Vacancies at Adcock Ingram

Key Job Outputs:

• Reviewing of data documented by laboratory personnel within laboratory notebooks, worksheets and instrument logbooks.
• Reviewing of documentation related to in-process, finished product, raw materials and stability testing in the laboratory
• Reviewing of audit trail to ensure that the electronic data generated is according to the applicable procedures.
• Performs review of analytical data and calculations associated with material testing, and analytical methods
• To priorities reviewing of analytical data to strict timescales and as per the emergency of release.
• Performs evaluation of Out of Specification with the laboratory analyst.
• Informs manager or designate of any critical data integrity or issue of irregularity.
• Review reagents, standards and standardized Solution in the “P” Book.
• Review the working and reference working Standards and verify that the correct grade and Potency has been used.
• Reviews that the Samples were taken from the correct sampling points and that testing was performed testing as per 03-15-23-004.
• Ensuring the Lab equipment in handled with care and non-abuse.
• Switching off the equipment when not in use.
• Ensuring cleanliness of the laboratory
• Follow Safety and GMP requirements as instructed
• Complying with Standard Operating Procedures (SOP’s)

Requirements

Required Learning: 

• BSc Degree or National Diploma in Chemistry
• 2 – 3 years Lab experience in Pharmaceutical Industry
• Knowledge of laboratory SOP’s
• Knowledge of pharmaceutical GMP
• Knowledge of using analytical instrumentation and data review
• Strong analytical and problem solving

go to method of application »

Requirements

• A Bachelor’s degree in Science with less than a year of relevant experience or a National Diploma in Analytical Chemistry with 2 to 3 years’ relevant experience.
• Relevant experience is considered as quality control (QC) testing of pharmaceutical products.
• Some knowledge and understanding of the tests conducted for pharmaceutical dosage forms including tablets, capsules, solutions, suspensions, creams and ointments.
• Some knowledge, understanding and application of a Quality Management System as relevant to QC testing. 
• Some experience in the review and interpretation of data generated during QC testing

Key Job Outputs

• To plan, organise and execute work as an individual contributor to fulfil the operational requirements of the Method Validations team, which includes:
• To accurately (first-time right) and timeously conduct QC testing for release of products to market on an ad-hoc basis.
• To compile raw data, certificates of analysis (COAs) and reports accurately, logically and with adequate scientific rigour.
• To initiate quality management documentation such as OOS investigations, deviations, change controls and corrective actions when required with practical, but scientific justifications, risk/impact assessments and root cause analyses.

CLOSING DATE 22 April 2026