both customer-provided and Plexus-developed test solutions. Defining and supporting calibration and preventative maintenance processes. Validating test systems/fixtures for compliance with ISO13485 and FDA 21 CFR 820 standards. Performing failure analysis and yield improvement actions on PCBAs and complete end products. Utilizing problem-solving More ❯
the business working closely with staff at all levels of the organisation. You will take a prominent role leading/driving internal and external ISO13485 and MHRA audits. There are a number of key projects led and supported by the quality team that need to be delivered … or pharmaceutical Quality Assurance, Senior Quality Assurance, Principal Quality Assurance Engineers or QA Specialists. All candidates should have strong experience leading or closely supporting ISO13485/MHRA audits, driving QA projects across a business and leading/coaching/mentoring junior colleagues in the QA function. Exposure to leading or More ❯
role in the business working closely with staff at all levels of the organisation. You will take a prominent role across internal and external ISO13485 and MHRA audits. There are a number of key projects led and supported by the broader quality team that need to be … are looking for an experienced medical device, life sciences or pharmaceutical Quality Assurance Engineer or Quality Assurance Specialist. Candidates should have some experience supporting ISO13485/MHRA audits, contributing to QA projects across a business and possess good generalist QA and some QC experience. Exposure or knowledge of FDA accreditation More ❯
