- Enlisted FDA regulatory and quality requirements for IVD devices- Created review checkpoints for the reviewers of blogposts, marketing videos, and webinars for social media- Conducted training sessions on how to review and edit articles for the company website.

- Drafted 3 Technical Documentations and 3 GSPRs for CE Submissions and authored 4 Clinical Evaluation Reports - Performed Gap Assessment and Change assessment for re-certification under MDD- Drew up Software Development Plan and SDLC templates IEC 62304: 2015-06- Well-versed with risk management activities, packaging and labeling, PMS and PMCF activities, UDI, GS1 Standards- Comprehensive understanding of IEC 60601-1, IEC 60601-1-2, ISO 10993 Series, ISO 15223-1

- Developed, reviewed, and updated course content on various Learning Management Systems such as BrightSpace, PFx, and Sakai.- Created 100+ effective storyboards for courses targeted towards master’s level students taught by professors from Harvard, MIT, Columbia University.- Created infographics and illustrations for courses created by a leading e-learning solutions provider.

- Market research for surgical equipment, cardiology, consumables, cosmetics, dental, etc.- Identification and Market Analysis for 80+ up-and-coming medical devices for B2B sales- End-to-end vendor onboarding and management

- Performed daily inspection of high-end devices and equipment in addition to troubleshooting, and repair- Performed Preventive Maintenance activities and administrative activities for AMC and CMC of devices and equipment