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About the Organisation
Head, Quality Assurance – Vaccine Division job at Dei BioPharma Ltd | Apply Now
Matuga, Uganda
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.
Are you looking for HSE jobs in Uganda 2025 today? then you might be interested in Head, Quality Assurance – Vaccine Division job at Dei BioPharma Ltd
Full Time
Deadline:
12 May 2025
Job Title
Head, Quality Assurance – Vaccine Division job at Dei BioPharma Ltd
Dei BioPharma Ltd
Job Description
The position involves oversight of the entire quality assurance (QA) system for vaccine production, covering viral, recombinant protein, and mRNA-based vaccines. The Head of QA will ensure compliance with international regulatory standards such as WHO TRS, EMA GMP Annexes, and US FDA 21 CFR. Responsibilities include product release decision-making, management of deviations, validation of cold chain logistics, and enforcement of data integrity principles (ALCOA+). The role requires leading cross-functional QA teams, overseeing facility qualification processes, and maintaining a culture of continuous improvement and risk-based quality management.
Duties, Roles and Responsibilities
Qualifications, Education and Competencies
See all details of the qualifications, competencies and education for this role under the "How to Apply" section below.
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How to Apply
Lead the development and execution of comprehensive QA systems for vaccine manufacturing.
Ensure full regulatory compliance with WHO, US FDA, EMA, and NDA Uganda requirements.
Oversee batch documentation, product release decisions, deviations, CAPA, and change controls.
Approve quality-critical documentation including SOPs, validation protocols, and master records.
Manage internal audits and coordinate external inspection readiness across the vaccine value chain.
Lead Quality Management Reviews (QMR) and drive KPI-based performance monitoring.
Provide QA oversight in facility qualification, cold chain validation, aseptic processes, and product stability.
Implement and enforce global data integrity and documentation harmonization practices.
Mentor and lead QA personnel across departments, fostering a high-performing quality culture.
Respond to regulatory queries and drive institutional readiness for global licensure and distribution.
Academic Qualifications:PhD in Biotechnology, Vaccine Development, Immunology, Pharmaceutical Sciences, or related field. Certification in GMP, Quality Systems, or Regulatory Affairs is an added advantage.
Experience:
Minimum of 15 years in biopharmaceutical or vaccine manufacturing, including at least 5 years in a senior QA leadership role.
Extensive experience in WHO Prequalification and regulatory compliance with EMA/FDA.
Strong technical background in vaccine manufacturing technologies: live attenuated, recombinant, and mRNA.
Proven leadership in aseptic validation, cold chain QA systems, and sterility assurance.
Competencies:
Strategic thinker with a solid understanding of global quality frameworks.
Strong leadership and mentoring skills.
Excellent problem-solving, documentation, and cross-functional collaboration abilities.
Demonstrated ability to foster a culture of quality and compliance.


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