quality engineer

consultant, qa/qc

customer care supervisor

customer service supervisor Jobs in Cairo

customer service supervisor

icqa supervisor, icqa

quality control supervisor

RATP Dev Mobility Cairo

<div>
 
 Job Purpose
 
 
 
 The Quality &amp; Continuous Improvement Supervisor is responsible for creating and overseeing all activities related to the definition, implementation, and continuous improvement of the Integrated Management System. The role supports the progression of the Quality Improvement strategy by analyzing information derived from service failures and implementing corrective actions to drive continuous improvement and reduce future failure demand across the business.
 
 
 
 Responsibilities/Duties
 
 
 
 
 Profil de candidat recherch&eacute; :
 
 
 
 
 Quality Management System (QMS) Implementation &amp; Control
 
 
 
 <ul>
 <li>
 Defining and implementing the Integrated/Quality Management System as per the ISO 9001:2015 standard requirements.
 </li>
 <li>
 Implementing the Integrated/Quality Management System as per the ISO 45001:2018 and 14001:2015 standard requirements.
 </li>
 <li>
 Designing and developing quality processes that support the business objectives.
 </li>
 <li>
 Ensure that the organization sets up and follows measurable quality objectives particularly relating to the quality of the service and customer satisfaction.
 </li>
 <li>
 Utilize and develop valid internal and external standards to measure quality.
 </li>
 <li>
 Provides content knowledge in the interpretation, implementation, and maintenance of all accreditations, national quality assurance standards or regulatory standards to match external requirements.
 </li>
 <li>
 Responsible for ISO 9001, 45001, and 14001 certifications.
 
 
 </li>
 </ul>
 
 Continuous Improvement (CI) &amp; Innovation
 
 
 
 <ul>
 <li>
 Works to promote quality improvement and innovation and monitor progress towards goals by collecting accurate, timely data to display the quality, cost, and service outcomes.
 </li>
 <li>
 Deploy and execute the Continuous Improvement Framework (CIF).
 </li>
 <li>
 Assist to implement effective continuous improvement (CI) training plans that develop and sustain a CI culture, ensuring a constant safety focus.
 </li>
 <li>
 Support the other departments by providing continuous improvement tools and methodology.
 </li>
 <li>
 Utilize analytical / statistical tools &amp; methods combined with the ability to select and apply them to make data-based decisions.
 </li>
 <li>
 Utilize Lean Six Sigma tools in quality improvement projects.
 </li>
 <li>
 Develop corrective actions and processes to drive continuous improvement.
 </li>
 <li>
 Maintains accountability for ongoing self-development activities, especially related to presentation facilitation and application of quality improvement activities.
 
 
 </li>
 </ul>
 
 Auditing &amp; Compliance
 
 
 
 <ul>
 <li>
 Assist in the Internal Audit Plan and be part of the Internal Audit Team.
 </li>
 <li>
 Assist and communicate major problems with other directorates on the RDMC Action Plan.
 </li>
 <li>
 Provides content knowledge in the interpretation, implementation, and maintenance of all accreditations, national quality assurance standards or regulatory standards to match external requirements.
 
 
 </li>
 </ul>
 
 Training &amp; Knowledge Sharing
 
 
 
 <ul>
 <li>
 Provide Quality Related training.
 </li>
 <li>
 Assist to implement effective continuous improvement (CI) training plans that develop and sustain a CI culture, ensuring a constant safety focus.
 
 
 </li>
 </ul>
 
 Other Responsibilities
 
 
 
 <ul>
 <li>
 Other duties and responsibilities might be assigned.
 
 
 </li>
 </ul>
 
 Safety Responsibilities
 
 
 
 <ul>
 <li>
 Promote a positive Safety culture within the workplace and attend any Safety-related meetings/briefings as required within the job role.
 </li>
 <li>
 Comply with the requirements of the Company Safety Policy.
 
