Production Section Head (Injection)

PT Oneject Indonesia; Desa Ciranjeng; On-site; IDR 200.000.000 - 300.000.000; Full time

Job summary

A leading medical device manufacturer is seeking a Production Supervisor to oversee syringe production, ensuring adherence to quality and GMP standards. The ideal candidate will have a Bachelor's degree in Industrial or Manufacturing Engineering and a strong background in Plastic Injection Molding. Responsibilities include managing production targets, resolving issues, and leading a team effectively. Candidates should possess good analytical skills and effective communication abilities, with proficiency in English as a plus. Willingness to be placed in Cikarang is required.

Qualifications

• Minimum Bachelor’s Degree in Industrial Engineering, Manufacturing Engineering or related field.
• Strong understanding of Plastic Injection Molding and manufacturing processes.
• Experience in medical device or pharmaceutical manufacturing is preferred.
• Good command of English, both written and verbal.

Responsibilities

• Supervise and control all syringe production activities.
• Ensure achievement of production targets.
• Monitor and resolve production issues.
• Prepare production reports with improvement recommendations.
• Ensure product quality meets specifications.
• Maintain cleanliness and condition of machines.
• Implement Health, Safety, and Environment (HSE) standards.
• Manage manpower planning and scheduling.
• Lead, coach, and evaluate team performance.
• Communicate effectively with internal stakeholders.
• Utilize time management and prioritization skills.
• Use Microsoft Office for reporting.

Skills

Understanding of Plastic Injection Molding

Analytical and problem-solving skills

Good command of English

Education

Bachelor’s Degree (S1) in Industrial Engineering or related

Tools

Microsoft Office

Job description

Qualifications

• Minimum Bachelor’s Degree (S1) in Industrial Engineering, Manufacturing Engineering or related field.
• Strong understanding of Plastic Injection Molding and manufacturing processes.
• Experience in medical device or pharmaceutical manufacturing is preferred.
• Good command of English, both written and verbal.
• Willing to be placed in Cikarang.

Job Responsibilities

• Supervise and control all syringe production activities in accordance with established procedures and GMP standards.
• Ensure achievement of production targets, including output, quality, and lead time.
• Monitor, analyze, and resolve production issues using strong analytical and problem‑solving skills.
• Prepare production reports and present improvement recommendations in a clear and structured manner.
• Ensure product quality meets specifications and customer requirements.
• Maintain cleanliness and proper condition of machines, work equipment, and production areas.
• Implement and monitor Health, Safety, and Environment (HSE) standards in the workplace.
• Manage manpower planning, including work scheduling, task allocation, and team rotation based on capability.
• Lead, coach, and evaluate team performance to ensure operational effectiveness.
• Communicate effectively with internal stakeholders and coordinate with related departments to support smooth production operations.
• Utilize time management and prioritization skills to ensure deadlines and production schedules are met.
• Use Microsoft Office and related software for reporting and operational monitoring.

Company Overview

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 exporting 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.