1,852 Qc Supervisor 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 Supervisor: 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 4 years experience in sterile vaccine / pharmaceutical / biotech manufacturing industry with QC Laboratory.
• At least 1 year experience at supervisor level.
• Experience in quality and regulatory compliance within a cGMP facility.
• Experience in aseptic (sterile) manufacturing is preferred.

KEY DUTIES & RESPONSIBILITIES OF THE ROLE:

• Driving continuous improvement plans and priorities through the implementation of appropriate tools or methodologies to proactively manage risk, reduce wastage and to improve quality on site.
• Planning and assisting with routine laboratory testing.
• Co-ordinating testing of Stability, analytical verification and/or analytical validation samples related to Biological testing and associated activities.
• Compiling data trends, data analysis and associated reports related to Biological testing to the correct standard and on time.
• Reviewing of laboratory raw data and logbooks, including OOS/MDDs and or OOT results from internal and/or external testing related to Biological testing.
• Ensuring that OOS/MDDs and OOT investigations are initiated and completed to the correct standard.
• Training and upskilling of analysts within Biological Testing.
• Training analysts on theoretical aspects of Biological testing with hands-on training approach by means of demonstration and supervision, using test methods, SOPs, and other documentation and formal assessments.
• Performing formal competency assessments of performance, (e.g., Endotoxin, etc.)
• Selecting analytical test equipment for procurement and participating in equipment qualification e.g., review of qualification documents from a Biological perspective.
• Assisting in writing and updating of material and product specifications and test methods and standard operating procedures related to Biological testing.
• Participating in the selection and procurement of analytical test equipment and participation in equipment qualification (e.g., review of qualification documents.)
• Adhering to Pharmaceutical Quality System (PQS) requirements (e.g., SOPs, CAPAs, Deviations, Risk Assessments, and Change Controls.)
• Participating in quality audits and close out gaps and findings.
• Participating in inspections, investigations, risk management and quality review exercises.
• Participating in Biological testing related to technology transfers from other vaccine manufacturers and other project activities.
• Ensuring that DMS queries are attended to and resolved within a reasonable time as the System Owner.
• Co-ordinating Data Integrity in the QC Laboratory with reference to Biological testing with new and upcoming technologies (e.g., LIMS, new hardware and software programs, new technologies), when necessary.
• Co-ordinating Biological Risk assessments in accordance with cGMP guidelines (e.g., ICH Q9, ICH Q10, etc.)
• Assisting with implementation of the site Containment and Control Strategy (CSS), with reference to Biological testing.

We are an equal opportunities employer and welcome applications from all qualified candidates.

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 Supervisor: 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 4 years' experience in sterile vaccine / pharmaceutical / biotech manufacturing industry with QC Laboratory.
• At least 1 year experience at supervisor level.
• Experience in quality and regulatory compliance within a cGMP facility.
• Experience in aseptic (sterile) manufacturing is preferred.

KEY DUTIES & RESPONSIBILITIES OF THE ROLE:

• Driving continuous improvement plans and priorities through the implementation of appropriate tools or methodologies to proactively manage risk, reduce wastage and to improve quality on site.
• Planning and assisting with routine laboratory testing.
• Co-ordinating testing of Stability, analytical verification and/or analytical validation samples related to Biological testing and associated activities.
• Compiling data trends, data analysis and associated reports related to Biological testing to the correct standard and on time.
• Reviewing of laboratory raw data and logbooks, including OOS/MDDs and or OOT results from internal and/or external testing related to Biological testing.
• Ensuring that OOS/MDDs and OOT investigations are initiated and completed to the correct standard.
• Training and upskilling of analysts within Biological Testing.
• Training analysts on theoretical aspects of Biological testing with hands-on training approach by means of demonstration and supervision, using test methods, SOP's, and other documentation and formal assessments.
• Performing formal competency assessments of performance, (e.g., Endotoxin, etc.)
• Selecting analytical test equipment for procurement and participating in equipment qualification e.g., review of qualification documents from a Biological perspective.
• Assisting in writing and updating of material and product specifications and test methods and standard operating procedures related to Biological testing.
• Participating in the selection and procurement of analytical test equipment and participation in equipment qualification (e.g., review of qualification documents.)
• Adhering to Pharmaceutical Quality System (PQS) requirements (e.g., SOPs, CAPA's, Deviations, Risk Assessments, and Change Controls.)
• Participating in quality audits and close out gaps and findings.
• Participating in inspections, investigations, risk management and quality review exercises.
• Participating in Biological testing related to technology transfers from other vaccine manufacturers and other project activities.
• Ensuring that DMS queries are attended to and resolved within a reasonable time as the System Owner.
• Co-ordinating Data Integrity in the QC Laboratory with reference to Biological testing with new and upcoming technologies (e.g., LIMS, new hardware and software programs, new technologies), when necessary.
• Co-ordinating Biological Risk assessments in accordance with cGMP guidelines (e.g., ICH Q9, ICH Q10, etc.)
• Assisting with implementation of the site Containment and Control Strategy (CSS), with reference to Biological testing.

