906 Quality Specialist jobs in South Africa

Overview:

To monitor and control Quality Systems and Processes to achieve Quality Standards and meet customer specific requirements (CSR’s).

Minimum Requirements:

• Grade 12 / School leaving certificate
• National Diploma Quality Management or Engineering
• Trained Auditor ISO 9001;2015; IATF 16949:2016 & VDA 6.3:2016
• 3-5 years’ experience within a similar role in the Automotive Industry

Key Performance Areas:

Quality Control:

• Establish and manage Critical Control Points in the Process
• Investigate all Quality non-conformances and track corrective actions
• Analyse the PPM's and defect trends and make recommendations
• Conduct Gauge MSA assessments on all measuring systems
• Determine the disposition of quarantined products (Pass, Reject or Rework)
• Manage and maintain the Quality Management System ensuring compliance with IATF 16949:2016 and VDA6
• Achieve Quality Assurance operational objectives by contributing information and analysis to strategic plans and reviews; preparing and completing action plans; implementing production, productivity, quality, and customer-service standards; identifying and resolving problems; completing audits; determining system improvements and implementing change
• Develop Quality assurance plans by conducting risk analysis; identifying critical control points and preventive measures; procedures, corrective actions, and verification procedures
• Validate quality processes by establishing product specifications and quality attributes; measuring production; documenting evidence & writing and updating quality assurance procedures
• Communicate and liaise with internal and external customers and foster relationships
• Facilitate containment at Customer Site, raise Quality Alert bulletins, and facilitate training on quality-related concerns
• Control of non-conforming products and the rework thereof
• Support quality production inspectors in making product-related decisions regarding quarantined products (Pass, Reject or Rework)
• Generate work instructions and product-specific documentation
• Facilitate the generation and updating of Flow Charts, Control Plans, and FMEA’s
• Responsible for facilitating Measurement System Analysis and Capability Studies
• Liaise with Stores Controller and Manufacturing Practitioner regarding Quality concerns
• Responsible for Supplier Development in liaison with Stores Controller and Manufacturing Practitioner
• Compile and maintain Audit Schedules (Dock & Product Audits, Manufacturing Process Audits (VDA 6.3:2016), Internal Systems Audits (IATF 16949:2016))
• Maintain & improve product quality by completing product, process, system, compliance, and surveillance audits & investigating customer complaints
• Coordinate Annual Quality Management reviews and keep records of meetings and quality objectives
• Compile Monthly Management Quality Reports
• Compile weekly yields reports
• Review Quality Risks and requirements in APQP activities
• Ensure compliance with process and Customer Specifications
• Complete Production Part Approval Process (PPAP)
• Investigate and implement countermeasures for continual quality improvement
• Monitor and measure customer feedback, complaints, and rejections to identify opportunities for improvement
• Conduct MSA studies
• Approve COC’s in absence of QM

Quality Management:

• Compile Quality Topics for Quality Awareness Training

Quality Assurance:

• Implement Quality Procedures and Work Instructions
• Maintain the Quality Assurance system
• Ensure compliance with Quality Policies, Procedures, and Work Instructions

Audits:

• Conduct internal Process audits (VDA 6.3:2016) and Product & Layout audits

Supply Quality Assurance (SQA):

• Specify Supplier Acceptable Quality Levels (AQL's) (Tolerances, Drawing requirements, Tooling, PPM's, etc.)
• Analyse Supplier Performance (Product Quality, Special Status, etc.) and make recommendations
• Notify Suppliers of non-conformances and initiate corrective actions

Information Management and Direction Focusing:

• Collate and analyse company data and management reports

Advanced Product Quality Planning (APQP):

• Review Quality Risks of APQP activities
• Ensure compliance with process and Customer Specifications
• Complete Production Part Approval Process (PPAP)
• Provide input to the Contract Review Process

Continuous Improvement:

• Maintain an updated Continuous Improvement Plan

People Management:

• Ensure an enabling climate/culture.
• Ensure a safe, secure and legal working environment.
• Manage individual, team, and departmental performance to achieve organisational objectives.
• Compile and update Performance Contracts and Individual Development Plans and facilitate individual career path planning.
• Determine the training needs of the Department.
• Conduct Performance Reviews and manage sub-standard performance.
• Coach and counsel people to ensure improved performance levels
• Ensure discipline is maintained in the department (absenteeism, lateness, overtime, misconduct, etc.)
• Resolve grievances and disputes

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Job Responsibilities

• Ensure that all products and processes are in accordance with Quality Standards and Customer specific requirements.
• Monitor and control Quality Systems and Processes to achieve Quality Standards and meet customer specific requirements (CSR’s).

