Quality Manager

Huge Dental; Tangerang; Sur place; IDR 180 000 000 - 240 000 000; Plein temps

Résumé du poste

Shandong Huge Dental Material Corporation in Tangerang, Indonesia seeks a qualified professional to lead the development and operation of the quality management and safety systems for medical device manufacturing. You will organize internal audits and management reviews, implement corrective and preventive actions, and drive quality improvements across functions.

The role requires a bachelor’s degree in quality-related fields and at least 3 years in quality management within medical devices or

Qualifications

• Bachelor’s degree or above in Quality Management, Biomedicine/Pharmaceuticals, Materials & Chemical Engineering, Law, or related majors.
• Over 3 years of quality management experience in the medical device or pharmaceutical manufacturing industry.
• Familiar with local laws and regulations and quality system supervision requirements.
• Meticulous and detail-oriented, with excellent writing skills, strong communication and coordination abilities, and strong execution.

Responsabilités

• Establish, maintain, and organize quality management system activities and certifications.
• Lead internal audits, management reviews, and corrective/preventive actions.
• Organize quality analysis meetings and track improvement measures.
• Supervise inspection processes, handle complaints and nonconforming products, and review quality data reports.

Connaissances

Quality management

Regulatory compliance

Documentation

Communication

Auditing

Formation

Bachelor's degree in Quality Management / related fields

Description du poste

• Responsible for the establishment, maintenance, and the organization, coordination, inspection, and assessment during the implementation and operation of the quality management system; responsible for the preparation, organization, and implementation of company quality certification;
• Responsible for the establishment, maintenance, and the organization, coordination, inspection, and assessment during the implementation and operation of the safety and occupational health management system;
• Under the leadership of the Management Representative, organize and implement internal audits and management reviews, and take corrective and preventive actions on the system;
• Organize quality analysis meetings, provide corresponding quality improvement requirements, and organize and track the implementation of quality improvement measures;
• Supervise and review the inspection process, complaints, nonconforming products, returns and exchanges, and quality anomaly handling measures, as well as review quality data analysis reports;

Job Requirements

• Bachelor's degree or above in Quality Management, Biomedicine/Pharmaceuticals, Materials & Chemical Engineering, Law, or related majors;
• Over 3 years of quality management experience in the medical device or pharmaceutical manufacturing industry;
• Familiar with local laws and regulations and quality system supervision requirements;
• Meticulous and detail-oriented, with excellent writing skills, strong communication and coordination abilities, and strong execution;

Proficiency in spoken Chinese or English preferred