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Job Summary

Job Title:
QC Analyst - Finished Product
Employer:
Dei BioPharma Ltd
Location:
Kampala, Uganda
Country:
Uganda
Contract Type:
Full Time
Job Category:
Medical jobs
Number of Positions:
1
Deadline:
Friday, 4 April 2025

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QC Analyst - Finished Product job at Dei BioPharma Ltd | Apply Now

Kampala, Uganda

Full Time

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

Deadline: 

4 Apr 2025

About the Organisation


DEI BioPharma Drugs and Vaccines Manufacturing Plant is a pioneering pharmaceutical company dedicated to the research, development, and production of high-quality, affordable medicines and vaccines to enhance public health and disease prevention. Recognized for its commitment to pharmaceutical excellence, the company has built a strong reputation for innovation, compliance with global quality standards, and contributions to healthcare advancement in Africa and beyond.

DEI BioPharma fosters a collaborative and research-driven work culture, offering employees professional development opportunities, cutting-edge facilities, and a supportive environment that promotes scientific innovation and teamwork. The company provides diverse job opportunities in biotechnology, pharmaceutical production, quality assurance, research and development, logistics, and administration, with flexible work arrangements to support efficiency and work-life balance. Established with a vision to revolutionize Africa’s pharmaceutical industry, DEI BioPharma has rapidly grown through strategic partnerships, regulatory approvals, and continuous investment in advanced manufacturing technologies.

Its innovation-driven business model integrates state-of-the-art production processes, data-driven research methodologies, and sustainable pharmaceutical solutions to ensure accessibility, affordability, and efficacy. With a vast operational reach, the company supplies essential drugs and vaccines to local and international markets, strengthening healthcare systems and pandemic preparedness. Rooted in core values of integrity, excellence, innovation, and social responsibility, DEI BioPharma remains committed to ethical business practices and long-term health impact.

Through Corporate Social Responsibility (CSR), the company actively engages in community health programs, vaccine accessibility initiatives, pharmaceutical education, and environmental sustainability projects. For more information about products, research initiatives, and career opportunities.

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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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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