Qualifications

• Grade 12
• National Diploma in Quality Management or Engineering related qualification
• Trained Auditor ISO 9001:2015; IATF 16949:2016 & VDA 6.3:2016
• Minimum 5 Years in a similar role within an Automotive/Manufacturing environment
• Skills: MS Office, Excel, Word, PowerPoint, Outlook
• Demonstrate an understanding of ISO/IATF and OEM Standards
• Demonstrate an understanding of Problem-Solving Techniques

Quality Management

• Conduct Quality investigations (Internal, Supplier, Customers)
• Maintain IATF 16949:2016 Certification

Quality Assurance

• Maintain the Quality Assurance system

Audits

• Conduct internal 1st party Process audits (VDA 6.3:2016), System Audits (IATF), Supplier Audits, Product / Dock audits

Supply Quality Assurance (SQA)

• Interact with all suppliers
• Approve all PSW/PPAP/ISIR for new projects/products/items

Customer Relations (External and Internal)

• Interact with internal and external customers regarding quality issues
• Investigate internal production, project, and customer laboratory test failures

Quality Control

• Investigate all Quality non-conformances and track corrective actions (Initiate, follow up and close)
• Make decisions on quarantined products (Pass, Reject or Rework)
• Manage and maintain the Quality Management System ensuring compliance with all applicable requirements contained in IATF 16949:2016 and VDA 6.3
• Achieve Quality Assurance operational objectives by contributing information and analysis to strategic plans and reviews; preparing and completing action plans; implementing production, productivity, quality, and customer-service standards; identifying and resolving problems; completing audits; determining system improvements and implementing change
• Communicate and liaise with internal and external customers and foster relationships
• Support quality production inspectors to make product-related decisions regarding quarantined products (Pass, Reject or Rework)
• Review, update, and approve Flow Charts, Control Plans, and FMEA’s
• Facilitate Measurement System Analysis and Capability Studies on all measuring equipment (CPK, CMK)
• Responsible for Supplier Development in liaison with Stores Controller and Manufacturing Practitioner
• Maintain & improve product quality by completing product, process, system, compliance, and surveillance audits & investigating customer complaints.
• Compile Monthly Management Quality Reports
• Compile weekly yield reports
• Approve COC’s

Advanced Product Quality Planning (APQP)

• Review Quality Risks of APQP activities
• Ensure compliance with process and Customer Specifications
• Complete Production Part Approval Process (PPAP) for all customers
• Provide input to the Contract Review Process

