Quality Systems Officer
ARC International Middle East LLC
Total des années d'expérience :21 years, 10 Mois
Prepare internal audits annual plan to assure compliance of standards ( ISO 9001, ISO 22000 requirements)
Execute ISO 9001& ISO 22000 internal audits for plant annually. Reporting audit findings to the relevant persons and follow up corrective and preventive actions execution
Responsible for maintenance & compliance to ISO 9001: 2008. & ISO 14001 Documentation & regular updating of Master Files, Quality records & its monthly/Quarterly review
Prepare department monthly reports for achievements compared with planned target and establish monthly action plan for the department and follow up execution of established plan
Creating Quality Awareness within the company & promoting Quality achievement & Performance Improvements across the organization by preparing and sharing the Monthly Newsletter.
To share awareness of customer requirements and any complaints to identify any areas that may need development or improvement by preparing & sharing Quality alert.
Conducting audit of ARC Company standard Like AIS and APS. It’s covering Lean, Reliability, Quality and safety standards.
Conducting training & Monitoring the projects of FMEA, VSM, SPC & Ergonomic Improvements.
Co-ordinate with other department improves the process with help of PDCA Philosophy.
Conducting 5S & Visual management Audits to improve work culture.
Oversee Lean transformation initiatives. Establish value stream relationships and continuous flow strategy. Develop program acceleration strategies, analyzed learning curves and strategic lean implementation plans by VSM & Process flow tools.
Initiated and facilitated Process Action for critical business activities. analyzed problem areas, recommended solutions, executed them, and evaluated their effectiveness with teams.
To help in preparation of SOP, related to Quality Assurance & manufacturing activities.
Skilled in planning and implementing new processes, procedures and tools for quality assurance testing, defect tracking, status reporting and problem resolution
Measure & Analysis the SMED process to improve job change time and improve productivity
Monitoring, Conducting and analysis SPC & R&R study.
Conduct safety risk assessments on departments with team and provide risk mitigation measures.
Provide HSE improvement proposals stating: the non-conformance, proposed corrective action, required resources for corrective action and plan of implementation.
Supervising all Quality Control related jobs, Inspection of Products, calibration of instruments required for Process Control & Product Control
Responsible for the development of product and process quality plans, including control plans, procedures, inspection plans, and other quality documentation
Member of Cross Functional Team to prepare PPAP for new product
Member of Cross Functional Team to prepare CONTROL PLAN, FMEA for existing and new
product
Initiate and/or participate in corrective action and problem solving activities.
Managed quality assurance activities and audits of supplier quality programs.
Supporting member of the Quality Team - provide specific guidance and direction to general staff as well as department managers, functional owners in implementation of the quality system and compliance with quality standards and regulations
Drive process improvement and problem solving thru 7 QC tools principals
Provides support in the way of development and evaluation of process capability, process control plans, analysis of out-of-control conditions and process audits.
Report on the performance of the quality system to executive management for review
Maintain the ISO 9001 Quality Management system.
Conducting Internal Audit for QMS & EMS as per plan.
Hosts & supports Internal, Customer and Third Party Audits as required
Vendor development and Evaluation
Maintain 5S on shop floor
Supervising all Quality Control related jobs, Inspection of Products, calibration of instruments required for Process Control & Product Control
Evaluating the product quality at every stage of processes.
Coordinated in conducting deep analysis to reduce the internal defects with a circle committee.
Ensuring compliance with production standards & continuous improvement in process capabilities during the manufacturing process.