Quality Assurance / Quality Control Jobs in Egypt 2026

Full Time 2 to 5 years Wuzzuf .com

Quality Auditor for Housekeeping

On-site - Egypt - Cairo 28 July 2026

Other

<h2>Key Responsibilities</h2><ul><li>Conduct housekeeping quality audits and inspections.</li><li>Ensure compliance with cleaning standards, SOPs, and HSE requirements.</li><li>Identify non-conformities and recommend corrective actions.</li><li>Prepare audit reports and monitor corrective action implementation.</li><li>Coordinate with Site Managers and Supervisors to improve service quality.</li><li>Verify proper use of cleaning equipment, chemicals, and consumables.</li><li>Support client inspections and continuous improvement initiatives.</li></ul>Requirements<ul><li>Bachelor's degree or relevant qualification.</li><li>2+ years of experience in housekeeping, quality assurance, or facility management.</li><li>Knowledge of housekeeping standards and quality auditing.</li><li>Proficiency in Microsoft Office.</li><li>Strong reporting and documentation skills.</li></ul><h2>Skills</h2><ul><li>Attention to detail.</li><li>Analytical and problem-solving skills.</li><li>Strong communication skills.</li><li>Time management and organization.</li><li>Teamwork and ability to work independently.</li></ul>

0 to 0 years Bayt

Lead QA/QC Engineer

On-site - Egypt 17 July 2026

Manufacturing & Production

<h2 class="h5">Job description</h2> <div class="t-break" data-jb-field="description"> Job Summary The Lead QA/QC Engineer - Construction and Contracting provides operational, technical, and functional leadership across construction and contracting activities while ensuring alignment with organizational standards, business objectives, and regulatory requirements. The role is responsible for driving performance, coordination, compliance, stakeholder engagement, and service delivery within the qa/qc function. The position supports continuous improvement initiatives, cost optimization, operational efficiency, and quality outcomes while collaborating closely with internal teams, contractors, clients, and business stakeholders. Job Responsibilities 1 Operational Management: Manage day-to-day qa/qc activities within the construction and contracting environment to ensure efficient execution, compliance with procedures, and achievement of operational targets while maintaining service quality and productivity standards. Planning and Coordination: Coordinate schedules, manpower, materials, contractors, and operational activities to ensure timely completion of tasks, projects, and deliverables in line with approved timelines and business requirements. Stakeholder Engagement: Liaise with internal departments, consultants, suppliers, subcontractors, clients, and operational teams to ensure smooth communication, issue resolution, and alignment on technical and operational requirements. Compliance and Governance: Ensure compliance with company policies, contractual obligations, regulatory standards, HSE requirements, and industry best practices applicable to the construction and contracting sector. Performance Monitoring: Monitor operational KPIs, productivity, service standards, and quality benchmarks while identifying gaps, implementing corrective actions, and driving continuous improvement initiatives. Reporting and Documentation: Prepare operational reports, technical records, progress updates, cost analyses, and management presentations to support decision-making, audit readiness, and business transparency. Resource Optimization: Support efficient utilization of manpower, equipment, budgets, materials, and operational resources to improve productivity, reduce waste, and optimize operational costs. Risk and Issue Management: Identify operational risks, technical challenges, delays, and performance issues while implementing mitigation measures and escalation processes to minimize business impact. Quality Assurance: Support the implementation of quality assurance and quality control procedures to ensure services, deliverables, and operational outputs meet company and client expectations. Continuous Improvement: Contribute to process enhancements, digital initiatives, workflow optimization, and operational excellence programs to improve efficiency, service delivery, and overall business performance. Job Responsibilities 2 Additional Responsibilities 3 Job Knowledge & Skills Sector Operations Knowledge: Strong understanding of operational requirements, standards, workflows, and regulatory expectations within the construction and contracting sector. Technical and Functional Expertise: Advanced knowledge of qa/qc processes, documentation, reporting standards, systems, and operational controls relevant to the role. Stakeholder Coordination: Ability to manage cross-functional communication, contractor coordination, client engagement, and team collaboration within fast-paced operational environments. Systems and Reporting: Proficiency in ERP systems, reporting tools, Microsoft Office applications, operational dashboards, and performance tracking methodologies. Problem Solving and Decision Making: Strong analytical, organizational, and decision-making capabilities with the ability to resolve operational issues and support business continuity. Job Experience Industry Experience: Proven experience within the construction and contracting sector handling operational, technical, project, or functional responsibilities related to the role. Operational Coordination Exposure: Demonstrated experience coordinating teams, contractors, stakeholders, resources, and service delivery activities within complex operational environments. Compliance and Performance Management: Experience supporting KPI management, reporting, process improvement, quality compliance, and operational efficiency initiatives. Competencies Leadership Resilience Quality Agility AI Fluency Material testing & Standard awareness L3 QA Audits L3 Quality Assurance L3 Statistical Quality Control L3 Sub-contractor Quality Management L3 Education </div>

0 to 0 years Bayt

Quality Control Manager

On-site - Egypt 22 July 2026

<h2 class="h5">Job description</h2> <div class="t-break" data-jb-field="description"> Job Summary The Quality Control Retail Manager is responsible for ensuring consistent operational excellence, compliance with company standards, and superior customer experience across all retail stores. The role oversees quality control processes, conducts store audits, monitors compliance with operational procedures, and drives continuous improvement initiatives to enhance overall retail performance. Key Responsibilities <ul><li>Develop and implement quality control standards and procedures across all retail locations.</li><li>Conduct regular store audits to ensure compliance with company policies, SOPs, visual merchandising standards, and operational guidelines.</li><li>Monitor customer service quality and ensure a consistent brand experience across all stores.</li><li>Evaluate store operations, identify performance gaps, and implement corrective action plans.</li><li>Monitor inventory management, stock accuracy, shrinkage, and loss prevention practices.</li><li>Ensure compliance with health, safety, and security regulations.</li><li>Analyze audit results, customer feedback, and operational KPIs to identify improvement opportunities.</li><li>Collaborate with Retail Operations, HR, Training, and Store Managers to improve operational performance.</li><li>Develop quality reports and present findings and recommendations to senior management.</li><li>Support new store openings by ensuring compliance with operational and quality standards.</li><li>Lead continuous improvement initiatives to enhance efficiency, productivity, and customer satisfaction.</li></ul> Qualifications <ul><li>Bachelor's degree in Business Administration, Retail Management, Quality Management, or a related field.</li><li>5–8 years of experience in retail operations or quality control, including at least 3 years in a managerial role.</li><li>Experience in retail chains, fashion, luxury, FMCG, or consumer goods is preferred.</li><li>Strong knowledge of retail operations, quality assurance, SOPs, and customer service standards.</li><li>Experience in conducting operational audits and compliance reviews.</li><li>Proficiency in Microsoft Office and ERP/POS retail systems.</li><li>Strong analytical, leadership, communication, and problem-solving skills.</li><li>Willingness to travel regularly between retail locations.</li></ul> </div>

