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COMPANY OVERVIEW
Our Client is world leader in providing superior health and safety protection solutions that enhance human well-being.
JOB RESPONSIBILITIES
Main Tasks:
Quality Management Systems
Our Client is world leader in providing superior health and safety protection solutions that enhance human well-being.
JOB RESPONSIBILITIES
Main Tasks:
Quality Management Systems
- Ensure that the Quality System is established, implemented, and maintained to meet the requirements of ISO 9001 and other relevant Quality Systems and PPE regulation.
- Report the Quality System effectiveness to Top Management and Management Team and make recommendation for improvements.
- Ensure the promotion of awareness of QMS, regulatory and customers’ requirements throughout the plant.
- Ensure that processes needed for the quality management systems are established, implemented, maintained and effective.
QMS Management Review
- Organize and conduct the scheduled QMS Management Review Meeting.
- Review the suitability and effectiveness of the Quality System.
QMS Internal Audit and external Audit
- Lead auditor of the local Internal Audit team
- Lead the team and ensure effectiveness of QMS Internal audits.
- Be the liaison person and Quality Management Representative for all external audits.
- Provide technical and quality advice related to process and product improvement.
Laboratory Testing and Calibration
- Ensure continued accreditation of QC Lab against ISO/IEC 17025.
- Administer the laboratory testing/ inspection activities which include incoming materials, in-process solutions/ compounds/ product, finished product and effluent testing as well as environment control.
- Provide necessary support in inter-plant product testing and benchmarking program.
- Administer the Calibration Program of the company concerning testing/ inspection and relevant measuring and process control equipment.
Subordinates
- Inventory, recommend and provide training to ensure the QA and Lab personnel have adequate skills to carry out their responsibilities and to consistently improve the quality of work.
- Recruit, promote and take disciplinary actions as the situation demands with respect to QA and lab personnel.
- Develop subordinates through training, delegation, coaching and other techniques to maintain organization effectiveness.
Others
- Coordinate the implementation of Global Procedures or standardization.
- Provide the necessary support for the new product, process and software validation.
- Be the liaison person among the marketing, technical support and manufacturing functions for product improvement and matching to the plant’s capability.
- Participate in and support continuous improvement initiatives.
- Work to standardize processes across factories.
- Participate in inter-plant audits as requested.
- Meet corporate compliance EMS and SHE requirements.
- Support implementation efforts of Six Sigma and World-Class Manufacturing in the plant.
- Participate in local Standards Committees where relevant.
- Any other duties as assigned by her Superior
JOB REQUIREMENTS
- Degree/ Diploma holder. Science or Polymer Science discipline is preferred.
- 5+ Experience in QA or related manufacturing environment. 2+ years in similar capacity
- A certified Lead Auditor – Quality Management System.
- Familiar with the Regulatory requirements for various type of gloves.
- Familiar with the Statistical Techniques, process Improvement Tools used in manufacturing process e.g. SPC, Six-Sigma.
- Extensive experience in handling external quality audits and internal audits.
- Experience in Customer Relation Management.
- Highly motivated and able to work independently. Excellent leadership.
- Good command of the English Language. Strong written and verbal communication skills.
- Good interpersonal and organizational skills.
- Ability to communicate across all levels internally/ externally and across geographies.
- Strong analytical skills and attention to details.
- Strong drive for results and commercial access.
- Team player.
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