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Job Title

Validation Engineer - Contract - Cork






Validation Engineer – 12 month contract. A validation Engineer is required for a dynamic and fast moving Medical Devices manufacturing plant in Cork. Scope. - Manufacturing a wide range of products this is an opportunity to work on a wide range of projects as part of a validation team. - The role is aimed primarily at process validation dealing with supplier and raw material changes across a range of departments, processes and devices. - A small proportion of equipment validation is also included. - This is a full time day shift contract. Key Duties and Responsibilities. - Draft and complete relevant protocols and reports in accordance with the site Master Validation plan. - Engage with relevant Engineering and Quality personnel to collate and evaluate the data and results of the execution and draft the validation reports. - Use knowledge of statistics to assist with validation developments and process improvements. - Support and manage projects on time, within budget and to meet business requirements. - Support Engineering and Manufacturing teams and lead investigations as required. - Provide guidance on and ensure compliance to relevant Quality standards and validation regulations. Requirements. - Strong demonstrated knowledge of and experience in documentation generation and control in a regulated manufacturing environment is required. - A good knowledge of statistical analysis is required. - A good knowledge of relevant standards including ISO 13458, cGMP etc is required. - Ability to work in a fast paced, dynamic environment and collaborate cross functionally is essential. - A Degree in Science or Engineering is required. - A minimum of three years relevant experience is required. For more information and a confidential discussion please call Nigel on 021 4221000 or submit your CV through this website. This job originally appeared on

Date Added

346 days ago