Role summary
Key ResponsibilitiesRegulatory Affairs:Ensure compliance with applicable medical device regulations (e.g., SAHPRA, FDA, EU MDR, ISO 13485, ISO 14971).Prepare, submit, and maintain product registrations, licenses, and approvals with regulatory authorities.Monitor regulatory changes and advise…
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SalesAIUI
- LOCATION
- Cape Town, Western Cape
- WORK MODE
- On-site
- JOB TYPE
- Full-time
- POSTED
- Oct 14, 2026
- CLOSING
- Nov 13, 2026
Source: Job Mail Public Jobs