Sterility Support Process Specialist

Biovac; Cape Town; On-site; ZAR 400 000 - 600 000; Full time

Job summary

A leading sterile vaccine manufacturer in Africa is seeking a Sterility Support Process Specialist to join their team in Cape Town. The ideal candidate will have a Bachelor's degree in microbiology or a related field and strong analytical skills to interpret data. Responsibilities include troubleshooting production issues, analyzing data, and delivering training on sterility concepts. The company embraces diversity and applies Employment Equity principles in its hiring processes.

Qualifications

• Bachelor's degree in a relevant field is required.
• Knowledge of aseptic manufacturing processes is essential.
• Strong analytical abilities for interpreting data are crucial.

Responsibilities

• Initiate testing and troubleshooting in the production environment.
• Analyze process data to drive improvements.
• Deliver training on sterility concepts.

Skills

Strong knowledge of microbiology

Analytical skills

Collaboration

Communication

Education

Bachelor's degree in Microbiology, Engineering, Biochemistry, Chemistry, or Pharmaceutical Sciences

Job description

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 Sterility Support Process Specialist to join a goal-oriented team.

QUALIFICATIONS NEEDED:

• Bachelors degree in microbiology, Engineering, Biochemistry, Chemistry, or Pharmaceutical Sciences or in a relevant field

NECESSARY EXPERIENCE & INDUSTRY KNOWLEDGE:

Minimum requirements:

• Strong knowledge of microbiology including both analytical and practical application.
• Analytical skills to interpret both quantitative and qualitative data.

Preferred requirements:

• Experience in a GMP manufacturing environment
• Experience with digital solutions to drive operational excellence

KEY DUTIES & RESPONSIBILITIES OF THE ROLE:

Core Technical Delivery:

• Take initiative on the production floor: test, troubleshooting, identify problems, and implement practical solutions.
• Analyze environmental and process data to spot trends and drive improvements.
• Ability to interpret both quantitative and qualitative data, especially from environmental monitoring.
• Technical proficiency in aseptic manufacturing processes, cleanroom operations, and contamination control.
• Communicate clearly and simply, making complex information accessible to all team members.
• Collaborate with people from diverse backgrounds and education levels.
• Develop and deliver training that simplifies complex sterility concepts.
• Foster a culture of continuous improvement and creative problem-solving.
• Maintain and review sterility assurance records and documentation.
• Support compliance with sterility processes and procedures.

Application Deadline: 31 December 2025

If you do not receive a response from us within three weeks of submitting your application, please understand that your application was not successful.

We believe in the magic of diversity within teams and to achieve this, we do apply Employment Equity principles during our selection process where this is necessary to achieve such diversity.

Disclaimer:

Dear Applicant, we appreciate your interest in joining our organization. It is imperative for us that you understand how we handle your information. We are committed to ensuring the security and confidentiality of the information you provide. Your personal details will be collected for the sole purpose of the application process and will be used strictly for that purpose. By applying, you acknowledge and consent to the collection, use, and protection of your personal information in accordance with our privacy policy. If you have any inquiries or concerns, our Human Capital department is available to provide clarification. We look forward to reviewing your application.