Remote Regulatory Data Specialist (RIM)

Medtronic plc; Bogotá; Híbrido; COP 60.000.000 - 90.000.000; Jornada completa

Descripción de la vacante

Medtronic plc in Bogotá, Colombia is seeking a Regulatory Information Management Analyst to support global regulatory data and processes in a remote working model. The role focuses on maintaining regulatory information within RIM systems, ensuring data quality, and supporting modernization initiatives across regions and time zones.

You will collaborate with Regulatory Affairs and IT teams to optimize submission structures, data attributes, and templates while delivering timely support to end

Formación

• Bachelor's degree in Life Sciences, Public Health, Business, or a related discipline.

Responsabilidades

• Serve as a primary point of contact for internal users of Regulatory Information Management systems, providing support and issue resolution.
• Create and maintain submission structures, regulatory records, and business data attributes within the RIM environment.
• Build and manage system templates, including submission assembly templates and related configurations.
• Perform data entry, data cleansing, and master data governance activities to ensure data accuracy and integrity.
• Support implementation and sustainment activities associated with the RIM modernization program.
• Participate in project meetings, providing status updates, identifying risks, and supporting mitigation activities for assigned deliverables.

Conocimientos

Regulatory information management

Data governance

Regulatory affairs processes

End-user support

Microsoft Excel

Educación

Bachelor's degree in Life Sciences or related

Herramientas

RIM systems

Microsoft Office

Descripción del empleo

Medtronic plc in Bogotá, Colombia is seeking a Regulatory Information Management Analyst to support global regulatory data and processes in a remote working model. The role focuses on maintaining regulatory information within RIM systems, ensuring data quality, and supporting modernization initiatives across regions and time zones.

You will collaborate with Regulatory Affairs and IT teams to optimize submission structures, data attributes, and templates while delivering timely support to end