 
 </li>
 </ul>
 
 Qualifications
 
 
 
 
 ESSENTIAL QUALIFICATIONS, KNOWLEDGE &amp; EXPERIENCE
 
 
 
 <ul>
 <li>
 Bachelor&rsquo;s degree in Engineering/Pharma or any related Fields.
 </li>
 <li>
 Demonstrated proficiency in the principles of Quality Assurance
 </li>
 <li>
 Demonstrated proficiency in the principles of HSE and environment
 </li>
 <li>
 Fluent in both Arabic and English.
 
 
 </li>
 </ul>
 
 Knowledge
 
 
 
 <ul>
 <li>
 Knowledge of ISO 9001, 14001, and 45001 standards.
 </li>
 <li>
 Knowledge of Internal Audit processes.
 </li>
 <li>
 Certified Lead Auditor is preferred for ISO 9001, 14001, and 45001.
 </li>
 <li>
 Lean Enterprise and Six Sigma methodologies.
 </li>
 <li>
 Root Cause Analysis.
 </li>
 <li>
 Statistical Process Control.
 </li>
 <li>
 Knowledge of quality improvement concepts and methodology.
 </li>
 <li>
 Demonstrated experience using problem-solving and Six Sigma statistical tools to solve problems.
 </li>
 <li>
 Strong IT skills and ability to learn and manage databases.
 
 
 </li>
 </ul>
 
 Experience
 
 
 
 <ul>
 <li>
 5 to 7 years of experience in Quality Management.
 </li>
 <li>
 Proven experience in building, deploying, and maintaining Integrated Management Systems (ISO 9001, 45001 &amp; 14001) is a must.
 
 
 </li>
 </ul>
 
 Desired Behaviors &amp; Experiences
 
 
 
 <ul>
 <li>
 Quality-Driven Mindset: Demonstrates a strong commitment to maintaining and enhancing quality standards across all processes, ensuring compliance with ISO requirements and promoting a culture of excellence.
 </li>
 <li>
 Continuous Improvement Orientation: Actively seeks opportunities to optimize systems and workflows by applying Lean Six Sigma and analytical tools to achieve measurable performance improvements.
 </li>
 <li>
 Attention to Detail: Maintains accuracy and consistency in data collection, documentation, and audit processes to ensure reliability and compliance with established standards.
 </li>
 <li>
 Collaboration &amp; Support: Works effectively with cross-functional teams, providing guidance, training, and support to ensure consistent application of quality and continuous improvement practices.
 </li>
 <li>
 Accountability &amp; Initiative: Takes ownership of assigned tasks and demonstrates initiative in identifying issues, developing corrective actions, and following through on implementation to achieve sustainable results.
 </li>
 <li>
 Analytical Thinking: Uses data and statistical tools to identify trends, root causes, and opportunities for improvement, making informed, evidence-based decisions.
 </li>
 <li>
 Commitment to Safety: Promotes and upholds a strong safety culture by integrating safety principles into all quality and improvement activities.
 </li>
 <li>
 Adaptability &amp; Learning: Continuously develops professional knowledge and skills to stay current with evolving standards, best practices, and industry requirements.
 </li>
 </ul>
</div>

Quality & Continuous Improvement Supervisor

Jamjoom Pharma

<div>
 
 Join Jamjoom Pharma as a Quality Control Manager &ndash; Quality Department
 
 
 
 <ul>
 <li>
 Are you a detail-oriented professional with a passion for quality control in the pharmaceutical industry? Jamjoom Pharma is looking for a Quality Control Manager to join our Quality team.
 </li>
 <li>
 As Quality Control Manager, you will oversee the QC Department, managing resources effectively to achieve organizational objectives and aligning strategic plans.
 
 
 </li>
 </ul>
 
 Key Responsibilities
 
 
 
