Fresh Jobs 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 AMD Chemistry Scientist to join a goal-oriented team.

QUALIFICATIONS NEEDED:

• Bachelors degree or diploma in Microbiology/Biochemistry/Chemistry/Process Engineering or equivalent.
• Recognition is given to Prior Learning and practical experience.

NECESSARY EXPERIENCE & INDUSTRY KNOWLEDGE:

• 2–3 years of hands-on High-Performance Liquid Chromatography (HPLC) experience, including method development, validation, and troubleshooting, preferably in a pharmaceutical, vaccine, or biologicals environment.
• Strong experience in the Product development of vaccines and/or biologicals and associated equipment.
• Proven hands-on expertise in HPLC, including method development, validation, and troubleshooting, preferably in a vaccine, biologicals, or pharmaceutical setting.
• Exposure and understanding of scientific principles that governs production of vaccines and /or biologicals.
• Knowledge of cGMP (SA, PIC, WHO) and GLP guidelines.
• Knowledge of bio-safety principles.
• Ability to work under biosafety level 3 containment.
• Experience in having faced successfully local quality audits would be an advantage.

KEY DUTIES & RESPONSIBILITIES OF THE ROLE:

• Laboratory Administration including Budgeting and Cost Control (Assists with group/ unit budgeting, follows a cost-conscious culture within own department/ group/ unit).
• Ensure services are delivered to all internal and/ or external stakeholders as defined and as per agreed timelines.
• Risk and Anticipation Mitigation to ensure that all work done is in accordance with current standards/processes and assist Senior Scientist/Group Leader to identify anticipated risks impacting group/ unit/ team.
• Develop and implement HPLC-based analytical methods to support in-process control, and final product characterization.
• Perform routine HPLC analysis, interpret data, and troubleshoot assays to ensure accuracy and reliability.
• Follow cGMP guidelines and ensure all Change Controls/ NCRs etc. are effectively managed to support QAs processes.
• Mitigate obvious risks on site and submit job cards to address facility issues/ risks as per the process set by Engineering.
• Close all actions assigned to self/ staff member as per EHS committee agreed deadlines.
• Responsible for providing assistance, guidance, problem solving or input to the operational departments as required and agreed.
• Responsible and accountable for the generation of applicable documentation in accordance with current scientific, GMP and GDP guidelines.
• Responsible for biological product and process development, which could include upstream (microbial cultivation) and down- stream processes (purification) and analytical method development (microbial, immunological, chemical).
• Responsible for experimental design, planning, execution, problem solving and recording.
• Assist with technology transfers from development to manufacturing (including manufacture of material to be used in clinical trials).
• Responsible and accountable for the generation of applicable documentation in accordance with current scientific, GMP and GDP guidelines.
• Driving Innovation and Continuous Improvement
• Compilation of Deviations, Change Controls, CAPAs

Application Deadline: 15 January 2026

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• 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 AMD Immunology Scientist to join a goal-oriented team.

QUALIFICATIONS NEEDED:

• Bachelors degree or diploma in Microbiology/Biochemistry/Chemistry/Process Engineering or equivalent.
• Recognition is given to Prior Learning and practical experience.

NECESSARY EXPERIENCE & INDUSTRY KNOWLEDGE:

• 2–3 years of hands-on Biological and molecular biology experience, including method development, validation, and troubleshooting, preferably in a pharmaceutical, vaccine, or biologicals environment.
• Strong experience in the Product development of vaccines and/or biologicals and associated equipment.
• Exposure and understanding of scientific principles that governs production of vaccines and /or biologicals.
• Knowledge of cGMP (SA, PIC, WHO) and GLP guidelines.
• Knowledge of bio-safety principles.
• Ability to work under biosafety level 3 containment.
• Experience in having faced successfully local quality audits would be an advantage.

KEY DUTIES & RESPONSIBILITIES OF THE ROLE:

