Posted:20 hours ago|
Platform:
On-site
Full Time
1. DEVELOP DOCUMENTS FOR SUBMISSION TO ETHICS COMMITTEE FOR CLINICAL TRIALS
2. CREATE DOCKETS FOR RESEARCH PAPERS, TECHNICAL REPORTS FOR HEALTH PARAMETERS LIKE GLUCOSE, HEMOGLOBIN, ECG ETC.
3. CREATING DOCUMENTS FOR CE CERTIFICATIONS
4. CREATING DOCUMENTS FOR ISO13485
5. CREATING DOCUMENTS FOR PATENTS
6. CREATING DOCUMENTS FOR FDA APPROVAL
7. ANALYTICAL REPORT AND ALGORITHM PREPARATIONS BASED ON CLINICAL TRIALS
8. BIO SAFETY REPORTS FOR MEDICAL DEVICES
9. CONDUCTING TRIALS, TESTS FOR MEDICAL DEVICES.
10. OTHER ACTIVITIES THAT WILL BE DEFINED BY TEAM.
Job Type: Full-time
Pay: From ₹270,000.00 per year
Experience:
Work Location: In person
miisky technovation pvt ltd
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