Sarupa Giri Verma

4+ years of expertise enhancing procedures, quality, and profitability in the aerospace and medical device industries. Experience in driving the and monitoring the supplier audit schedule, following up on the audit scheduling, conducting the audit, reporting the audit, and concluding the audit. Proficiency in checking that the products and services of the company follow to internal policies and business requirements. Have strong experience with Medical devices and Aerospace standards like AS9100, MILSTD, ISO 13485, ISO 9001:2015, ISO 14971, QSR 21 CFR Part 820 (198, 200), ISO 14971, ISO 11607, FDA standards and compliance, Requirement Specifications, designing Requirement Traceability Matrix (RTM), Supplier Corrective Actions (SCARs). Resourceful, analytical, and detail-oriented with the ability to finish several projects.

I am working as a Supplier Quality Engineer in Q-Tech Corporation. Where my day to day responsibilities are performed root cause analyses for any defects, nonconformities, and other quality failures, and encouraged follow-up on the completion of supplier CAPA actions and supplier process improvement initiatives. I am also solely responsible for keeping track of the supplier audit schedule, following up on the audit scheduling, carrying out the audit, and reporting and closing out audit. Moreover, I led supplier and internal audits in adherence for the compliance to AS9100 and ISO 9001 regulations and standards to ensure the effective implementation of Quality Management System.

I have completed my Bachelor in Respiratory Therapist in 2018, where my main focus was studying regarding the medical devices components such as Catheter, Ventilator etc. I have vast knowledge regarding Catheter and expert in Adult and Children immunization. I am working towards my next goal is to become Certified Quality Auditor (CQA).