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Crewe, Cheshire
Principal Validation Specialist
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Salary: £45000 - £50000 per annum + + Benefits |
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Overview
Principal Validation Specialist- £45,000-50,000 - Cheshire A leading Pharmaceutical Manufacturer based in Cheshire are seeking an experienced Validation Specialist for a 12 Month Fixed Term Contract. We will be looking for the individual to be able to develop and execute qualification & validation protocols. The Principal Validation Specialist will also generate reports to support the implementation of site projects. This is a great opportunity to join a leading manufacturing organisation in the North West who are deemed as experts within the Validation world. Whats on offer? Salary up to £50,000 Great career progression working for a leading Pharma Manufacturer Generous benefits package Major Responsibilities / Accountabilities: Developing validation master plans, protocols, reports and to generate related summary reports Support site engineering project managers in developing and reviewing and approving URS documents, specifications, assessments, acceptance criteria and test/inspection requirements and any other related validation procedures Assist in pre-qualification commissioning activities Execute installation, operational and performance qualification protocols and related documentation. Ownership of any related Q&V deviations to resolution and closure Owning, initiating and updating as required Q&V related change controls, events, CAPAs and improvement actions Qualification/ Skills & Attributes: Knowledge of HSE within a Pharmaceutical organisation Life Sciences degree is beneficial 3-5 Years minimum experience of working within Validation Technical writing experience Compliance & regulatory background within pharma If you would like to be considered for the position please submit an application or contact Sarah Kesaulija on 01179 309 708 This job was originally posted as www.totaljobs.com/job/89677843