0 to 0 years Bayt

Quality Control Manager

On-site - Egypt 26 June 2026

Manufacturing & Production

<h2 class="h5">Job description</h2> <div class="t-break" data-jb-field="description"> Viatris Egypt S.A.EViatris is a global healthcare company uniquely positioned to bridge the traditional divide between generics and brands, combining the best of both to more holistically address healthcare needs globally. With a mission to empower people worldwide to live healthier at every stage of life, we provide access at scale, currently supplying high-quality medicines to approximately 1 billion patients around the world annually and touching all of life's moments, from birth to the end of life, acute conditions to chronic diseases. We have been included on number of award lists that demonstrate the impact we are making.   Every day, we rise to the challenge to make a difference and here’s how the “Quality Control Manager” role will make an impact: Key responsibilities for this role include: <ul><li>Responsible for the QC laboratory functions (Chemical, Stability, Methodology, Raw material, Packaging & Microbiology) and the corresponding documentation to support the timely disposition of products and materials</li><li>The laboratory function encompasses raw material, packaging, Stability, finished product testing, method validation and QC Compliance.</li><li>Manage the overall Quality control release and disposition of incoming materials and finished products.</li><li>Performing routine Gemba walks in QC Labs to ensure GMP and safety practices are strictly followed</li><li>Review and approval of Laboratory out-of-specification and failure investigations</li><li>Support regulatory inspections and audits and address findings</li><li>Track and evaluate Quality Control KPIs, identifying trends and leading improvement initiatives to enhance performance and compliance and present to Quality Council</li><li>Review and approval of the entire SOPs relating to Quality control tasks and ensure understanding and implementation of these SOPs.</li><li>Responsible for closing the gaps between Viatris Quality Policies, regulatory requirements and compliance practices.</li><li>Responsible for ensuring implementation and sustaining QC data integrity program and ALCOA+ on laboratory level and ensure data integrity implementation throughout lab operations</li><li>Support laboratory colleagues in all aspects of their work to achieve the completion of tests and/or investigations in a timely manner as well as maintaining an updated knowledge base in the technical, operations, company policy and regulatory fields.</li><li>Facilitate continuous improvement in QC day-to-day operations and general systems and will actively support achievement of site goals.</li><li>Responsible for QC resource planning including preparation of budgets and monitoring budget adherence with QO manager.</li><li>Coaching and developing QC colleagues to achieve high performance.</li><li>Implementation of Viatris Operational Excellence standards and facilitating PHE (Production Health Evaluation), HEP (Human Error Performance) and Continuous Improvement Projects</li><li>Ensuring compliance with Pharmacopeial requirements and up to date with Pharmacopeial notifications and updates</li><li>Leading and guiding QC inspection readiness</li><li>Review and approve the protocol and the results of the Analytical Method Transfer Exercise (AMTE) locally (for the new analysts) and for other locations.  Also, responsible for receiving and implementing AMTE for the new product manufacturing.</li><li>Ensure implementation of all the stability (Ongoing and Accelerating stability) programs, including review and approval of the stability reports.</li><li>Review and Approve the Validation of new developed test procedures.</li><li>Review and Approve the Validation protocols and reports</li><li>Preparing and ensuring the execution of the development plan (IDP) for QC colleagues</li><li>Encourage the QC members in applying RFT projects for M1, M2, and M3 and follow up these projects.</li><li>Ensure that safety guidelines are implemented and followed in QC lab</li><li>Active implementation of Critical Quality Notifications and Notification to Management procedures.</li><li>Delegate for Site Quality Operation Head in case of his/her absence (if needed).</li><li>Delegating Finished goods Section Head, Microbiology Section Head, Raw Materials Section Head, QC Compliance Section Head or Quality Control Section Head (Stability and Methodology) in case of absence.</li><li>Being eligible to be registered as QC Manager according to EDA requirements and legislation</li></ul>The minimum qualifications for this role are: <ul><li>Bachelor’s degree in Pharmaceutical Sciences is a must</li><li>Minimum 10 years’ experience in QC lab operations</li><li>cGMP & cGLP Extensive Knowledge</li><li>Data Integrity and ALCOA+ Knowledge</li><li>Good understanding of the pharmaceutical regulatory process.</li><li>Complying with EDA legislation for QC Manager registration</li></ul>The following documents to be available: <ul><li>Experience letter(s) for 10 years of relevant experience in QC</li><li>Original certificate confirming the pharmacist’s position regarding mandatory assignment (Taklif)</li><li>Valid Pharmacy Syndicate Membership Card</li></ul>The essential personal qualifications for this role are: <ul><li>Six Sigma Knowledge and Green Belt holder is a plus. </li><li>Good command of English both written and spoken.</li><li>Excellent problem-solving and investigative skills</li><li>Experience in handling regulatory audits and inspections</li><li>Logical thinking.</li><li>Management and decision-making skills.</li><li>High analytical skills.</li><li>Communication & high interpersonal skills.</li><li>Good planning skills.</li><li>Time Management skills.</li></ul>At Viatris, we offercompetitivesalaries, benefitsandan inclusive environment where you can use your experiences, perspectives and skills to help make an impact on the lives of others. Viatris is an Equal Opportunity Employer. </div>

