Aspen Pharma Group
Quality Pharmacist
Skills
13 days ago
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Important information
Contract type:
Permanent
Location:
Gqeberha, South Africa
Work mode:
Onsite
Published on:
14 October 2026
What they need
Responsible for ensuring that pharmaceutical products and manufacturing processes meet GMP, regulatory, quality and company requirements. The role reviews and approves quality documentation, supports product release, manages quality risks and ensures that deviations, CAPAs and changes are properly controlled.
Main Responsibilities
- Review and approve batch and quality documentation.
- Release finished products in line with GMP and regulatory requirements.
- Monitor manufacturing processes for quality and compliance.
- Investigate deviations, quality issues and process problems.
- Support and review CAPAs, change controls and risk assessments.
- Review and approve production and QC changes.
- Conduct and support quality inspections and compliance checks.
- Review Annual Product Quality Reviews (APQRs).
- Manage retention samples according to requirements.
- Maintain accurate quality records and documentation.
- Prepare and provide quality reports.
- Identify quality risks and recommend corrective or preventive actions.
- Provide guidance and support to Production and other relevant teams.
- Ensure SOPs, GMP requirements and regulatory standards are consistently followed
Job Requirements Qualification:
- BPharm Degree.
- Registered with the South African Pharmacy Council (SAPC).
Experience:
- Approximately 2 years' pharmaceutical manufacturing experience.
- Experience in Quality Assurance, GMP and pharmaceutical quality systems.
- Experience with batch release, deviations, CAPA and change control is advantageous
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