OverviewWe’re currently recruiting for an exciting opportunity with a Pharmaceutical organization based in Cork. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do.DutiesCompile relevant documentation from contractors, suppliers, and other departments for inclusion in reports.Prepare reports for executed protocols for review and approval.Initiate and implement change control activities in accordance with site procedures.Track and resolve exceptions/events/deviations.Prioritize MSAT activities in line with the project schedule.Co-ordinate document review and approval.Collate and organize files for turnover to QADC.Assist in the development of training material.Participate in cross-functional teams as required.Deputise for the Manager or other team member where required.Domestic and international travel may be required.Education & ExperienceBachelors Degree in a scientific/technical discipline requiredCleaning Validation Experience.Experience in a large molecule facility.Experience in other Validation areas (e.g. Process Validation Support (e.g. Mixing Studies, Media Challenge), Thermal Validation, Process Validation).How to ApplyIf interested in this posting please feel free to contact Seán McCarthy on +353 (0)87 798 8480 or sean.mccarthy@lifescience.ie for further information.
#J-18808-Ljbffr