47 Qc Analyst jobs in South Africa

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: Chemistry to join a goal-oriented team.

QUALIFICATIONS NEEDED:

• Diploma or degree in Analytical Chemistry, Biotechnology, Biochemistry or equivalent
• Recognition is given to Prior Learning and practical experience

NECESSARY EXPERIENCE & INDUSTRY KNOWLEDGE:

• At least 1 - 3 years experience within the pharmaceutical/ biotech manufacturing/ vaccine manufacturing / quality control or similar position.
• Demonstrated competency in laboratory skills, including documentation.
• Experience in quality and regulatory compliance within a cGMP facility.

KEY DUTIES & RESPONSIBILITIES OF THE ROLE:

• Implementation of new tests and new technologies and participation in the qualification of related equipment.
• Test development, verification and validation.
• Participation in technology transfers from other vaccine manufacturers and other project activities.
• Maintaining laboratory operations at cGMP standards to ensure quality, safety and regulatory compliance.
• Stock control.
• Equipment monitoring and maintenance.
• Contributing to drafting, updating, proof reading and editing of procedures.
• Sampling of utilities
• Routine testing (including utilities testing, raw material, in process, final product testing and stability).
• Peer review of laboratory raw data.
• Equipment calibration and maintenance adherence
• Compiling laboratory reports.
• Completing trend analysis templates as laboratory results are obtained.
• Participate in departmental audits and implement corrective actions where relevant.
• 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 in line with SOPs and DI principles of ALCOA+.

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.

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: Chemistry to join a goal-oriented team.

QUALIFICATIONS NEEDED:

• Diploma or degree in Analytical Chemistry, Biotechnology, Biochemistry or equivalent
• Recognition is given to Prior Learning and practical experience

NECESSARY EXPERIENCE & INDUSTRY KNOWLEDGE:

• At least 1 - 3 years’ experience within the pharmaceutical/ biotech manufacturing/ vaccine manufacturing / quality control or similar position.
• Demonstrated competency in laboratory skills, including documentation.
• Experience in quality and regulatory compliance within a cGMP facility.

KEY DUTIES & RESPONSIBILITIES OF THE ROLE:

• Implementation of new tests and new technologies and participation in the qualification of related equipment.
• Test development, verification and validation.
• Participation in technology transfers from other vaccine manufacturers and other project activities.
• Maintaining laboratory operations at cGMP standards to ensure quality, safety and regulatory compliance.
• Stock control.
• Equipment monitoring and maintenance.
• Contributing to drafting, updating, proof reading and editing of procedures.
• Sampling of utilities
• Routine testing (including utilities testing, raw material, in process, final product testing and stability).
• Peer review of laboratory raw data.
• Equipment calibration and maintenance adherence
• Compiling laboratory reports.
• Completing trend analysis templates as laboratory results are obtained.
• Participate in departmental audits and implement corrective actions where relevant.
• 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 in line with SOPs and DI principles of ALCOA+.

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.

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.

BioVac is a leading sterile vaccine manufacturer based in Africa, with the core purpose of "protecting life". We are seeking to hire four dynamic, passionate, confident, proactive, and meticulous QC Analysts for Biological Testing to join our goal-oriented team.

• Degree or diploma in Immunology, Biotechnology, Biochemistry, or equivalent.
• Recognition is given to prior learning and practical experience.

• 1-3 years of experience in vaccine, pharmaceutical, or biotech manufacturing industry with QC Laboratory.
• Competency in laboratory skills, including documentation.
• Experience with quality and regulatory compliance within a cGMP facility.
• Experience in aseptic (sterile) manufacturing is preferred.
• Knowledge of molecular and immunoassays such as ELISA, protein quantification, blotting assays, etc.

