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About the Organisation
Analytical Method Development Specialist job at Dei BioPharma Ltd | Apply Now
Matugga, 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 Analytical Method Development Specialist job at Dei BioPharma Ltd
Full Time
Deadline:
12 May 2025
Job Title
Analytical Method Development Specialist job at Dei BioPharma Ltd
Dei BioPharma Ltd
Job Description
This role involves working closely with formulation scientists, regulatory affairs, quality control, and production teams to develop robust, reproducible, and regulatory-compliant analytical methods. The specialist will perform validation in accordance with ICH Q2(R2) guidelines and ensure methods are transferable for routine quality control and suitable for regulatory dossier submissions. Duties also include handling complex analytical challenges, maintaining data integrity, and supporting audit readiness.
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
Design and validate analytical methods using HPLC, UV-Vis, FTIR, GC, and dissolution techniques.
Draft and execute method development and validation protocols aligned with ICH guidelines.
Conduct forced degradation studies and stability-indicating method development.
Optimize method parameters to ensure accuracy, precision, and robustness.
Troubleshoot analytical issues and refine existing methods.
Coordinate method transfer and training with QC and QA teams.
Maintain detailed records and ensure compliance with ALCOA+ principles.
Support CTD Module 3 (P.5 and S.4) documentation for regulatory submissions.
Oversee calibration, qualification, and maintenance of analytical instruments.
Contribute to regulatory inspections and continuous improvement initiatives.
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Bachelor’s degree in Analytical Chemistry, Industrial Chemistry, Pharmacy, or a related scientific field.
Master’s degree in Analytical Chemistry or Pharmaceutical Analysis is an added advantage.
4–6 years of hands-on experience in analytical method development in a pharmaceutical R&D or QC setting.
Proficiency in using analytical instruments (HPLC, UV, FTIR, GC, dissolution testers).
In-depth knowledge of ICH Q2(R2), USP/BP/Ph. Eur. standards, and method validation lifecycle.
Experience in stability studies and impurity profiling.
Strong understanding of GMP/GLP and regulatory submission processes.
Excellent problem-solving, documentation, and teamwork skills.
