Production Assistant Manager

Bachelor’s degree in Industrial Engineering, Mechanical Engineering, or Pharmacy.

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 ensure the availability and readiness of raw materials, equipment, and manpower 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 check sheets, 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.
• Coordination 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.

How many years' experience do you have as an Assistant Production Manager?

Manufacturing, Transport & Logistics Not specified

PT. Oneject Indonesia is a Medical Devices manufacturer produces Auto Disable Syringes.

As a pioneer of AD syringes manufacturer in Indonesia in providing safe injections, PT. Oneject Indonesia has contributed to reduce the number of standard syringes, which are produced and distributed in Indonesia. Our product is the market leader of AD syringes in Indonesia with 90% market share.

PT. Oneject Indonesia is growing continuously, not only in Indonesia. We have been exported our AD syringes to Asian countries and ready to enter the European market. We ensure the quality of the products at each stage of the production process starting with the selection of medical grade raw materials, the complete manufacturing process to the point of finished product. The products are monitored and controlled by our QC Department as per requirement of ISO 9001:2015 and ISO 13485:2016, in cooperation with our R&D Department, in order to continuously monitor the improvement, innovation and thereby increase our product quality.

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