• Implementing new tests and technologies, and participating in equipment qualification related to Biological testing.
• Performing biological testing for analytical development, verification, and validation.
• Participating in technology transfers and other project activities from a biological perspective.
• Maintaining laboratory operations to cGMP standards to ensure quality, safety, and compliance.
• Controlling biological stock and monitoring equipment maintenance.
• Drafting, updating, proofreading, and editing procedures related to biological testing.
• Sampling utilities, routine and non-routine testing of raw materials, in-process samples, final products, and stability samples.
• Reviewing laboratory raw data and compiling reports.
• Performing trend analysis based on laboratory results.
• Participating in audits and implementing corrective actions.
• Handling OOS/OOT investigations related to biological testing, ensuring timely completion.
• Managing DMS queries as System Owner and escalating issues appropriately.
• Escalating quality issues and ensuring effective communication.
• Assisting with the implementation of the Containment Control Strategy.
• Ensuring data recording, review, and storage adhere to ALCOA+ principles.
• Promoting a culture of data integrity and compliance.
• Executing paper-based, hybrid, and computerized data handling.

Application Deadline: 11 August 2025

If you do not receive a response within three weeks, your application was not successful.

Disclaimer: We value your interest. Your information will be handled securely and confidentially, used solely for the application process, in accordance with our privacy policy. For inquiries, contact our Human Capital department. We look forward to reviewing your application.

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 x4 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.

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.

• Degree or diploma in Immunology, Biotechnology, Biochemistry, or equivalent.
• Recognition is given to prior learning and practical experience.

• 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.

• 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.

A client based in KZN - Durban North is looking for a Quality Control Assistant

• Must have his own transport.
• Will be based in Dube Tradeport, KZN
• Overtime & standby will be required
• Work is shift work - 12 hour shifts both day and night on rotation
• High quality working environment

Minimum Qualifications :

• Matric math’s HG pass
• Minimum 3 years’ experience in quality control (not industry specific)
• Preferred Experience :
• Rapid Global Risk software proficiency
• Ritescan scanning experience

Capabilities :

• Of strong character, not to be intimidated by other department members
• Pass eye test, which will include test for colour blindness
• Confident and able to make decisions
• Strong team player (cohesive, approachable, good at communicating)
• High attention to detail
• Able to handle a physical job, i.e. climbing ladders, picking up boxes, spend a lot of time on your feet
• Able to work under pressure, be able to solve problems and adapt when necessary
• Good written and verbal articulation ability
• Able and willing to work long hours
• Willing to participate in stock takes
• Strong ability to adhere to systems and procedure

Duties :

• Controlling and issuing labels to jobs
• Issuing signed standards to jobs and controlling signed standard room
• Constand updating of signed standards (signed by the QC manager)
• Ensuring QC boards are attached to each machine for each job change
• Verifying correct material is issued to jobs
• Scanning completed jobs out of WIP
• Monitoring Operations-process control, factory floor, qc station.
• Reporting incidents on Rapid software.
• Packing list to be put up- (new boards to be designed)
• Ensure manufactured stock meets mandated quality standards – per company policy Eliminate production delays due to poor quality of bought in stock or work in progress stock
• Always maintain quality control SOP and AQL control document – online checks required
• Have an intimate knowledge of Company product and what constitutes good quality
• Supply product that meets quality standards as agreed with the customers
• Engage with other team members cohesively, so that quality becomes a team responsibility, and all understand they are responsible for delivery thereof
• Complete required training on time and in a manner that allows you to affect what you have learnt in your daily duties
• Use all software mandated by the Company
• Always act in a manner that is aligned with company duties

Quality Control Assistant • Durban, South Africa

A well-established manufacturing company within the fruit industry has an exciting opportunity available for a Quality Control Manager at their Stellenbosch facility.

Requirements :

• Degree in Food Science or equivalent
• Experience in developing fruit quality assurance specifications
• 5 – 10 years’ experience within a FMCG manufacturing environment.

Quality Manager • Stellenbosch

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• Quality Inspections and Testing:
• Conduct regular inspections of supplier raw materials and at various stages of the manufacturing process to ensure compliance with quality standards and specifications. Perform testing and measurements using calibrated equipment to verify product functionality, safety, and reliability. Record and document inspection results, test data, and any deviations from quality standards.

