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.