Posted to MedZilla on 4/28/2017


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.

Job Role:

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.

Job Requirements:

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.

To Apply:

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.
In case you have difficulty in applying or if you have any questions, please call Will Hitchcock on +44 203 0789 554 or upload your CV on our website
A full job description is available on request.
ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

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  considered, please do so. Applications for all positions are subject to each employer's specific requirements.