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 retainedfor 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:

Providing best practice day-to-day manufacturing pharmaceutical services to manage workflow, production and Document Procedure Compliance so as to ensure safe and efficacious medicines are manufactured. To comply with cGMP, MCC guidelines, SOP's and adhere to batch documentation instructions at all the times.

Key Outputs:

Managing Pharmacist Assistants Proper documentation of manufactured and packaged pharmaceutical products. Perform Line Openings and Closures in manufacturing & packing lines. Prepare weekly production scheduling of product. Auditing batch documents for QA closure and release Assist in preparing Annual Product Quality Reviews Initiate and close off CAPAs and Non-Conformances. Ensure regulatory compliance Safety, Health and Environmental Standards. Manufacturing process including line checks. Regulatory & Document Compliance Handling of non-conforming production, both inbound, WIP and produced batches Documenting of Deviations, CAPA's and Change Control on Caliber Audits & Continuous Improvement Development of Team's technical capabilities Lead / Champion change overs, line opening, line closing, Lead and be the chief accountable officer for GMP and Micro compliance in the area on shift On line and in line testing resulting in approval of batch documentation and Provisional releases Submission of full production manufacturing tickets and supporting documentation within one hour of batch completions Ability to identify, execute and prioritize work tasks/projects Excellent interpersonal, communication skills and team oriented Strong problem solving and troubleshooting capabilities


B. Pharm Degree Registered with South African Pharmacy Council Preferably 2-3 years' experience in Pharmaceutical Production in a Manufacturing environment cGMP skills Computer Literacy - MS Office (proficient in Excel, Word and Power Point)

Closing Date:

27 August 2025