More jobs:
Quality Management Systems Pharmacist; JHB North
Job in
Johannesburg, 2000, South Africa
Listed on 2026-02-08
Listing for:
Aspen Pharma Group
Full Time
position Listed on 2026-02-08
Job specializations:
-
Quality Assurance - QA/QC
-
Healthcare
Data Scientist, Medical Science
Job Description & How to Apply Below
Job Location : Johannesburg, Gauteng, South Africa Final date to receive applications : February 16, 2026
OBJECTIVE OF ROLE- The role undertakes responsibility for the pharmaceutical tasks within the quality management systems (QMS) function of the Quality department for Pharmacare Limited, ensuring QMS and company compliance with sound quality assurance (QA) principles and requirements, Aspen Group and Third-Party Alliance partner policies and procedures and in accordance with Good ‘X’ Practice (GxP) guidelines, The Pharmacy Act, Act 53 of 1974 as amended, the Medicines and Related Substances Act, Act 101 of 1965 as amended, and any other relevant legislation and guidelines relating to the import, export, manufacture, packing, testing, warehousing and distribution of medicines in South Africa and the Southern African Development Community (SADC), thereby ensuring that the products meet the intended quality, safety and efficacy standards and requirements as required of the marketing authorisation (MA) holding entity, Pharmacare Limited.
- To perform pharmaceutical tasks within the Quality department under the direction of the Quality Lead - Quality Management Systems. This includes the Quality Management System, Product Quality Review (PQR), Waste Management, Product Quality Complaints, Inspections, Self-Inspections, Trend Analysis, Risk Management, Training, and associated functions as per GxP and company Standard Operating Procedures
- Execute daily tasks according to the relevant standard operating procedures and work instructions.
- Adhere to agreed Key Performance Indicators (KPIs)
- Support the continuous development and improvement of the Quality function while upholding the Aspen core values
- Operate computer systems by capturing data, printing standard reports, etc.
- Perform reconciliations of data.
- Update and maintain systems, databases and trackers
- Generate reports as per instruction.
- Collate data for ad hoc requests
- Verify and interpret the accuracy of data and audit documentation.
- Obtain the necessary signatures for all relevant documentation
- Manage and utilise resources effectively to keep processes cost effective
- Provide quality support for the SA and SADC Commercial, Supply Chain, Value Chain, and enablement functions (e.g. Regulatory, Finance), as it relates to QMS matters
- Maintain good relations and communications with all members of the team and respond politely and in a timely fashion to internal and external customers.
- Work with all members of staff to maintain and develop the positive progressive culture within Aspen.
- Display a professional attitude when responding to customers and responding to enquiries in a timely manner
- Manage projects as per guidance from the line manager and within agreed time frames
- Provide regular feedback on progress of projects and highlight any issues that require the line manager’s attention
- Adhere to company policies and procedures
- Participate in training programmes
- Keep abreast of developments in best practice, and all QMS related activities
- Maintain a high and up-to-date level of QMS and therapy area knowledge by attending conferences, training courses, and reading relevant medical and scientific literature
- Any other duties as assigned by line manager or head of department
- Maintain templates and lists
- Maintain accurate filing and retrieval of documentation
- Perform any other administrative tasks relating to your work as and when required
- Responsible for quality management system activities, including change controls, deviations, corrective and preventative actions (CAPAs), quality risk management and assessments, customer product quality complaints, annual product quality reviews, training, product recalls/withdrawals, self-inspections, internal/external audits of Pharmacare, regulatory intelligence and documentation such as standard operating procedures (SOPs)/work instructions and reports.
- Compile, review and update SOPs and related documentation (e.g. Work Instructions, standard forms, trackers and all relevant Quality Management System documents) related to work function to ensure compliance with…
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