201 Quality Director jobs in South Africa
Associate Director, Global Quality Assurance
Posted 4 days ago
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IAVI Cape Town, Western Cape, South Africa
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Associate Director, Global Quality AssuranceIAVI Cape Town, Western Cape, South Africa
Join to apply for the Associate Director, Global Quality Assurance role at IAVI
Job Title: Associate Director, Global Quality Assurance
Location: Nairobi, Kenya, Cape Town, South Africa; Remote-South Africa, Remote-Uganda, Remote-Nigeria, New York, New York; US - Remote Considered; United Kingdom – Remote; OR Amsterdam, Netherlands
Reporting to: Senior Director, Clinical Quality Assurance
Position Summary:
Are you a Quality focused leader in clinical development, passionate about bringing forward public health solutions?
IAVI is seeking an experienced and detail oriented Associate Director, Quality Assurance who will ensure compliance of clinical development operations to IAVI and industry standards. The Associate Director will facilitate the Clinical Development group’s participation in the IAVI quality management system where appropriate processes, procedures, and controls are established to ensure clinical research is conducted according to IAVI and industry standards.
Key Responsibilities:
- Support Project Teams with the development of quality management plans relevant to the specific project(s);
- Support and prepare Project Teams for regulatory inspections and external Sponsor audits;
- Serves as the GCP point person for the IAVI electronic QMS, and Clinical Trial Systems, development and implementation;
- Develop and implement QMS compliance assessments for the GCP component of the QMS;
- Develop and implement an eTMF inspection readiness assessment plan for all IND studies;
- Participate in executing the audit plan as delegated;
- Provide training to GCP Operations on best practices and trends as indicated;
- Oversees implementation of GCP CAPAs and conduct the required effectiveness checks;
- Perform other tasks as assigned by the manager.
Education and Work Experience:
- Masters Degree or equivalent in Clinical Research and/or Public Health or related field is required.
- Minimum 10 years of experience in clinical research is required of which at least 3 in Quality Assurance is required.
- Certification as GCP Auditor and/or Post Graduate Qualification in Quality Management is highly preferred.
Qualifications and Skills:
- Strong knowledge and understanding of industry standards and research operations as pertinent to vaccine development is required.
- Experience working with quality management systems is required.
- Experience working with electronic data and records in CFR21Part11 compliant environments is highly desirable.
- Experience as auditor of public health trials is highly desirable.
- Experience working in remote-, virtual-, global-, teams, is highly desirable.
- Ability to travel to research sites throughout the Africa region at up to 30%.
Organizational Overview:
IAVI is a nonprofit scientific research organization dedicated to addressing urgent, unmet global health challenges including HIV and tuberculosis. Our mission is to translate scientific discoveries into affordable, globally accessible public health solutions. Through scientific and clinical research in Africa, India, Europe, and the U.S., IAVI is pioneering the development of biomedical innovations designed for broad global access. We develop vaccines and antibodies in and for the developing world and seek to accelerate their introduction in low-income countries. IAVI programs and partnerships are grounded in the regions of the world where the disease burden is the greatest, and our approach emphasizes sustainability. Our network of clinical research center partners in Africa and India helps strengthen in-country research capacity and supports the training and education of the next generation of scientists. The global impact of our science includes fundamental contributions to understanding the biology of HIV infection, which IAVI and others are applying toward advancing vaccine science and immunology. IAVI accelerates scientific discovery and development by fostering unique collaborations among academia, industry, local communities, governments, and funders to explore new and better ways to address public health threats that disproportionately affect people living in poverty. Our global reach, including a clinical research network in five countries in sub-Saharan Africa and in India, has allowed us to make fundamental contributions to understanding the epidemiology, transmission, virology, and immunology of HIV. This work played a key role in facilitating the design of promising HIV vaccine candidates, as well as the discovery of broadly neutralizing antibodies that are now being advanced as promising approaches for HIV prevention. Our integrated capabilities in vaccine and antibody discovery, development, and clinical research take advantage of bio-pharmaceutical industry expertise to accelerate the development and testing of prevention methods for HIV and other diseases. Through the Product Development Center, we support external researchers with technical and scientific expertise to accelerate the development of their own products.
