Regulatory Affairs Specialist | Johnson & Johnson Medtech | Riyadh - Ksa
J&J FAMILY OF COMPANIES
Riyadh, Saudi Arabia
Not specified (assumed to be onsite based on location)
Launch medical device products in saudi arabia
Prepare registration and re-registration files
Manage sfda meetings and submissions
Johnson & Johnson is seeking a Regulatory Affairs Specialist for their MedTech division in Riyadh, Saudi Arabia. The role focuses on the registration and compliance of medical devices in the Saudi market, requiring strong regulatory knowledge and communication skills
Job Summary
The primary purpose of this role is to launch medical device products in the Saudi Arabia market while ensuring full compliance with regulatory registration and importation guidance.
Responsibilities include preparing and submitting product files, managing SFDA meetings, supporting distributors, and conducting copy reviews for promotional materials on time.
Johnson & Johnson MedTech offers an inclusive work environment where employees are respected for their diversity and merit while working towards breakthroughs in healthcare innovation.
Matching Summary
Match Score: 75
Johnson & Johnson is seeking a Regulatory Affairs Specialist for their MedTech division in Riyadh, Saudi Arabia. The role focuses on the registration and compliance of medical devices in the Saudi market, requiring strong regulatory knowledge and communication skills.
Skills & Requirements
Must-have
Launch medical device products in Saudi Arabia
Prepare registration and re-registration files
Manage SFDA meetings and submissions
Update regulatory tracking systems
Conduct copy review for promotional materials
Nice-to-have
Experience with regional projects
Strong analytical reasoning skills
Detail-oriented execution focus
Process oriented approach
Effective presentation and communication
Key Requirements
Bachelor's degree in Biomedical Engineering or Sciences