SUMMARY OF JOB FUNCTION: Required to perform quality assurance activities for the Wafer fabrication development and manufacturing teams. The site develops and manufactures Indium Phosphide wafers, processing them through to individual chips. KEY RESPONSIBILITIES: QMS Implementation and Maintenanc e:Develop, implement, and maintain the company’s Quality Management System (QMS) in compliance with ISO 9001 and TL900 0.Manage and oversee all aspects of the QMS, ensuring it is effectively integrated across all departments and function s.Ensure the QMS documentation is up-to-date and accessibl e.Compliance and Auditin g:Conduct internal audits to assess compliance with QMS procedures, identify non-conformities, and initiate corrective and preventive action s.Support external audits and ensure timely resolution of any audit finding s.Process Improvemen t:Continuously assess the effectiveness of the QMS and implement improvements to optimize processe s.Work cross-functionally to ensure all departments follow established quality standards and practice s.Analyse quality performance metrics and identify areas for improvemen t.Facilitate PFME AsTraining and Suppor t:Provide QMS training to staff and ensure proper understanding of quality requirements, procedures, and best practice s.Support teams in implementing QMS changes and improvement s.Act as a liaison between various departments, ensuring quality objectives are aligned across the organizatio n.Documentation Control and Reportin g:Manage and control all quality-related documentation, ensuring it is accurate, secure, and compliant with regulation s.Track and report key performance indicators (KPIs) for QMS performance and quality initiative s.Prepare detailed reports for senior management on quality trends, audits, and improvement initiative s.Problem Solvin g:Support internal 8D process and coordinate 8D meeting s.Address customer complaints or concern s. Qualificati ons:Educat ion:Bachelor’s degree in Engineering, Quality Management, or a related fi eld.Certifications (Preferr ed):Certified Quality Auditor, Certified Quality Engineer (CQE), or other relevant certificati ons.Core Tools (FMEA, SPC, MSA)VDA 6.3 Experi ence:Minimum 5-7 years’ experience in a quality management or QMS role, preferably within a manufacturing or production environ ment.Previous experience of working within a cleanroom environment (Prefe rred)Previous working experience with Oracle, Agile or PROMIS (or similar sys tems) S kills:Strong understanding of quality management systems, particularly ISO 9001, IATF 16949, or equivalent stan dards.Experience in conducting internal audits, managing non-conformities, and applying CAPA princ iples.Familiarity with continuous improvement methodologies such as Six Sigma, Lean, or K aizen.Strong problem-solving and analytical skills, with the ability to assess processes and drive c hange.MS Office – Inc. Word, Excel, Email and Powe rPointCalibration Experience (Pref erred) PERSONAL REQUIR EMENTS:Strong attention to detail with excellent organizational and documentation skills.Ability to integrate quickly into an existing team, and able to demonstrate having strong inter-personal communication skillsTarget ori entatedCapable to work independently on give n tasksDue to rural location of the site and not being served by public transport – own transportation is es sential Lumentum Technology UK Ltd is an Equal Opportunities Employer