Full Time 8 to 10 years Wuzzuf .com

Quality Control Manager

On-site - Egypt - Cairo 9 July 2026

Education & Training

About the CompanyWe are a well-established Petroleum Services company providing specialized solutions to the Oil & Gas industry. Our expertise includes OCTG Services, API & Premium Connection Rethreading, Machine Shop Manufacturing, Repair, Bucking Operations, Welding, Hard banding, and related workshop and field services. Job PurposeWe are seeking an experienced Quality Control Manager to lead all Quality Control activities across workshop and field operations. The successful candidate will ensure that all inspection, testing, manufacturing, repair, welding, and threading activities fully comply with customer specifications, API standards, and company quality requirements while leading a high-performing quality team. Key Responsibilities<ul><li>Lead and manage all Quality Control Engineers, Supervisors, and Inspectors.</li><li>Develop and implement inspection and testing plans for all operational activities.</li><li>Oversee quality control activities related to OCTG, Machine Shop Manufacturing, API & Premium Connection Rethreading, Repair, Bucking, Welding, Hardbanding, Cleaning, and Field Services.</li><li>Ensure compliance with API specifications, ISO requirements, customer specifications, and Premium Connection standards.</li><li>Supervise dimensional inspection, thread inspection, welding inspection, NDT coordination, and final product release.</li><li>Review and approve inspection reports, quality dossiers, certificates, and final release documentation.</li><li>Ensure calibration, traceability, and control of inspection and measuring equipment.</li><li>Coordinate customer inspections and third-party inspection activities.</li><li>Investigate non-conformities, customer complaints, and field failures while leading RCA and CAPA activities.</li><li>Monitor QC KPIs and implement initiatives to reduce defects, rework, and quality costs.</li><li>Collaborate closely with QA, Operations, Engineering, and HSE teams to improve product quality and operational performance.</li><li>Develop and mentor QC personnel to ensure technical competency and operational excellence.</li><li>Regular travel to company workshops and operational sites is required.</li></ul>

0 to 0 years Naukri Gulf

Quality Control Manager

On-site - Egypt - Cairo 26 June 2026

Research & Development

<section>Job DescriptionRoles & Responsibilities<div class="paragraph">Responsible for the QC laboratory functions (Chemical, Stability, Methodology, Raw material, Packaging & Microbiology) and the corresponding documentation to support the timely disposition of products and materials The laboratory function encompasses raw material, packaging, Stability, finished product testing, method validation and QC Compliance. Manage the overall Quality control release and disposition of incoming materials and finished products. Performing routine Gemba walks in QC Labs to ensure GMP and safety practices are strictly followed Review and approval of Laboratory out-of-specification and failure investigations Support regulatory inspections and audits and address findings Track and evaluate Quality Control KPIs, identifying trends and leading improvement initiatives to enhance performance and compliance and present to Quality Council Review and approval of the entire SOPs relating to Quality control tasks and ensure understanding and implementation of these SOPs. Responsible for closing the gaps between Viatris Quality Policies, regulatory requirements and compliance practices. Responsible for ensuring implementation and sustaining QC data integrity program and ALCOA+ on laboratory level and ensure data integrity implementation throughout lab operations Support laboratory colleagues in all aspects of their work to achieve the completion of tests and/or investigations in a timely manner as well as maintaining an updated knowledge base in the technical, operations, company policy and regulatory fields. Facilitate continuous improvement in QC day-to-day operations and general systems and will actively support achievement of site goals. Responsible for QC resource planning including preparation of budgets and monitoring budget adherence with QO manager. Coaching and developing QC colleagues to achieve high performance. Implementation of Viatris Operational Excellence standards and facilitating PHE (Production Health Evaluation), HEP (Human Error Performance) and Continuous Improvement Projects Ensuring compliance with Pharmacopeial requirements and up to date with Pharmacopeial notifications and updates Leading and guiding QC inspection readiness Review and approve the protocol and the results of the Analytical Method Transfer Exercise (AMTE) locally (for the new analysts) and for other locations. Also, responsible for receiving and implementing AMTE for the new product manufacturing. Ensure implementation of all the stability (Ongoing and Accelerating stability) programs, including review and approval of the stability reports. Review and Approve the Validation of new developed test procedures. Review and Approve the Validation protocols and reports Preparing and ensuring the execution of the development plan (IDP) for QC colleagues Encourage the QC members in applying RFT projects for M1, M2, and M3 and follow up these projects. Ensure that safety guidelines are implemented and followed in QC lab Active implementation of Critical Quality Notifications and Notification to Management procedures. Delegate for Site Quality Operation Head in case of his/her absence (if needed). Delegating Finished goods Section Head, Microbiology Section Head, Raw Materials Section Head, QC Compliance Section Head or Quality Control Section Head (Stability and Methodology) in case of absence. Being eligible to be registered as QC Manager according to EDA requirements and legislation</div></section><section>Desired Candidate ProfileThe minimum qualifications for this role are: Bachelor s degree in Pharmaceutical Sciences is a must Minimum 10 years experience in QC lab operations cGMP & cGLP Extensive Knowledge Data Integrity and ALCOA+ Knowledge Good understanding of the pharmaceutical regulatory process. Complying with EDA legislation for QC Manager registration The following documents to be available: Experience letter(s) for 10 years of relevant experience in QC Original certificate confirming the pharmacist s position regarding mandatory assignment (Taklif) Valid Pharmacy Syndicate Membership Card The essential personal qualifications for this role are: Six Sigma Knowledge and Green Belt holder is a plus. Good command of English both written and spoken. Excellent problem-solving and investigative skills Experience in handling regulatory audits and inspections Logical thinking. Management and decision-making skills. High analytical skills. Communication & high interpersonal skills. Good planning skills. Time Management skills.</section>

Full Time 0 to 0 years Elsewedy Electric jobs

Senior Quality Control Engineer

On-site - Egypt 27 July 2026

<div ><table cellspacing="0" cellpadding="0" hspace="0" vspace="0"><tbody><tr><td valign="top" align="left">·         Supervise and manage all Quality Control functions in the workplace and manage a team of QC engineers and inspectors for day-to-day QC functions.·         Interface and coordinate with clients for QC matters and coordinate with third party inspection agencies for all related inspection activities.·         Act as a coordination point for ISO internal and external audits·         Plan and undertake Subcontractor audits and reviews of Sub contractor quality control programs.·         Supervise Soil investigation and batching plant assessment.·         Coordinate with the Clients and subcontractors for carrying out field compaction test on soil, cube tests & slump tests on concrete and the various third-party tests on soil and concrete.·         Supervise pre-concrete inspections and ensure that the formwork, rebar’s and the concrete placing are in accordance with the approved drawings and international standards.·         Supervise Inspection of Concreting, Fireproofing and Asphalt paving.·         Supervise Inspection of Building works.</td></tr></tbody></table></div>Lead the land surveyors by carrying out constant checks in levels and coordinates and ensure that they are in accordance with the project specifications.

