Quality Control Staff - Medical Device Manufacturing Industry

Key Responsibilities:

• Perform incoming, in-process, and final product inspections in accordance with approved procedures.

• Ensure    products   meet    defined   specifications,    quality    standards,   and   regulatory requirements.

• Conduct testing and measurement activities using appropriate inspection tools and equipment.

• Document inspection results accurately in quality records and reports.

• Identify and report non-conformities to the QC Supervisor.

• Support investigation of quality issues and assist in corrective and preventive actions (CAPA).

• Ensure compliance with Good Manufacturing Practice (GMP) and ISO 13485 requirements.

• Maintain cleanliness and orderliness of the production and warehouse and inspection areas.

• Participate in internal audits and continuous improvement initiatives.

Qualifications:

• Minimum Bachelor’s Degree (S1) in Pharmacy, Biomedical Engineering, Chemical Engineering, Medical Laboratory Technology, or other related fields

• Fresh graduates are welcome to apply

• Basic understanding of quality control processes and inspection methods.

• Familiar with GMP and knowledge of ISO 13485 is an advantage.

• Able to use basic measuring instruments (e.g., caiper, micrometer, etc.).

• Strong attention to detail and analytical thinking.

• Good documentation and reporting skills.

• Proficient in Microsoft Office.

• Able to work independently and in a team environment.

• Willing to work in shifts if required.

• Willing to be placed in Cikarang, West Java

• Non-smoker (mandatory requirements)