A Day in the Life

The purpose of the position is to ensure regulatory compliance for the region of responsibility, managing projects and assignments to ensure that Medtronic therapies are approved. Enabler for internal customers.

Internship details:

Start date: 4 November 2024
Duration: 12 months
Location: Johannesburg
Working hours: 40 h/week
Working model: hybrid

Responsibilities may include the following and other duties may be assigned:

Support in coordination and preparation of document packages for regulatory submissions from all Operating Units and departments for countries across the region
Support in compiling all materials required in submissions, license renewal and annual registrations
Network across departments to ensure that products are approved for the market
Monitor and improves tracking/control systems
Perform post market requirements

Required knowledge:

Recently graduated with a degree in Logistics, Management or Regulatory Affairs 
Ability to communicate effectively in English
Strong MS office skills

Would be a plus:

System Analysis Program experience
Team player

Physical Job Requirements

The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.