0 to 0 years Bayt

Senior Quality Control Engineer

On-site - Egypt 13 July 2026

Manufacturing & Production

<h2 class="h5">Job description</h2> <div class="t-break" data-jb-field="description"> ·Supervise and manage all Quality Control functions in the workplace and manage a team of QC engineers and inspectors for day-to-day QC functions. ·Interface and coordinate with clients for QC matters and coordinate with third party inspection agencies for all related inspection activities. ·Act as a coordination point for ISO internal and external audits ·Plan and undertake Subcontractor audits and reviews of Sub contractor quality control programs. ·Supervise Soil investigation and batching plant assessment. ·Coordinate with the Clients and subcontractors for carrying out field compaction test on soil, cube tests & slump tests on concrete and the various third-party tests on soil and concrete. ·Supervise pre-concrete inspections and ensure that the formwork, rebar’s and the concrete placing are in accordance with the approved drawings and international standards. ·Supervise Inspection of Concreting, Fireproofing and Asphalt paving. ·Supervise Inspection of Building works. Lead the land surveyors by carrying out constant checks in levels and coordinates and ensure that they are in accordance with the project specifications. ·Bachelor Degree of Electrical Engineering. ·Team leadership. ·Holder of IPMA certificate. ·Conflict and grievance resolution. ·Related Field Experience:3 to 5 years ·Preferred Requirements: oISO Lead Auditor Training. Any additional qualification to the Engineering degree </div>

Full Time 0 to 0 years Elsewedy Electric jobs

Senior Quality Control Engineer

On-site - Egypt 12 July 2026

<div ><table cellspacing="0" cellpadding="0" hspace="0" vspace="0"><tbody><tr><td align="left">·         Undertake QC functions in the workplace for daily QC activities.<o\:p></o\:p>·         Conduct inspection of raw materials, bought out items and review of Material Test Certificates (MTC) and the specification requirements.<o\:p></o\:p>·         Interface and coordinate with clients for QC matters and coordinate with third party inspection agencies for all related inspection activities.<o\:p></o\:p>·         Prepare Quality Control procedures/work instruction, ITP (Inspection Test Plans) according to project/client requirements and follow-up for its approval and monitor the implementation.<o\:p></o\:p>·         Plan and supervise Subcontractor inspection activities and reviews of Sub Contractor QC performance.<o\:p></o\:p>·         Supervise staff for reporting, recording and inspection activities.<o\:p></o\:p>·         Preparation of final QC dossier for handing over to the client and maintain proper filling system (as per Organization procedure) with full traceability for retrieving the document.<o\:p></o\:p>·         Have a proactive approach in problem solving.<o\:p></o\:p>·         Knowledge and experience in all QC related activities in Piping/Pipe line, Equipment, Tanks, Painting, Fireproofing & Insulation.<o\:p></o\:p>·         Verification of Piping and pipeline Test packages.<o\:p></o\:p>·         Conduct all QC related activities in Plumbing, HVAC, static& rotating equipment installation, Firefighting system and Painting (for C&I Project).<o\:p></o\:p>·         To coordinate Non-Destructive Testing (NDT) activities and review of NDT reports.<o\:p></o\:p></td></tr></tbody></table></div>Read and interpret the various drawings used in the projects for executing the work.

0 to 0 years Naukri Gulf

Quality Control Engineer

On-site - Egypt - Egypt 16 July 2026

Research & Development

<section>Job DescriptionRoles & Responsibilities<div class="paragraph">Job SummaryThe Quality Control (QC) Engineer is responsible for ensuring that construction and engineering works comply with project specifications, approved drawings, applicable codes, and quality standards. The role involves conducting inspections, monitoring work execution, identifying non-conformities, and ensuring corrective actions are implemented to achieve the required quality objectives.Key Responsibilities<ul><li>Implement the project Quality Control Plan (QCP) and Inspection and Test Plans (ITPs).</li><li>Inspect materials, equipment, and workmanship to ensure compliance with project specifications and approved drawings.</li><li>Conduct site inspections and witness testing activities for mechanical, electrical, civil, or architectural works, as applicable.</li><li>Prepare and submit Inspection Requests (IRs) and coordinate inspections with consultants and clients.</li><li>Identify, document, and report non-conformities (NCRs) and monitor corrective and preventive actions.</li><li>Review material approvals, method statements, shop drawings, and quality documentation before construction activities.</li><li>Verify that only approved materials are used on site.</li><li>Monitor contractors and subcontractors to ensure compliance with quality standards and project requirements.</li><li>Maintain quality records, inspection reports, test results, and as-built documentation.</li><li>Participate in internal and external quality audits.</li><li>Coordinate with project engineers, consultants, and clients to resolve quality-related issues.</li><li>Ensure testing and commissioning activities are performed according to approved procedures.</li><li>Support project handover by ensuring all quality documentation is complete and approved.</li><li>Promote continuous improvement in quality processes and construction practices.</li></ul></div></section><section>Desired Candidate ProfileQualificationsBachelor s degree in Engineering (Mechanical, Civil, Electrical, or related discipline).Professional certifications in Quality Management (e.g., ISO 9001 Lead Auditor/Internal Auditor) are an advantage.5+ years of experience in quality control within construction, MEP, industrial, or infrastructure projects.Technical Skills<ul><li>Strong understanding of QA/QC principles and quality management systems.</li><li>Knowledge of ISO 9001 standards and quality documentation.</li><li>Familiarity with international codes and standards relevant to the discipline (e.g., ASME, ASTM, NFPA, ASHRAE, ACI, IEC).</li><li>Ability to read and interpret engineering drawings and specifications.</li><li>Experience preparing NCRs, inspection reports, ITPs, and material inspection records.</li><li>Proficiency in Microsoft Office and AutoCAD; knowledge of BIM software is an advantage.</li></ul>Soft Skills<ul><li>Strong analytical and problem-solving abilities.</li><li>Excellent communication and reporting skills.</li><li>High attention to detail and accuracy.</li><li>Good organizational and documentation skills.</li><li>Ability to work collaboratively with multidisciplinary teams.</li><li>Effective time management and ability to meet project deadlines.</li></ul></section>

