QUALITY ASSURANCE OFFICER - IPQA
Kampala Pharmaceutical Industries (1996) Ltd.
Quality Control & Assurance
Job Summary
KPI is looking for a qualified Quality Assurance Officer, in charge of IPQA/GMP Monitoring, Dispensing, monitoring of Raw Materials and Packaging Materials, FGS stores, Utilities / Services, AHU Areas, and housekeeping.
- Minimum Qualification : Bachelors
- Experience Level : Mid level
- Experience Length : 3 years
Job Description/Requirements
KPI is looking for a qualified Quality Assurance Officer, in charge of IPQA/GMP Monitoring, Dispensing, monitoring of Raw Materials and Packaging Materials, FGS stores, Utilities / Services, AHU Areas, and housekeeping.
Key Deliverables
- Inspecting all manufacturing areas, equipment and systems including housekeeping daily to ensure that they comply with cGMP in all aspects of suitability of manufacturing medicines.
- Monitor and ensure that there is proper and correct documentation of all production activities and records are updated online.
- Review BMRs online to verify that all production stages have been completed in accordance with SOPs and all signatures and dates of persons performing and checking activities are in place.
- Monitoring and controlling of manufacturing environment including housekeeping practices which include personal hygiene and cleanliness of manufacturing premises.
- To approve or reject equipment/ machinery based on qualification processes.
- To approve or reject processes based on process validation.
- Monitoring compliance with cGMP requirements.
- Carrying out In-process Quality Control Checks like friability, uniformity of mass, disintegration tests, moisture content, hardness, and thickness tests of all products.
- Calibration and Qualification of all production equipment.
- Monitoring and ensuring that the environmental conditions like temperature, pressure and relative humidity are within specifications hence don’t affect the quality of the products.
- Ensuring safety of personnel during manufacturing and packaging.
- Monitoring and ensuring good documentation practices are complied with throughout GMP documentations.
- Identifying, and investigation of deviations in manufacturing processes.
- Observing preventive maintenance, qualification, calibration programs of production equipment, systems and In Process laboratory equipment.
Qualifications and Experience:
- Bachelor of Science Technology- chemistry/ BSc. Chemical Engineering / BSc. Industrial chemistry or BSc. Pharmaceutical sciences, B.Pharmacy.
- At least 3 years’ experience in QA / QC Operations. Experience in pharmaceutical manufacturing environments will be an added advantage
Skills / Competencies:
- Basic QA/QC Knowledge
- Analytical Skills
- Flexibility
- Team player
- Attention to Detail
How to Apply:
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