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Validation Officer job at Dei BioPharma Ltd | Apply Now
Are you looking for Healthcare jobs in Uganda 2025 today? then you might be interested in Validation Officer job at Dei BioPharma Ltd
Kampala, Uganda
Full Time
About the Organisation
The DEI BioPharma Drugs and Vaccines Manufacturing Plant, which is located at Matugga in Wakiso District, was launched on July 6, 2021, by President Yoweri Museveni and then Kenyan Vice President (now President) William Ruto.
Dei BioPharma Ltd is a leading pharmaceutical company committed to ensuring the highest standards of quality and regulatory compliance in all aspects of our manufacturing processes.
Job Title
Validation Officer job at Dei BioPharma Ltd
Dei BioPharma Ltd
Job Description
Job Title: Validation Officer
Job Type: Full-Time
Industry: Pharmaceutical
Category: Healthcare
Company: Dei BioPharma Ltd
Application Deadline: Friday, April 4, 2025
Location: Kampala, Uganda
Job Posting Date: Friday, March 28, 2025
The Validation Officer is responsible for executing validation activities and maintaining all validation-related documentation to ensure compliance with regulatory requirements.
Duties, Roles and Responsibilities
Prepare, review, and execute process validation protocols and reports.
Conduct validation activities in accordance with the Validation Master Plan.
Develop and implement validation procedures, as well as documentation control systems.
Manage the change control process and evaluate the impact on validated systems.
Implement and manage Continued Process Verification (CPV) programs and annual monitoring.
Perform cleaning validation and hold time studies.
Ensure compliance with GMP standards and maintain readiness for audits.
SERVICES
COMMERCIAL
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INDUSTRIAL
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RESIDENTIAL
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COMMERCIAL
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INDUSTRIAL
SERVICES
RESIDENTIAL
SERVICES
COMMERCIAL
SERVICES
COMMERCIAL
SERVICES
COMMERCIAL
SERVICES
COMMERCIAL
SERVICES
INDUSTRIAL
SERVICES
RESIDENTIAL
Qualifications, Education and Competencies
Education: Bachelor's degree in Chemistry, Pharmacy, Pharmaceutical Sciences, or Chemical Engineering.
Experience: At least 2 years of experience 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 recruitment@deibiopharma.com 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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