# Regulatory Affairs Associates at Dawa Life Sciences

Canonical URL: https://primejobalerts.com/jobs/regulatory-affairs-associates-at-dawa-life-sciences

Company: Dawa Life Sciences

Category: Accounting

Location: Kenya

Work type: Full-time

Work arrangement: On-site

Published: 2026-08-06

Expires: 2026-08-12

## Job Description

Regulatory Affairs Associates at Dawa Life Sciences

View Jobs in Science

/

View Jobs at Dawa Life Sciences

Posted: Aug 6, 2026

Deadline: Aug 12, 2026

Save

Email

@gmail.com@yahoo.com@outlook.com

Never pay for any notarisation, certificate or assessment as part of any recruitment process. When in doubt, contact us

We are continuously upgrading to new technologies and implementing robust processes to ensure we deliver best-in-quality products to our communities

Read more about this company

Regulatory Affairs Associates

Job Type Full Time

Qualification BA/BSc/HND , Diploma

Experience 4

- 5 years
Location Nairobi

Job Field Pharmaceutical

### 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

Ideal Candidate Requirements

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.

Check how your CV aligns with this job

## Requirements

Apply by email: careers@dawalifesciences.com

## Apply

Use the canonical Prime Job Alerts page for full application instructions and source verification.
