Regulatory Affairs Specialist Job Corevix
Medical Jobs. Corevix Jobs
At COREVIX, we are committed to redefining the aesthetics industry across East Africa by enhancing access to the world’s finest beauty and wellness innovations. Through a network of premium medical spas and a portfolio of high-quality consumables, we deliver cutting-edge treatments, advanced technology, and expert-driven solutions. Guided by excellence, innovation, and a customer-centric approach, we strive to inspire confidence, transform lives, and shape the future of aesthetics in the region.
Role Description
This is a full-time on-site role for a Regulatory Affairs Specialist located in Nairobi County, Kenya. The Regulatory Affairs Specialist will be responsible for preparing and submitting regulatory documents, ensuring compliance with regulatory requirements, managing regulatory submissions, and staying up-to-date with regulatory affairs. The Specialist will also liaise with different departments to ensure all regulatory documentation is accurate and meets relevant standards.
Qualifications
- Experience with Regulatory Documentation and Regulatory Submissions
- Knowledge of Regulatory Compliance, Regulatory Requirements, and Regulatory Affairs
- Strong attention to detail and excellent organizational skills
- Ability to work collaboratively and communicate effectively with cross-functional teams
- Bachelor’s degree in a relevant field such as Life Sciences, Pharmacy, or Chemistry
- At least 2 years of experience in regulatory affairs or a related field
- Proficiency with regulatory software and data management systems
- Fluency in English and Swahili would be an advantage
How to Apply
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