Qualifications: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.