Quality Validation Engineer

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Quality and Validation Engineer-Cleanroom Manufacturing

Liverpool

Excellent salary plus benefits

Are you an experienced Quality Engineer with working knowledge of of ISO 13485 and ISO 14971, looking for an exciting opportunity with a fast growing pharmaceutical manufacturer.

The position offers excellent working conditions, job security and really superb job satisfaction.

Part of the goal of the position will be to enable the business achieve BS EN ISO 15378:2017 as a supplier for Primary packaging materials for medicinal with a view of becoming fully cGMP compliant by 2023 so there is something really worthwhile to work towards.

The roleFull time permanent position working Mon-Fri working in the pharmaceutical/cleanroom manufacturing sectorBuild and maintain the quality system for the cleanroom operationGuide the business towards compliance to applicable standards such as ISO, FDA-QSR and GMP.The personWoirking experience to include practical application of ISO 13485, ISO 14971 and FDA Quality System Regulation CFR 21 Part 820.GMP experience mandatory. .Applied technical knowledge of Qualitative and Quantitative data analysis, and statistical tools.Project Management experience/qualificationsThis is a superb opportunity to join a company at exactly the right time