Sowmya Naidu Sunkara

Sowmya Naidu Sunkara

Project Coordinator Qa/Ra Labelling @ Teleflex

About Sowmya Naidu Sunkara

Sowmya Naidu Sunkara is a Project Coordinator QA/RA Labelling at Teleflex in Athlone, County Roscommon, Ireland, with a background in quality assurance and pharmaceutical sciences.

Title

Sowmya Naidu Sunkara holds the position of Project Coordinator QA/RA Labelling at Teleflex. In this role, she coordinates with various teams to secure IPNs and GTINs for product labeling, manages the master product code/SKU list for medical devices, and maintains label tracking metrics for bi-weekly and monthly meetings.

Company

Currently, Sowmya Naidu Sunkara is employed at Teleflex in Athlone, County Roscommon, Ireland. Her responsibilities include coordinating with EUDAMED, Regulatory, and other teams to ensure accurate and compliant labeling of medical products. Previously, she has worked with companies such as TestReach, NIBRT, and MANKIND PHARMA LTD.

Education and Expertise

Sowmya Naidu Sunkara has a solid educational background in pharmaceuticals and biopharmaceutical technology. She studied Pharmaceutical Sciences at Athlone Institute of Technology, obtaining expertise in Biopharmaceutical Technology. Prior to this, she studied at Raghu College Of Pharmacy, completing her education there over four years.

Professional Experience

Before her current role at Teleflex, Sowmya Naidu Sunkara served as a Remote Invigilator at TestReach for 3 months and a Trainee at NIBRT National Institute for Bioprocessing Research and Training for 2 months. Additionally, she worked as a Quality Assurance Analyst for MANKIND PHARMA LTD for 2 years, where she gained extensive experience in quality assurance in Visakhapatnam, India.

Project Coordination in QA/RA Labelling

In her role at Teleflex, Sowmya Naidu Sunkara oversees multiple facets of QA/RA labelling. She processes DCOs in Agile and other document control systems for regulatory submission, collaborates with operations Procurement Team leads and other stakeholders to process SQAs and SAFs documents, and generates Label Change Request forms to initiate updates by labeling design centers. Her role is crucial in ensuring the accuracy and regulatory compliance of product labels.

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