• Laboratory Administration including Budgeting and Cost Control (Assists with group/ unit budgeting, follows a cost-conscious culture within own department/ group/ unit).
• Ensure services are delivered to all internal and/ or external stakeholders as defined and as per agreed timelines.
• Risk and Anticipation Mitigation to ensure that all work done is in accordance with current standards/processes and assist Senior Scientist/Group Leader to identify anticipated risks impacting group/ unit/ team.
• Develop and implement biological and molecular-based analytical methods to support in-process control, and final product characterization.
• Perform routine biological and molecular analysis, interpret data, and troubleshoot assays to ensure accuracy and reliability.
• Follow cGMP guidelines and ensure all Change Controls/ NCRs etc. are effectively managed to support QAs processes.
• Mitigate obvious risks on site and submit job cards to address facility issues/ risks as per the process set by Engineering.
• Close all actions assigned to self/ staff member as per EHS committee agreed deadlines.
• Responsible for providing assistance, guidance, problem solving or input to the operational departments as required and agreed.
• Responsible and accountable for the generation of applicable documentation in accordance with current scientific, GMP and GDP guidelines.
• Responsible for biological product and process development, which could include upstream (microbial cultivation) and down- stream processes (purification) and analytical method development (microbial, immunological, chemical).
• Responsible for experimental design, planning, execution, problem solving and recording.
• Assist with technology transfers from development to manufacturing (including manufacture of material to be used in clinical trials).
• Responsible and accountable for the generation of applicable documentation in accordance with current scientific, GMP and GDP guidelines.
• Driving Innovation and Continuous Improvement
• Compilation of Deviations, Change Controls, CAPAs.

Application Deadline: 15 January 2026

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• 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 AMD Senior Scientist to join a goal-oriented team.

QUALIFICATIONS NEEDED:

Required:

• PhD or MSc with at least 1-2 years experience in relevant discipline

Experience needed to deliver the role seamlessly:

• 2 years experience in vaccine / biotech / pharmaceutical industry or equivalent would be advantageous.
• 1 year supervisory experience in product development or a cGMP environment.
• Exposure and understanding of scientific principles that governs production of vaccines and /or biologicals.
• Quality & regulatory compliance knowledge, i.e. SAPHRA and WHO.
• GDP and IP management knowledge preferable.
• Experience in technology transfer would be advantageous.
• Knowledge of cGMP (SA, PIC, WHO) and GLP guidelines.
• Experience in having faced successfully local quality audits would be an advantage.

KEY DUTIES & RESPONSIBILITIES OF THE ROLE:

Core Technical Delivery:

• Laboratory Administration including Budgeting and Cost Control (Assists with group/ unit budgeting, follows a cost-conscious culture within own department/ group/ unit)
• Ensure services are delivered to all internal and/ or external stakeholders as defined and as per agreed timelines.
• Risk and Anticipation Mitigation to ensure that all work done is in accordance with current standards/processes and assist Senior Scientist/Scientist o identify anticipated risks impacting group/ unit/ team.
• Follow cGMP guidelines and ensure all Change Controls/ NCRs etc. are effectively managed to support QAs processes.
• Mitigate obvious risks on site and submit job cards to address facility issues/ risks as per the process set by Engineering.
• Close all actions assigned to self/ staff member as per EHS committee agreed deadlines.
• Responsible for providing assistance, guidance, problem solving or input to the operational departments as required and agreed.
• Responsible and accountable for the generation of applicable documentation in accordance with current scientific, GMP and GDP guidelines.
• Responsible for biological product and process development, which could include upstream (cultivation) and down- stream processes (purification) and analytical method development (microbial, immunological, chemical).
• Responsible for experimental design, planning, execution, problem solving and recording.
• Accountable for specified deliverables within projects according to agreed timelines.
• Assist with technology transfers from development to manufacturing (including manufacture of material to be used in clinical trials).
• Responsible and accountable for the generation of applicable documentation in accordance with current scientific, GMP and GDP guidelines.
• Driving Innovation and Continuous Improvement
• Driving Quality Risk Management
• Managing Deviations, Change Controls, CAPAs
• Quality Objectives: Drive the quality objectives.
• Communication:
• Ensure a timely and effective communication.
• Escalate quality issues to the appropriate levels of management.

People Management

• Align departmental focus areas and outputs to the business objectives.
• Conduct business, cross functional and departmental planning and execute activities within own scope of accountability.
• Adequate capacity planning and performance delivery in line with strategic, tactical, and operational plans
• Role profiling, goal setting and performance management of managers and staff within the department.
• Develop and implement a knowledge management infrastructure within the department to ensure Intellectual Property is effectively maintained.
• Growth, succession & retention of departmental talent.
• Accountability for own and team's personal and professional learning & development to ensure technical and leadership bench strength within the department.
• Ensure accurate and documented delegation of ongoing operational activities in the event of key staff members absence in line with the related policies and SOPs.
• Conduct effective employee relations in accordance with labour legislation, company policies and procedures and address any performance and conduct concerns and risks timeously.
• Ensure that Occupational and other risks related to roles within the department are defined and mitigated.

Application Deadline: 15 January 2026