Regulatory Affairs Specialist | Johnson & Johnson Medtech | Riyadh - Ksa
Johnson & Johnson Medtech
Riyadh, Saudi Arabia
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Sfda registration and submission
Medical device product launch
Variation submission management
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Johnson & Johnson Medtech is seeking a Regulatory Affairs Specialist in Riyadh, Saudi Arabia, to oversee the registration and compliance of medical device products in the local market. The ideal candidate should have a background in biomedical engineering or sciences, along with at least two years of relevant experience.
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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 variation submissions, and coordinating SFDA meetings either directly or through distributors.
The candidate must maintain updated regulatory tracking systems, handle certificate renewals, and provide critical support to commercial teams during tender processes.
Matching Summary
Match Score: 75
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Johnson & Johnson Medtech is seeking a Regulatory Affairs Specialist in Riyadh, Saudi Arabia, to oversee the registration and compliance of medical device products in the local market. The ideal candidate should have a background in biomedical engineering or sciences, along with at least two years of relevant experience.
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Skills & Requirements
Must-have
SFDA registration and submission
Medical device product launch
Variation submission management
Promotional material copy review
Tender support for commercial teams
Nice-to-have
Regional project involvement
Analytical reasoning skills
Detail-oriented execution focus
Strong presentation abilities
Process oriented mindset
Key Requirements
Bachelor's degree in Biomedical Engineering or Sciences
Minimum 2 years of experience in Regulatory Affairs