QA Validation Specialist – Dublin – Biopharmaceutical
CV-Library – Dublin – United Kingdom – My Client based in Dublin is a Global Biopharmaceutical Manufacturer with a need for 2 QA Validation Specialists for two different contracts on site: 6 month contract 12 month contract The QA Validation Specialist would be responsible for ensuring that the relevant level of validation is executed for new systems. The QA Validation Specialist will co-ordination review and support the execution of validation activities. The role reports to the Validation Project Lead Roles and Responsibilities: Responsible for drafting, reviewing and approving commissioning and qualification documentation for new systems and equipment. This may include the development of user and function requirements, support of factory/site acceptance testing, commissioning, and development of performance qualification documents Assisting in determining project schedules and the relevance of appropriate levels of validation. Ensuring Data Integrity per 21 CFR Part 11 / Annex 11 Requirements. Responsibl… – Permanent – Full-timeApply for this job.