We are supporting a well established, global healthcare business, who produce a cutting-edge and very critical medical product to recruit a new Quality/CI Engineer to join their team. The business are very well invested, and have seen a lot of growth in recent years, with significant amounts of R&D activity within the business. This role will work within their Quality department reporting into the Quality Engineering Manager, but will also work very closely with the Operational team - and you will be responsible for supporting and conducting NCR's, Deviations and CAPA's, but with a strong emphasis on this role being to drive Lean, CI and Process Improvement activities within the business. The key responsibilities for the Quality/CI Engineer will involve: Ensuring a strong link between the Quality and Production team is established - carrying out QA/QC reviews, inspections of manufacturing processes. Drive the implementation of Continuous Improvement activities across the business Supporting the business' wider validation tasks, particularly process and equipment related activities. Involvement with new product development initiatives CAPA investigations and reporting Supporting with Product Release and Batch Control tasks The ideal candidate for the Quality/CI Engineer role will have the following background: Good experience working in a Quality department, and with a good understanding of quality systems/processes as well as CI/Process Improvement. Ideally, will have worked within the Pharmaceutical, Medical Device, Biotechnology sector and have a good understanding of GMP/ISO 13485 environments We are also open to considering candidates who come from manufacturing environments with a strong Lean/CI emphasis (ie. Automotive/Engineering) Degree qualified in a Science or Engineering related subject - or have significant professional experience in this area. This role is commutable from: Brighton, Hove, Worthing, Littlehampton, Shoreham by-Sea...