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Pharmaceutical Regulatory Affairs Manager Job Vacancy in Gitarama, Rwanda – Healthcare & Regulatory Compliance
CDI30 days ago
Job Description
Nyagatare, Rwanda
CDI
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Position: Biomedical Device Regulatory Affairs Manager Company: Medtronic Rwanda Location: Nyagatare, Rwanda Experience: 5-8 years Education: Master’s degree in Biomedical Engineering, Regulatory Affairs, Life Sciences, or related field Employment Type: Full-time Industry: Medical Technology & Regulatory Compliance Department: Regulatory Affairs & Quality Assurance Vacancies: 1 Company Overview Medtronic Rwanda is the regional subsidiary of Medtronic plc, a global leader in medical technology, services, and solutions. With operations spanning over 150 countries, Medtronic is dedicated to alleviating pain, restoring health, and extending life for millions of people worldwide. In Rwanda, we are committed to advancing healthcare through innovative medical devices and technologies, collaborating with healthcare providers, regulatory bodies, and communities to improve patient outcomes. Our presence in Nyagatare supports Rwanda’s vision for enhanced medical infrastructure and access to cutting-edge healthcare solutions. We foster a culture of integrity, inclusion, and collaboration, empowering our team to make a meaningful impact in the medical technology sector. As we expand our regulatory and compliance operations in East Africa, we seek passionate professionals to join our mission-driven organization. Job Overview We are seeking a highly skilled Biomedical Device Regulatory Affairs Manager to lead our regulatory compliance and submission strategies for medical devices in Rwanda and the broader East African region. This role is critical in ensuring that our innovative medical technologies meet all local and international regulatory requirements, facilitating timely market access and patient availability. The successful candidate will navigate complex regulatory landscapes, engage with the Rwanda Food and Drugs Authority (Rwanda FDA) and other regulatory bodies, and develop comprehensive regulatory pathways for new and existing products. This position offers a unique opportunity to shape the regulatory framework for advanced medical devices in a rapidly evolving healthcare market. If you are passionate about regulatory science and improving healthcare access, we encourage you to explore this career opportunity. For
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