Location: White River, South Africa
Closing Date: 31 December 2025
Apply Link: 👉 APPLY NOW
Role Purpose
Carry out defined quality assurance and quality control activities to support and optimise the overall quality standards within the organisation.
Required Qualifications
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Grade 12 / NQF Level 4
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BSc Degree (advantageous)
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Minimum 3 years QA/QC experience in the pharmaceutical industry
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Strong knowledge of cGMP, regulatory guidelines, and ISO standards
Required Skills & Abilities
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Computer literate (Microsoft Word & Excel)
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Ability to work independently and within a team
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Excellent written communication and document management
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Exceptional attention to detail
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Strong time management skills
Role Responsibilities
Quality Assurance
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Compile, review, and close out quality incidents (OOS, non-conformances, deviations, change controls, CAPAs)
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Compile and review SOPs and work instructions
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Perform GDP and GMP compliance checks during manufacturing
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Coordinate and conduct internal and supplier audits
Documentation
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Issue document numbers and manage QMS document control
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Distribute, retrieve and archive documents
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Maintain version control and official document copies
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Log quality incidents
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Compile reports such as APQR and QMR
Training
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Prepare training plans and training matrices
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Coordinate the company training programme
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Prepare and file records and training presentations
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Create general employee training awareness
Trending
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Track and trend QMS data (OOS, deviations, CAPAs, change controls, etc.)
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Analyse product-related data such as yields and deviations