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QC Analyst - Raw Material job at Dei BioPharma Ltd | Apply Now
Are you looking for Healthcare jobs in Uganda 2025 today? then you might be interested in QC Analyst - Raw Material 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 the highest standards of quality and compliance in the healthcare industry.
Job Title
QC Analyst - Raw Material job at Dei BioPharma Ltd
Dei BioPharma Ltd
Job Description
Job Title: QC Analyst - Raw Material
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 - Raw Material will be responsible for sampling, testing, and releasing raw materials while ensuring full compliance with Good Manufacturing Practice (GMP) standards in the laboratory environment.
Duties, Roles and Responsibilities
Perform sampling and testing of raw materials using approved analytical methods.
Monitor the shelf life of raw materials and schedule re-testing as necessary.
Develop and maintain material specifications, test methods, and standard operating procedures (SOPs).
Prepare SOPs for raw material sampling and testing procedures.
Maintain accurate analytical records and retention samples.
Compile and report monthly Key Performance Indicators (KPIs) for the Raw Material Laboratory.
Ensure proper maintenance, calibration, and functioning of analytical equipment.
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INDUSTRIAL
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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 QC raw material testing within the pharmaceutical industry.
Knowledge: Strong understanding of GMP, GLP, GDP, and regulatory guidelines (FDA, EMA, WHO).
Skills:
Proficiency in analytical laboratory techniques.
Strong documentation and record-keeping skills.
A compliance-oriented mindset with a focus on quality assurance.
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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