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 via :
ic.eightfold.ai
