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2 Technology Transfer Officer – Quality Control job at Quality Chemical Industries Limited
Posted by: great-volunteer
Posted date: 2025-Oct-03
Location: kampala, Kampala, Uganda
2 Technology Transfer Officer – Quality Control 2025-10-03T07:33:23+00:00 Quality Chemical Industries Limited https://cdn.ugashare.com/jsjobsdata/data/employer/comp_11748/logo/download%20(2).png https://www.qcil.com/ FULL_TIME kampala Kampala 00256 Uganda Manufacturing Science & Engineering 2025-10-08T17:00:00+00:00 Uganda 8 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
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 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 JOB-68df7c43de3b0 Vacancy title:
2 Technology Transfer Officer – Quality Control Jobs at:
Quality Chemical Industries Limited Deadline of this Job:
Wednesday, October 8 2025 Duty Station:
kampala | Kampala | Uganda Summary
Date Posted: Friday, October 3 2025, Base Salary: Not Disclosed 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: 36 Level of Education: bachelor degree Job application procedure
Interested in applying for this job? qcil.com&form%5Bvalid-to%5D=Wednesday,%20October%208%202025">Click here to submit your application now.
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