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Contact Info
James Cassidy
Life Science

+353 1 5079250
james.cassidy@lifescience.ie
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Details

Validation Engineer


Reference:JCHQ00001203 Location: Galway
Qualification:DegreeExperience:5-7 Years
Job Type:Fixed Term ContractSalary: Not Disclosed
May be suitable for: Validation Engineer, Process Engineer

Validation Engineers required by a leading medical devices company based in Galway for a 12 month contract.

Key Job Responsibilities:

Generate validation documentation (URS, IQ, OQ, PQ and process characterisation studies & validation reports) and assist in the execution of protocols for equipment, process, utilities, methods and computerised systems.
Generate collection plans for the qualification and acceptance of incoming components including product sub assemblies.
Troubleshoot validation issues associated with the validation project and provide feedback to the product/process design team.
Ensure consistency on validation/qualification approach across systems and projects. Review and approve changes to equipment, process, utilities, methods and computerised systems to ensure the validation status of equipment is maintained.
Ensure validation documents are up-to-date (primarily project MVPs and key inputs).
Manage the execution of the product/process validation as per the MVP and project plan.
Work directly with customer validation representatives to define inputs and requirements to the MVP.
Ensure all results and data are correct and follow-up on any gaps or discrepancies.
Liaise with the Engineering function to ensure that equipment validation requirements are maintained from Purchase to Qualification of new technology equipment.
Provide guidance and direction in the preparation and execution of validation activities, including carrying out training to staff across various functions.
Maintain validation procedures and templates up to date, focusing on continuous improvement.

Job Requirements:

Degree in Science/Engineering with 3+ years experience in a similar role within the Medical Devices or related Healthcare industry.
Strong knowledge of ISO and FDA quality requirements.
Good understanding of validation concepts and documentation.
Strong communication skills, including ability to advise and influence.
Excellent attention to detail and report-writing ability
Proven ability to work on own initiative.
Highly organized with strong ability to prioritize tasks.
A general knowledge and experience of statistical analysis methods is an advantage.
If you would like further Information you can contact the recruiter directly:

James Cassidy | Tel: +353 (0) 1 5079250