Job Title: Quality Assurance Inspectors (4 Fresher Jobs)
Organisation: Dei BioPharma Ltd
Duty Station: Matugga, Wakiso, Uganda
About the Company:
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. Our state-of-the-art manufacturing facility, situated in Matugga, Wakiso district, Uganda, shall produce high-quality medicines across a wide range of therapeutic areas.
Job Summary: The Quality Assurance Inspector is responsible for providing line-level oversight of manufacturing, packaging, and warehousing operations to ensure adherence to current Good Manufacturing Practices (cGMP), Standard Operating Procedures (SOPs) and regulatory compliance.
The role involves conducting real-time in-process checks, monitoring cleanliness and status labelling, verifying equipment readiness, inspecting documentation accuracy, and ensuring deviations are promptly escalated.
QA Inspectors play a critical role in enforcing product quality, data integrity and compliance throughout production activities. The ideal candidate should demonstrate keen attention to detail, a strong understanding of GMP operations and the ability to act decisively within a regulated environment.
Key Duties and Responsibilities:
- Perform in-process checks during manufacturing, filling, compression, coating and packaging operations.
- Verify correct line clearance, material status labeling and equipment readiness before and after batch operations.
- Ensure adherence to approved BMRs, packaging instructions, and cleaning procedures.
- Monitor compliance with gowning, hygiene and contamination control practices in production areas.
- Identify, document and escalate any deviations, non-conformances, or equipment malfunctions.
- Conduct inspections of raw materials, packaging materials and finished goods during handling and storage.
- Support implementation of data integrity principles (ALCOA+) across documentation and operations.
- Maintain real-time documentation of inspections, logbook entries and QA observations.
- Participate in GMP training sessions and contribute to audit and inspection readiness.
- Work closely with Production and Quality Control to ensure product quality and compliance are maintained at every stage.
Qualifications, Skills and Experience:
- Diploma or degree in Pharmacy, Industrial Chemistry, Quality Assurance, or a related field from a recognized institution.
Experience and Competencies:
- Minimum of 2–3 years of experience in pharmaceutical production or QA roles.
- Sound understanding of cGMP, data integrity, and GDP requirements.
- Strong observational skills and attention to detail.
- Ability to work on shifts and across multiple production zones.
- Good communication and documentation skills.
- Proactive in identifying quality risks and enforcing compliance on the shop floor.
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 [email protected] 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 5:00 PM
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