 <ul>
 <li>
 Approve QC department&rsquo;s SOPs, protocols, specifications, test methods, and worksheets for starting (raw and packaging) materials, products, stability and microbiology.
 </li>
 <li>
 Review and approve analytical methods validation, verification, and method transfer reports
 </li>
 <li>
 Review raw data of raw materials, packaging materials, stability and products testing
 </li>
 <li>
 Assure data integrity and review audit trail of instruments within the QC
 </li>
 <li>
 Approve analytical test reports for raw materials, packaging, finished products and microbiology
 </li>
 <li>
 Review and approve materials specifications for starting (raw and packaging) materials, finished products, stability and microbiology
 </li>
 <li>
 Prepare and review technical analysis (CADC) files submitted to EDA for registration purposes
 </li>
 <li>
 Review process validation and cleaning validation protocols, reports, and approve biowaiver study reports
 </li>
 <li>
 Authorize purchase requests and oversee procurement of QC instruments and chemicals to meet growing demands
 </li>
 <li>
 Deploy organizational policies and develop QC plans aligned with company objectives
 </li>
 <li>
 Lead recruitment and training of QC staff to build a high-performing team
 </li>
 <li>
 Attend audits, ensure compliance, and implement corrective and preventive actions (CAPA)
 </li>
 <li>
 Review maintenance contracts with external partners
 </li>
 <li>
 Prepare the required yearly needs of the instruments (CAPEX), operational expenses (OPEX) and headcounts.
 </li>
 <li>
 Design and implement training programs to enhance staff capabilities
 
 
 </li>
 </ul>
 
 Qualifications &amp; Experience
 
 
 
 <ul>
 <li>
 Bachelor&rsquo;s degree in pharmacy
 </li>
 <li>
 Minimum of 10+ years of professional experience in Quality Control within the pharmaceutical industry as quality control professional
 </li>
 <li>
 Strong command of the English language
 </li>
 <li>
 Proficiency in Microsoft Office and Minitab Statistical Software
 </li>
 <li>
 In-depth knowledge of test method validation, GLP and GMP standards
 
 
 </li>
 </ul>
 
 Why Join Us?
 
 
 
 
 At Jamjoom Pharma, you&rsquo;ll be part of a dynamic team committed to innovation, compliance, and excellence. This is your opportunity to make a lasting impact on product quality and contribute to the growth of one of the region&rsquo;s leading pharmaceutical companies
 
</div>

Quality Control Manager

Innovo Group

<div>
 Role Purpose
 
 The Quality Control Manager leads the development, implementation, and continual improvement of the Quality Management System (QMS) across all construction projects. This role ensures that all activities, materials, and workmanship comply with contractual requirements, international standards, and regulatory obligations. Acting as the primary authority on quality matters, the Manager drives a culture of excellence, oversees quality teams, and works closely with project leadership, consultants, and clients to deliver defect-free projects, reduce risks, and safeguard Innovo Group&rsquo;s reputation for high standards.
 
 Key Accountabilities
 <ul>
 <li>
 
 Lead, implement, and continuously improve the company&rsquo;s QMS in compliance with ISO 9001 and relevant standards.
 
 </li>
 <li>
 
 Ensure full audit compliance (internal, client, third-party) and timely closure of non-conformities.
 
 </li>
 <li>
 
 Approve and maintain quality procedures, method statements, ITPs, and related documentation.
 
 </li>
 <li>
 
 Oversee and enforce project quality assurance activities to ensure compliance with drawings, specifications, and codes.
 
 </li>
 <li>
 
 Direct inspection, testing, and verification processes to ensure material and workmanship quality.
 
 </li>
 <li>
 
 Manage major quality issues and implement corrective and preventive actions with project teams.
 
 </li>
 <li>
 
 Mentor and guide quality staff to ensure consistent application of company quality standards.
 
 </li>
 <li>
 
 Represent Innovo Group in client, consultant, and regulatory quality meetings.
 
 </li>
 <li>
 
 Coordinate with Project, Engineering, Procurement, and HSE teams to align quality goals with project delivery.
 
 </li>
 <li>
 
 Review and approve quality reports, NCRs, CARs, and dashboards for management and clients.
 
 </li>
 <li>
 
 Monitor KPIs, analyze trends, and recommend improvements to enhance efficiency and reduce rework.
 
 </li>
 <li>
 
 Ensure proper control, traceability, and readiness of all quality documentation for final handover.
 
 </li>
 <li>
 
 Develop and deliver training programs on quality standards and continuous improvement.
 
 </li>
 <li>
 
 Promote a culture of accountability, learning, and best practices across all projects.
 
