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
APPLY USING THE LINK BELOW:
Internship – Regulatory Affairs at Medtronic
