LSC have a requirement for a Cleaning Validation Technical Specialist to join our team at biopharmaceutical client based in Dublin.
As the Cleaning Validation Technical Specialist you will be required to:
-Author, and maintain the Cleaning/Validation Master Plan to support the startup of the multi-product drug substance manufacturing facility.
-Development and/or optimize cleaning (CIP) cycles/methods/recipes for buffer and media preparation systems, upstream (bioreactors) and downstream equipment trains, parts washers and supporting process equipment.
-Generate and execute cleaning validation protocols, plans and reports as required.
-Work closely with colleagues within the Technical Services team, and with Quality, Commissioning, -Manufacturing Operation, and Automation MCS to ensure CIP recipes, batch record instruction and standard work practices meet the needs of startup, technology transfer, and routine manufacturing timelines in the context of cleaning validation.
-B.Sc. in Biochemistry, Biology, Chemistry or equivalent, or B.Eng. Process or Chemical Engineering.
-2 – 4 years’ experience in Cleaning verification/validation / Technical Services / Manufacturing / Technical Development/Quality Support in pharma.
Contact Kathy on 021 4777329 or email@example.com for further details on this and more validation roles.