#J-18808-Ljbffr

De van oudsher Dommelsche Bierbouwerij in Dommelen is de brouwerij waar het bekende Dommelsch bier wordt gebrouwen. Tegenwoordig is het bedrijf onderdeel van AB In Bev en worden er meerdere grote biermerken gebrouwen waaronder Jupiler, Hertog-Jan, Dommelsch en nog vele andere grote merken. Hier ben je verantwoordelijk voor de veiligheid, kwaliteit, netheid en de lopende processen. Je krijgt de nodige opleiding om volledig inzetbaar te zijn op alle onderdelen van de afdeling Quality!Functiebeschrijving Als Quality Specialist ben je zowel voor onze brouwerij in Dommelen als in Arcen mede verantwoordelijk voor de implementatie, borging en opvolging van de kwaliteitsprocedures en -vereisten. Je bent de drijvende kracht voor het audit- en continue verbeteringsproces, met speciale aandacht voor hygiëne en voedselveiligheid. Dit alles in nauwe samenwerking met de diverse afdelingen en de gecentraliseerde diensten. Je werkzaamheden bestaan o.a. uitDe implementatie en opvolging van interne en externe kwaliteitsaudits en het opstellen van actieplannen Coördinatie van verbetering van de kwaliteitsprocessen en opvolging van deze projecten ter ondersteuning en verbetering van de KPIs In stand houden en verbeteren van de quality management systemen (HACCP, FCA, VPO) en volgen van de CCP's en voedselveiligheid Een continue kritische analyse van de kwaliteitsresultaten van de diverse processen en verbeteringsacties Berekening en de rapportering van een aantal kwaliteitsindexen + preventieve en correctieve acties hieromtrent Opvolging van de relevante wettelijke aspecten in verband met de kwaliteitsmanagementsystemen Functie-eisen Jij bet iemand met gedegen kennis van de operationele activiteiten in een brouwerij omgeving en aantoonbare leidinggevende ervaring. Ben jij sterk analytisch er probleemoplossend ingesteld, met een ruime bagage aan creativiteit en passie voor implementaties van innovatieve ideeën? Heb jij daarnaast goede kennis van de informaticasystemen zoals o.a.: Excel, Word, Sigma, Outlook en Power Point en ben jij resultaatgericht, met grote aandacht voor details zowel kwalitatief als kwantitatief? Dan zoeken zij jou! Daarnaast beschik je over:HBO werk- en denkniveau verkregen door opleiding of werkervaring (bij voorkeur een afgeronde opleiding aan de HAS). Sterke leiderschapsvaardigheden: een charismatisch en dynamisch persoon met sterke communicatieve vaardigheden Zelfstandigheid en efficiëntie in het stellen van prioriteiten in functie van de werkdruk Arbeidsvoorwaarden Hele mooie functie binnen een mooie brouwerij die onderdeel is van de grootste brouwerijketen van de wereld: Ab In Bev. Zij bieden naast een boel verantwoordelijkheden ook een mooi bedrijf om in te werken en goede voorwaarden:Uitdagende functie in dagdienst Een salaris op basis van leeftijd en ervaring, ingeschaald volgende de HAY systematiek Diverse opleidingsmogelijkheden #J-18808-Ljbffr

Job Responsibilities Ensure that all products and processes are in accordance with Quality Standards and Customer specific requirements. Monitor and control Quality Systems and Processes to achieve Quality Standards and meet customer specific requirements (CSR’s). Qualifications Grade 12 National Diploma in Quality Management or Engineering related qualification Trained Auditor ISO 9001:2015; IATF 16949:2016 & VDA 6.3:2016 Minimum 5 Years in a similar role within an Automotive/Manufacturing environment Skills: MS Office, Excel, Word, Power Point, Outlook Demonstrate an understanding of ISO/IATF and OEM Standards Demonstrate an understanding of Problem-Solving Techniques Quality Management Conduct Quality investigations (Internal, Supplier, Customers) Maintain IATF 16949:2016 Certification Quality Assurance Maintain the Quality Assurance system Audits Conduct internal 1st party Process audits (VDA 6.3:2016), System Audits (IATF), Supplier Audits, Product / Dock audits Supply Quality Assurance (SQA) Interact with all suppliers Approve all PSW/PPAP/ISIR for new projects/products/items Customer Relations (External and Internal) Interact with internal and external customers regarding quality issues Investigate internal production, project, and customer laboratory test failures Quality Control Investigate all Quality non-conformances and track corrective actions (Initiate, follow up and close) Make decisions on quarantined products (Pass, Reject or Rework) Manage and maintain the Quality Management System ensuring compliance with all applicable requirements contained in IATF 16949:2016 and VDA 6.3 Achieve Quality Assurance operational objectives by contributing information and analysis to strategic plans and reviews; preparing and completing action plans; implementing production, productivity, quality, and customer-service standards; identifying and resolving problems; completing audits; determining system improvements and implementing change Communicate and liaise with internal and external customers and foster relationships Support quality production inspectors to make product-related decisions regarding quarantined products (Pass, Reject or Rework) Review, update, and approve Flow Charts, Control Plans, and FMEA’s Facilitate Measurement System Analysis and Capability Studies on all measuring equipment (CPK, CMK) Responsible for Supplier Development in liaison with Stores Controller and Manufacturing Practitioner Maintain & improve product quality by completing product, process, system, compliance, and surveillance audits & investigating customer complaints. Compile Monthly Management Quality Reports Compile weekly yield reports Approve COC’s Advanced Product Quality Planning (APQP) Review Quality Risks of APQP activities Ensure compliance with process and Customer Specifications Complete Production Part Approval Process (PPAP) for all customers Provide input to the Contract Review Process #J-18808-Ljbffr