 </li>
 </ul>
 Qualifications, Experience, Knowledge &amp; Skills
 <ul>
 <li>
 Bachelor&rsquo;s degree in civil engineering, Construction Management, or a related discipline.
 </li>
 <li>
 Minimum
 
 10&nbsp;years of proven experience
 
 in Quality Assurance/Quality Control within large-scale construction projects, with at least
 
 5 years in a managerial/supervisory role
 
 .
 </li>
 <li>
 In-depth knowledge of construction codes, specifications, and international quality standards (ISO 9001, ASTM, ACI, BS, etc.).
 </li>
 <li>
 Demonstrated experience in planning, leading, and closing internal, client, and third-party audits.
 </li>
 <li>
 Proficiency in MS Office Suite and quality management systems/software.
 </li>
 <li>
 Strong leadership, communication, and team management skills with the ability to influence stakeholders at all levels.
 </li>
 <li>
 Solid problem-solving, analytical, and decision-making capabilities under pressure.
 </li>
 <li>
 Professional certifications in Quality Management (e.g., ISO 9001 Lead Auditor, Six Sigma, or equivalent) are highly desirable.
 </li>
 </ul>
</div>

Quality Project Manager - Cairo

<div>
 Join Jamjoom Pharma as a
 
 Junior IPC Manager &ndash; Quality Department
 
 
 
 Are you detail-oriented, driven, and passionate about
 
 quality assurance in the pharmaceutical industry
 
 ? Jamjoom Pharma is seeking a dedicated
 
 Junior IPC Manager
 
 to join our Quality team and contribute to our mission of delivering excellence in healthcare.
 
 
 
 Key Responsibilities
 
 
 
 <ul>
 <li>
 Team Leadership &amp; Management: Lead, train, and develop the IPC team of Officers and Analysts. Schedule activities, manage workloads, and foster a culture of quality and accountability.
 </li>
 <li>
 System Management: Oversee the entire IPC system, including sampling plans, testing procedures, documentation, and trend analysis for all manufacturing stages (from dispensing to packaging).
 </li>
 <li>
 Quality Assurance: Ensure all in-process tests are performed accurately, on time, and documented as per SOPs.
 </li>
 <li>
 Deviation &amp; OOS Management: Immediately investigate and report any failures, Out-of-Specification (OOS) results, or process deviations. Initiate and support root cause analysis and corrective/preventive actions (CAPA).
 </li>
 <li>
 Compliance: Guarantee that all IPC activities strictly adhere to cGMP, GLSP, data integrity principles (ALCOA+), and company SOPs. Serve as a point of contact during internal and external regulatory audits.
 </li>
 <li>
 Continuous Improvement: Analyze data to identify trends, potential risks, and opportunities for process optimization. Drive initiatives to improve efficiency, reliability, and quality of IPC operations.
 </li>
 <li>
 SOP &amp; Documentation: Review, update, and authorize IPC-related Standard Operating Procedures (SOPs), batch records, and forms. Ensure all documentation is complete, accurate, and maintained.
 </li>
 <li>
 Cross-Functional Collaboration: Work closely with Production, Quality Control (QC), Quality Assurance (QA), and Engineering departments to resolve issues and ensure seamless production flow.
 </li>
 <li>
 Equipment &amp; Lab Management: Ensure IPC instruments and equipment are calibrated, maintained, and suitable for use.
 
 
 </li>
 </ul>
 
 Qualifications &amp; Experience
 
 
 
