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Quality Assurance Inspector job at Dei BioPharma Ltd. | Apply Now
Matugga, Uganda
Full Time
Are you looking for HSE jobs in Uganda 2025 today? then you might be interested in Quality Assurance Inspector 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 Inspector job at Dei BioPharma Ltd.
Dei BioPharma Ltd.
Job Description
This role provides hands-on oversight across multiple pharmaceutical manufacturing operations to guarantee that processes are conducted in line with regulatory requirements, SOPs, and internal quality standards. The QA Inspector conducts real-time checks on equipment readiness, cleanliness, material handling, documentation accuracy, and personnel hygiene compliance. By escalating deviations and supporting corrective actions, the Inspector helps uphold product safety and audit readiness. The ideal candidate is meticulous, well-versed in cGMP, and committed to ensuring the highest levels of regulatory compliance in a dynamic production environment.
Duties, Roles and Responsibilities
Conduct in-process quality checks during manufacturing, filling, compression, coating, and packaging.
Verify equipment cleanliness, readiness, and correct labeling before and after batch operations.
Monitor production activities for adherence to BMRs, SOPs, and packaging instructions.
Observe hygiene practices, gowning, and contamination control in all production areas.
Identify, document, and escalate deviations and non-conformances.
Inspect raw materials, packaging components, and finished products during storage and handling.
Ensure proper implementation of ALCOA+ data integrity principles across documentation.
Record real-time observations and maintain logbooks and QA reports.
Participate in internal audits, trainings, and compliance improvement initiatives.
Collaborate with Production and QC teams to uphold product quality and regulatory standards.
Qualifications, Education and Competencies
Academic Qualifications:
Diploma or Degree in Pharmacy, Industrial Chemistry, Quality Assurance, or a related technical field.
Experience and Competencies:
At least 2–3 years of experience in a pharmaceutical manufacturing or QA environment.
Strong understanding of cGMP, GDP, and data integrity principles.
Excellent attention to detail and problem-solving skills.
Able to work shifts and across different production zones.
Strong communication skills and ability to document findings clearly.
Proactive and decisive in identifying risks and ensuring compliance.
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.