QC Analyst: Microbiology

Biovac; Wes-Kaap; On-site; ZAR 300,000 - 420,000; Full time

Job summary

A leading vaccine manufacturer in Africa is looking for a dynamic QC Analyst: Microbiology. The role requires a degree in Microbiology or related fields and 1-3 years of experience in the pharmaceutical manufacturing industry. Key responsibilities include implementing microbiology tests, maintaining cGMP standards, and ensuring compliance with quality regulations. The application deadline is August 11, 2025.

Qualifications

• 1-3 years experience in vaccine or pharmaceutical manufacturing industry.
• Experience in quality and regulatory compliance within a cGMP facility.
• Demonstrated competency in laboratory skills, including documentation.

Responsibilities

• Implement new tests and technologies related to Microbiology testing.
• Maintaining laboratory operations at cGMP standards.
• Contributing to drafting and updating procedures related to Microbiology testing.

Skills

Laboratory skills

Quality compliance

Aseptic manufacturing knowledge

Microbiology testing

Education

Degree or diploma in Microbiology / Biotechnology / Biochemistry or equivalent

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 QC Analyst: Microbiology to join a goal-oriented team.

QUALIFICATIONS NEEDED:

• Degree or diploma in Microbiology / Biotechnology / Biochemistry or equivalent.
• Recognition is given to Prior Learning and practical experience.

NECESSARY EXPERIENCE & INDUSTRY KNOWLEDGE:

• At least 1- 3 years’ experience in vaccine / pharmaceutical / biotech manufacturing industry with QC Laboratory.
• Demonstrated competency in laboratory skills, including documentation.
• Experience in quality and regulatory compliance within a cGMP facility.
• Experience in aseptic (sterile) manufacturing is preferred.
• Knowledge of Sterility testing, Growth promotion, Micro Identification, Environmental monitoring and utilities testing is preferred.

KEY DUTIES & RESPONSIBILITIES OF THE ROLE:

• Implementing new tests and new technologies and participation in the qualification of related equipment related to Microbiology testing.
• Performing Microbiology testing, for analytical development, analytical verification, and analytical validation activities.
• Participating in technology transfers from other vaccine manufacturers and other project activities from a Microbiology perspective.
• Maintaining laboratory operations at cGMP standards to ensure quality, safety, and regulatory compliance.
• Controlling stock related to Microbiology.
• Monitoring equipment and maintenance of Microbiology equipment.
• Contributing to drafting, updating, proof reading and editing of procedures related to Microbiology testing.
• Sampling of utilities, routine, and non-routine.
• Microbiology testing, routine, and non-routine (including utilities testing, raw material, in process, final product testing and stability).
• Reviewing of laboratory raw data related to Microbiology testing.
• Compiling laboratory reports related to Microbiology testing.
• Completing trend analysis templates as laboratory results are obtained from a Microbiology perspective.
• Participate in departmental audits and implement corrective actions where relevant.
• Actively involved with OOS and/or OOT investigation related to Microbiology testing (internal or external testing) and ensuring that OOS and/or OOT investigations are completed on time, and to the correct standard.
• Ensure that DMS queries are attended to within a reasonable time as the System Owner and escalated to Laboratory Supervisors and management.
• Ensuring timely and effective communication by escalating quality issues to the appropriate levels of management, including DMS excursions.
• Assisting with implementation of the Containment Control Strategy (CCS) for the site.
• Ensure all laboratory data is recorded, reviewed, and stored in accordance with ALCOA+ principles (Attributable, Legible, Contemporaneous, Original, Accurate, Complete, Consistent, Enduring, and Available).
• Analysts promote a good culture of data integrity and ensure compliance within the laboratory.
• Execute proper paper based, hybrid and computerized data handling.

Application Deadline: 11 August 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.

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.