IAVI CORE VALUES:
- Dedication to the Mission: We are committed to the translation of scientific discoveries into affordable, globally accessible public health solutions.
- Innovative Evolution: We are committed to solving complex problems in creative and innovative ways, learning from our mistakes and successes and never giving up
- Integrity: We are committed to meeting the highest ethical and professional standards in everything we do and to taking responsibility for our actions to earn respect
- Collaboration: We are committed to embracing diversity, the power of global teamwork and the belief that by working as one we can make a difference
Disclaimer: Nothing in this job description restricts management's right to assign or reassign duties and responsibilities to this job at any time. The above statements are intended to describe the general nature and level of work being performed by individuals assigned to this position. They are not intended to be an exhaustive list of all duties, responsibilities and skills required of personnel so classified. This document does not create an employment contract, implied or otherwise, other than an “at-will” relationship. IAVI is an equal opportunity employer and applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.
IAVI IS AN EQUAL OPPORTUNITY EMPLOYER dedicated to fostering a diverse and inclusive global organization. We recognize that a variety of backgrounds and perspectives enriches our work and strengthens our ability to achieve our mission. IAVI is committed to recruiting, developing, and retaining individuals through a merit-based approach. At IAVI, we celebrate the spectrum of colleagues’ experiences and believe that dedication to our mission above all is essential to our success as a scientific non-profit organization focused on global health.
IAVI is an equal opportunity employer. It is IAVI’s policy to provide equal opportunity without regard to race, citizenship, color, sex, gender identity or expression, age, height, weight, disability (including physical and mental conditions unrelated to job performance), religion, creed, caste, home language, ancestry, national origin, pregnancy, marital or partnership status, sexual orientation, status as a protected veteran, ethnicity, genetic information, predisposing genetic characteristic, status as a victim of domestic violence, stalking and sex offenses, HIV status, or any other status protected by applicable federal, state, or local laws.
Compensation and Benefits Information for US-Based Candidates:
Annual base salary for this position is: $140,000.00 - 155,000.00
Please note, there may be some variation based on experience level. In addition, this position offers competitive benefits including: generous retirement savings plan employer contributions; competitive health, dental and vision insurance plans; competitive paid time off policy; potential for annual bonuses based on performance; and other benefits. More information can be found on IAVI's career page.
Compensation And Benefits Information for NON-US Based Candidates:
Salary is paid in local currency, and is commensurate and competitive with the local labor market
Please note, there may be some variation based on experience level. In addition, this position offers competitive benefits such as annual bonus, generous retirement savings plan, competitive health insurance benefits, and other benefits.
Seniority level- Seniority level Mid-Senior level
- Employment type Full-time
- Job function Quality Assurance, Research, and Science
- Industries Biotechnology Research and Pharmaceutical Manufacturing
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#J-18808-LjbffrQuality Control Superintendent
Posted 1 day ago
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Join to apply for the Quality Control Superintendent role at Sea Harvest Group Ltd .
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The role involves ensuring that all aspects of Food Safety and Quality Control, as outlined in the company's Food Safety/Quality Management Systems, are properly initiated, implemented, and maintained, particularly concerning frozen incoming materials.
Seniority level- Entry level
- Full-time
- Management and Manufacturing
- Fisheries
Quality Control Supervisor
Posted 4 days ago
Job Viewed
Job Description
We are seeking two accomplished Quality Control Supervisors : one to drive compliance and regulatory initiatives, and the other to lead QC operations, optimising efficiency and process excellence. Both roles are pivotal to ensuring our products consistently meet rigorous quality and safety requirements. Reporting directly to the QC Manager, these positions offer the opportunity to work in a dynamic, fast-paced environment while collaborating across teams to uphold our commitment to quality.
Qualifications, Experience & Competencies
- Degree or Diploma in Analytical Chemistry, Biochemistry, Food Technology, or related field.
