Dei BioPharma Ltd is a biotech and pharmaceutical research firm duly incorporated in Uganda, specializing in the development and manufacture of innovative medicines and vaccines. Our state-of-the-art manufacturing facility, situated in Matugga, Wakiso district, Uganda, shall produce high-quality medicines across a wide range of therapeutic areas.

Job Summary: To execute validation activities and maintain all validation-related documentation in compliance with regulatory requirements.

Key Duties and Responsibilities:

Prepare, review, and execute process validation protocols and reports
Conduct validation activities according to the Validation Master Plan
Develop and implement validation procedures and documentation control systems
Manage change control processes and evaluate impacts on validated systems
Implement Continued Process Verification (CPV) programs and annual monitoring
Perform cleaning validation and hold time studies
Ensure compliance with GMP standards and maintain audit readiness

Qualifications, Skills and Experience:

Education: Bachelor’s degree in Chemistry, Pharmacy, Pharmaceutical Sciences, or Chemical Engineering
Experience: Minimum 2 years in pharmaceutical manufacturing or validation
Knowledge: Strong understanding of GMP and regulatory requirements

How to Apply:

All interested candidates who meet the required qualifications and experience are invited to submit their CVs, Cover Letter & Academic documents (addressed to the Head Human Capital)

All Application documents should be merged as one document in PDF or .DOC / .DOCX, which should not exceed 10MB

Applications should be sent by email to This vacancy has closed — applications are no longer acceptedApplications closedSee open jobs at Dei BioPharma → with the JOB TITLE IN THE SUBJECT LINE.

Deadline: 4th April 2025

NB: Should you not hear from us within fourteen (14) days from the closing date of this advertisement, you may consider your application to be unsuccessful.

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