Adcock Ingram Critical Care (Pty) Limited 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:
This may include analysis of raw material, bulk, imported, finished products and stability samples to ensure compliance to specifications prior to release. The supervision of personnel and workload during the shift will also be required. Ensure that the scope of practice is met regarding current Good Laboratory Practice in line with local requirements.
Key Job Outputs:
- Perform release analysis on samples
- Timeous execution and investigating OOS.
- Trouble shooting in various laboratory equipment
- Review own and work of other analysts to ensure accuracy and compliance
- Conform to specified guidelines
- Reviewing of Analytical report and laboratory notebook.
- Reviewing and updating SOP’s, Analytical methods and specification when required.
- Reports generated as testing is completed
- Reports are accurate and of high quality
- Ensure that procedures are maintained in a GLP compliant manner
- Ensure careful use of consumables to prevent wastage and maintain sufficient stock levels
- HPLC, UPLC and other instrument (UV, AA & Flame etc.) with understanding of related substances.
- Understanding of data integrity management during HPLC analysis
- Assisting in analytical techniques training when required.
- Liaising with production personnel on OOS during production of batches
- Ensure all required samples are tested during the shift
Closing date: 15 August 2025
- BSc Chemistry degree / National Diploma or BTech Analytical Chemistry or equivalent
- 4 or more years pharmaceutical laboratory testing experience
- Broad knowledge of GMP regulations and Good Laboratory Practices
- Knowledge of commonly used analytical laboratory methods as well as knowledge of USP / BP Compendia methods.
- Computer Literacy – MS Office (proficient in Excel, Word, and Power Point)