 <ul>
 <li>
 Bachelor&rsquo;s degree in pharmacy
 </li>
 <li>
 Minimum of +10 years of hands-on experience in a pharmaceutical manufacturing environment, with at least 3 years in a supervisory or managerial role within IPC, Quality Control, or Production.
 </li>
 <li>
 Proven expertise in solid dosage forms (tablets, capsules) and/or liquid, semi-solid, sterile products is highly desirable.
 </li>
 </ul>
 <ul>
 <li>
 Technical Skills:
 </li>
 <li>
 In-depth knowledge of cGMP, WHO-GMP, ICH guidelines, and pharmaceutical manufacturing processes.
 </li>
 <li>
 Strong understanding of statistical process control (SPC) and quality management systems (QMS).
 </li>
 <li>
 Proficiency in using pharmaceutical manufacturing and laboratory equipment.
 </li>
 <li>
 Excellent documentation skills and familiarity with electronic document management systems (EDMS).
 </li>
 <li>
 Soft Skills:
 </li>
 <li>
 Strong leadership, problem-solving, and decision-making abilities.
 </li>
 <li>
 Excellent communication and interpersonal skills.
 </li>
 <li>
 High level of integrity, attention to detail, and a results-oriented mindset.
 </li>
 <li>
 Ability to work under pressure and manage multiple priorities.
 </li>
 </ul>
</div>

Junior IPC Manager

PepsiCo

<div>
 
 Responsibilities
 
 
 
 <ul>
 <li>
 Conduct daily &amp; weekly reconciliation on consumables/consignments and ensure that they are logged on SAP.
 </li>
 <li>
 Validate stock in CoMan on a daily basis and ensure that it is reported to the SP&amp;L team to coordinate with raw material suppliers for smooth operations.
 </li>
 <li>
 Validate BOMs of Gold item by item &amp; ensure that codes are properly matched with SKU codes.
 </li>
 <li>
 Coordinate deployment of FG from CoMan warehouse to DCs on a daily basis.
 </li>
 <li>
 Ensure raw material receiving data is submitted on SAP and share receiving documents with the WH team.
 </li>
 <li>
 Process invoices and credit notes on Aqulla.
 </li>
 <li>
 Conduct periodical witness sessions/Proficiency testing of CoMan laboratory testing in a timely manner to ensure accurate laboratory testing of the CoMan Lab team as per PepsiCo standards to mitigate any risk of poor lab testing. (E)
 </li>
 <li>
 Carry out periodical checks on finished products as per the standard sampling protocol &amp; testing to ensure that finished products are compliant with product specifications (e.g., product quality, packaging quality). (D)
 </li>
 <li>
 Manage customer complaints &amp; ensure that they are investigated by the CoMan team. Review corrective actions with tracking &amp; monitoring of CoMan customer complaints. (D)
 </li>
 <li>
 Develop &amp; report CoMan Quality KPIs to the business to ensure that CoMan is compliant with PepsiCo standards. (E)
 </li>
 <li>
 Coordinate &amp; schedule external audits (AIB/GFSI) on CoMan facilities, review audit reports &amp; ensure that there is a solid action plan based on audit nonconformities. (E)
 </li>
 <li>
 Ensure that key food safety contingency protocols are compliant (e.g., ensure that mock recalls are conducted periodically&mdash;forward or backward&mdash;for effective product traceability if needed). (D)
 </li>
 <li>
 Train &amp; coach the CoMan team on PepsiCo food safety standards as well as product quality procedures. (E)
 </li>
 <li>
 Ensure the receiving of raw &amp; pack materials at the CoMan facility. Validate quantities delivered vs. delivery receipts/documents against the delivery schedule shared by the SP&amp;L team to ensure that CFI pays for what has been received as per the receiving key control.
 </li>
 <li>
 Ensure submission of material received on SAP &amp; ensure SAP records are updated for every delivery to enable manufacturing backflush.
 </li>
 <li>
 Validate raw material rejections at the time of receiving to avoid any manipulation by CoMan for selective receiving. Conduct double testing on potatoes to confirm the rejection reason.
 </li>
 <li>
 Coordinate the return of defective raw materials through validating quantities, defects &amp; quarantine.
 </li>
 <li>
 Ensure phasing of pricing (Gold) per material change on the ground through isolation, reporting &amp; proper consumption &amp; FG segregation.
 </li>
 <li>
 Conduct physical counts on raw materials &amp; share stock reports with SP&amp;L for proper production &amp; material planning to ensure smooth operations.
 </li>
 <li>
 Coordinate operational consumables &amp; ensure delivery of consumables from the spare parts store to CoMan in a timely manner to ensure smooth &amp; uninterrupted operations.
 </li>
 <li>
 Reconcile operational consumables &amp; consignments to validate consumption vs. standard rates to charge CoMan for extra consumption.
 </li>
 <li>
 Review product GRs on SAP to ensure that all products manufactured in the CoMan facility have been recorded on SAP for invoice issuing.
 </li>
 <li>
 Run MUV calculations based on the physical count of raw material &amp; FG; then validate actual consumption vs. BOMs on SAP to ensure that material consumption is not deviated from the standard.
 </li>
 <li>
 Calculate MUV deviations through material standard/period cost; then review with the Control team to charge CoMan on deviated consumption through CN.
 </li>
 <li>
 Process invoices, credit &amp; debit notes on Aqulla/NGDI &amp; match delivery records vs. GRs on SAP to ensure proper payment to CoMan for the exact amount of FG at the correct price.
 </li>
 <li>
 Verify quantities of material waste &amp; ensure that they are real waste to avoid any manipulation by CoMan &amp; waste collection suppliers. Ensure that waste is recorded on SAP on a daily basis as per GCS standards.
 </li>
 <li>
 Ensure that commercial weight is being fulfilled by CoMan packaging machines to ensure that there are no discrepancies.
 </li>
 <li>
 Coordinate FG deployment as per production &amp; deployment plans &amp; ensure that GRs match product receiving on SAP.
 </li>
 <li>
 Enter CoMan operational, quality &amp; performance/sustainability KPIs on the CoMan automation dashboard system for the Egypt BU.
 </li>
 <li>
 Enter AU, TE &amp; NE on the daily scorecard in line with the outstanding balance of CoMan from SAP records.
 </li>
 <li>
 Review &amp; validate the calculation of carton conversion into tons to verify the cost per carton vs. tons in the contract to ensure that CFI pays the proper rate as per the contract before PO release/amendments.
 </li>
 <li>
 Collect waste selling documents &amp; calculate waste refunds for CoMan by ingredient to ensure issuing of electronic invoices and/or debit notes according to toll manufacturing agreements.
 </li>
 <li>
 Review all BOMs of Gold phasing by ingredient &amp; consumption vs. standard to ensure no gain/loss of phased packaging material.
 </li>
 <li>
 Calculate stoppage claims per material &amp; conclude cost.
 </li>
 <li>
 Ensure that there are no near-to-expiry items in CoMan stock &amp; ensure that the raw material planning team takes action to move them from CoMan premises.
 </li>
 <li>
 Ensure that CoMan quality &amp; food safety is implemented in CoMan operations &amp; processes.
 </li>
 <li>
 Report daily downtime, material efficiency &amp; submit daily scorecards to be circulated with stakeholders.
 </li>
 <li>
 Ensure that the deployment plan is executed to avoid stoppages in CoMan due to high stock.
 
