Sneha Joshi

About Sneha Joshi

Sneha Rajendra Joshi | Regulatory Affairs Professional Regulatory Affairs and Quality professional with a strong background in the pharmaceutical, medical device, and digital health sectors. My experience spans regulatory strategy, regulatory submissions, quality systems, clinical research, and pharmacovigilance.I have supported various regulatory submissions for medical devices and drug products, including work on regulatory documentation, quality processes, and compliance with U.S. FDA and global regulations. My background also includes safety data reporting, risk assessment, and process improvement for regulatory and quality functions.Previously, I worked on global pharmacovigilance projects, managing adverse event reporting and collaborating with regulatory authorities to ensure compliance with international safety and reporting standards. My experience also includes regulatory research, documentation, and quality system development in line with industry regulations and guidelines.I hold a Master of Science in Regulatory Affairs from Northeastern University (GPA 3.97/4.0) and a Bachelor’s degree in Pharmacy, complemented by certifications in Good Clinical Practice (GCP), EU-MDR, and Six Sigma.I am passionate about regulatory science, patient safety, and working across multidisciplinary teams to bring safe and effective healthcare products to market. Regulatory Strategy & Submissions Medical Devices, Drugs & Digital Health Pharmacovigilance & Drug Safety Quality Systems & Risk Management Regulatory Research & Intelligence Compliance & Process ImprovementLet’s connect!

Experience

1. Product Complaint Analyst i

   Boston Scientific

   Nov 2025 — Present · Marlborough, MA, US

Education

• Vivekanand Education Societys College of Pharmacy Sindhi Society Chembur Mumbai 400 071

  Bachelor of Pharmacy - BPharm, Pharmacy

  2015 — 2019

• Northeastern University

  Master of Science - MS, Regularory Affairs