Akbar Jilani

Sr Executive Post Market Surveillance| Post Marketing Surveillance|ISO 13485 FDA Medical Device Regulation For QMS|Medical Device Vigilance officer|Medical Device Complaint Handling

Role
Sr Executive Product Surveillance at Vantive
Location
Gurugram, HR, IN
LinkedIn followers
500 followers
Manufacturing & ProductionView LinkedIn profile

About Akbar Jilani

Working as a Medical Device Safety & Vigilance Associate. PROFESSIONAL STRENGTHS…

Experience

  1. Sr Executive Product Surveillance

    Vantive

    Nov 2024 — Present · Gurugram, IN

    Medical Device Complaint Management: Expertise in managing and monitoring medical device complaints, ensuring compliance with EU MDR guidelines, and reporting adverse events and malfunctions.2. Vigilance Reporting: Active involvement in EU MDR vigilance reporting, including timely submission of Manufacturer Incident Reports (MIR) and compliance with regulatory requirements. Complaint Handling: Proficient in various stages of complaint handling such as intake, Medical Device Reporting (MDR), investigations, and quality assurance.4. Complaint Intake Management: Experienced in handling mailbox complaints, assigning cases to the team, and ensuring complaint creation within established timelines (3 days).5. TrackWise Documentation: Skilled in creating complaints in TrackWise, conducting due diligence by following up with reporters for missing information, and ensuring accuracy in complaint records.6. Complaint Approvals: Verified complaint information, created associated records (e.g, Complaint Evaluation, EU MDR Decision Tree, and MIR), and ensured adherence to regulatory standards.7. Defective Sample Handling: Monitored defective sample status and coordinated shipping to investigation plants via UPS, ensuring proper tracking and documentation.8. Investigation Coordination: Assigned complaint evaluations to investigation plants, followed up for timely results, and ensured thorough resolution of issues.9. EU MDR Decision Tree (DT) Processing: Evaluated complaints using ARPC and DVAD codes to determine reportability per EU MDR 2017/45 guidelines.10. Vigilance Report Drafting: Drafted, reviewed, and submitted initial, combined, and final vigilance reports (MDR and MIR) to regulatory authorities within prescribed timelines (e.g, 15 days for initial reports).11. Customer Communication: Prepared and sent customer response letters (CRLs), providing investigation results and root cause analysis for complaints.12. Good customer service skills.

Education

  • Sikkim University, Gangtok

    Bachelor of Pharmacy - B.Pharm

    2016 — 2020

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Akbar Jilani — Sr Executive Product Surveillance at Vantive in Gurugram, HR, IN | Unifers