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: Biological Testing to join our 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 of experience in vaccine, pharmaceutical, or biotech manufacturing industry within a 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 with molecular- and immunoassays such as ELISA testing, protein quantification assays, blotting assays, etc.
Key Duties & Responsibilities:
- Implementing new tests and technologies, and participating in the qualification of related equipment for Biological testing.
- Performing biological testing for analytical development, verification, and validation activities.
- Participating in technology transfers and project activities from a biological perspective.
- Maintaining laboratory operations at cGMP standards to ensure quality, safety, and regulatory compliance.
- Controlling stock related to biological materials.
- Monitoring and maintaining biological equipment.
- Drafting, updating, proofreading, and editing procedures related to biological testing.
- Sampling utilities, and conducting routine and non-routine testing (raw materials, in-process, final product, stability).
- Reviewing laboratory raw data and compiling reports related to biological testing.
- Performing trend analysis as results are obtained.
- Participating in departmental audits and implementing corrective actions.
- Managing OOS and OOT investigations related to biological testing, ensuring timely and standard-compliant completion.
- Attending to DMS queries promptly as the System Owner, escalating issues as necessary.
- Escalating quality issues and ensuring effective communication within the team.
- Assisting with the implementation of the Containment Control Strategy (CCS).
- Recording, reviewing, and storing all laboratory data in accordance with ALCOA+ principles.
- Promoting a culture of data integrity and compliance.
- Executing data handling in paper, hybrid, and computerized formats.
Application Deadline: 11 August 2025
If you do not receive a response within three weeks, your application was not successful.
Disclaimer:
We are committed to protecting your personal information. By applying, you agree to our privacy policy regarding data collection and use. For inquiries, contact our Human Capital department. We look forward to reviewing your application.