Overview
Quality Assurance Intern Jobs in Southern Suburbs at Pharma Dynamics
KEY RESPONSIBILITIES
Operational efficiency
- Contribute to the creation and implementation of best practices processes and procedures to aid and improve operational performance and timeous release of product to market
- Contribute to timeous implementation of QA projects
Operational activities:
- Manage the compilation of lot releases on LR App in line with release priorities
- Assist with the release of printed packaging components and ensure all colour standards are current and filed
- Ensure the timeous recording of any stock for destruction and the coordination of the destruction process
- Assist with the capturing of data and the maintenance of QA registers
- Assist with the compilation and/or closure of CCP’s and Issue Logs
- Liaise with suppliers as and when required
- Assist with the update and circulation of standard operating procedures within the department
- Assist with Product quality review links, sign offs and coordination/compilation of documents as and when required
- Assist with the management of reference standards and columns for existing products and new launches
- Coordinate and/or obtain quotes for consumables as/when required
- Ensure all invoices received from laboratories are checked against approved pricelists and processed for approval
- Assist with the compilation of monthly QA reports to HOD
- Assist with the coordination of technical and/or other agreements for signature
- Provide the necessary QA information to Compliance and Regulatory Affairs as and when required
- Assist with launch activities in line with business priorities
- Assist with compilation of minutes and actions as and when required
- To carry out any other administrative duty as and when required
Good Manufacturing practice (GMP)
- Maintain all GMP principles in line with departmental Quality System and SAHPRA requirements
Documentation & Systems Management
Documentation
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- Assists with SOP tracking and compilation
- Assists with monthly status reports
Systems
- Drive accuracy and efficiency of the departmental eDMS
- Ensure ongoing compliance with GMP requirements
PRE-REQUISITES
- B.Sc. Degree or equivalent scientific qualification
- Minimum 3 years’ working experience in an administrative capacity
- Basic knowledge of the quality environment within the pharmaceutical industry
Title: Quality Assurance Intern
Company: Pharma Dynamics
Location: Southern Suburbs
