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Stability Chamber Operator job at Dei BioPharma Ltd. | Apply Now
Matugga, Uganda
Full Time
Are you looking for Quality Control jobs in Uganda 2025 today? then you might be interested in Stability Chamber Operator 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
Stability Chamber Operator job at Dei BioPharma Ltd.
Dei BioPharma Ltd.
Job Description
The Stability Chamber Operator will oversee the proper handling of pharmaceutical samples within stability chambers, maintaining controlled temperature and humidity conditions. Responsibilities include monitoring, documentation, labeling, and sample management for long-term and accelerated stability studies. The role also involves ensuring the functionality of stability chambers, addressing equipment alarms, supporting audits, and collaborating with quality and development teams.
Duties, Roles and Responsibilities
Operate and monitor stability chambers in compliance with ICH guidelines and internal SOPs.
Conduct regular checks on temperature, humidity, and other environmental parameters.
Schedule and organize stability sample pulls based on predefined protocols.
Label and place stability samples ensuring traceability and documentation.
Perform preliminary visual inspections of samples and coordinate further testing.
Maintain accurate records of chamber usage, sample log-ins, and environmental deviations.
Perform routine preventive maintenance and initiate service requests for stability chambers.
Participate in the qualification and requalification of chambers.
Ensure all stability documentation is accurate, traceable, and compliant.
Collaborate with QC, QA, and Product Development teams to ensure effective execution of stability programs.
SERVICES
COMMERCIAL
SERVICES
INDUSTRIAL
SERVICES
RESIDENTIAL
Qualifications, Education and Competencies
Academic Qualifications:
Diploma or Bachelor’s degree in Pharmaceutical Sciences, Industrial Chemistry, Laboratory Technology, or a related scientific field from a recognized institution.
Experience and Competencies:
Minimum of 2–4 years of relevant experience in a pharmaceutical or regulated manufacturing environment.
Experience working with controlled environmental chambers and understanding of ICH stability requirements.
Familiarity with GDP, cGMP, and laboratory operations related to sample handling and documentation.
Ability to interpret temperature/humidity monitoring charts and respond to deviations.
Basic understanding of Good Laboratory Practices (GLP) and documentation control systems.
Attention to detail, reliability, and ability to work independently.
Experience supporting audits and inspections is an added advantage.
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.
