Regulatory Post-Market Surveillance & Vigilance Specialist
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Regulatory Post-Market Surveillance & Vigilance Specialist with 4+ years of medical device complaint handling experience (8+ years total professional experience), specializing in global regulatory reporting (eMDR, EU MDR, FDA 21 CFR Part 820/803/806) and ISO 13485-compliant QMS. Skilled in preliminary complaint classification, IMDRF risk coding (Hazard, Harm, Severity), product analysis review, MDSAP-aligned documentation, and cross-functional collaboration. Proven track record in process improvement, audit readiness, and high-accuracy complaint file closure.
Vigilance Specialist - Medtronic Engineering & Innovation Center - Hyderabad, India
(2022-06)
Senior Technical Support Associate - Tech Mahindra - Hyderabad, India
(2018-09 - 2022-06)
Customer Service Executive - HSBC - Visakhapatnam, India
(2017-01 - 2018-09)
Bachelor of Technology (B.Tech) - Computer Science Engineering - MVGR College of Engineering (2016)