 
 </li>
 </ul>
 
 Qualifications
 
 
 
 <ul>
 <li>
 Food Safety Expereience
 </li>
 <li>
 Certified as a Safety Auditor
 </li>
 <li>
 Total Quality Approach
 </li>
 <li>
 Experience in Quality Control Management of similar position.
 </li>
 <li>
 Technical Knowledge of Quality Management System &amp; concepts.
 </li>
 <li>
 Knowledge of Statistical Process Control techniques.
 </li>
 <li>
 Strong interpersonal &amp; analytical skills
 </li>
 <li>
 Fluent English language
 </li>
 <li>
 Computer literate.
 </li>
 <li>
 in Chemistry or Food science / Technology
 </li>
 <li>
 Spent the last 3 years in a similar capacity
 </li>
 <li>
 Communication Skills
 </li>
 <li>
 Planning &amp; Organizing
 </li>
 <li>
 Problem Solving
 </li>
 <li>
 Excellent command of English language (Scientific English is a plus)
 </li>
 <li>
 Accuracy &amp; Attention to Details
 </li>
 <li>
 Internal / External Customer Focus
 </li>
 <li>
 Accountable, Assertive &amp; Adaptable
 </li>
 <li>
 Forward thinking, Motivating &amp; Growing people
 </li>
 <li>
 Collaborative &amp; living our values
 </li>
 </ul>
</div>