Overview: To monitor and control Quality Systems and Processes to achieve Quality Standards and meet customer specific requirements (CSR’s). Minimum Requirements: Grade 12 / School leaving certificate National Diploma Quality Management or Engineering Trained Auditor ISO 9001;2015; IATF 16949:2016 & VDA 6.3:2016 3-5 years’ experience within a similar role in the Automotive Industry Key Performance Areas: Quality Control: Establish and manage Critical Control Points in the Process Investigate all Quality non-conformances and track corrective actions Analyse the PPM's and defect trends and make recommendations Conduct Gauge MSA assessments on all measuring systems Determine the disposition of quarantined products (Pass, Reject or Rework) Manage and maintain the Quality Management System ensuring compliance with IATF 16949:2016 and VDA6 Achieve Quality Assurance operational objectives by contributing information and analysis to strategic plans and reviews; preparing and completing action plans; implementing production, productivity, quality, and customer-service standards; identifying and resolving problems; completing audits; determining system improvements and implementing change Develop Quality assurance plans by conducting risk analysis; identifying critical control points and preventive measures; procedures, corrective actions, and verification procedures Validate quality processes by establishing product specifications and quality attributes; measuring production; documenting evidence & writing and updating quality assurance procedures Communicate and liaise with internal and external customers and foster relationships Facilitate containment at Customer Site, raise Quality Alert bulletins, and facilitate training on quality-related concerns Control of non-conforming products and the rework thereof Support quality production inspectors in making product-related decisions regarding quarantined products (Pass, Reject or Rework) Generate work instructions and product-specific documentation Facilitate the generation and updating of Flow Charts, Control Plans, and FMEA’s Responsible for facilitating Measurement System Analysis and Capability Studies Liaise with Stores Controller and Manufacturing Practitioner regarding Quality concerns Responsible for Supplier Development in liaison with Stores Controller and Manufacturing Practitioner Compile and maintain Audit Schedules (Dock & Product Audits, Manufacturing Process Audits (VDA 6.3:2016), Internal Systems Audits (IATF 16949:2016)) Maintain & improve product quality by completing product, process, system, compliance, and surveillance audits & investigating customer complaints Coordinate Annual Quality Management reviews and keep records of meetings and quality objectives Compile Monthly Management Quality Reports Compile weekly yields reports Review Quality Risks and requirements in APQP activities Ensure compliance with process and Customer Specifications Complete Production Part Approval Process (PPAP) Investigate and implement countermeasures for continual quality improvement Monitor and measure customer feedback, complaints, and rejections to identify opportunities for improvement Conduct MSA studies Approve COC’s in absence of QM Quality Management: Compile Quality Topics for Quality Awareness Training Quality Assurance: Implement Quality Procedures and Work Instructions Maintain the Quality Assurance system Ensure compliance with Quality Policies, Procedures, and Work Instructions Audits: Conduct internal Process audits (VDA 6.3:2016) and Product & Layout audits Supply Quality Assurance (SQA): Specify Supplier Acceptable Quality Levels (AQL's) (Tolerances, Drawing requirements, Tooling, PPM's, etc.) Analyse Supplier Performance (Product Quality, Special Status, etc.) and make recommendations Notify Suppliers of non-conformances and initiate corrective actions Information Management and Direction Focusing: Collate and analyse company data and management reports Advanced Product Quality Planning (APQP): Review Quality Risks of APQP activities Ensure compliance with process and Customer Specifications Complete Production Part Approval Process (PPAP) Provide input to the Contract Review Process Continuous Improvement: Maintain an updated Continuous Improvement Plan People Management: Ensure an enabling climate/culture. Ensure a safe, secure and legal working environment. Manage individual, team, and departmental performance to achieve organisational objectives. Compile and update Performance Contracts and Individual Development Plans and facilitate individual career path planning. Determine the training needs of the Department. Conduct Performance Reviews and manage sub-standard performance. Coach and counsel people to ensure improved performance levels Ensure discipline is maintained in the department (absenteeism, lateness, overtime, misconduct, etc.) Resolve grievances and disputes #J-18808-Ljbffr

