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Ankit Kanojia

Hey I am on Medial • 23d

Certified ISO 13485 Internal Auditor with 6+ years of comprehensive experience in Quality Assurance (QA) within the medical device industry. Proven expertise in implementing and maintaining Medical Device Quality Management Systems (MDQMS) as per ISO 13485 standards. Highly skilled in handling internal and external audits, regulatory compliance, CAPA, NC handling, risk management, and document control. Successfully led QA processes across the product lifecycle—from design and development to manufacturing and post-market surveillance. Adept at coordinating with cross-functional teams, regulatory bodies, and third-party auditors to ensure product and process quality. Seeking challenging QA roles where I can contribute my deep knowledge of MDQMS, continuous improvement, and quality systems to support organizational growth and regulatory success. looking for the job opportunity

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