- Minimum 5 years experience in an analytical laboratory within the pharmaceutical / beauty / cosmetic sectors, including supervisory exposure.
- Solid understanding of Quality Management Systems (ISO 9001, ISO 22716, SANAS 1841).
- Experience in artwork review is advantageous.
- Knowledge of GLP and GMP; experience with HPLC is beneficial.
- Strong communication skills at all levels.
- Highly detail-oriented, goal-driven, dependable, and proactive.
Key Technical Skills & Responsibilities
- Oversee compliance with GMP, ISO, and internal standards.
- Approve laboratory data, artwork, and product specifications.
- Manage item codes and BOMs in Syspro.
- Lead non-conformance investigations and support production teams.
- Supervise QC team activities and maintain instrument calibration and verification.
- Coordinate quality inspections, environmental monitoring, and outsourced analyses.
- Develop, implement, and refine QC procedures and SOPs.
Looking for a role that aligns with your package expectations, job level, or industry expertise? Apply now via our career portal :
Create a job alert for this searchQuality Control Supervisor • CapeTown, South Africa
#J-18808-LjbffrQuality Control Analyst
Posted 4 days ago
Job Viewed
Job Description
Analytical Chemistry / Bio-Medical / Bio-Technology / BSc degree(biomedicine) / B Pharm degree
Pharmaceutical experience preferred
Experienced and skilled HPLC technician
Raw material testing experience
Job Duties :
Perform a variety of simple to complex routine and non-routine tests to evaluate the quality of raw material(s)
Compiles, interprets and documents data from testing processes to confirm compliance with established standards or identify deviations / OOS (Out of Specifications).
Ensures completion of delegated tasks by agreed completion dates.
Maintain and manage accurate and precise documentation.
Operation of analytical laboratory instrumentation.
Ensure regulatory compliance with GLP and GMP environment.
Comply with standard procedures.
Interact with Operations and Quality Assurance.
Maintain a safe laboratory work environment.
Ensure adequate stocking of laboratory reagents, reference standards and consumables by monitoring stock levels and ensuring timeous ordering.
Salary :
Basic of : R25000 - R30 000
Overtime is paid when it is necessary to work on a weekend(not often)
How to apply :
Create a job alert for this searchQuality Analyst • East Rand/Bedford View/Germiston/Isando, South Africa
#J-18808-LjbffrQUALITY CONTROL OFFICER
Posted 4 days ago
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Job Description
Our client in the Electrical Construction (Renewable) industry are seeking a dedicated Quality Officer to join their electrical construction team, specializing in renewable energy projects. This role requires a multi-disciplinary technical background and proven experience in quality control processes within the renewable energy sector. The successful candidate will be responsible for ensuring all project activities meet stringent quality standards and regulatory requirements.
Key Responsibilities
Quality Control & Assurance
- Implement and maintain comprehensive quality control processes throughout project lifecycle
- Conduct regular quality inspections and audits on electrical, mechanical, and civil construction activities
- Monitor compliance with project specifications, industry standards, and regulatory requirements
- Identify quality issues and implement corrective and preventive actions
- Prepare detailed quality reports and maintain quality documentation systems
Documentation & Process Management
- Manage MRFI (Material Request for Information) and RFI (Request for Information) processes
- Develop and maintain quality control procedures and work instructions
- Ensure all quality documentation is accurate, complete, and properly filed
- Coordinate with project teams to resolve technical queries and quality concerns
- Maintain comprehensive quality records and databases
Standards Compliance
- Ensure compliance with ISO quality management standards
- Implement Eskom quality processes and requirements where applicable
- Monitor adherence to renewable energy industry quality standards
- Conduct internal quality audits and assessments
- Support external audits and regulatory inspections
Stakeholder Communication
- Liaise with project managers, engineers, contractors, and clients on quality matters
- Participate in project meetings and provide quality status updates
- Communicate quality requirements to construction teams
- Coordinate with suppliers and vendors on quality specifications
- Provide training and guidance to project personnel on quality procedures
- Identify opportunities for quality process improvements
- Analyze quality data and trends to prevent recurring issues
- Recommend best practices and lessons learned
