Quality Control Analyst at Adcock Ingram

Requirements

• At a minimum, a Bachelor’s Degree in Science or a National Diploma in Analytical Chemistry with 5 to 8 years relevant experience.
• Relevant experience is considered as quality control (QC) and stability testing of pharmaceutical products.
• Experience with execution and review of validation/ verification protocols and reports
• Experience in the review and interpretation of data generated during testing.
• Some knowledge of Risk, CAPA, Deviations, OOS and Change control management as relevant to QC testing. 
• Proficiency in MS Word, MS Excel and compilation of scientific justifications, based on data evaluation.

Key Job Outputs

To plan, organise and execute work as an individual contributor to fulfil the operational requirements of the Analytical department, which includes:

•  Analysis of products, stability and lab trials
• Compilation of method verification and method validation protocols and reports
• Execution of method verification and method validation
• To accurately process and review raw data related to analysis
• To review quality management documentation such as OOS investigations, deviations, change controls and corrective actions when required with justifications, risk/impact assessments and root cause analysis.
• Maintain QC-related QMS documentation system, when required.
• Execution of additional laboratory responsibilities such as calibration, verification of instruments, maintenance of chemical store, as required.

CLOSING DATE 12 MAY 2026