Validation Engineer

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My Client, a well-established pharmaceutical company based in Wicklow are looking for a Validation Engineer to join their team.This role would see you working in a cross-functional environment supporting both the Quality Assurance and Regulatory Affairs teams. You will be responsible for the performance and execution of Production and Cleaning Validation. The primary focus of the role will be on validation transfers of existing products to new equipment within the site. As Validation Engineer you will;Responsibility for the co-ordination of Process Validation, Cleaning Validation activity and Equipment Validation and maintaining validation/qualification status in the Production Department.Preparation and execution of validation and re-validation protocols and reports, (IQ / OQ / PQ), for the validation of equipment, systems, products and projects.Responsible for Investigating and resolving deviations associated with validation studies.Acting as the primary point of contact for all Production related Validation matters as well as internal and external compliance audits or regulatory inspectionsProcess Validation regulatory requests relating to the VMP Education & Experience;A minimum of two years' validation experience within the Pharmaceutical/Medical Devices IndustryDegree level qualification in a scientific or relevant discipline This is a great opportunity to join an excellent company with a well known reputation as a great place to work!Excellent salary and benefits package available with this role! To find out more about Real please visit www.realstaffing.comReal Staffing, a trading division of SThree Partnership LLP is acting as an Employment Agency in relation to this vacancy| Registered office | 1st Floor, 75 King William Street, London, EC4N 7BE, United Kingdom | Partnership Number | OC387148 England and Wales