Job Description
GerTEK is an engineering consultancy company specialising in project management, talent solutions and commissioning qualification and validation services (CQV) to the life sciences and technology sectors. We partner with many of the world's largest life science & technology companies who entrust in us to deliver their most strategic and important projects with our technically strong personnel ensuring all important activities meet both current requirements and client's needs. We are recruiting throughout Ireland for highly experiencedProcess Engineersto join our leading global healthcare client based in Co. Sligo Job Requirements Provide engineering support to all manufacturing and control system related issues. Tasks include, daily trouble shooting, optimisation, cost reduction, training and coaching of manufacturing personnel. Execution of process development on existing products or new late-stage clinical products including scale up to plant equipment. Support Capital project design and review activities, particularly Single use equipment items & setup and/or process improvements. Provide technical support for the aseptic filling and lyophilization of biological drug product. Work closely with the global science and quality teams, on the process development of suitable future products Responsible for ensuring that own work complies with GMP, Data Integrity and Good Documentation Practice (GDP) and is undertaken in accordance with applicable procedures. Identifying continuous improvement activities and leading or participating in cross-functional teams to implement. Supporting activities in the areas of cost reduction, process efficiency and operational excellence. Develop and manage strong relationships across teams to remove barriers, or time lags while performing effectively within own working groups to achieve favourable outcomes for the business. Key Requirements Degree educated in chemical engineering, process engineering or related technical discipline. 3 year's plus professional experience within a Biopharmaceutical environment. Relevant experience of fill finish, batch processing, technical transfers, scale up, commissioning and validation in a cGMP pharmaceutical / biologics industry. Experience in new product introductions to Biologic facilities a distinct advantage Demonstrated project management skills, including the ability to deliver projects on schedule, within budget, and meeting the predefined quality requirements are required. Benefits Highly competitive salaries / hourly rates Career development Mentorship programs Hands-on training Good working culture On-site parking To start the process click the Continue to Application or Login/Register to apply button below.