Real R

Validation Specialist (BB-D7CE2)

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My client, a well-known pharmaceutical company based in Co.Wicklow, are looking for a Validation Specialist to join their Validation team.You will be a part of the wider quality department, and will work closely with production on validation activities.As Validation Specialist, you will be responsible for;Co-ordination of Process Validation, Cleaning Validation activity and Equipment Validation in the Production DepartmentPreparation 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 VMPContribute to achievement of VMP and site targets Education & Experience:Degree level qualification in a scientific or relevant disciplineA minimum of three years' validation experience within the Pharmaceutical/Medical Devices Industry is required.Company Culture:You will be joining a team that has an excellent reputation on the market as a great place to work. You will join an experienced team of quality professionals where the aim is professional development and delivering high quality standards.There is a great culture on site with open and transparent ways of working.*Excellent salary and benefits package on offer with this role*To find out more about Real please visit Real 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 | OC(phone number removed) England and Wales

calendar_today17 hours ago

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