Number of vacancies: Two (2)
Location: Dawa Life Sciences, Ruaraka
Brief Job Description:
We are looking for a highly driven, detail-oriented, and tech-savvy Regulatory Affairs AI-Powered Intern to accelerate our dossier preparation and submission pipeline using AI and digital tools. This fast-paced, high-learning role offers hands-on exposure to real pharmaceutical regulatory systems, where the intern will help streamline dossier compilation, improve documentation consistency, and support efficient, compliant regulatory submissions. This role is ideal for a high-potential life sciences graduate who is eager to build strong Regulatory Affairs fundamentals, develop practical industry skills, and fast-track their growth into a top-tier Regulatory Affairs professional while delivering measurable impact.
Key Responsibilities
AI-Enabled Regulatory Acceleration
Leverage AI tools (ChatGPT, document parsing, OCR, automation) to:
- Draft dossier modules summaries
- Extract, organize, and cross-reference content from multiple documents
- Create submission checklists
- Compile regulatory documentation
- Cross-check dossier completeness and consistency
- Support accelerated dossier preparation and submission while ensuring accuracy, quality and compliance
- Reduce dossier compilation time from days to hours through AI
- Collaborate with the Regulatory Affairs team to meet submission requirements and timelines
- Supporting multi-country registrations across East Africa
Qualifications and Experience:
Must Have: Minimum Requirements
To be considered, these minimum requirements must be evident on your resume.
- Degree in: Pharmaceutical Sciences, Biotechnology, Biomedical Sciences, Life Sciences, Computer Science, Engineering or Data Science
- Ability to execute tasks efficiently and deliver results within the shortest time.
- Tech-savvy and comfortable using AI tools daily