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QA Administrator
Adcock IngramZA11 days ago
Job descriptionTyping and formatting of Standard Operating Procedures, Manufacturing documents, Packaging documents, QA Packaged Product Inspection Reports and all other QA related documentation. Printing of master documentation and circulating for approval. Scanning of approved master documentation into the Master Scanned Document folder on the QA drive. Maintaining the Master Scanned Document folder on the QA drive with the latest document versions. Archiving of superseded document versions in their respective superseded folders on the QA drive. Archiving of all master documents. Maintaining master and department SOP files. Updating all QMS registers and maintaining files. Maintaining of the QA Department documentation system. Self-inspection findings follow-up and updates on the QA drive. Sample Inspection for APQR’s. Post Imports sample inspection and maintenance of Post Imports registers. Document review Customer complaints Projects Assisting with issuing of Manufacturing documents, Packaging documents and Attachments. Assisting with any other QA related activities. Adherence to all QA standards. Matric Post Matric qualification will be an advantage Computer Literacy-MS Office (proficient in Excel, Word and PowerPoint) General administration experience cGMP skills 3 years’ experience in Pharmaceutical environment Basic QA and pharmaceutical knowledge Production / Manufacturing jobs
Job title : QA Administrator
Job Location : Western Cape,
Deadline : October 18, 2025
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Administrator • ZA