QC Microbiology Technician at Biovac

• BIOVAC is one of the leading sterile vaccine manufacturers rooted in Africa, with our core purpose being to "protect life". We are looking to hire a dynamic, passionate, confident, proactive and meticulous QC Microbiology Technician to join a goal-oriented team.

QUALIFICATIONS NEEDED:

• Matric/ Grade 12 or equivalent.

NECESSARY EXPERIENCE & INDUSTRY KNOWLEDGE:

• At least 1 years experience within the pharmaceutical/ biotech manufacturing/ vaccine manufacturing / quality control or similar position.

OTHER REQUIREMENTS:

• Routine shift work, occasional after-hours availability required based on operational requirements.
• Reliable transport that enables you to work all the required shifts.
• Ability to work in cleanrooms (Grades A–D) under full gowning (If you have respiratory issues or health concerns that may impede your ability to work under strict gowning requirements we need to know in advance).
• High levels of concentration and ability to perform repetitive tasks accurately.

KEY DUTIES & RESPONSIBILITIES OF THE ROLE:

Duties below are not an exhaustive list, additional duties may be required based on operation requirements.

• Assist in day-to-day laboratory operation requirements.
• Sampling of utilities and environmental monitoring.
• Stock control and receipt
• Monitoring and sanitisation of purified water
• Equipment monitoring and maintenance.
• Assist with sample reception
• Contributing to drafting, updating, proof reading, editing of procedures.
• Compiling laboratory reports.
• Maintaining laboratory operations at cGMP standards to ensure quality, safety and regulatory compliance.
• Participate in investigations.
• Participate in departmental audits and implement corrective actions where relevant.
• Building own, team and sites GMP Knowledge and Compliance
• Participate in achieving the company.
• Participate in building a sustainable Quality Culture on site and proactive mitigate risks that may negatively impact quality or escalate these appropriately.
• Ensuring that the department is audit ready through closing out audit findings timeously
• Advocate continuous improvement
• Strong understanding of data integrity compliance/practise in a GMP environment.

Application Deadline: 06/02/2026