Dei BioPharma Ltd
Dei BioPharma Ltd is a biotech and pharmaceutical research firm duly incorporated in Uganda, specializing in the development and manufacture of innovative medicines and vaccines.
The development of our drugs and vaccines manufacturing facility was commissioned on July 6, 2021, by President Yoweri Museveni and Kenya President William Ruto (then Vice President).
The state-of the art facility is situated in Matugga, Wakiso district. Uganda, and shall produce high quality medicines across a wide range of therapeutic areas.
These include malaria, cancer, generies, beta lactums, non betalactums, nutraceuticals, podies.
The manufacturing facility is gearing to produce one billion doses of mRNA vaccines guided by the most stringent global CMP including the US FDA, EU (EMA) and the World Health Organization (WHO) standards.
Announcement Number: DB/05/2025/PD05
Position Tile: Production Officer – Compression (Number of positions: 03)
Opening Period: 05/05/2025 – 05/12/2025
Series/Grade: L (3)
Salary: Competitive
Who May Apply: All Interested Applicants
Duration Appointment: Indefinite, subject to successful completion of probationary period
Supervisory Position: None
Job Summary:
The Production Officer Compression is responsible for supervising the ablet compression process in the manufacturing of oral solid dosage forms, ensuring compliance with approved Batch Manufacturing Records (BMRs), Standard Operating Procedures (SOPs) and current Good Manufacturing Practices (GMP). The role involves operating and monitoring rotary tablet press machines, adjusting compression parameters (weight, hardness, thickness), conducting in-process checks and ensuring batch integrity and equipment readiness. The officer will coordinate with QA, engineering and maintenance teams to resolve deviations, optimize productivity and ensure timely execution of production schedules. The ideal candidate should have in-depth knowledge of compression processes, tooling management, machine troubleshooting and regulatory compliance within a GMP-regulated pharmaceutical environment.
Key Duties and Responsibilities:
1. Supervise the tablet compression process in line with approved Batch Manufacturing Records (BMRs) and production plans.
2. Operate and monitor tablet compression equipment including single and double rotary tablet presses.
3. Set and adjust compression parameters such as tablet weight, thickness, hardness and turret speed to achieve batch specifications.
4. Conduct and document in-process quality checks including weight variation, hardness, friability and tablet appearance.
5. Ensure compliance with GMP documentation practices, including logbooks, equipment cleaning records and deviation reports.
6. Coordinate with maintenance and engineering teams to resolve equipment issues and perform preventive maintenance tasks.
7. Ensure proper cleaning, setup and changeover of equipment to avoid cross-contamination and maintain batch integrity.
8. Participate in product scale-up, validation and troubleshooting activities.
9. Train and supervise compression operators, ensuring safety, producivity and adherence to procedures.
10. Maintain high standards of housekeeping, hygiene and operational discipline within the compression area.
Academic Qualifications:
Bachelor’s degree or Higher Diploma in Pharmacy, Industrial Chemistry, Mechanical Engineering or a related technical field from a recognized institution.
Experience and Competencies:
1. Minimum of 3-4 years of hands on experience in pharmaceutical tablet compression operations under GMP.
2. Proficient in operating rotary compression machines and performing minor mechanical adjustments.
3. Familiarity with compression tooling (punches/dies), machine troubleshooting and in-process quality control.
4. Strong understanding of GMP, ALCOA+ principles and production documentation.
5. Demonstrated ability to lead small teams and coordinate across departments.
6. Experience in validation and scale-up activities is an added advantage.
All applicants under consideration will be required to pass medical and security certifications.
EQUAL OPPORTUNITY EMPLOYER: Dei BioPharma Ltd, provides equal opportunity and fair and equitable treatment in employment to all people without regard to race, color, religion, sex, national origin, age, disability, political affiliation or marital status.
HOW TO APPLY:
All interested candidates who meet the required qualifications and experience are invited to submit their CVs, Cover Letter & Academic documents (addressed to the Human Resources Manager)
All Application documents should be merged as one document in PDF or DOC / DOCX, which should not exceed 10MB
Applications should be sent by email to recruitment@deibiopharma. com with the JOB TITLE IN THE SUBJECT LINE
Should you not hear from us within twenty one (21) days from the closing date of this advertisement, you may consider your application to be unsuccessful
Deadline: 12th May 2025 by 5:00PM