Mediclinic Southern Africa Corporate Office Stellenbosch South Africa

Closing date: 10 / 09 / 2025

Number of positions: 1

Recruiter name: Lerato Khati

Reference number: 63082

Workplace Type: Hybrid

Permanent

Please note if you are an internal employee on a fixed term contract please apply using an external candidate profile and not your employee profile

Overview

Main purpose of job: To implement drive and sustain clinical quality within the emergency medical environment.

Key responsibilities

• Set implement and manage operational clinical plans aligned with Emergency Medicine strategy
• Oversee clinical performance in the emergency medical environment and provide operational support
• Provide specialist expertise and support to emergency centres
• Build and maintain key stakeholder relationships

Education

ESSENTIAL EDUCATION : Registered / Professional Nursing qualification

DESIRED EDUCATION : Registered / Professional Nursing qualification

Experience

ESSENTIAL MINIMUM EXPERIENCE : Minimum 5 to 10 years clinical experience of which 3 5 should be in a Specialist function / SME-role such as Unit or branch Manager Patient Safety Risk Management

Experience in the private emergency medicine environment

Job skills and knowledge

• Data analysis and interpretation skills
• Infection prevention and control knowledge
• Computer literacy (MS Office package)
• Clinical risk management
• Stakeholder management
• Nursing functional knowledge
• Relevant nursing legislation
• Training and facilitation methodologies
• Healthcare industry knowledge
• Continuous improvement and quality assurance methodologies
• Communication skills
• Research reporting writing and presenting
• Staff and process analysis and optimisation

All applicants will be considered with the understanding that preference will be given in accordance with the Employment Equity Plan of Mediclinic Southern Africa as well as internal applicants / employees that meet the minimum requirements.

Please note if you are an internal employee on a fixed term contract please apply using an external candidate profile and not your employee profile

Required Experience: Unclear Seniority

Key Skills

Quality Assurance,FDA Regulations,Data Collection,Food Safety Experience,ISO 9001,Mobile Devices,Root cause Analysis,Quality Systems,OSHA,Food Processing,Quality Management,cGMP

Vacancy: 1

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Overview

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.

Responsibilities

Purpose:

The Commercial Quality Specialist is responsible for independently providing Commercial Quality support within the affiliate, covering quality system requirements related to pharmaceutical products, medical devices, combination products, biologics. Key responsibilities include authorizing the release for sale of products that meet AbbVie quality and regulatory standards, administering the product returns process, and assisting with handling Product Quality Complaints when needed. The role also involves supporting the Quality Assurance Manager in managing affiliate documentation, quality systems, and the training matrix for the Quality Assurance Department to ensure compliance with all procedures, legislative requirements, and AbbVie global policies. Additional areas of support include overseeing Storage and Distribution, addressing potential quality events or product shortages, managing Supplier Controls and Product Quality Reviews, participating in Risk Management, Agency inspections/internal audits, CAPA (Corrective and Preventive Actions), and fulfilling overall Quality Manual requirements. This ensures that all product, process, or system-related quality activities from receipt of final product through distribution align with Corporate, governmental, and local regulations.

Responsibilities:

