Bhavya Chintala

Background

About Bhavya Chintala

R&D Mechanical Engineer with 7years 2months of experience in Product development and sustenance engineering for medical devices and Master Data Management. Skilled in design control procedures per ISO 13485, FDA CFR part 820, CAD tools (Auto CAD, SolidWorks & CATIA V5) Product Development, Good in understanding Manufacturing drawings (GD & T). Sound knowledge and experience Design Verification and Validation, Analyzing Test reports and Protocols, Technical Documentation, Corrective and Preventive Action (CAPA), Defect Prevention Analysis (DPA), Root cause Analysis & 5-Why Analysis. Positions:>Holding Positions related to Data Mining, Master Data Management, Supplier change control, Process validation and verification, Quality deliverables to support EU MDR >Hands on experience in Risk Management activities as per ISO 14971, FDA and ISO regulations Current works: Working on multiple projects for Neurovascular devices like Catheters, Implants, Stents Etc, used for Medication, such as: Process and design verification and validation, Gaps assessment in Process Validation, Supplier change control, Quality deliverables to support EU MDR requirements