Full Time 0 to 0 years Elsewedy Electric jobs

Quality Control Engineer

On-site - Egypt 14 hours ago

<div ><table cellspacing="0" cellpadding="0" hspace="0" vspace="0"><tbody><tr><td align="left">·         Analyze Test specifications and monitors test implementation during production stages till the final product stage.<o\:p></o\:p>·         Getting approval from QC Manager for order fixing form (OFF) to start the Manufacturing process.<o\:p></o\:p>·         Follow up the order cycle with the designated department till it reaches the planning department to get information such as machine loading, delivery time, machine time/man hour.<o\:p></o\:p>·         Request Quality control procedure and test report from QA department. <o\:p></o\:p>·         Follow up order cycle with production department and manage quality control according to quality control procedures. <o\:p></o\:p>·         Coordinate with warehouse department to allocate the final product in the specified quality area to ensure it is not being transferred or shipped to any clients at this stage. <o\:p></o\:p>·         Communicate with Technical Department to agree on the packing required to ship this transformer. <o\:p></o\:p>·         Send technical specifications to Packaging department in the production warehouse for execution. <o\:p></o\:p>·         Send technical documents to the testing lab to start the testing process including drawings, technical datasheet and shipment details. <o\:p></o\:p>·         Follow up on test results to obtain the required certificate. <o\:p></o\:p>·         Send shipment request to shipping department to launch the shipment process to the final destination in case of exporting. <o\:p></o\:p></td></tr></tbody></table></div>Update project plan with all actual project stages and saved on the project’ technical file.

0 to 0 years Bayt

Quality Control Analyst

On-site - Egypt 26 June 2026

Manufacturing & Production

<h2 class="h5">Job description</h2> <div class="t-break" data-jb-field="description"> Viatris Egypt S.A.EViatris is a global healthcare company uniquely positioned to bridge the traditional divide between generics and brands, combining the best of both to more holistically address healthcare needs globally. With a mission to empower people worldwide to live healthier at every stage of life, we provide access at scale, currently supplying high-quality medicines to approximately 1 billion patients around the world annually and touching all of life's moments, from birth to the end of life, acute conditions to chronic diseases. We have been included on number of award lists that demonstrate the impact we are making.   Every day, we rise to the challenge to make a difference and here’s how the “Quality Control Analyst” role will make an impact: Key responsibilities for this role include: <ul><li>Conduct routine and non-routine analyses of in-process materials, finished goods, and stability samples in a timely manner.</li><li>Interpret test results and compare them with established specifications and control limits.</li><li>Conduct chemical and physical laboratory tests to perform qualitative and quantitative analyses.</li><li>Complete documentation required to support testing activities, including data capture forms, equipment logbooks, and inventory records.</li><li>Ensure compliance with Data Integrity principles and Good Documentation Practices (GDP) in all laboratory activities.</li><li>Prepare technical reports, graphs, and charts to document experimental results.</li><li>Participate in out-of-specification (OOS), out-of-trend (OOT), and laboratory failure investigations.</li><li>Provide quality control data required for regulatory submissions, as applicable.</li><li>Investigate and report questionable or atypical test results to the supervisor.</li><li>Perform data entry and trend analysis activities.</li><li>Execute activities related to process validation, cleaning validation, and instrument qualification under supervision, as applicable.</li><li>Support the preparation and execution of SOPs, calibration protocols, validation protocols, and qualification documents (IQ, OQ, and PQ) related to laboratory activities.</li><li>Ensure implementation of Viatris Policies and requirements applicable to laboratory operations.</li><li>Monitor reference standards inventory and expiry status.</li><li>Monitor inventory and expiry status of laboratory stock items, including reagents, glassware, filters, and other laboratory consumables.</li><li>Support the review and revision of Quality Control SOPs, as assigned.</li><li>Participate in continuous improvement initiatives, including Lean and Six Sigma projects.</li><li>Support QC compliance activities related to Viatris Policies, internal audits, EDA actions, and data integrity requirements.</li></ul>Experience and Knowledge <ul><li>Working knowledge of current Good Manufacturing Practices (cGMP) and current Good Laboratory Practices (cGLP), with particular emphasis on Quality Control operations.</li><li>Knowledge of analytical laboratory techniques and laboratory instrumentation, including pH meters, UV-Visible spectrophotometers, High-Performance Liquid Chromatography (HPLC), and reagent preparation.</li><li>Familiarity with laboratory investigations, data integrity requirements, and Good Documentation Practices (GDP) is preferred.</li><li>Experience with laboratory computerized systems and electronic data management is an advantage.</li><li>Knowledge of pharmaceutical testing requirements, specifications, and regulatory expectations is preferred.</li></ul>Minimum Qualifications for this Role <ul><li>Bachelor's degree in Pharmacy, Chemistry or Pharmaceutical Sciences.</li><li>1–2 years of experience in a pharmaceutical Quality Control laboratory.</li><li>Good command of the English language, both written and spoken.</li><li>Strong technical writing, documentation, and communication skills.</li><li>Proficiency in Microsoft Office applications (Word, Excel, and PowerPoint).</li><li>Strong organizational, analytical, and problem-solving skills, with the ability to work independently and effectively within a team environment.</li><li>Ability to manage multiple priorities, work under pressure, and meet deadlines.</li></ul>At Viatris, we offercompetitivesalaries, benefitsandan inclusive environment where you can use your experiences, perspectives and skills to help make an impact on the lives of others. Viatris is an Equal Opportunity Employer. </div>

