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Quality Assurance Officer job at Dei BioPharma Ltd | Apply Now
Matugga, Uganda
Full Time
Are you looking for Medical jobs in Uganda 2025 today? then you might be interested in Quality Assurance Officer job at Dei BioPharma Ltd
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
Quality Assurance Officer job at Dei BioPharma Ltd
Dei BioPharma Ltd
Job Description
The Quality Assurance Officer ensures that all aspects of the manufacturing process adhere to current Good Manufacturing Practices (cGMP), Good Documentation Practices (GDP), and internal Standard Operating Procedures (SOPs). Responsibilities include reviewing and approving batch manufacturing and packaging records, conducting in-process quality checks, and participating in deviation and complaint investigations. The role supports validation and qualification activities and contributes to document control, change management, and internal/external audit readiness. The QA Officer also provides training to staff and promotes continuous improvement initiatives. The role requires thorough knowledge of pharmaceutical regulations including WHO, NDA, and US FDA standards.
Duties, Roles and Responsibilities
The Quality Assurance Officer ensures that all aspects of the manufacturing process adhere to current Good Manufacturing Practices (cGMP), Good Documentation Practices (GDP), and internal Standard Operating Procedures (SOPs). Responsibilities include reviewing and approving batch manufacturing and packaging records, conducting in-process quality checks, and participating in deviation and complaint investigations. The role supports validation and qualification activities and contributes to document control, change management, and internal/external audit readiness. The QA Officer also provides training to staff and promotes continuous improvement initiatives. The role requires thorough knowledge of pharmaceutical regulations including WHO, NDA, and US FDA standards.
SERVICES
COMMERCIAL
SERVICES
INDUSTRIAL
SERVICES
RESIDENTIAL
Qualifications, Education and Competencies
Bachelor’s degree in Pharmacy, Industrial Chemistry, Quality Management, or a related scientific discipline
Minimum of 3–4 years of experience in pharmaceutical quality assurance within a GMP-regulated facility
Proficient in batch record review, deviation and CAPA management, and document control
Sound knowledge of WHO GMP, ICH guidelines, and regulatory compliance
Strong analytical, communication, and organizational skills
Ability to collaborate with cross-functional teams and work independently
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.
