Engineering & Production Assisten Manager

We are looking for an experienced professional to lead our Engineering and Production activities for Medical Devices Manufacturing, while ensuring that production processes run efficiently, consistently, and in compliance with the quality standards of the medical device industry.

Key Responsibilities

• Work closely with the superior to plan resource requirements for engineering and production activities.

• Plan, coordinate, and supervise maintenance programs (preventive, predictive, and corrective) to keep machines ready for operation and minimize downtime.

• Handle PLC programming, modification, and troubleshooting, as well as production machine control systems.

• Manage the operation, setup, and maintenance of high-precision part machines to maintain accuracy and consistency of production output.

• Analyze and resolve electrical and mechanical issues on both machinery and facilities/buildings.

• Prepare and maintain technical documentation, including machine specifications, operational SOPs, maintenance schedules, and repair records.

• Analyze cycle time and machine capacity to achieve efficient production processes and meet targets.

• Monitor production activities and provide technical support to ensure smooth operations.

• Drive continuous improvement in work methods, machinery/equipment, and production processes.

• Ensure that products meet applicable quality standards and regulations.

Qualifications

• Minimum Bachelor’s degree in Electrical Engineering/Mechatronics Engineering, or Industrial Engineering.

• At least 5 years of experience in the Pharmaceutical/Medical Devices/Automotive/Electronics manufacturing industry.

• Strong knowledge of electrical and mechanical systems of industrial machinery.

• Proficient in PLC programming and troubleshooting, as well as machine programming.

• Experienced in handling high-precision part production machines.

• Comprehensive understanding of the end-to-end production process.

• Good understanding of TPM, TQM, and OEE concepts.

• Knowledge of ISO standards (ISO 13485 preferred), GMP, and Halal Product Assurance System (SJPH).

• Good command of English, both spoken and written.

• Strong analytical and problem-solving skills.

• Hardworking, adaptable, committed, dedicated, and possesses high integrity.

• Able to work under pressure and collaborate effectively in a team.

• Willing to be placed in Depok, West Java.