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QC Analyst – Raw Materials job at Dei BioPharma Ltd | Apply Now
Matugga, Uganda
Full Time
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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 – Raw Materials job at Dei BioPharma Ltd
Dei BioPharma Ltd
Job Description
The QC Analyst – Raw Materials is tasked with receiving, sampling, and conducting analytical testing on incoming raw materials using validated methods and pharmacopeial standards (USP, BP, Ph. Eur.). The analyst will use techniques including HPLC, UV, and IR to confirm identity, purity, and quality. The role also includes preparing reagents and standards, calibrating instruments, recording and analyzing results, and preparing Certificates of Analysis. The analyst must follow cGMP, GLP, and internal SOPs while supporting audit readiness, quality investigations, and continuous improvement initiatives.
Duties, Roles and Responsibilities
Receive, log, and sample incoming raw materials per approved protocols.
Conduct physical, chemical, and instrumental analysis of raw materials.
Adhere to pharmacopeial standards (USP, BP, Ph. Eur.) and validated test methods.
Record raw data, test results, and generate Certificates of Analysis (CoAs).
Identify out-of-specification results and document deviations as necessary.
Operate, calibrate, and maintain analytical equipment including HPLC, UV, and FTIR.
Prepare reagents, volumetric solutions, and reference standards.
Support internal audits, continuous improvement, and staff training.
Maintain GLP/cGMP compliance and uphold data integrity principles.
SERVICES
COMMERCIAL
SERVICES
INDUSTRIAL
SERVICES
RESIDENTIAL
Qualifications, Education and Competencies
Academic Qualifications:
Bachelor’s degree in Pharmacy, Pharmaceutical Sciences, Analytical Chemistry, Industrial Chemistry, or related field from a recognized institution.
Postgraduate certification in Quality Control, Analytical Method Development, or Regulatory Sciences is an added advantage.
Experience and Competencies:
3–5 years’ experience in a pharmaceutical analytical lab.
Skilled in analytical method validation as per ICH Q2(R2).
Experience with analytical instruments (HPLC, UV-Vis, FTIR, Dissolution Tester).
Strong understanding of compendial methods and regulatory guidelines (NDA Uganda, WHO PQ, US FDA).
Demonstrated audit readiness and adherence to ALCOA+ principles and cGMP.
Ability to generate and interpret CoAs and technical reports.
Familiarity with SOPs, documentation practices, and lab safety standards.
How to Apply
ONLINE APPLICATION ONLY!
Interested candidates are advised that applications for this position must be submitted online. To apply please click the “Apply” button below.
