Job Requirements:
Demonstrated success in delivering results on time with Quality.
Participate in testing and development of medical device by following regulations and standards (IEC62304, ISO13485, ISO14971, IEC 60601)
Follow Medical device software testing process and customer specific needs in testing process.
Support external lab testing like TUV, UL
Writing test protocols for safety critical medical devices.
Follow development practice by using the tools such as IBM DOORS, RQM, JIRA, Github etc.
Work Experience
3-6 years’ renal care device experience in writing and reviewing test cases/protocols for safety critical medical devices.
Experience on Medical devices or software test cycle
Exposure in IEC62304 standards in embedded medical devices following IEC 60601
Experience in Manual & Automation testing
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