Qc jobs in Indonesia

Bachelor’s degree in Industrial Engineering or Mechanical Engineering.

Minimum 4–5 years of experience in manufacturing, preferably in the medical device industry.

Strong knowledge of production systems, Lean Manufacturing, Total Productive Maintenance (TPM), and quality control.

Proven leadership and problem-solving skills, with the ability to manage, coach, and develop production teams.

• Lead production teams for medical devices.
• Direct and coordinate production personnel to ensure efficient and smooth operations.
• Monitor team performance, ensure compliance with GMP and quality standards, and maintain workplace safety.
• Achieve production targets through effective team management.

• Prepare annual technical work plans and ensure achievement of production goals.
• Develop annual production plans with measurable objectives and timelines aligned to company targets.
• Monitor progress, evaluate implementation, and identify risks or obstacles.
• Implement corrective actions to ensure efficient execution.

• Ensure availability of materials, resources, and production-ready machines.
• Coordinate with relevant departments to guarantee raw materials, equipment, and manpower are ready for production.
• Monitor inventory levels and machine readiness to support continuous operations.
• Prevent production delays by ensuring all resources are prepared and in optimal condition.

• Supervise all production stages from start to finish.
• Ensure operations comply with GMP, safety regulations, and company quality standards.
• Identify deviations or non-compliance issues and implement corrective actions to maintain production integrity.

• Review defects, scrap, and downtime to identify root causes.
• Implement corrective and preventive actions to improve production efficiency and product quality.

• Direct, train, and provide coaching to Section Heads, Officers/Leaders, and Operators.
• Enhance team skills, performance, and overall productivity.

• Oversee production documentation, including checksheets, output reports, traceability records, and daily forms.
• Ensure all documentation is accurate and meets compliance and quality standards.
• Collaborate with QA for inspections, approvals, and quality improvement initiatives.
• Coordinate with QA to ensure compliance with standards and enhance production output.
• Collaborate with Engineering, Maintenance, and Warehouse for design changes, troubleshooting, machine reliability, and material readiness.
• Ensure smooth and continuous production operations by resolving technical issues and maintaining equipment reliability.

PT. Oneject Indonesia is a Medical Devices manufacturer producing Auto Disable Syringes. As a pioneer of AD syringes manufacturer in Indonesia, we provide safe injections and have contributed to reducing the number of standard syringes. Our product is the market leader of AD syringes in Indonesia with 90% market share.

We are growing continuously, not only in Indonesia, exporting to Asian countries and ready to enter the European market. We ensure quality of the products at each stage of the production process, from selection of medical grade raw materials, through the complete manufacturing process to finished product. Our QC Department monitors and controls products per ISO 9001:2015 and ISO 13485:2016, in cooperation with our R&D Department, to continuously improve innovation and product quality.