Vacancy title:
Technology Transfer Officer

[Type: FULL_TIME, Industry: Manufacturing, Category: Computer & IT]

Jobs at:
Quality Chemical Industries Limited

Deadline of this Job:
Friday, September 26 2025

Duty Station:
Uganda | Kampala | Uganda

Summary
Date Posted: Wednesday, September 24 2025, Base Salary: Not Disclosed

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JOB DETAILS:

Key Responsibilities:

• Carry out comparative dissolution studies for test products and reference comparator products to assure pharmaceutical equivalence
• Carry out cleaning validation for new products that are developed at Formulation Development
• Carry out analytical method validations and verifications and compile reports for the same to the Formulation Development to assure the consistency of the developed analytical method
• Perform Analytical Method Transfer during transfer of the products from Formulation Development to Manufacturing
• Carry out accelerated and long-term stability studies as well as compile reports of the same
• Conduct impurity profiling of drug substances including the identification and quantification of impurities
• Assist the Formulation Development Quality Chemical Officers in developing analytical methods, such as spectroscopy-based methods, chromatographic methods or dissolution methods amongst others
• Assist the Formulation Development Officers in conducting experiments, analysing results and preparing reports for various pharmaceutical formulations developed
• Execute and report experimental work related to biopharmaceutical characterization in support of drug product development
• Participate in the evaluation of new analytical techniques in the area of pre-formulation sciences, automated workflows and biorelevant testing
• Create and review specifications in the SAP system
• Handle ERP System/ SAP for specification generations and Trackwise system for deviation and complaints
• Prepare SOPs, FMECAs, protocols, and any other documents assigned by the line manager from time to time
• Any other job responsibility/ assignment given by Supervisor/ Manager deemed fit within your jurisdiction

Qualifications and Experience Required 

• Bachelor’s Degree in Chemistry, Chemical Engineering, Industrial Chemistry, or Science Technology (Chemistry), or any other science related field
• Minimum of 3 years’ experience in Quality Control in a manufacturing plant or standard recognized laboratory
• Familiar with pharmaceutical regulations and guidelines, such as Good Manufacturing Practices (GMP) and International Council for Harmonization (ICH) guidelines
• Certification in Quality Management or Quality Assurance is an added advantage
• Good teamwork, interpersonal skills and adherence to Quality Management Systems
• Self-starter, flexible and able to work well under pressure at work
• Proficiency in Excel and its basic formulae, and in PowerPoint presentations
• Familiar with the various analytical tools like the Pareto Chart, Waterfall, Pie Charts, Bar Charts and Line Charts
• Be observant, creative and innovative in line with the business needs
• Able to work Shifts program as per business needs

Work Hours: 8

Experience in Months: 24

Level of Education: bachelor degree

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