Bachelor's or Master's degree in Engineering, Biomedical, Life Sciences, or a related field.
Minimum of 6 years of experience in risk management within the medical device industry.
In-depth knowledge of ISO 14971 and global regulatory requirements (FDA, EU MDR / IVDR, TGA, etc.).
Strong background in risk analysis tools : FMEA, FTA, HACCP, etc.
Experience with Class II / III medical devices preferred.
Excellent problem-solving, analytical, and decision-making skills.
Strong communication and leadership skills.
Experience working in cross-functional, global teams.
Certifications such as RAC, CQE, or Six Sigma are a plus.
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Risk Management • India
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