Full Time 3 to 5 years Wuzzuf .com

Architecture Quality Control Engineer

On-site - Egypt - Cairo 16 July 2026

Research & Development

<ul><li>Inspect and monitor finishing works on site (flooring, wall finishes, ceilings, joinery, painting, etc.) to ensure compliance with approved drawings and specifications.</li><li>Prepare and follow up on Quality Control checklists for each finishing stage before handover.</li><li>Identify defects or non-conformities and issue NCRs (Non-Conformance Reports), following up until resolved.</li><li>Coordinate with site engineers and contractors to correct quality issues before proceeding to the next stage.</li><li>Review materials and finishes delivered to site against approved samples and specifications.</li><li>Prepare periodic quality inspection reports for project management.</li><li>Ensure compliance with architectural quality standards and specifications throughout execution.</li></ul>RequirementsEducation Bachelor's degree in Architecture or Civil Engineering Experience 3 – 5 yearsBackground Must have solid hands-on experience specifically in finishing works on siteSoftware AutoCAD (preferred) – Microsoft Office (Word, Excel, PowerPoint)Language Good written and spoken English for technical documentation

Full Time 0 to 2 years Wuzzuf .com

Quality Control Engineer

On-site - Egypt - Cairo 28 July 2026

Engineering

<ul><li>Prepare project QA/QC documents according to project requirements, installation and fabrication sequence .</li><li>Prepare and implement internal quality audits .</li><li>Conduct site inspection .</li></ul>Requirements<ul><li>BSc in Civil Engineering or Production Engineering or Architecture Engineering.</li><li>0-2 years of experience in QC field.</li><li>Ability to read and understand contracts / project specifications.</li></ul>

Full Time 0 to 0 years Gulf Talnet

Quality Control Engineer

On-site - Egypt - Cairo 24 July 2026

Sales

<h4>Job description</h4> Follow the implementation of quality control procedure by inspecting, testing & qualifying received components to maintain product quality level & cost. Establish quality manual of each component with all standards & specifications to effectively control the process of components’ receiving. Qualify new introduced suppliers, materials and components to ensure compliance with specifications & standards. Measure suppliers’ performance level periodically based on evaluation criteria to enhance components quality level. Set development plans for approved suppliers through audits & visits to improve suppliers quality level and ensure high quality level for received components. Set plans for periodic audits on warehouses to ensure the implementation of related procedures and standards. Measure plant performance against agreed KPIs & objectives to identify areas for improvement. Audit the performance of manufacturing & production processes by inspecting & testing random samples from manufactured & produced products to maintain product quality level & cost. Investigate & troubleshoot production & manufacturing issues and set agreed actions with operations team to achieve product & process quality level. Monitor, investigate & troubleshoot market returns issues and set responsibilities & needed actions to enhance customer satisfaction level. Measure skills of QC team and set training plans based on skills matrix to improve technical skills level for both production and QC teams and encourage them towards continuous improvement and innovation. Ensure that workflows, processes, and products comply with safety regulations to maintain safe working area. <h4>Skills description</h4> Technical skills <ul> <li>Good knowledge of production & manufacturing techniques.</li> <li>Very good knowledge of problem solving, statistical tools & techniques.</li> <li>Basic knowledge for A/C product features.</li> <li>Lean Six Sigma knowledge is added plus.</li> <li>ISO 9001:2015 knowledge is added plus.</li> </ul>

Full Time 3 to 5 years Wuzzuf .com

Quality Control Analyst

On-site - Egypt - Giza 9 July 2026

Information Technology

Are you a meticulous problem-solver with a passion for perfection in technology? We are seeking an exceptional Quality Control Analyst to join our dynamic team in Giza, Egypt. This is your chance to play a pivotal role in ensuring the flawless delivery of cutting-edge IT and telecommunications solutions. As an integral part of our on-site team, you will champion quality, drive innovation, and directly impact our products' excellence.<ul><li>Overview: As a Quality Control Analyst, you will be the guardian of our product quality, meticulously examining software and systems to identify defects and ensure adherence to the highest standards. Your expertise will be crucial in safeguarding the integrity and performance of our IT and telecom offerings.</li><li>Key Responsibilities:<ul><li>Design and execute comprehensive test plans and test cases for software and system functionalities.</li><li>Perform various types of testing, including functional, regression, performance, and integration testing across different platforms.</li><li>Identify, document, and track defects rigorously using advanced defect tracking systems, collaborating closely with development teams for resolution.</li><li>Contribute to the continuous improvement of our Quality Assurance processes and methodologies.</li><li>Participate actively in all phases of the Software Development Life Cycle (SDLC) within an Agile framework.</li><li>Analyze test results and provide detailed reports on product quality and release readiness.</li></ul></li><li>Skills & Technologies: This role demands a strong foundation in Quality Assurance and Quality Control principles. You will leverage your expertise in Engineering, alongside practical experience with Test Automation tools, performing thorough Manual Testing, and working with databases using SQL. Familiarity with Defect Tracking systems, Agile Methodologies, and Performance Testing is essential.</li><li>Growth Opportunities: Embark on a journey of continuous learning and professional advancement. We are committed to fostering your growth through challenging projects, access to advanced training, and opportunities to lead quality initiatives. Elevate your career in a rapidly evolving technological landscape.</li><li>Team & Culture: Join a collaborative, innovative, and supportive environment where your contributions are valued, and your voice is heard. Our team in Giza is driven by a shared commitment to excellence and a passion for pushing technological boundaries.</li><li>Impact: Your work will directly influence the reliability and quality of our products, enhancing user experience and solidifying our reputation as a leader in IT and telecommunications. Be the critical link in delivering exceptional solutions to our customers.</li></ul>

