Quality Supervisor - Medical Equipment - Jakarta (B-125623)

RGF HR Agent Indonesia; Pluit; On-site; IDR 200.000.000 - 300.000.000; Full time

Job summary

A medical equipment company in Jakarta is seeking a Quality Supervisor to manage QMS compliance and oversee quality inspections. The ideal candidate will have a Bachelor's degree in Engineering and at least 3 years of experience in a QA/QC role within the medical equipment manufacturing field. Proficiency in English and knowledge of ISO and GMP standards is required. This role involves significant leadership and analytical skills.

Qualifications

• Minimum 3 years as Quality (QA/QC) Senior Staff in Medical Equipment Manufacture company.
• Proficient in related ISO, GMP, and quality tools.

Responsibilities

• Manage and maintain the QMS in compliance with ISO and regulatory requirements.
• Oversee quality inspections for materials and production.
• Lead internal audits and implement CAPA actions.

Skills

Leadership

Analytical skills

Communication skills

Conversational English

Education

Bachelor's degree in Engineering

Tools

ISO standards

GMP

CAPA

FMEA

SPC

Job description

Quality Supervisor - Medical Equipment - Jakarta (B-125623)

Our client is a Medical Equipment company. Currently, they are looking for a Quality Supervisor.

Responsibilities

• Manage and maintain the QMS in compliance with ISO and regulatory requirements.
• Oversee quality inspections for incoming materials, in-process production, and finished medical devices.
• Lead internal audits, handle non-conformities, and implement CAPA actions.
• Monitor quality performance and drive continuous improvement initiatives.
• Supervise QA/QC staff and coordinate quality activities with production and engineering teams.
• Review and approve quality documentation and support regulatory compliance.
• Other tasks as assigned.

Requirements

• Min. Bachelor's degree in Engineering.
• Min. Conversational English proficiency.
• Min. 3 years as Quality (QA/QC) Senior Staff in Medical Equipment Manufacture company.
• Knowledge of related ISO, GMP, and quality tools (CAPA, FMEA, SPC).
• Excellent analytical, leadership, and communication skills.

Preferred

• Able to speak Mandarin.
• Working experience in Chinese company.

Only CV in English will be processed