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QA Officer – Medical Diagnostic Devices 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 QA Officer – Medical Diagnostic Devices 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
QA Officer – Medical Diagnostic Devices job at Dei BioPharma Ltd
Dei BioPharma Ltd
Job Description
The Quality Assurance Officer – Medical Diagnostic Devices is responsible for ensuring the quality and compliance of manufacturing processes and diagnostic products. This includes the review and approval of batch manufacturing records, conducting in-process quality checks, and managing non-conformities and CAPAs. The QA Officer plays a key role in supporting internal and external audits, maintaining controlled documentation systems, ensuring adherence to quality systems, and training teams on GMP, ISO 13485, and documentation protocols. The officer ensures the company remains audit-ready and all activities meet the requirements of relevant health and safety standards.
Duties, Roles and Responsibilities
Review and approve batch records, QC data, and documentation for diagnostic product batches
Ensure full compliance with ISO 13485, cGMP, and regulatory requirements in production and QA processes
Conduct in-process checks and verify environmental monitoring and line clearance
Manage non-conformances, deviations, product complaints, and CAPA processes
Participate in validation and qualification (IQ/OQ/PQ) of products, processes, and equipment
Maintain and control quality documentation including SOPs, BMRs, and forms
Conduct internal audits and support external regulatory or supplier audits
Review CoAs, inspection checklists, and QC results for product release
Promote Good Documentation Practices (GDP) and ALCOA+ data integrity principles
Train QA and production teams on quality procedures, hygiene, and compliance standards
Qualifications, Education and Competencies
Bachelor’s degree in Biomedical Engineering, Industrial Chemistry, Medical Laboratory Technology, Quality Assurance, or a related scientific field
Certification in ISO 13485 or internal auditing is an added advantage
3–5 years of experience in QA within medical device, diagnostics, or pharmaceutical manufacturing environments
Strong understanding of ISO 13485, cGMP, GDP, and IVD regulatory requirements
Practical experience with audits, CAPA systems, and quality documentation
Familiarity with cleanroom standards, aseptic manufacturing, and batch review
Strong attention to detail, organizational skills, and ability to work under compliance demands
Excellent communication and teamwork skills
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.