Application Deadline: 14 October 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 Supervisor: 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 4 years experience in sterile vaccine / pharmaceutical / biotech manufacturing industry with QC Laboratory.
• At least 1 year experience at supervisor level.
• Experience in quality and regulatory compliance within a cGMP facility.
• Experience in aseptic (sterile) manufacturing is preferred.

KEY DUTIES & RESPONSIBILITIES OF THE ROLE:

• Driving continuous improvement plans and priorities through the implementation of appropriate tools or methodologies to proactively manage risk, reduce wastage and to improve quality on site.
• Planning and assisting with routine laboratory testing.
• Co-ordinating testing of Stability, analytical verification and/or analytical validation samples related to Biological testing and associated activities.
• Compiling data trends, data analysis and associated reports related to Biological testing to the correct standard and on time.
• Reviewing of laboratory raw data and logbooks, including OOS/MDDs and or OOT results from internal and/or external testing related to Biological testing.
• Ensuring that OOS/MDDs and OOT investigations are initiated and completed to the correct standard.
• Training and upskilling of analysts within Biological Testing.
• Training analysts on theoretical aspects of Biological testing with hands-on training approach by means of demonstration and supervision, using test methods, SOPs, and other documentation and formal assessments.
• Performing formal competency assessments of performance, (e.g., Endotoxin, etc.)
• Selecting analytical test equipment for procurement and participating in equipment qualification e.g., review of qualification documents from a Biological perspective.
• Assisting in writing and updating of material and product specifications and test methods and standard operating procedures related to Biological testing.
• Participating in the selection and procurement of analytical test equipment and participation in equipment qualification (e.g., review of qualification documents.)
• Adhering to Pharmaceutical Quality System (PQS) requirements (e.g., SOPs, CAPAs, Deviations, Risk Assessments, and Change Controls.)
• Participating in quality audits and close out gaps and findings.
• Participating in inspections, investigations, risk management and quality review exercises.
• Participating in Biological testing related to technology transfers from other vaccine manufacturers and other project activities.
• Ensuring that DMS queries are attended to and resolved within a reasonable time as the System Owner.
• Co-ordinating Data Integrity in the QC Laboratory with reference to Biological testing with new and upcoming technologies (e.g., LIMS, new hardware and software programs, new technologies), when necessary.
• Co-ordinating Biological Risk assessments in accordance with cGMP guidelines (e.g., ICH Q9, ICH Q10, etc.)
• Assisting with implementation of the site Containment and Control Strategy (CSS), with reference to Biological testing.

Application Deadline: 14 October 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.

Genpact City of Johannesburg, Gauteng, South Africa

Genpact is an advanced technology services and solutions company that delivers lasting value for leading enterprises globally. Through our deep business knowledge, operational excellence, and cutting-edge solutions – we help companies across industries get ahead and stay ahead. Powered by curiosity, courage, and innovation, our teams implement data, technology, and AI to create tomorrow, today. Get to know us at genpact.com and on LinkedIn, X, YouTube, and Facebook.

Inviting applications for the role of Management Trainee - Quality (Premium Customer Care Voice)

• New Hire Trainings and Refresher Sessions: Leads NHT program in line with client provided Training content to equip new hires with required knowledge on client processes and tools. Leads the Nesting team of Customer Service & Payment Support specialists to achieve performance goals to be assessed ready for movement to Operations
• Quality Monitoring: Evaluate and audit calls/cases handled by team members to check quality health of the team, providing feedback and implementing improvement plans as necessary to bring in required improvement.
• Refresher Trainings and Process Knowledge Tests: Conduct regular training sessions to enhance the skills and knowledge of the team in line with new process updates and check retention through PKTs
• Compliance Assurance: Ensure all collection activities comply with industry regulations and company policies.
• Reporting: Prepare and present regular reports on team’s training and quality performance, challenges, and achievements to senior management.
• Customer Interaction: Handle escalated customer issues and complaints, ensuring a high level of customer satisfaction during no new hire batches to stay update to date with process changes
• Process Improvement: Identify opportunities for process improvements and implement changes to enhance efficiency and effectiveness.
• Adhering to client defined Process Flows: Ensuring all operations activities during customer interactions comply with relevant process flows

• Minimum Qualifications / Skills: Work Experience - Candidate with two years of experience working on US financial services and Minimum of 4 years of experience in a voice role
• Leadership: Ability to inspire and lead new hire batches and Production teams towards achieving common goals in direction of knowledge management and retention.
• Problem-Solving: Strong analytical skills to identify issues and develop effective solutions.
• Communication: Excellent verbal and written communication skills to interact with team members and customers effectively.
• Adaptability: Ability to work in a 24x7 fast-paced environment and adapt to changing priorities.
• Education Qualification: Graduate or Post Graduate in any field
• Special Skills: Advanced knowledge of MS Word & Excel; ability to work in a fast-paced environment with quality and timeline standards; high integrity; ability to work effectively in a team; relevant experience with international IB/ OB Voice process; mandatory experience in Training and/or Quality function as Process Trainer and/or Quality Auditor

• Be a transformation leader – Work at the cutting edge of AI, automation, and digital innovation
• Make an impact – Drive change for global enterprises and solve business challenges that matter
• Accelerate your career — Get hands-on experience, mentorship, and continuous learning opportunities
• Work with the best – Join 140,000+ bold thinkers and problem-solvers who push boundaries every day
• Thrive in a values-driven culture – Our courage, curiosity, and incisiveness - built on a foundation of integrity and inclusion - allow your ideas to fuel progress

Come join the tech shapers and growth makers at Genpact and take your career in the only direction that matters: Up. Let’s build tomorrow together.

