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 47 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 multifunctional teams
Disclaimer: Drjobpro.com is only a platform that connects job seekers and employers. Applicants are advised to conduct their own independent research into the credentials of the prospective employer.We always make certain that our clients do not endorse any request for money payments, thus we advise against sharing any personal or bank-related information with any third party. If you suspect fraud or malpractice, please contact us via contact us page.