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Pharmaceutical Regulatory Affairs Manager Job Vacancy in Gitarama, Rwanda – Healthcare & Regulatory Compliance

Novartis Rwanda
📍 GitaramaCDI🗓️ 29 days ago

Job Description

Gitarama
CDI

Your safety comes first — read before you go. Taf4All only lists job offers published by third parties. We are not the employer, we do not conduct these recruitments, and we cannot guarantee what happens once you make contact — you deal directly with the person or company behind the offer, at your own risk.

Position: Pharmaceutical Regulatory Affairs Manager Company: Novartis Rwanda Location: Gitarama, Rwanda Experience: Minimum 7 years in pharmaceutical regulatory affairs, with at least 3 years in a managerial role within Sub-Saharan Africa Education: Master’s degree in Pharmacy, Pharmaceutical Sciences, Regulatory Affairs, or related field. Additional certification in Regulatory Affairs (RAC) preferred Employment Type: Full-time Industry: Healthcare & Pharmaceutical Department: Regulatory Affairs & Compliance Vacancies: 1 Company Overview Novartis Rwanda is a leading global medicines company operating at the forefront of healthcare innovation in Rwanda. We use innovative science and digital technologies to create transformative treatments in areas of great medical need. Our mission is to reimagine medicine to improve and extend people’s lives, and we are committed to bringing life-saving and life-enhancing pharmaceuticals to the Rwandan population. As part of our expansion in East Africa, we are establishing a robust regulatory affairs hub in Gitarama to ensure compliance with Rwanda Food and Drugs Authority (FDA) regulations and facilitate timely access to innovative medicines. We offer exceptional Career Opportunities in Rwanda for professionals dedicated to advancing public health through regulatory excellence. Job Overview We are seeking an experienced Pharmaceutical Regulatory Affairs Manager to lead our regulatory strategy and submissions in Rwanda. This senior role is critical for ensuring all Novartis products meet local regulatory requirements for registration, licensing, and post-marketing surveillance. The successful candidate will serve as the primary liaison with the Rwanda FDA and other health authorities, managing the entire product lifecycle from clinical trial applications to market authorization and renewals. This position represents a unique Job Vacancy in Rwanda for regulatory professionals seeking to impact healthcare delivery at a national level. You will join a dynamic team committed to bringing innovative therapies to patients while maintaining the highest standards of regulatory compliance. For

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