Assistant Quality Manager
location_onKuala Ketil, Kedah, Malaysiaschedule6 jam lalu
badgePekerjaan:Sepenuh masa
historyPengalaman minimum:5+ tahun
schoolPendidikan:Ijazah sarjana muda
Penerangan kerja
Job Responsibilities
- Assist the Quality Manager in overseeing the company's quality management system and daily quality-control activities.
- Lead and supervise the Quality Assurance and Quality Control teams to ensure products meet company, customer and regulatory requirements.
- Develop, implement and maintain quality procedures, work instructions and inspection standards.
- Monitor incoming materials, production processes and finished products to ensure compliance with quality specifications.
- Investigate customer complaints, product defects and non-conformance issues.
- Lead root-cause analysis and implement corrective and preventive actions (CAPA).
- Coordinate internal, customer, supplier and regulatory audits.
- Monitor supplier quality performance and work with suppliers to resolve quality-related issues.
- Analyse quality data and prepare reports on defect rates, customer complaints, audit findings and improvement actions.
- Work closely with Production, Engineering, Procurement and other departments to improve product and process quality.
- Conduct quality training and promote continuous improvement throughout the organisation.
- Ensure quality records and documentation are properly maintained and controlled.
- Support compliance with relevant quality standards and regulatory requirements.
- Perform other quality-related duties assigned by management.
Requirements
- Diploma or Bachelor's Degree in Quality Management, Engineering, Manufacturing or a related discipline.
- At least 5 years of quality-related experience in a manufacturing environment.
- Experience in the medical device or healthcare manufacturing industry will be an added advantage.
- Previous supervisory or team-management experience is preferred.
- Good understanding of Quality Assurance, Quality Control, CAPA, root-cause analysis and continuous improvement.
- Familiarity with ISO 9001; knowledge of ISO 13485 or relevant medical-device regulations will be advantageous.
- Experience handling internal, supplier, customer or regulatory audits.
- Able to use quality tools such as 8D, 5 Why, Fishbone Analysis, SPC and FMEA.
- Good command of Mandarin and Bahasa Malaysia to communicate with relevant employees, suppliers and stakeholders.
- Strong leadership, analytical, communication and problem-solving skills.
- Detail-oriented, responsible and able to work effectively across different departments.
- Open to candidates of all genders and ages.
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