3 Production Officer – Oral Liquids
2025-05-09T08:40:00+00:00
Dei BioPharma
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https://deibiopharma.com/
FULL_TIME
Matugga
Uganda
00256
Uganda
Healthcare
Healthcare
2025-05-12T17:00:00+00:00
Uganda
8
Summary:
The Production Officer Oral Liquids will be responsible for overseeing the end-to-end manufacturing of oral liquid dosage forms such as syrups, suspensions and solutions in compliance with current Good Manufacturing Practices (cGMP). This includes supervising batch manufacturing operations, ensuring adherence to approved Batch Manufacturing Records (BMRs), coordinating with quality and engineering teams and ensuring process efficiency, product quality, and regulatory compliance. The role requires hands-on experience with mixing vessels, filtration systems and filling lines as well as sound knowledge of process validation, documentation, and deviation management. The ideal candidate should be technically competent, detail-oriented, and capable of leading teams in a sterile or classified manufacturing environment.
Key Duties and Responsibilities:
- Supervise and execute the manufacturing process for oral liquid formulations including syrups, suspensions and solutions as per approved Batch Manufacturing Records (BMRs).
- Prepare and verify raw materials, equipment and documentation prior to production initiation.
- Operate and monitor liquid preparation equipment including mixing tanks, homogenizers and filtration systems.
- Ensure process parameters such as mixing speed, temperature and pH are maintained within validated ranges.
- Oversee bulk transfer of finished liquids to holding tanks or filling lines and coordinate filling activities with the packaging team.
- Perform in-process checks for clarity, volume, pH and homogeneity and take necessary corrective actions when required.
- Maintain accurate records of production operations, cleaning activities and any deviations or non-conformances.
- Ensure cleaning and sanitization of equipment and production areas are performed in line with SOPs and cleaning validation requirements.
- Participate in scale-up, process validation and technology transfer of new liquid formulations.
- Promote safety, cGMP compliance and continuous improvement initiatives within the production team.
Academic Qualifications:
Bachelor’s degree or Higher Diploma in Pharmacy, Industrial Chemistry, Chemical Engineering or a related technical field from a recognized institution.
Experience and competencies:
- Minimum of 3–4 years of hands-on experience in oral liquid production within a GMP-regulated pharmaceutical or related facility.
- Familiarity with oral liquid processing equipment, cleaning protocols and cGMP documentation.
- Strong understanding of liquid formulation science and ability to troubleshoot production deviations.
- Proven ability to manage production teams and coordinate with QA, maintenance and logistics departments.
- Excellent documentation, communication and team leadership skills.
Supervise and execute the manufacturing process for oral liquid formulations including syrups, suspensions and solutions as per approved Batch Manufacturing Records (BMRs). Prepare and verify raw materials, equipment and documentation prior to production initiation. Operate and monitor liquid preparation equipment including mixing tanks, homogenizers and filtration systems. Ensure process parameters such as mixing speed, temperature and pH are maintained within validated ranges. Oversee bulk transfer of finished liquids to holding tanks or filling lines and coordinate filling activities with the packaging team. Perform in-process checks for clarity, volume, pH and homogeneity and take necessary corrective actions when required. Maintain accurate records of production operations, cleaning activities and any deviations or non-conformances. Ensure cleaning and sanitization of equipment and production areas are performed in line with SOPs and cleaning validation requirements. Participate in scale-up, process validation and technology transfer of new liquid formulations. Promote safety, cGMP compliance and continuous improvement initiatives within the production team.
Bachelor’s degree or Higher Diploma in Pharmacy, Industrial Chemistry, Chemical Engineering or a related technical field from a recognized institution. Experience and competencies: Minimum of 3–4 years of hands-on experience in oral liquid production within a GMP-regulated pharmaceutical or related facility. Familiarity with oral liquid processing equipment, cleaning protocols and cGMP documentation. Strong understanding of liquid formulation science and ability to troubleshoot production deviations. Proven ability to manage production teams and coordinate with QA, maintenance and logistics departments. Excellent documentation, communication and team leadership skills.
JOB-681dbf6014dd5
Vacancy title:
3 Production Officer – Oral Liquids
[Type: FULL_TIME, Industry: Healthcare, Category: Healthcare]
Jobs at:
Dei BioPharma
Deadline of this Job:
Monday, May 12 2025
Duty Station:
Matugga | Uganda | Uganda
Summary
Date Posted: Friday, May 9 2025, Base Salary: Not Disclosed
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JOB DETAILS:
Summary:
The Production Officer Oral Liquids will be responsible for overseeing the end-to-end manufacturing of oral liquid dosage forms such as syrups, suspensions and solutions in compliance with current Good Manufacturing Practices (cGMP). This includes supervising batch manufacturing operations, ensuring adherence to approved Batch Manufacturing Records (BMRs), coordinating with quality and engineering teams and ensuring process efficiency, product quality, and regulatory compliance. The role requires hands-on experience with mixing vessels, filtration systems and filling lines as well as sound knowledge of process validation, documentation, and deviation management. The ideal candidate should be technically competent, detail-oriented, and capable of leading teams in a sterile or classified manufacturing environment.
Key Duties and Responsibilities:
- Supervise and execute the manufacturing process for oral liquid formulations including syrups, suspensions and solutions as per approved Batch Manufacturing Records (BMRs).
- Prepare and verify raw materials, equipment and documentation prior to production initiation.
- Operate and monitor liquid preparation equipment including mixing tanks, homogenizers and filtration systems.
- Ensure process parameters such as mixing speed, temperature and pH are maintained within validated ranges.
- Oversee bulk transfer of finished liquids to holding tanks or filling lines and coordinate filling activities with the packaging team.
- Perform in-process checks for clarity, volume, pH and homogeneity and take necessary corrective actions when required.
- Maintain accurate records of production operations, cleaning activities and any deviations or non-conformances.
- Ensure cleaning and sanitization of equipment and production areas are performed in line with SOPs and cleaning validation requirements.
- Participate in scale-up, process validation and technology transfer of new liquid formulations.
- Promote safety, cGMP compliance and continuous improvement initiatives within the production team.
Academic Qualifications:
Bachelor’s degree or Higher Diploma in Pharmacy, Industrial Chemistry, Chemical Engineering or a related technical field from a recognized institution.
Experience and competencies:
- Minimum of 3–4 years of hands-on experience in oral liquid production within a GMP-regulated pharmaceutical or related facility.
- Familiarity with oral liquid processing equipment, cleaning protocols and cGMP documentation.
- Strong understanding of liquid formulation science and ability to troubleshoot production deviations.
- Proven ability to manage production teams and coordinate with QA, maintenance and logistics departments.
- Excellent documentation, communication and team leadership skills.
Work Hours: 8
Experience in Months: 36
Level of Education: bachelor degree
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