Senior Pharmaceutical QA Auditor — GMP/GDP Expert & CAPA Lead

Placements24

Soweto

On-site

ZAR 600,000 - 900,000

Full time

7 days ago
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Benefits offered by this job

Medical aid
Retirement fund
Professional development
Structured environment

Job summary

Placements24 in Soweto, Gauteng, is seeking a highly experienced Pharmaceutical Quality Assurance Auditor to ensure regulatory compliance across manufacturing sites, suppliers and quality systems.

The role requires a Bachelor’s degree in Pharmacy or Chemistry and 4–6 years in QA/QC with auditing experience. You will identify non-conformities, recommend CAPAs, and contribute to the QMS integrity and safety of medicines.

Qualifications

  • Bachelor's degree in Pharmacy, Chemistry or related scientific discipline.
  • 4–6 years in pharma QA or QC with auditing experience.
  • Knowledge of GMP, GDP and pharmaceutical regulatory requirements.
  • Experience conducting internal and supplier audits.
  • Strong report writing and communication skills.

Responsibilities

  • Plan, conduct, and report on internal and external audits of manufacturing facilities, quality control laboratories, warehouses, and suppliers.
  • Assess compliance with GMP, GDP, and other regulatory requirements (e.g., SAHPRA).
  • Identify non-compliance issues and deviations, document findings, and recommend CAPAs.
  • Follow up on the implementation and effectiveness of CAPAs.
  • Review and approve quality-related documents, including SOPs and batch records.
  • Contribute to the continuous improvement of the QMS.

Skills

Auditing
Regulatory knowledge
Analytical skills

Education

Bachelor's degree in Pharmacy/ Chemistry

Job description

Placements24 in Soweto, Gauteng, is seeking a highly experienced Pharmaceutical Quality Assurance Auditor to ensure regulatory compliance across manufacturing sites, suppliers and quality systems.

The role requires a Bachelor’s degree in Pharmacy or Chemistry and 4–6 years in QA/QC with auditing experience. You will identify non-conformities, recommend CAPAs, and contribute to the QMS integrity and safety of medicines.

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