
- Generates validation documentation (protocols/reports) and provides assistance with the execution of protocols for computerised equipment and systems.
- Participates in the change control process advising on CSV issues, as appropriate
- Hands on role in the development and execution of DQ, IQ, OQ and PQ activities.
- Ensures projects are managed in compliance with all required Sanofi and legal requirements (Health & Safety, cGMP, construction, environmental etc).
- Designs, implements and executes validation studies for manufacturing and control equipment. Additional responsibilities for critical systems and facilities as well as validation studies to satisfy regulatory compliance.
- Provide technical assistance on current US FDA and EU validation requirements for lyophilization, aseptic processing and sterilisation.
- Ensure that the validation status of equipment and systems are in compliance with cGMP at all times.
- Maintain validation documentation through the
- Approval and implementation of changes to relevant systems and assist in generating validation/ revalidation plans
- Generate/review/approve execution of the validation/revalidation plan.
- Review and approval of site change controls
- Ensure compliance to cGMP at all times
- Initially 100% onsite; after the first few months, up to two days per week remote working may be possible (on of the working days needs to be Monday or Friday)
- Degree in Science (Chemistry, Micro. or Pharmacy preferred) or Engineering (Chemical/Mech/Elec
- 3-5 years experience working in a Healthcare manufacturing environment – ideally part of which would be in the pharmaceutical sector.
- 2-3 years experience in validation environment
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