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Job Summary

Job Title:
QA Officer – Medical Diagnostic Devices
Employer:
Dei BioPharma Ltd
Location:
Matugga, Uganda
Country:
Uganda
Contract Type:
Full Time
Job Category:
Medical jobs
Number of Positions:
2
Deadline:
Monday, 12 May 2025

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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

Deadline: 

12 May 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

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

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SERVICES

COMMERCIAL

SERVICES

INDUSTRIAL

SERVICES

RESIDENTIAL

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.

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