• Responsible for the integration of local quality regulations for drugs, biologics, device and/or combination products.
• Design effective quality systems, procedures and/or processes within cross functional teams to ensure compliance as well as efficiency throughout our quality systems.
• Maintain and ensure the effectiveness of the Quality Management System in the affiliate, supporting quality control, assurance, and regulatory compliance activities by Monitoring metrics and KPIs to ensure compliance.
• Authorize timely release of products to the market and manage retention samples in line with Quality Assurance procedures. Work on assessments to determine compliance to processes, procedures and regulations to identify potential gaps and mitigate and implement improvements.
• Support all activities governed by Good Storage and Distribution Practices including monitoring of controlled temperature and cold chain shipments.
• Administer customer returns according to the Return Goods procedure.
• Support the effective management of Product Quality Complaints at the affiliate.
• Act as the Training Coordinator for the Quality Assurance department, ensuring compliance with all required training activities.
• Initiate exception reports and manage CAPAs (Corrective and Preventive Actions) and effectivity checks as identified by the current Non-Conformance procedures.
• Initiate Change Plans and oversee related tasks to resolution.
• Assist in preparing quality reports for quarterly management reviews and participate in Product Quality Reviews.
• Support the supplier management program by maintaining updated lists of local TPMS and vendors, qualifying suppliers/customers, evaluating supplier performance, monitoring supplier quality issues, and coordinating timely failure investigations.
• Conduct assigned internal quality audits and external audits according to the audit schedule, supporting the affiliate’s audit program.
• Assist with risk management activities, including participation in risk meetings and verifying the implementation of risk mitigation in products and processes.
• Contribute to writing, reviewing, maintaining, and approving Standard Operating Procedures for the Quality department.
• Support documentation maintenance and control as per applicable procedures.
• Act as Deputy Responsible Pharmacist during the absence of the Responsible Pharmacist. Represent Commercial Quality in cross functional teams, projects and programs, as assigned by management.

Qualifications

• Bachelor’s Degree in Pharmacy
• Registration with the South African Pharmacy Council (SAPC)
• At least two years’ experience in a quality assurance, GMP or GDP environment preferred.
• Excellent knowledge of computerized systems, familiarity with SAP, TrackWise, ComplianceWire and OneVault.
• Full understanding of local GxP requirements including regulations and standards affecting device, biologics, pharmaceutical products.
• General knowledge and understanding of AbbVie MD, pharmaceutical, biologic products and regulations
• Ability to support projects as a team member as assigned by manager
• Experience working in both a team setting and independently. Works well with manager guidance to complete tactical objectives while able to manage own time effectively.
• Make decisions in collaboration with management
• Acts as an owner - uses available resources to independently complete assigned tasks

Additional Information

Key Stakeholders: Local Affiliate Staff, Commercial QA team, Regulatory/Competent Authority, Suppliers/Service Providers.

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.

US & Puerto Rico only - to learn more, visit

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

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Quality Specialist (Plant)

Our client in the automotive industry is currently seeking a Quality Specialist (Plant) to join their team in Durban. This is a full-time, permanent position with a competitive salary and benefits.

As a Quality Specialist, you will be responsible for managing the Quality department, ensuring that all products and processes are in accordance with Quality Standards and Customer specific requirements.

Duties & Responsibilities

• Manage the Quality department.
• Ensure that all products and processes are in accordance with Quality Standards and Customer specific requirements.
• Monitor and control Quality Systems and Processes to achieve Quality Standards and meet customer specific requirements (CSRs).
• Conduct Quality investigations (Internal, Supplier, Customers).
• Maintain IATF 16949:2016 Certification.

Desired Experience & Qualification

• Minimum 5 years in a similar role within an Automotive/Manufacturing environment.
• National Diploma in Quality Management or Engineering related qualification.
• Trained Auditor ISO 9001:2015, IATF 16949:2016 & VDA 6.3:2016.

#J-18808-Ljbffr

Quality Specialist (Plant)

Our client in the automotive industry is currently seeking a Quality Specialist (Plant) to join their team in Durban. This is a full-time, permanent position with a competitive salary and benefits.

As a Quality Specialist, you will be responsible for managing the Quality department, ensuring that all products and processes are in accordance with Quality Standards and Customer specific requirements.

Duties & Responsibilities

• Manage the Quality department.
• Ensure that all products and processes are in accordance with Quality Standards and Customer specific requirements.
• Monitor and control Quality Systems and Processes to achieve Quality Standards and meet customer specific requirements (CSRs).
• Conduct Quality investigations (Internal, Supplier, Customers).
• Maintain IATF 16949:2016 Certification.

Desired Experience & Qualification

• Minimum 5 years in a similar role within an Automotive/Manufacturing environment.
• National Diploma in Quality Management or Engineering related qualification.
• Trained Auditor ISO 9001:2015, IATF 16949:2016 & VDA 6.3:2016.

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