Vacancy title:
QC Stability & Documentation Officer

[Type: FULL_TIME, Industry: Pharmaceutical, Category: Science & Engineering, Manufacturing & Warehouse, Business Operations]

Jobs at:
Apeiron Consultancy Ltd

Deadline of this Job:
Monday, August 31 2026

Duty Station:
Kampala | Kampala

Summary
Date Posted: Thursday, August 20 2026, Base Salary: Not Disclosed

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JOB DETAILS:

Background

Apeiron Consultancy Ltd is recruiting for a leading pharmaceutical manufacturing company across multiple QA, QC, CSV, GMP, and laboratory roles.

Responsibilities

The QC Stability & Documentation Officer manages the full lifecycle of stability studies and prepares related technical documentation.

• Oversee Stability Studies: Oversee the full lifecycle of stability studies, including sample tracking, pulls, shipments, and ensuring all work adheres to Data Integrity principles.
• Author Documentation: Author and review GMP-compliant documentation, specifically focusing on stability protocols, reports, and process change controls.
• Prepare Stability Reports: Prepare Stability Summary Reports (SSR) and track stability study status, report timelines, and documentation activities.
• Manage Deviations: Manage deviations and laboratory investigation reports.
• Coordinate with Teams: Coordinate with QC, QA, and cross-functional teams for data collection, review, and approval of stability documentation.

Additional Information

If you meet the requirements, this could be your next career opportunity.

Work Hours: 8

Experience in Months: 12

Level of Education: bachelor degree

Job application procedure
Interested in applying for this job? Click here to submit your application now.

Subject: Job Title – Full Name

Closing Date: 31 August 2026

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