Quality Assurance Pharmacist Assistant – Compliance Focus

Biovac; Cape Town; On-site; ZAR 300,000 - 420,000; Full time

Job summary

Biovac is seeking a QA Pharmacist Assistant to support quality assurance activities in a cGMP environment. You will handle document administration for release, review batch records, and assist with QA release processes and audits at our facility in Cape Town.

Minimum qualification includes Post Basic Pharmacist Assistant with 2–3 years in pharma quality or sterile manufacturing. Knowledge of SAHPRA guidelines and regulatory compliance is essential.

Qualifications

• At least 2–3 years’ experience in pharmaceutical / vaccine or sterile manufacturing / quality assurance.
• Experience in quality management systems within a cGMP facility.
• Knowledge of pharmaceutical legislation is preferred.
• Experience in aseptic (sterile) manufacturing is a plus.

Responsibilities

• Document Administration for Release documents.
• Record Administration, archiving, and filing of release documents.
• Batch book issuing and retrieval.
• Data base management and report generation for product release.
• General Administration including filing, scanning, and audits support.
• Measurement, analysis and improvement initiatives and cross‑functional projects.

Skills

Quality Systems

GMP Knowledge

Documentation Management

SOPs

Education

Matric / Grade 12 or equivalent

Post Basic Pharmacist Assistant

Tools

Database management

Job description

Biovac is seeking a QA Pharmacist Assistant to support quality assurance activities in a cGMP environment. You will handle document administration for release, review batch records, and assist with QA release processes and audits at our facility in Cape Town.

Minimum qualification includes Post Basic Pharmacist Assistant with 2–3 years in pharma quality or sterile manufacturing. Knowledge of SAHPRA guidelines and regulatory compliance is essential.