Quality Assurance Officer - Wildlife Pharmaceuticals

Role Purpose:Carry out specifically defined activities in terms of quality guarantees and/or quality assurance systems with the aim of contributing to the optimisation of quality within the organisation.Required Role Qualifications:Grade 12 or NQF Level 4BSc Degree advantageousMinimum of 3 years’ QA/QC experience in pharmaceutical industryGood knowledge of cGMP, regulatory guidelines and ISO standardsRequired Role Skills and Abilities:Computer literate with an excellent grasp of Microsoft Word and ExcelWork independently while also being a team player.Effective written communication & excellent document managementExcellent attention to detailGood time management skillsRequired Role Responsibilities:Quality assurance:Assist in the compilation, review and close out of quality incidents, e.g. OOS, non-conformances, deviations, change controls, CAPA’s, andAssist in the compilation and review of SOPs and work instructions.Perform GDP and GMP compliance checks during manufacturing.Coordinate and conduct internal audit and supplier audits.Documentation:Issue document numbers.Issue, distribute and retrieve QMS documents.Compile and/or review documents.Maintain document version control including creating official copies; superseding and obsoleting QMS documents.Logging of quality incidents e.g. OOS, non-conformances, deviations, change controls, CAPA’s etc.Compile reports e.g. APQR & QMR.Training:Prepare the training plan and training matrix.Coordinate the training programmePrepare and file training records.Prepare training presentations.Create general employee training awareness.Trending:QMS data, e.g. OOS, non-conformances, deviations, change controls, CAPA’s, and deviations.Product data i.e. yields, OOS, deviations, CAPA’s, change control etc.White RiverPublished Date: 13 November 2025Closing Date: 31 December 2025