Deskripsi Pekerjaan
Are you a seasoned Quality Assurance professional looking to make a significant impact with a global leader in precision manufacturing? Nolato is seeking a highly skilled and dynamic Quality Manager to join our team in Penang. In this pivotal role, you will be the guardian of our quality standards, driving excellence across our production processes while ensuring strict adherence to international regulatory requirements.
As our Quality Manager, you will lead the implementation and maintenance of the Quality Management System (QMS), ensuring we remain compliant with ISO 13485 and IATF 16949 standards. You will champion a culture of continuous improvement, manage complex audit programs, and serve as the primary quality liaison for our high-profile customers and strategic suppliers. If you are passionate about process optimization, data-driven decision-making, and leading high-performing teams, we invite you to advance your career with us.
Tanggung Jawab
- Oversee and maintain the Quality Management System (QMS) in accordance with ISO 13485 and IATF 16949 standards.
- Lead and facilitate internal and external quality audits, ensuring full compliance and prompt closure of non-conformities.
- Manage the CAPA (Corrective and Preventive Action) process to drive root cause analysis and permanent resolution of quality issues.
- Lead and mentor the quality team, fostering a culture of ownership and high-performance quality standards.
- Collaborate with cross-functional departments to drive continuous improvement in production efficiency and product reliability.
- Manage supplier quality performance, conducting evaluations and audits to ensure materials meet strict specifications.
- Serve as the key point of contact for customer quality concerns, providing technical support and resolution reports.
Kualifikasi
- Bachelor’s degree in Engineering, Quality Management, or a related technical field.
- Minimum of 5-8 years of experience in a Quality Management role within a high-precision manufacturing environment.
- Deep understanding and hands-on experience with ISO 13485 (Medical Devices) and IATF 16949 (Automotive) standards.
- Proven track record in leading successful regulatory and customer audits.
- Expertise in quality core tools (APQP, PPAP, FMEA, MSA, SPC).
- Strong leadership skills with the ability to motivate, develop, and supervise quality personnel.
- Excellent problem-solving skills, with a focus on CAPA, 8D, and lean manufacturing principles.
- Fluent in English and local languages, with strong stakeholder management capabilities.