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Electronic QA/QC Supervisor

Salary undisclosed

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Company Description

Elitech Technovision, located in Surabaya, is a company that produces electromedical equipment with the brand Elitech. The company meets the requirements of ISO9001:2015, ISO13485:2016, and CPAKB.

Job Description:

  • Develop, implement, and maintain the Quality Management System (QMS) in compliance with ISO 13485 and Good Electromedical Manufacturing Practice (CPAKB).
  • Conduct internal and external audits to ensure compliance with regulations and quality standards.
  • Oversee and evaluate Quality Control (QC) processes to ensure products meet specified standards and requirements.
  • Collaborate with the Production and R&D teams to improve product quality and manufacturing processes.
  • Manage quality documentation, including procedures, policies, and inspection records.
  • Analyze quality data and identify areas for improvement to enhance efficiency and effectiveness.
  • Address and resolve quality-related issues, implementing corrective and preventive actions as needed.
  • Coordinate with external parties such as auditors, regulatory bodies, and customers on quality-related matters.

Qualifications:

  • Bachelor’s degree/diploma in Electrical Engineering.
  • Experience in electronics or electromedical manufacturing is required.
  • Strong knowledge of Quality Control, Quality Assurance, and Quality Management Systems.
  • Experience with Good Electromedical Manufacturing Practice (CPAKB) is a plus.
  • Proven experience in quality auditing, both internal and external.
  • Excellent attention to detail, analytical, and problem-solving skills.
  • Ability to work independently and collaboratively in a team environment.
  • Experience with electromedical equipment is an advantage.

Company Description

Elitech Technovision, located in Surabaya, is a company that produces electromedical equipment with the brand Elitech. The company meets the requirements of ISO9001:2015, ISO13485:2016, and CPAKB.

Job Description:

  • Develop, implement, and maintain the Quality Management System (QMS) in compliance with ISO 13485 and Good Electromedical Manufacturing Practice (CPAKB).
  • Conduct internal and external audits to ensure compliance with regulations and quality standards.
  • Oversee and evaluate Quality Control (QC) processes to ensure products meet specified standards and requirements.
  • Collaborate with the Production and R&D teams to improve product quality and manufacturing processes.
  • Manage quality documentation, including procedures, policies, and inspection records.
  • Analyze quality data and identify areas for improvement to enhance efficiency and effectiveness.
  • Address and resolve quality-related issues, implementing corrective and preventive actions as needed.
  • Coordinate with external parties such as auditors, regulatory bodies, and customers on quality-related matters.

Qualifications:

  • Bachelor’s degree/diploma in Electrical Engineering.
  • Experience in electronics or electromedical manufacturing is required.
  • Strong knowledge of Quality Control, Quality Assurance, and Quality Management Systems.
  • Experience with Good Electromedical Manufacturing Practice (CPAKB) is a plus.
  • Proven experience in quality auditing, both internal and external.
  • Excellent attention to detail, analytical, and problem-solving skills.
  • Ability to work independently and collaboratively in a team environment.
  • Experience with electromedical equipment is an advantage.