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QC Analyst - Finished Product job at Dei BioPharma Ltd | Apply Now
Are you looking for Medical jobs in Uganda 2025 today? then you might be interested in QC Analyst - Finished Product 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.
Job Title
QC Analyst - Finished Product job at Dei BioPharma Ltd
Dei BioPharma Ltd
Job Description
Job Title: QC Analyst - Finished Product
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 QC Analyst - Finished Product will be responsible for conducting quality control testing of semi-finished and finished pharmaceutical products, ensuring compliance with GMP standards, and supporting efficient laboratory operations.
Duties, Roles and Responsibilities
Perform chemical analysis of semi-finished products, finished products, and stability samples using approved methods.
Develop and execute stability protocols and method validation studies.
Manage laboratory inventory, including reagents and HPLC columns.
Prepare and update standard test methods, product specifications, and standard operating procedures (SOPs).
Generate and analyze monthly KPI reports related to finished product testing.
Collaborate with quality assurance and production teams to maintain product compliance and quality standards.
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COMMERCIAL
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INDUSTRIAL
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RESIDENTIAL
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COMMERCIAL
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INDUSTRIAL
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RESIDENTIAL
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COMMERCIAL
SERVICES
COMMERCIAL
SERVICES
COMMERCIAL
SERVICES
COMMERCIAL
SERVICES
INDUSTRIAL
SERVICES
RESIDENTIAL
Qualifications, Education and Competencies
Education: Bachelor’s degree in Pharmaceutical Sciences or Analytical Chemistry (Master’s preferred).
Experience: 2-3 years of experience in a pharmaceutical quality control laboratory.
Regulatory Knowledge: Thorough understanding of GMP, GLP, GDP, and international guidelines (FDA, EMA, WHO).
Technical Skills:
Advanced analytical techniques.
Expertise in method validation.
Strong documentation and record-keeping practices.
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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