Pharma QA Specialist — Audits, CAPA & Process Improvement

Placements24

Rustenburg

On-site

ZAR 600,000 - 900,000

Full time

2 days ago
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Benefits offered by this job

Competitive salary package
Health insurance
Retirement savings plan
Life insurance
Training and development
Stable work environment

Job summary

Placements24 is seeking a Pharmaceutical Quality Assurance Specialist to join the Rustenburg team. The role focuses on ensuring quality across the product lifecycle, performing audits, reviewing documentation, and driving CAPA and process improvements.

You will work with the QA team to maintain GMP compliance, support regulatory inspections, and contribute to continuous quality enhancements in a leading pharmaceutical manufacturer.

Qualifications

  • Bachelor’s degree in a relevant science field required.
  • Minimum 4 years of QA experience in pharma industry.
  • Solid understanding of GMP and SAHPRA/regulatory guidelines.
  • Experience with CAPA, deviations, and QMS documentation.

Responsibilities

  • Conduct internal audits of manufacturing processes and systems for GMP compliance.
  • Review and approve batch records and validation protocols.
  • Investigate deviations and OOS results; implement CAPA actions.
  • Support external regulatory audits and inspections with proper documentation.
  • Lead quality improvement initiatives and maintain QMS procedures.
  • Update training materials and ensure ongoing QA compliance.

Skills

GMP knowledge
CAPA
QMS experience
Audit experience
Regulatory liaison

Education

Bachelor's degree in Pharmacy, Chemistry, Biology or related

Tools

Quality management systems

Job description

Placements24 is seeking a Pharmaceutical Quality Assurance Specialist to join the Rustenburg team. The role focuses on ensuring quality across the product lifecycle, performing audits, reviewing documentation, and driving CAPA and process improvements.

You will work with the QA team to maintain GMP compliance, support regulatory inspections, and contribute to continuous quality enhancements in a leading pharmaceutical manufacturer.

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