Regulatory Affairs Intern at Medtronic

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.