- Support the development of quality management systems
- Contribute to quality policy development and implementation
Technical Background
- Multi-disciplinary technical qualification in electrical, mechanical, or civil engineering
- Minimum 5+ years experience developing, implementing and maintaining QA / QC plans for utility scale solar PV projects
- Demonstrated experience on solar PV construction projects with aggregate capacity exceeding 100MW
- At least one project with individual capacity greater than 10MW
- Understanding of solar PV systems, components, and installation methodologies
Industry Experience
- Minimum 5+ years experience in developing, implementing and maintaining quality assurance and quality control plans on utility scale solar PV projects
- Proven track record on PV plant construction with aggregate peak capacity of more than 100MW
- Experience on at least one PV plant with capacity exceeding 10MW
- Understanding of utility-scale solar project construction phases and methodologies
- Knowledge of solar PV equipment, installation procedures, and grid connection requirements
Standards & Processes
- Comprehensive understanding of international codes and standards applicable to solar PV projects
- Knowledge of local South African codes and standards including SANS, NRS, and Grid Code requirements
- Understanding of Eskom quality processes and requirements (advantageous)
- Experience with MRFI and RFI processes and management
- Knowledge of IEC standards for solar PV systems and components
Administrative & Communication Skills
- Excellent administrative skills with attention to detail
- Strong written and verbal communication abilities
- Fluent in English (speaking, reading, writing)
- Proficient in Microsoft Office Suite and quality management software
- Ability to prepare clear, concise reports and documentation
Personal Attributes
- Strong analytical and problem-solving skills
- Attention to detail and accuracy
- Ability to work independently and as part of a team
- Proactive approach to quality management
- Adaptability to changing project requirements
- Professional demeanour and integrity
Preferred Qualifications
- National Diploma or Bachelor's degree in Engineering or related technical field
- Quality management certification (ISO 9001 Lead Auditor or similar)
- Previous experience in utility-scale renewable energy projects
- Knowledge of South African electrical and construction regulations
- Experience with quality management software systems
Key Performance Areas
- Maintain zero non-conformances through proactive quality management
- Ensure 100% compliance with project quality requirements
- Timely resolution of all MRFIs and RFIs
- Accurate and complete quality documentation
- Effective communication with all project stakeholders
- Continuous improvement of quality processes and procedures
Working Conditions
- Site-based work environment with office support
- May require travel to multiple project locations
- Interaction with construction teams and equipment
- Adherence to strict safety protocols and procedures
- Flexible working hours to accommodate project requirements
This role offers excellent opportunities for professional growth within the renewable energy sector, with exposure to cutting-edge technology and industry best practices. The successful candidate will gain valuable experience in quality management systems and renewable energy project delivery.
Application Requirements
Candidates must provide :
- Detailed CV highlighting relevant quality control experience with detail of the projects
- Copies of relevant qualifications and certifications
- References from previous renewable energy or construction projects
Quality Control Officer • Centurion, Gauteng, ZA
#J-18808-LjbffrQuality Control Analyst
Posted 4 days ago
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Job Description
Our client is seeking an experienced Quality Control Analyst to join their company in Gauteng
Location : Germiston Gauteng
Job Requirements :
Analytical Chemistry / Bio-Medical / Bio-Technology / BSc degree(biomedicine) / B Pharm degree
Pharmaceutical experience preferred
Experienced and skilled HPLC technician
Raw material testing experience
Job Duties :
Perform a variety of simple to complex routine and non-routine tests to evaluate the quality of raw material(s)
Analyse raw materials, intermediate products, finished products, validation samples.
Compiles, interprets and documents data from testing processes to confirm compliance with established standards or identify deviations / OOS (Out of Specifications).
Ensures completion of delegated tasks by agreed completion dates.
Maintain and manage accurate and precise documentation.
Operation of analytical laboratory instrumentation.
Ensure regulatory compliance with GLP and GMP environment.
Comply with standard procedures.
