# Regulatory Affairs Associates Job Dawa Life Sciences Nairobi, Kenya

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Company: Dawa Life Sciences Nairobi, Kenya

Category: Accounting

Location: Kenya

Work type: Full-time

Work arrangement: On-site

Published: 2026-08-06

Expires: 2026-09-20

## Job Description

### Key Responsibilities

- Prepare, review, and submit product dossiers, and upload them correctly on each authority’s portal.

- Manage variations and renew product licences on time so our products stay on the market.

- Coordinate the design and approval of packaging artwork, labels, inserts, and leaflets, making sure each country’s labelling rules are met.

- Work with Production, PD, QA, and QC on BMRs, stability data, validation reports, and Methods of Analysis so our filings match what we actually do.

- Follow changes in pharmaceutical regulations in Kenya and the region and advise the business early on what they mean for us.

- Be the main contact for questions from regulators and pull together clear technical responses with the relevant departments.

- Obtain GMP certificates and import/export permits on time and keep all records audit-ready.

### Qualifications and Experience

- To be highly considered, these minimum requirements must be evident on your resume.

- Diploma or bachelor’s degree in pharmacy (B.Pharm), Chemistry, Industrial Chemistry, Biochemistry, Pharmaceutical Sciences, or related science.

- 4–5 years’ Regulatory Affairs experience in pharmaceutical manufacturing, including preparing dossiers for African markets.

- Registration with the Pharmacy and Poisons Board or a relevant professional body.

- Good knowledge of GMP, GLP, and GDP, and of regional regulatory portals and document management systems.

- Strong technical writing, communication, and teamwork skills, with good analytical and organizational ability.

### How to Apply

Send CV and Cover Letter to careers@dawalifesciences.com by

## Requirements

Apply by email: careers@dawalifesciences.com

## Apply

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