Biovac, 1 Job Post – Quality Assurance Graduate

  • Full Time
  • Western Cape

Biovac

X3 Quality Assurance Graduate

Company: Biovac

Location: Western Cape, South Africa

Job type: Graduate Program

Contract: 24 months (fixed term)

About the Job

Biovac is one of Africa’s leading manufacturers of sterile vaccines. Our mission is to “protect life”. We are looking for a proactive, detail‑oriented, and enthusiastic Graduate – Quality Assurance to join our dynamic team.

Purpose of the Role

  • Support the line manager and team members in day‑to‑day activities.
  • Provide ongoing feedback to stakeholders on tasks and projects.
  • Ensure compliance with the Related Substances Act 101 of 1965, the Pharmacy Act 53 of 1974, and Biovac’s internal policies and procedures.
  • Promote teamwork and help achieve team deliverables.
  • Apply cGMP principles across quality operations.
  • Participate in a rotational program across Quality, Quality Assurance, Validation, Training, and Quality Control.
  • Deliver quality system services that meet pharmaceutical standards (SA GMP, PIC/S, WHO).
  • Plan and carry out QA functions aligned with best practice standards.

Key Duties & Responsibilities

  • Assist with data collection, research, and learning about the company’s processes.
  • Rotate through departments to gain exposure and identify improvement opportunities.
  • Take on business‑focus projects, research solutions and present findings.
  • Propose improvements and support the implementation of quality policies and procedures.
  • Help Validate equipment, processes and systems per industry standards.
  • Contribute to quality control activities: testing of raw materials, in‑process and finished products.
  • Analyze data, collaborate on quality issue resolution and close out CAPAs, deviations and incidents.
  • Use the e‑QMS (Trackwise) to close tickets, monitor dashboards and drive trend analysis.
  • Create automated reports for QMS items, APQRs and stakeholder requirements.
  • Support the local training program and build sustainable cGMP knowledge.
  • Ensure audit readiness and close audit findings on time.
  • Advocate continuous improvement and reduce the number of deviations, incidents and CAPAs.

Qualifications Needed

  • University degree or diploma in a relevant field (Life Sciences, Chemistry, Pharmacy, etc.).
  • Basic understanding of regulatory requirements and quality systems.
  • Excellent communication, organisation and analytical skills.
  • Team player with a proactive attitude and willingness to learn.
  • Ability to adapt to a rotating program and multi‑disciplinary projects.

Application Deadline

05 December 2025

Disclaimer

Dear Applicant, we value your privacy. Any personal information you share will be used solely for the application process and protected in accordance with our privacy policy. If you have questions, please contact our Human Capital department. We appreciate your interest and look forward to reviewing your application.

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How to Apply

To apply for this position, visit the following link:

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