Interact with Operations and Quality Assurance.
Maintain a safe laboratory work environment.
Ensure adequate stocking of laboratory reagents, reference standards and consumables by monitoring stock levels and ensuring timeous ordering.
Salary :
Basic of : R25000 - R30 000
Overtime is paid when it is necessary to work on a weekend(not often)
How to apply :
- Follow the link to our jobseeker’s page- https : / / measuredability.com / jobs-2 /
- Search for the job title.
- Click apply to submit your CV.
Quality Control Assistant
Posted 4 days ago
Job Viewed
Job Description
To ensure that all materials and processes adhere strictly to customer specifications and internal quality standards, and to oversee the implementation and compliance of quality systems within the production division.
- PRINCIPAL ACCOUNTABILITIES
Accountabilities
Key Performance Indicators (KPIs)
Support in determining, negotiating, and agreeing upon in-house quality procedures, standards, and specifications
Clearly documented quality procedures aligned with ISO and customer expectations
Ensure adherence to quality, health, and safety standards across the plant
Zero non-conformities and audit failures; reduced incident reports
Monitor and ensure that manufacturing processes comply with defined quality standards
Regular inspections, compliance audits, and corrective actions documented and implemented
Conduct and document quality testing (pre-production, in-process, and final product)
100% completion of quality checklists and sampling reports
Follow established procedures, ISO guidelines, and maintain proper documentation
ISO compliance and audit-readiness at all times
Act as a catalyst for continuous improvement in quality and operational efficiency
Number of improvement initiatives implemented per quarter; measurable performance improvements
Lead, manage and motivate quality control staff to meet departmental goals
Achievement of departmental KPIs; performance reviews and development plans completed on time
Monitor and document critical control points (CCPs) regularly
Accurate and timely CCP logs with corrective actions recorded
Ensure customer requirements and service standards are understood and implemented
Positive customer feedback; low rate of quality-related returns or complaints
- INTERACTIONS
Internal :
- Production Department
- Purchase / Procurement
- Planning and Production Control (PPC)
- Maintenance and R&D (as applicable)
External :
- Customers and end-users (for quality audits, complaints, and resolution)
- Raw material vendors and external testing laboratories
- Certification bodies (for ISO or regulatory audits)
- SKILLS AND KNOWLEDGE
Educational Qualifications :
- Post Graduate Diploma in Plastics Technology / CIPET or
- Diploma in Plastics / Mechanical Engineering or related field
Relevant Industry Experience :
- 5–7 years of experience in a Packaging Manufacturing Industry with hands-on exposure to Quality Control and Assurance
Technical Skills :
- In-depth knowledge of packaging processes (lamination, extrusion, printing, slitting, sealing)
- Experience with lab instruments and testing procedures (tensile strength, bond strength, GSM, COF, WVTR, etc.)
- Proficiency in ISO 9001 / ISO 22000 / HACCP and other quality management systems
- Skilled in preparing audit documentation, process documentation, and quality SOPs
Behavioral Skills :
- Strong analytical and problem-solving ability
- Detail-oriented with a commitment to accuracy and process compliance
- Effective communicator and team leader
- Ability to manage cross-functional teams under pressure
Quality Control Assistant • Centurion, South Africa
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Quality Control Assistant
Posted 4 days ago
Job Viewed
Job Description
To ensure that all materials and processes adhere strictly to customer specifications and internal quality standards, and to oversee the implementation and compliance of quality systems within the production division.
- PRINCIPAL ACCOUNTABILITIES
- INTERACTIONS
- Production Department
- Purchase / Procurement
- Planning and Production Control (PPC)
- Maintenance and R&D (as applicable)
- Customers and end-users (for quality audits, complaints, and resolution)
- Raw material vendors and external testing laboratories
- Certification bodies (for ISO or regulatory audits)
- SKILLS AND KNOWLEDGE
- Post Graduate Diploma in Plastics Technology / CIPET or
- Diploma in Plastics / Mechanical Engineering or related field
- 5–7 years of experience in a Packaging Manufacturing Industry with hands-on exposure to Quality Control and Assurance
- In-depth knowledge of packaging processes (lamination, extrusion, printing, slitting, sealing)
- Experience with lab instruments and testing procedures (tensile strength, bond strength, GSM, COF, WVTR, etc.)