0 to 0 years Naukri Gulf

Quality Control Analyst

On-site - Egypt - Cairo 26 June 2026

Research & Development

<section>Job DescriptionRoles & Responsibilities<div class="paragraph">Conduct routine and non-routine analyses of in-process materials, finished goods, and stability samples in a timely manner. Interpret test results and compare them with established specifications and control limits. Conduct chemical and physical laboratory tests to perform qualitative and quantitative analyses. Complete documentation required to support testing activities, including data capture forms, equipment logbooks, and inventory records. Ensure compliance with Data Integrity principles and Good Documentation Practices (GDP) in all laboratory activities. Prepare technical reports, graphs, and charts to document experimental results. Participate in out-of-specification (OOS), out-of-trend (OOT), and laboratory failure investigations. Provide quality control data required for regulatory submissions, as applicable. Investigate and report questionable or atypical test results to the supervisor. Perform data entry and trend analysis activities. Execute activities related to process validation, cleaning validation, and instrument qualification under supervision, as applicable. Support the preparation and execution of SOPs, calibration protocols, validation protocols, and qualification documents (IQ, OQ, and PQ) related to laboratory activities. Ensure implementation of Viatris Policies and requirements applicable to laboratory operations. Monitor reference standards inventory and expiry status. Monitor inventory and expiry status of laboratory stock items, including reagents, glassware, filters, and other laboratory consumables. Support the review and revision of Quality Control SOPs, as assigned. Participate in continuous improvement initiatives, including Lean and Six Sigma projects. Support QC compliance activities related to Viatris Policies, internal audits, EDA actions, and data integrity requirements.</div></section><section>Desired Candidate ProfileWorking knowledge of current Good Manufacturing Practices (cGMP) and current Good Laboratory Practices (cGLP), with particular emphasis on Quality Control operations. Knowledge of analytical laboratory techniques and laboratory instrumentation, including pH meters, UV-Visible spectrophotometers, High-Performance Liquid Chromatography (HPLC), and reagent preparation. Familiarity with laboratory investigations, data integrity requirements, and Good Documentation Practices (GDP) is preferred. Experience with laboratory computerized systems and electronic data management is an advantage. Knowledge of pharmaceutical testing requirements, specifications, and regulatory expectations is preferred.Minimum Qualifications for this Role<ul><li>Bachelor's degree in Pharmacy, Chemistry or Pharmaceutical Sciences.</li><li>1 2 years of experience in a pharmaceutical Quality Control laboratory.</li><li>Good command of the English language, both written and spoken.</li><li>Strong technical writing, documentation, and communication skills.</li><li>Proficiency in Microsoft Office applications (Word, Excel, and PowerPoint).</li><li>Strong organizational, analytical, and problem-solving skills, with the ability to work independently and effectively within a team environment.</li><li>Ability to manage multiple priorities, work under pressure, and meet deadlines.</li></ul></section>

0 to 0 years Bayt

Senior Supervisor, Quality Control

On-site - Egypt 7 July 2026

Manufacturing & Production

<h2 class="h5">Job description</h2> <div class="t-break" data-jb-field="description"> Job Purpose: To manage activities related to the quality control unit within the quality department including management of tests in products analysis, overseeing procedures, training direct reports, allocating workloads and troubleshooting any problems in order to detect any defects or issues in products before they are released into the market.  Duties & Responsibilities: <ul> <li>Recommends improvements to departmental policy and directs the implementation of procedures and controls covering all areas of Quality activity so that all relevant procedural/legislative requirements are fulfilled while delivering a quality, cost- effective service to customers</li> <li>Supervises the day-to-day operations of Quality section to ensure that work processes are implemented as designed and comply with established policies, processes and procedures</li> <li>Manages laboratory activities for assigned functions and projects to create short- and long-term work plans, assignments and milestones for direct reports. </li> <li>Supervises training activities for their teams to ensure they have the proper tools to achieve the identified objectives, maximize their potential and improve their individual effectiveness in meeting business needs. </li> <li>Manages the support for other departments in executing investigations and preparing deficiency letter responses to ensure efficient registration process for Hikma products. </li> <li>Supports activities related to analytical method transfers for the assigned projects to ensure efficient transfer of projects between sites. </li> <li>Reviews technical documents, including validation protocols and reports, reference standard qualifications protocols/ reports, analytical test procedures, Certificates of Analysis; technical reports, change controls and investigations report to ensure the documents are up to standards and comply with regulations. </li> <li>Standardizes processes throughout the laboratory to ensure compliance to cGMP’s and current SOP’s. </li> <li>Participates in the management of analytical procedure development and reviewal to ensure that they conform to current and appropriate scientific, compendial and regulatory standards and are suitable for use for their intended purpose.</li> <li>Develops and implements procedures, systems and training activities to develop an appropriate level of scientific expertise within laboratory to ensure the successful execution of project work to current pharmaceutical industry technical standards and to maintain compliance with cGMP’s.</li> <li>Manages troubleshooting activities for any potential faced issues to ensure keeping records of such issues and finding the best solution to solve them</li> <li>Prepares departmental reports of quality timely and accurately to meet company and department requirements, policies and standards</li> <li>Job Location: Beni Swief City</li> </ul> Qualifications: <ul> <li>Bachelor’s degree in pharmacy.</li> <li>Minimum 11 years of experience in pharmaceutical industry.</li> <li>Excellent leadership, communication, and problem-solving skills.</li> <li>Excellent organizational and leadership skills</li> <li>Sterile Pharmaceutical background is a must.</li> <li>In depth understanding of Quality Control procedures and relevant legal standards.</li> </ul> </div>