• Quality Control Procedures:
• Develop, implement, and maintain quality control procedures and work instructions for manufacturing processes. Establish sampling plans, acceptance criteria, and inspection methods to ensure consistent product quality. Monitor adherence to quality control procedures and provide guidance to production teams as needed.
• Non-Conformance Management:
• Identify and document non-conformities, defects, or deviations from quality standards during inspections and testing. Investigate root causes of non-conformities and implement corrective and preventive actions to address quality issues. Track and monitor the effectiveness of corrective actions to prevent recurrence of non-conformities.
• "Continuous Improvement Initiatives:
• Identify opportunities for process improvements and efficiency gains in quality control procedures and manufacturing processes. Participate in continuous improvement projects and quality improvement teams to enhance product quality and reduce defects. Use quality tools and methodologies such as Six Sigma, Lean Manufacturing, and Root Cause Analysis to drive process improvements."
• Regulatory Compliance:
• Ensure compliance with regulatory requirements and standards related to product quality, safety, and environmental protection. Stay updated on industry regulations, standards, and quality management system requirements to ensure adherence to all applicable requirements. Collaborate with regulatory affairs and compliance teams to address any quality-related regulatory issues or requirements.
• Documentation and Reporting:
• Maintain accurate records and documentation of quality control activities, inspection results, test data, and non-conformities. Prepare quality reports, trend analyses, and performance metrics to track quality performance and communicate findings to management and stakeholders. Ensure documentation complies with regulatory requirements and internal quality management system (QMS) standards.
  

• Acceptance of Products:
• Decide whether to accept or reject product batches based on quality inspection results and adherence to specifications.
• Implementation of Corrective Actions:
• Determine appropriate corrective actions to address non-conformities, defects, or deviations from quality standards identified during inspections and testing.
• Approval of Supplier Quality:
• Decide whether to approve or reject suppliers based on their ability to meet quality requirements and performance standards.
• Changes to Quality Control Procedures:
• Decide whether to update or revise quality control procedures, work instructions, or sampling plans to improve effectiveness and efficiency.
• Investigation of Quality Incidents:
• Determine the root causes of quality incidents, complaints, or customer returns and decide on appropriate corrective and preventive actions.
• Resource Allocation for Quality Improvement:
• Decide on resource allocation for quality improvement initiatives, such as training, equipment upgrades, or process improvements. Decide on actions to ensure compliance with regulatory requirements, standards, and quality management system (QMS) requirements.
  

• Technical Competence:
• Understanding of manufacturing processes, materials, and specifications. Proficiency in using quality control tools, equipment, and testing methods relevant to electrical components.
• Knowledge of industry standards and regulations related to electrical product safety and quality.
• Analytical Skills:
• Ability to analyze data, test results, and quality metrics to identify trends, patterns, and areas for improvement.
• Problem-Solving Abilities:
• Aptitude for identifying root causes of quality issues and implementing effective corrective and preventive actions.
• Capacity to troubleshoot quality-related problems and make timely decisions to address them.
• Attention to Detail:
• Meticulous attention to detail is crucial for conducting thorough inspections, testing, and documentation of quality control activities.
• Ability to identify even minor deviations from quality standards and specifications.
• Communication Skills:
• Effective communication skills, both verbal and written, to convey quality expectations, report findings, and collaborate with cross-functional teams.
• Quality Management System (QMS) Knowledge:
• Familiarity with quality management principles and practices, including ISO 9001 standards and quality assurance methodologies.
• Understanding of QMS requirements, documentation standards, and procedures for maintaining compliance.
• Ability to ensure compliance with regulatory requirements and maintain up-to-date knowledge of industry regulations.
• Commitment to continuous improvement and quality excellence through the implementation of quality improvement initiatives and best practices.
• Teamwork and Collaboration:
• Ability to collaborate effectively with production teams, engineers, quality assurance personnel, suppliers, and other stakeholders to achieve quality objectives.
  

• Quality Management or Quality Control qualification (National Diploma or higher preferred)
• Minimum 5 years of experience in the cable or electrical component manufacturing industry
• In-depth knowledge of cable manufacturing processes and quality requirements
• Proficient in the use of measurement tools (multi-meters, callipers, hi-pot testers, micrometres, etc.)
• Familiar with ISO standards (e.g., ISO 9001), Six Sigma, and Kaizen methodology
• Strong analytical and root-cause analysis skills
• Competent in drafting technical reports and documentation
• High attention to detail
• Ability to work independently and make objective decisions.
• Strong written and verbal communication skills
• Excellent organizational and time management abilities
• Uncompromising integrity and commitment to quality
• Initiative-taking, assertive, and able to stand firm under pressure.