- Proficiency in ISO 9001 / ISO 22000 / HACCP and other quality management systems
- Skilled in preparing audit documentation, process documentation, and quality SOPs
- Strong analytical and problem-solving ability
- Detail-oriented with a commitment to accuracy and process compliance
- Effective communicator and team leader
- Ability to manage cross-functional teams under pressure
Accountabilities
Key Performance Indicators (KPIs)
Support in determining, negotiating, and agreeing upon in-house quality procedures, standards, and specifications
Clearly documented quality procedures aligned with ISO and customer expectations
Ensure adherence to quality, health, and safety standards across the plant
Zero non-conformities and audit failures; reduced incident reports
Monitor and ensure that manufacturing processes comply with defined quality standards
Regular inspections, compliance audits, and corrective actions documented and implemented
Conduct and document quality testing (pre-production, in-process, and final product)
100% completion of quality checklists and sampling reports
Follow established procedures, ISO guidelines, and maintain proper documentation
ISO compliance and audit-readiness at all times
Act as a catalyst for continuous improvement in quality and operational efficiency
Number of improvement initiatives implemented per quarter; measurable performance improvements
Lead, manage and motivate quality control staff to meet departmental goals
Achievement of departmental KPIs; performance reviews and development plans completed on time
Monitor and document critical control points (CCPs) regularly
Accurate and timely CCP logs with corrective actions recorded
Ensure customer requirements and service standards are understood and implemented
Positive customer feedback; low rate of quality-related returns or complaints
Internal :
External :
Educational Qualifications :
Relevant Industry Experience :
Technical Skills :
Behavioral Skills :
Quality control operator
Posted 7 days ago
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Job Description
Summary:
Perform quality control checks on products before processing to ensure compliance with company standards and supplier requirements. Conduct inspections on all item being processed and address defects, deviations, or non-conformities.
Key Responsibilities:
- Inspect products, materials before processing stage.
- Ensuring daily demand targets of parcels being processed are met.
- Identify and isolate non-conforming products or materials. Notify production staff and manager of quality issues.
- Collaborate with production teams to resolve quality problems.
- Maintain a clean and organized work environment.
Requirements:
- High school matric.
- 1-2 years of warehousing operations experience and knowledge of quality control principles.
- Analytical and problem-solving skills. Attention to detail and accuracy is crucial.
- Effective communication and teamwork skills. Ability to work in a fast-paced environment.
- Basic computer skills (e.g., data entry, reporting).
Quality Control Executive
Posted 7 days ago
Job Viewed
Job Description
- Support in determining, negotiating, and agreeing on in-house quality procedures, standards, and/or specifications.
- Ensure quality and health and safety.
- Ensure that manufacturing processes comply with standards at the plant level.
- Follow established procedures, I.S.O guidelines, and rules, and maintain proper documentation.
- Act as a catalyst for change and improvement in performance and quality.
- Manage staff in the function to ensure productivity.
Key Performance Indicators
- Determine the in-house quality procedure, standards, and/or specifications.
- Conduct various tests as per the standard before manufacturing starts, during the course (online) of production, and perform final quality checks before the final products are delivered to customers.
- Assess customer requirements and ensure that these are met by setting customer service standards.
- Act as a catalyst for change and improvement in performance and quality.
- Follow I.S.O guidelines and rules and other quality parameters to ensure compliance with the audit.
- Ensure the critical control points are monitored and recorded regularly as per the departmental process.
Qualifications
- B.E/B. Tech in Mechanical Engineering.
- Minimum relevant experience of 3-8 years.
Skills
- In-depth technical knowledge.
- Sound knowledge of mechanical maintenance and total preventive maintenance.
- Experience in managing various quality initiatives in the plant.
ISO (International Organisation for Standardisation), Customer Service, Quality Control
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