Quality Assurance Officer job at Kampala Pharmaceutical Industries (KPI) | Apply Now

Conduct daily inspections of manufacturing areas, equipment, and systems to ensure full compliance with cGMP standards.

Ensure accurate and timely documentation of all production activities; maintain up-to-date online records.

Review Batch Manufacturing Records (BMRs) to verify adherence to SOPs and confirm that all required signatures and dates are in place.

Monitor cleanliness, personal hygiene, and overall housekeeping in the manufacturing environment.

Prepare qualification protocols and perform equipment qualifications (DQ/IQ/OQ/PQ/RQ); approve or reject equipment based on qualification results.

Draft and implement process validation protocols; perform process validations and approve/reject processes based on validation outcomes.

Conduct in-process quality control checks, including friability, disintegration, uniformity of mass, hardness, moisture content, and thickness testing.

Monitor environmental conditions such as temperature, pressure, and humidity to ensure product quality is not compromised.

Review and verify completeness of manufacturing and laboratory records.

Identify and investigate deviations in manufacturing processes.

Maintain robust documentation systems including proper filing, archiving, and control of GMP documents.

Develop and update Standard Operating Procedures (SOPs) for QA and related departments.

Issue, stamp, and distribute controlled documents (SOPs, protocols, specifications).

Prepare and issue batch manufacturing and packaging records (BMRs/BPRs) in line with the production plan, assigning unique batch numbers and coordinating with the production team.