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