Job Description

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:

This may include analysis of raw material, bulk, imported, finished products and stability samples to ensure compliance to specifications prior to release. Ensure that the scope of practice is met with regard to current Good Laboratory Practice in line with local and international requirements.

Key Job Outputs:

Perform routine testing as per relevant Test Methods and procedures for Raw Materials, In Process samples, Finished Products, Stability, Post Importation:


Carry out analysis following method of analysis and ensuring that technical data generated meets specification and obtain release within the agreed timelines. Evaluate data to ensure compliance to release specification. Generation of analytical test data reports. Conducting investigations required for out-of-specification results together with supervisor. Assist other sections such as Raw Materials and stability with analysis when necessary, or when it's required.

Documentation Compiling and Review


Ensure that all documented activities are in compliance with guidelines and procedures Total Quality Management (GMP, GLP and ICH): Ensure that scientific integrity of data is maintained Able to review own work to ensure accuracy, completeness and compliance with departmental procedures. Ensure that all documented activities are in compliance with guidelines and procedures. Report deviations and out of specification results immediately.

Utilization of Resources


Ensure that procedures are maintained in a GLP compliant manner Dynamic planning and communication with regards to utilization of human capital and equipment resources Ensure careful use of consumables to prevent wastage and maintain sufficient stock levels Utilize training sessions and available current literature


National Diploma/BSc Degree in Chemistry/ analytical chemistry and/or equivalent Minimum of 1 - 2 experiences in the Pharmaceutical Industry Proactive Attention to detail Verbal and written communication Technical Skills Team Player Problem solving and decision-making skills

Closing Date:

09 December 2025