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2 Job openings at Hexamed Technologies India Private Limited
Biomedical Engineer – Quality Assurance / Quality Control

Hyderābād

1 years

INR 2.4 - 3.6 Lacs P.A.

On-site

Full Time

Quality Control (QC): Perform routine inspections, calibrations, and validations of medical devices and hospital equipment. Monitor and document performance and safety metrics of equipment. Maintain and update equipment service history and maintenance logs. Ensure preventive maintenance is conducted on schedule and documented. Regulatory & Compliance: Ensure equipment complies with national and international regulations (CDSCO, AERB, BIS, etc.). Support documentation and filing for certifications, licenses, and renewals. Review and approve technical specifications from suppliers/vendors. Technical Support: Provide troubleshooting support for technical and operational issues related to biomedical equipment. Coordinate with vendors, engineers, and OEMs for repair, replacement, and calibration. Evaluate new medical technologies and support procurement processes. Ensure adherence to ISO 13485, NABH, CE, and other relevant regulatory and safety standards. Conduct root cause analysis and implement corrective and preventive actions (CAPA) for product/process deviations. Assist in internal and external audits and ensure timely closure of non-conformities. Job Type: Full-time Pay: ₹20,000.00 - ₹30,000.00 per month Benefits: Health insurance Schedule: Day shift Fixed shift Morning shift Supplemental Pay: Yearly bonus Education: Bachelor's (Preferred) Experience: total work: 1 year (Preferred)

Biomedical Engineer - Quality Assurance / Quality Control

hyderabad, telangana

1 - 5 years

INR Not disclosed

On-site

Full Time

As a Quality Control (QC) professional, you will be responsible for conducting routine inspections, calibrations, and validations of medical devices and hospital equipment. Your role will involve monitoring and documenting the performance and safety metrics of equipment, as well as maintaining and updating equipment service history and maintenance logs. It will be essential to ensure that preventive maintenance is conducted on schedule and properly documented. In the area of Regulatory & Compliance, you will play a crucial role in ensuring that the equipment complies with national and international regulations such as CDSCO, AERB, and BIS. You will be responsible for supporting the documentation and filing for certifications, licenses, and renewals, as well as reviewing and approving technical specifications from suppliers/vendors. Your Technical Support responsibilities will include providing troubleshooting support for technical and operational issues related to biomedical equipment. You will need to coordinate with vendors, engineers, and OEMs for repair, replacement, and calibration tasks. Additionally, you will be involved in evaluating new medical technologies and supporting procurement processes while ensuring adherence to ISO 13485, NABH, CE, and other relevant regulatory and safety standards. As part of your role, you will be required to conduct root cause analysis and implement corrective and preventive actions (CAPA) for product/process deviations. You will assist in internal and external audits and ensure timely closure of non-conformities. This is a Full-time job opportunity that offers health insurance benefits, a Day shift, Fixed shift, Morning shift schedule, and a Yearly bonus. The preferred educational qualification for this position is a Bachelor's degree, and the preferred total work experience required is 1 year. If you are looking for a challenging role where you can contribute to ensuring the quality and compliance of medical equipment while providing technical support and maintaining regulatory standards, this position might be the right fit for you.,

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