QC Analyst: Biological Testing (x3)

Biovac; Wes-Kaap; On-site; ZAR 300,000 - 450,000; Full time

Job summary

A leading vaccine manufacturer in Africa is seeking a QC Analyst specializing in Biological Testing. The ideal candidate has 1-3 years of experience in the vaccine or biotech industry and strong laboratory skills. Responsibilities include implementing tests, performing biological testing, and ensuring compliance with cGMP standards. Join a dynamic team focused on protecting life.

Qualifications

• 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.

Responsibilities

• Implement new tests and technologies related to Biological testing.
• Perform Biological testing, including routine and non-routine testing.
• Maintain laboratory operations at cGMP standards.

Skills

Documentation skills

Laboratory skills

Quality compliance

Aseptic manufacturing

Education

Degree or diploma in Immunology / 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 x3 QC Analyst: Biological Testing to join a goal-oriented team.

QUALIFICATIONS NEEDED:

• Degree or diploma in Immunology / 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 and experience if molecular- and immunoassays such as ELISA testing, protein quantification assays, blotting assays, etc.

KEY DUTIES & RESPONSIBILITIES OF THE ROLE:

• Implementing new tests and new technologies and participation in the qualification of related equipment related to Biological testing,
• Performing Biological testing, for analytical development, analytical verification, and analytical validation activities,
• Participating in technology transfers from other vaccine manufacturers and other project activities from a Biological perspective,
• Maintaining laboratory operations at cGMP standards to ensure quality, safety, and regulatory compliance,
• Controlling stock related to Biological,
• Monitoring equipment and maintenance of Biological equipment,
• Contributing to drafting, updating, proof reading and editing of procedures related to Biological testing,
• Sampling of utilities, routine, and non-routine,
• Biological testing, routine, and non-routine (including utilities testing, raw material, in process, final product testing and stability).
• Reviewing of laboratory raw data related to Biological testing,
• Compiling laboratory reports related to Biological testing,
• Completing trend analysis templates as laboratory results are obtained from a Biological perspective,
• Participate in departmental audits and implement corrective actions where relevant.
• Actively involved with OOS and/or OOT investigation related to Biological 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.