Internship – Regulatory Affairs at Medtronic

Begin your life-long career of exploration, innovation, and championing healthcare access and equity for all. Join a healthcare technology company that alleviates pain, restores health, and extends life for more than two people every second.

A Day in the Life

• Prepares submissions, for new products for Delve markets and any other allocated – ensures adequate follow up with Agencies timely approval for market release
• Provides tender support for Delve  markets .
• Works within RA team to support all relevant  OU regulatory needs
• Helps providing an on-going support to Delve commercial teams for  all regulatory issues and questions
• Communicates and interfaces primarily with internal contacts. May communicate with regulatory agencies in conjunction with line manager
• Keeps abreast of regulatory procedures and changes in regulatory environment and communicate to the RA Line function
• Supports in developing solutions to a variety of technical problems of moderate scope and complexity. Participates in planning and recommends solutions in problem solving discussions

Must Haves:

• Recent graduate
• Degree in Life Sciences, Pharmacy, Pharmaceutical Sciences
• Knowledge of MS Office tools
• Flexible and adaptable to changing priorities
• Innovative
• Able to establish objectives and achieve results
• Good interpersonal skills
• Motivated, driven, committed

Nice to Have

• Experience in regulatory affairs with medical devices
• Able to communicate effectively to with various stakeholders
• Able to plan, manage and execute projects within budget and on schedule

Program details:

• Start date: February
• Full-time (40 hours per week)
• Based in Nairobi, Kenya
• Work model: in the office