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Regulatory Affairs Associate Job Tasa Pharma
Tasa Pharma
Nairobi 🇰🇪 Kenya
Posted about 6 hours ago (24 Oct 2026) Updated about 6 hours ago
Job Description
The Regulatory Affairs Associate ensures that all pharmaceutical products comply with local and international regulations. They prepare and submit dossiers to health authorities, monitor legislative changes, and advise internal teams on compliance matters. The role also supports cross‑functional projects to maintain product quality and market authorization.
Qualifications & Requirements
- • Bachelor’s Degree in Pharmacy, Life Sciences, or a related field
- • 2–4 years of experience in regulatory affairs within the pharmaceutical industry
- • Strong knowledge of local and international regulatory guidelines
- • Excellent written and verbal communication skills
- • Ability to manage multiple projects and meet tight deadlines
Required Skills
Responsibilities
- • Monitor regulatory updates and assess impact on product pipelines
- • Prepare and submit registration dossiers and amendments to health authorities
- • Liaise with internal teams to ensure compliance throughout product development
- • Maintain accurate records of all regulatory communications
- • Provide guidance on labeling, advertising, and post‑market surveillance requirements