Quality Assurance Officer

Full Time13 hours ago
Employment Information

About the Organisation

Abacus Parenteral Drugs Limited (APDL), established in 2006, is East Africa’s largest manufacturer of parenteral drugs, specializing in Large Volume Parenterals (LVPs) and Small Volume Parenterals (SVPs). Operating from a state-of-the-art facility in Mukono, Uganda, APDL produces a wide range of intravenous fluids, ear, eye, and nasal drops, and injectables using innovative blow-fill-seal technology to ensure product purity. Recognized by the Indian Business Forum as the Top Company in the Manufacturing Sector, APDL employs over 200 skilled professionals in a dynamic work environment, offering opportunities for professional growth. 

The company’s business model focuses on delivering high-quality, affordable pharmaceuticals through a robust distribution network serving local and regional markets. Guided by core values of integrity, teamwork, and efficiency, APDL supports community-focused corporate social responsibility programs. For more information, visit .

Job Summary

The Quality Assurance Officer at APDL will perform quality assurance tasks to ensure compliance with cGMP and regulatory standards, maintaining high-quality production processes.

Roles, Duties, and Responsibilities

  • Develop and implement protocols for process and cleanliness validation
  • Investigate complaints, recalls, and deviations
  • Distribute controlled documents such as SOPs, CAPA forms, and QC reports
  • Monitor cleaning, temperature mapping, warehouse hygiene, and environmental controls
  • Verify that received materials meet standards
  • Ensure all departments adhere to established SOPs
  • Participate in quality rounds, audits, and validation (Gemba walks)
  • Conduct in-process checks, ensure line clearance, and monitor labeling
  • Ensure accurate, real-time data entry and documentation
  • Participate in schedules for external calibration and thermal mapping

Health and Safety Duties

  • Identify and address operational hazards
  • Conduct toolbox safety talks and ensure workplace safety

Authorities

  • Distribute controlled documents
  • Report deviations and ensure line clearance
  • Accept or reject starting materials

Qualifications, Education, and Competencies

  • BSc in Chemistry, Pharmacy, or a related field
  • Experience in the pharmaceutical or healthcare field is an advantage

Required Training

  • Training in basic safety, Good Manufacturing Practices (GMP), and record-keeping

How to Apply

Qualified and interested candidates should email their CV and academic qualifications to .

Apply Now

Only shortlisted candidates will be contacted. If you do not hear from us, please consider your application unsuccessful.

Deadline: 30 October 2025, 5:00 PM

Skills
Quality Assurance
Apply Now

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