Summary
Date Posted: Tuesday, January 17, 2023 , Base Salary: Not Disclosed

JOB DETAILS:

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

Job Experience: No Requirements

Work Hours: 8

Level of Education: Bachelor Degree

Job application procedure

Interested and qualified? Go to Medtronic on medtronic.eightfold.ai to apply

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