0 to 0 years Naukri Gulf

Senior Supervisor, Quality Control

On-site - Egypt - Egypt 7 July 2026

Research & Development

<section>Job DescriptionRoles & Responsibilities<div class="paragraph">Job Purpose: To manage activities related to the quality control unit within the quality department including management of tests in products analysis, overseeing procedures, training direct reports, allocating workloads and troubleshooting any problems in order to detect any defects or issues in products before they are released into the market.Duties & Responsibilities:<ul><li>Recommends improvements to departmental policy and directs the implementation of procedures and controls covering all areas of Quality activity so that all relevant procedural/legislative requirements are fulfilled while delivering a quality, cost- effective service to customers</li><li>Supervises the day-to-day operations of Quality section to ensure that work processes are implemented as designed and comply with established policies, processes and procedures</li><li>Manages laboratory activities for assigned functions and projects to create short- and long-term work plans, assignments and milestones for direct reports.</li><li>Supervises training activities for their teams to ensure they have the proper tools to achieve the identified objectives, maximize their potential and improve their individual effectiveness in meeting business needs.</li><li>Manages the support for other departments in executing investigations and preparing deficiency letter responses to ensure efficient registration process for Hikma products.</li><li>Supports activities related to analytical method transfers for the assigned projects to ensure efficient transfer of projects between sites.</li><li>Reviews technical documents, including validation protocols and reports, reference standard qualifications protocols/ reports, analytical test procedures, Certificates of Analysis; technical reports, change controls and investigations report to ensure the documents are up to standards and comply with regulations.</li><li>Standardizes processes throughout the laboratory to ensure compliance to cGMP s and current SOP s.</li><li>Participates in the management of analytical procedure development and reviewal to ensure that they conform to current and appropriate scientific, compendial and regulatory standards and are suitable for use for their intended purpose.</li><li>Develops and implements procedures, systems and training activities to develop an appropriate level of scientific expertise within laboratory to ensure the successful execution of project work to current pharmaceutical industry technical standards and to maintain compliance with cGMP s.</li><li>Manages troubleshooting activities for any potential faced issues to ensure keeping records of such issues and finding the best solution to solve them</li><li>Prepares departmental reports of quality timely and accurately to meet company and department requirements, policies and standards</li></ul>Job Location: Beni Swief City</div></section><section>Desired Candidate Profile<ul><li>Bachelor s degree in pharmacy.</li><li>Minimum 11 years of experience in pharmaceutical industry.</li><li>Excellent leadership, communication, and problem-solving skills.</li><li>Excellent organizational and leadership skills</li><li>Sterile Pharmaceutical background is a must.</li><li>In depth understanding of Quality Control procedures and relevant legal standards.</li></ul></section>

0 to 0 years Naukri Gulf

Regional QC Manager

On-site - Egypt - Egypt 17 July 2026

Research & Development

<section>Job DescriptionRoles & Responsibilities<div class="paragraph">Lead and govern TAGADDOD s regional quality control laboratories and testing systems to ensure reliable, accurate, compliant, and operationally supportive laboratory performance across all operating entities. The role exists to strengthen product quality assurance, laboratory governance, testing reliability, and data integrity through disciplined laboratory management and full compliance with ISO 17025 requirements. This role ensures laboratory operations evolve from isolated testing activities into an integrated quality-control and operational reliability enabler aligned with TAGADDOD s transformation strategy and Prime operating maturity journey.Responsibilities1- Laboratory Governance & Quality Control Management<ul><li>Lead regional laboratory and quality control governance across all entities and operating sites.</li><li>Govern laboratory operations, testing activities, and quality control systems to ensure disciplined execution and testing reliability.</li><li>Ensure laboratory governance supports operational stability, customer confidence, and product quality assurance.</li></ul>2- ISO 17025 Governance &Compliance<ul><li>Lead implementation, deployment, and governance of ISO 17025 requirements across all laboratories.</li><li>Ensure full compliance with ISO 17025 requirements including method validation, traceability, calibration, uncertainty management, and laboratory competence.</li><li>Govern laboratory documentation, records, and controlled testing procedures in alignment with ISO 17025 standards.</li></ul>3- Laboratory Operations &Testing Reliability<ul><li>Ensure reliable, accurate, and timely laboratory testing and reporting across all entities.</li><li>Govern sample handling, testing discipline, result integrity, and laboratory workflow effectiveness.</li><li>Ensure laboratory operations support production continuity and operational decision- making.</li><li>Govern laboratory testing prioritization and service responsiveness to support operational continuity and business needs.</li></ul>4- Laboratory Competence & Technical Qualification<ul><li>Govern laboratory competency frameworks and technical qualification requirements.</li><li>Ensure laboratory personnel competence, authorization discipline, and sustained technical capability.</li></ul>Calibration, Validation &Data Integrity<ul><li>Govern laboratory equipment calibration, testing traceability, and measurement reliability.</li><li>Ensure laboratory data integrity, testing accuracy, and controlled reporting systems.</li><li>Lead method validation and measurement uncertainty governance activities.</li></ul>5- Quality Assurance & Operational Support<ul><li>Ensure laboratory and QC activities support approved product quality specifications and customer requirements.</li><li>Coordinate with Operations, Planning & Warehouse, Procurement, and QHSE functions to ensure aligned quality execution and operational support.</li><li>Support RCA and CAPA investigations related to product quality, process instability, and recurring quality deviations.</li></ul>6- Audit & Compliance Support<ul><li>Support IMS audit rhythm and laboratory audit readiness across all entities.</li><li>Ensure laboratory compliance with legal, regulatory, customer, certification, and ISO requirements.</li><li>Monitor laboratory process compliance through structured audit and verification activities.</li></ul>7- Transformation & Continuous Improvement Enablement<ul><li>Partner with QHSE and Transformation & Continuous Improvement functions to support laboratory governance maturity and quality improvement initiatives.</li><li>Ensure disciplined adoption of approved laboratory transformation initiatives and quality governance programs.</li><li>Support laboratory digitalization, testing visibility, and reporting systems to strengthen operational decision quality.</li><li>Support laboratory digitalization and laboratory information management systems (LIMS) to strengthen testing visibility and data reliability.</li></ul>8- Leadership & Capability Development<ul><li>Lead and develop regional laboratory teams and country QC leadership.</li><li>Promote a culture of testing discipline, accountability, data integrity, and operational partnership.</li><li>Build laboratory capability, technical competence, and succession readiness across entities.</li><li>Govern laboratory operating rhythm and laboratory review cadence across all entities.</li><li>Govern laboratory equipment suitability, readiness, and lifecycle support requirements.</li></ul></div></section><section>Desired Candidate Profile<ul><li>Bachelor's degree in Quality Management, Engineering, Science, or a related field.</li><li>Minimum 10 years of experience in Quality Control with at least 7 years in a managerial role overseeing multiple sites or regions.</li><li>Proven experience in chemicals, oils or detergents industries.</li><li>Strong knowledge of quality management systems and standards (ISO 17025, ISO 9001, or Integrated Management Systems).</li><li>Proven experience in leading quality teams and managing audits.</li><li>Excellent leadership, communication, and interpersonal skills.</li><li>Ability to analyze complex data and drive decision-making.</li><li>Proficiency in quality tools and software.</li><li>Willingness to travel across the region as needed.</li></ul></section>

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