Job Description

Adcock Ingram Holdings Limited and its Subsidiaries ("we", "us") is committed to protecting and respecting your privacy. Our Privacy Notice sets out the basis on which personal information collected inter alia from you, social media, recruitment agencies and our website, will be processed by us. The Privacy notice is available on our website www.adcock.co.za.
One of the conditions under the Protection of Personal Information Act 4 of 2013 (POPIA) provides that candidates have the right to be informed about the collection and use of their personal information,
In the course of your application: we may

• collect personal information that may be used to identify potential professional opportunities other than the job you have applied for but of which we think might be of interest to you.
• use your Personal Information to confirm references or background checks you have provided us.
• request your consent to participate in aptitude tests or recruitment assessments.

We also use your personal information to respond to your inquiries, to verify your information and to share information with you.
Your personal information will be securely stored by the Human Capital Department and it will be retained for a period of up to 12 months as of the closure of the application procedure if your application is unsuccessful, and in case of a successful application and you are hired, your data will be transferred to your personal employee file.
By applying for this position, you consent to us processing your personal information.
We reserve the right to make an appointment. If you have not heard from us within 30 (thirty) days of the closing date, please accept that your application was unsuccessful. Correspondence will be entered into only with shortlisted candidates.
Job Purpose:
To review analytical data for the disposition of batches with attention to data integrity
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)

Closing date 20 August 2025
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