Jackson Hogg are delighted to be supporting a specialist systems integration business on the appointment of a Senior Validation Engineer. We are looking for experienced Validation Engineers with a passion for solving problems, engineers who take responsibility for delivering great results, who pay attention to detail but drive for progress, who understand what “Success looks like” and are not afraid to put themselves out there for the benefit of customers. Responsibilities Provide a positive proactive experience to our customers, by delivering great quality work, on time and budget so that they can benefit from your skills and experience. The work will need you to understand the customer’s problems, and key drivers for the changes that are to be made and ensure that you deliver the work on time and in a way that helps the customer resolve their issues. You will be working across some of our most valued customers’ manufacturing sites you'll be taking responsibility for ensuring that manufacturing processes, packing operations, equipment, cleaning, utilities/facilities, computer and analytical methods are fully validated to meet the expected and operational requirements, GMP and regulatory requirements. Your communications skills will be excellent ensuring clear and concise stakeholder communications both internally and externally. About You You'll have working knowledge in Computerised Systems Validation (CSV) and/or Computer Software Assurance (CSA) within the Biotech/Med Device/ Pharmaceutical (FDA/MHRA regulated industries). Must have working knowledge of cGMP, GxP, GAMP5, FDA 21 CFR Part 11, Eudralex Annex 11 and Data Integrity Regulations. Additional experience working in pharmaceutical or medical devices manufacturing and packing. Working knowledge of Eudralex Annex 15, Eudralex Annex 1, ISO 13485, ISO 14971 and ISO 62304 would also be desirable. If this sounds like something you would be interested in, apply today