QC Stability & Documentation Officer
Full-time
Expires In -2 weeks
Kampala
Duty Station -
Kampala
Bachelor's Degree
1 year
experience
Manufacturing
Science & Engineering
Job Details
The QC Stability & Documentation Officer manages the full lifecycle of stability studies and prepares related technical documentation for a leading pharmaceutical manufacturing company, recruited via Apeiron Consultancy Ltd. Duty station is Kampala, Uganda. Employment Type: Full-time. Work Hours: 8. Salary: Not Disclosed.
Key Duties and Responsibilities
- Oversee the full lifecycle of stability studies, including sample tracking, pulls, shipments, and ensuring all work adheres to Data Integrity principles.
- Author and review GMP-compliant documentation, specifically focusing on stability protocols, reports, and process change controls.
- Prepare Stability Summary Reports (SSR) and track stability study status, report timelines, and documentation activities.
- Manage deviations and laboratory investigation reports.
- Coordinate with QC, QA, and cross-functional teams for data collection, review, and approval of stability documentation.
Qualifications, Skills and Requirements
- Bachelor's degree (Level of Education: bachelor degree).
- Minimum of 1 year experience in stability studies, QC documentation or related pharmaceutical quality operations.
- Knowledge of GMP-compliant documentation, stability protocols and Data Integrity principles.
- Experience authoring and reviewing stability reports, protocols and change controls.
- Strong coordination and documentation skills with ability to work cross-functionally with QC and QA teams.