Asavari Dandekar

Expertise In Product Development & Engineering Leadership. at IZiel Healthcare

Asavari Dandekar (PMP) has extensive experience in the healthcare industry, having worked in various engineering and project management roles at companies like IZiel Healthcare, Medtronic, Philips Healthcare, and GE Healthcare. With a background in Computer Science, Asavari's expertise lies in leading medical device software projects for compliance with regulations and standards, requirements analysis, development and testing, safety and security risk analysis, and Agile Project Management. Prior roles include responsibilities such as owning product development, managing cross-functional teams, collaborating with customers and stakeholders, and driving program delivery with quality and on-time execution.

Location

Bengaluru, India

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IZiel Healthcare

IZiel Healthcare is an Engineering & Regulatory Services provider working successfully for global medical device manufacturers from our offices in USA & India. Our engineers are trained as per Design for Six Sigma – Black Belt Level and have completed various projects in Design, Process Validation, QMS Documentation, Regulatory Approvals & Acquisition Integration for Class I, IIa, IIb & III Products. We leverage statistical & data-driven methods, domain knowledge & robust work planning methodology to achieve an optimized product development processes for guaranteed success. IZiel Healthcare provides services in: Design - Systems Engineering and Requirements Management - Transfer Function Development - Predictive Engineering - 3D Modelling & Finite Element Analysis (FEA) - Design Controls Process & Software Validation - PVMP - IQ, OQ, PQ - Test Method Validation (TMV) - Productivity Improvement - Software Validation (IEC 62304) Risk Management - ISO 14971 based Risk Management - FMEA and FTA Based Product Risk Analysis - Quantitative Risk Management Expertise Quality Management Systems and CAPA - QMS Documentation with Procedures & Templates - CAPA (Corrective & Preventive Action) Regulatory - USFDA & CE Approvals - MDD – MDR Conversion - Clinical Evaluation Report (CER) - European Authorised Representative (EAR) Remediation - Resolve Observations (Form 483), Warning Letters etc - Product Remediation Training - Training – DFSS Methodologies and Engineering Topics


Headquarters

Pune, India

Employees

51-200

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