Msra Shweta Parwe's Location
Boston, MA, US
Msra Shweta Parwe's Work
- Associate Director Regulatory and QMS @ Teva Pharmaceuticals
- Regulatory and QMS Sr. Manager @ Teva Pharmaceuticals
- Regulatory and QMS Manager @ Teva Pharmaceuticals
- Product Coordinator- Regulatory Affairs @ Teva Pharmaceuticals
- Regulatory Affairs Co-op @ Teva Pharmaceuticals
- Regulatory Affairs Co-op @ Gecko Health Innovations Inc. (Acq. by Teva Pharmaceuticals)
Msra Shweta Parwe's Education
- Northeastern University
Master of Science (MS) (Regulatory Affairs in Drugs, Medical Devices and Biologics)
2014 - 2016 - Harrisburg University of Science and Technology
Master of Science - MS (Project Management)
2017 - 2019 - University of Mumbai
Bachelor of Engineering (B.E.) (Biotechnology)
2010 - 2014
Msra Shweta Parwe's Skills
- Regulatory Documentation
- Informed Consent
- SOP development
- eCTD
- Regulations
- NDA
- Microsoft Excel
- Biotechnology
- Project Management
- Microsoft Word
Msra Shweta Parwe's Summary
Msra Shweta Parwe, based in Boston, MA, US, is currently a Associate Director Regulatory and QMS at Teva Pharmaceuticals, bringing experience from previous roles at Teva Pharmaceuticals. Msra Shweta Parwe holds a 2014 - 2016 Master of Science (MS) in Regulatory Affairs in Drugs, Medical Devices and Biologics @ Northeastern University. With a robust skill set that includes Regulatory Documentation, Informed Consent, SOP development, eCTD, Regulations and more, Msra Shweta Parwe contributes valuable insights to the industry. Msra Shweta Parwe has 1 email on RocketReach.
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