Italy, QA Technical Writer, Pharmaceutical QA_WH_11462-MZ
Our client, a multinational pharmaceutical manufacturer, is currently seeking a QA Technical Writer to join them at their site in Southern Italy.
The role will involve writing technical documents such as Validation Master Plan (VMP), Process Validation Protocol (PVP), Process Validation Report (PVR), Cleaning Validation Protocol (CVP) Cleaning Validation Report (CVR), Validation Summary Report (VSR), IQ, OQ protocols and reports of equipments (reactors, centrifuges etc.), IQ, OQ, PQ protocols and reports of nitrogen, air-handling systems, PW (process water), Qualification of facilities and utilities.
The successful candidate will have a proven track record in writing technical documentation in a clear and easily understandable manner. Prior experience of working in the pharmaceutical sector is essential.
Please visit our website at www.proclinical.com