Location(s): Gurugram, Haryana, India ⋅ Haryana, India
Experience Level(s): Senior
Field(s): Data & Analytics
Work Flexibility: Hybrid
What you will do-
Understanding of end-to-end complaint lifecycle
Collect data from multiple sources such as Trackwise and translate the data into meaningful Power BI Dashboards and visualizations
Author and peer review Post market plans/reports on JR products sold worldwide.
Provide technical expertise in data analysis, data preparation and performance monitoring
Build, manage and maintain reports, dashboards and visualizations as needed
Communicate key findings to business partners and leadership throughout the organization
Help develop automated solutions for dashboard and report generation
Generate and analyze metrics and make recommendations as required
Generate data for Competent Authorities (FDA, BSI and other regulatory bodies).
What you need-
Required-
Experience on Post Market Surveillance as per US FDA & EU MDR; Quality Management (ISO 13485 or 21 CFR 820) and experience with TrackWise and Microsoft Project
Minimum 4-7 years of experience in Medical Device domain
Understanding on Medical Device Risk Management
Strong Analytical and Statistical Skills (proficient in Advance Excel, Power BI. Tableu, Minitab)
Preferred-
Ability to influence and motivate the cross functional team.
Project management experience and experience to lead & achieve global process improvement efforts.
Experience of working with multiple teams and collaborating across geographically spread multi-functional teams