Genpact is an Equal Opportunity Employer and considers applicants for all positions without regard to race, color, religion or belief, sex, age, national origin, citizenship status, marital status, military/veteran status, genetic information, sexual orientation, gender identity, physical or mental disability or any other characteristic protected by applicable laws. Genpact is committed to creating a dynamic work environment that values respect and integrity, customer focus, and innovation.

Genpact does not charge fees to process job applications and applicants are not required to pay to participate in our hiring process in any other way. Examples of such scams include purchasing a 'starter kit,' paying to apply, or purchasing equipment or training.

• Seniority level: Associate
• Employment type: Full-time
• Job function: Quality Assurance and Training
• Industries: Business Consulting and Services and Outsourcing and Offshoring Consulting

Randburg, Gauteng, South Africa 6 days ago

City of Johannesburg, Gauteng, South Africa 1 week ago

• Internal QMS
• Quality Management
• Continuous Improvement
• Training and Education
• Design Development and Support
• Incoming Material
• Manufacturing Quality
• Fabricators certification
• Measurement Equipment
• Preventive Maintenance
• Storage and Packing
• Updating and managing the QM database

• ASME, ISO 9001:2005, ISO 3834 Part 2, API 510, PER , API
• Flange management: Tag verification of tags, Hot torque verification, Correctness of blinding
• Verification of all Hot work requirements
• Validation of NDE Reports
• PMI requirements for both Hot & Cold Work
• Coating requirements
• Insulation requirements
• Conduct vendor validation audit
• Verification of workshop adherence to ISO 3834 Part 2
• Verification of contractors Internal QMS
• Writing of Audit report and close out reports. Reporting to management
• Verification of the corrective actions and close out of findings

• Adding and editing work orders
• Adding Audits to the QM database
• Sign off on corrective actions from Audit

• Review Contractors Event Quality Plan
• Review Contractor QC Trackers
• Verify the validity of the associated EWR (Engineering Work Request), TAW (Turnaround Additional Work) and PL(line) number and Work Order within the QMDb (Quality Management database)

• Tracking of all exception items
• QM signoff of contractor packs
• Tracking of TAW
• Adding Audits into the database
• Managing Redline drawings
• Reporting QM Status and statistics to management

• Conducting audits based on contractors QMS
• Manage and track QC data books within Quality Management Database
• Review Contractors Welding and QC tracker
• Capture audits, exception items, PMI reports and redline drawings
• Review, audit and sign-off QC Packs
• Requirements:

• 10-15 years relevant experience
• Minimum 5 years petrochemical experience
• SAIW Level 2
• Lead Auditors Training
• ISO 9001:2015, 3834 Training
• Project Management / Quality
• Position requires good knowledge and skills pertaining to all relevant computer applications including standard PC applications such as Word, Excel, Outlook

An opportunity has become available with one of our clients for a Quality Management System Officer to join the Bellville-based Manufacturer of private label beauty care products.

The company is seeking a talented person who aspires to a Quality Assurance career in a manufacturing environment. This is not a "Lab" type position.

Key Performance areas are:

• Writing and updating SOPs and Work Instructions to maintain the Document Library.
• Creating material and running training and assessment of staff on SOPs and Work Instructions.
• Setting the Training Schedule and maintaining the training database.
• Scheduling and carrying out Internal Audits and documenting and managing the resolutions of CAPAs arising from audits.
• Supporting the Technical Manager regarding external and customer audits and resulting CAPAs.

Qualifications and Experience:

• Diploma at NQF 7 level or relevant Degree
• Minimum of 2 years relevant working experience in a similar or associated role in a manufacturing environment

The right person will have the motivation, skills and professional and work ethic to support this challenging role that requires a combination of education, knowledge and experience in a factory facility.

Essential Functions

• Set up of QC for new process / clients requiring extensive interaction with clients to understand and capture all requirements
• Closely work with operations team and clients to continuously benchmark processes, baseline performance and target setting
• Incubation of Quality Program in Healthcare South Africa processes.
• Perform ongoing reviews to ensure compliance to QSD to all certification and internal / client requirements
• Facilitate and identify potential areas for improvement and actively participate in improvement initiatives and drive incremental improvements through AIM.
• Ensure the effective running and accurate data of process performance aligned with SLA targets
• Coordinate with the Black Belts and Process owners to ensure improvement exercises (Six Sigma Projects, AIM, etc) continue to happen in the processes.
• Train / mentor AMs and QCAs and operations teams on quality tools and concepts
• Responsible for working closely with clients and operations team to carry out process improvement activities and facilitate best practice sharing and driving standardization.