Validation Engineer

Team Horizon is seeking a Validation Engineer for our client’s Technical Operations team in the Northwest. This is a fixed term contract for 12 months and will report to the Validation Team Lead. * This role is a fully on-site position in Ireland, are you willing to relocate? * Do you have authorisation to work in the EU? Why you should apply: * This role will provide you the opportunity to get exposure to a broad range of validation activities on site, and you * You will be responsible for co-ordinating the development and maintenance of the company’s validation program in compliance with all applicable regulatory and company requirements. What you will be doing: * Co-ordinate, implement and participate in the site Validation Program. * Ensure all computerised systems are qualified in compliance with Data Integrity policies and regulatory requirements. * Co-ordinate / direction and participate in the validation of site equipment, facilities, utilities, processes and software in compliance with company policies, FDA, European cGMP and GAMP standards. * Generate/maintain Validation Master Plans. * Generate /maintain Project Validation Plans. * Generate validation plans, write protocols and final reports to cGMP standard. * Review / approve of protocols and final reports as required. * Manage validation change control process. * Adhere to and support all EHS & E standards, procedures and policies. What you need to apply: * 3rd level qualification in a relevant engineering or scientific discipline. * A minimum of 2 years’ experience in a cGMP regulated pharmaceutical manufacturing environment. * High level of attention to detail and mental concentration, to ensure accuracy and compliance. Excellent communications skills with the ability to write protocols and reports. * Proven problem-solving skills and the ability to adapt to new regulatory requirements. * This role is a fully on-site position in Ireland, are you willing to relocate? * Do you have authorisation to work in the EU?