Posted:3 months ago|
Platform:
Work from Office
Full Time
Role & responsibilities 1. Handling of Facility, equipment and utility qualification activities. 2. Preparation and review of Quality SOPs. 3. Handling of Vendor management. 4. Good knowledge in ISPE, EMA, FDA 21 CFR & ICH guidelines. 5. Handling of QMS elements. 6. Handling of equipment breakdowns. 7. Experience in HVAC, EMS and BMS qualification activities. 8. Having process knowledge is an added advantage. Department: Biotech Development Quality Assurance(DQA) Experience: 2-7 years Qualification: M.Sc, B.Pharma & M.Pharma Preferably from Biotech Companies. Please share resume to below mentation mail id dinesh.baratam@msnlabs.com
MSN Group
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3.0 - 8.0 Lacs P.A.