CoMan Operations Associate

Ishraaq Foundation for Community Development

<div>
 Role Summary
 <ul>
 <li>
 Supervise day-to-day electronics production for EEUN products (e.g., chargers, cables, accessories, light electronics). Ensure
 
 output, quality, ESD compliance, process discipline, and documentation
 
 . Lead operators/technicians, enforce SOPs, and drive continuous improvement.
 </li>
 </ul>
 
 
 
 Key Responsibilities1) Production Execution
 <ul>
 <li>
 Run daily production plan: manpower allocation, line balancing, takt time, shift targets.
 </li>
 <li>
 Ensure timely completion of work orders with minimal defects and rework.
 </li>
 <li>
 Coordinate material availability with warehouse/supply chain (kitting, shortages, FIFO).
 </li>
 </ul>
 2) People Supervision
 <ul>
 <li>
 Supervise operators, technicians, and line leaders: attendance, training, productivity, discipline.
 </li>
 <li>
 Conduct on-job training and enforce standard work instructions.
 </li>
 </ul>
 3) Quality &amp; Process Control
 <ul>
 <li>
 Enforce QC gates: incoming, in-process, final inspection.
 </li>
 <li>
 Control defects via root cause analysis (5-Why, basic CAPA), reduce rework/scrap.
 </li>
 <li>
 Maintain production records, traceability, and QC checklists.
 </li>
 </ul>
 4) ESD &amp; Safety Compliance
 <ul>
 <li>
 Implement and audit ESD controls: wrist straps, mats, grounding, ionizers (if used), storage.
 </li>
 <li>
 Ensure PPE and basic safety compliance; maintain clean and organized work areas (5S).
 </li>
 </ul>
 5) Equipment &amp; Tooling Oversight
 <ul>
 <li>
 Ensure proper use/calibration of tools (torque drivers, testers, microscopes, power supplies).
 </li>
 <li>
 Coordinate maintenance and report abnormalities early.
 </li>
 </ul>
 6) Continuous Improvement
 <ul>
 <li>
 Improve throughput and quality using small Kaizen changes: fixture improvements, better work sequence, visual management, mistake-proofing (poka-yoke).
 </li>
 <li>
 Support NPI (new product introduction) trials and stabilize processes.
 </li>
 </ul>
 Requirements
 <ul>
 <li>
 Diploma/BSc in Electronics, Electrical, Mechatronics, Industrial Engineering, or similar.
 </li>
 <li>
 
 3&ndash;7 years
 
 in electronics manufacturing/assembly, with
 
 1&ndash;3 years
 
 as supervisor/line leader.
 </li>
 <li>
 Strong understanding of:
 </li>
 <li>
 Assembly processes, soldering basics (if applicable), inspection standards
 </li>
 <li>
 Basic QC tools, defect tracking, rework control
 </li>
 <li>
 ESD discipline and factory documentation
 </li>
 <li>
 Comfortable with KPIs, shift reporting, and hands-on floor management.
 </li>
 </ul>
 KPIs
 <ul>
 <li>
 Output vs plan (daily/weekly)
 </li>
 <li>
 First Pass Yield (FPY) / defects per unit
 </li>
 <li>
 Rework and scrap rate
 </li>
 <li>
 Line downtime
 </li>
 <li>
 Attendance and productivity per operator
 </li>
 <li>
 On-time delivery (OTD)
 </li>
 <li>
 ESD audit compliance
 </li>
 </ul>
 
 
 
</div>

Electronics Production Supervisor

Solmax

<div>
 
 Overview
 
 
 
 The Lab Chemist will perform routine and specialized testing of raw materials, in-process samples, and finished polyethylene products in accordance with approved methods and specifications, ensuring product quality, compliance with standards, and adherence to the company&rsquo;s Integrated Management System (IMS) requirements.
 
 
 
 Responsibilities
 
 
 
 <ul>
 <li>
 Conduct routine testing of raw materials and finished products in accordance with approved ASTM, ISO, and internal methods.
 </li>
 <li>
 Perform testing on in-process and finished products as per the Product Technical Data Sheet, Solmax Quality Plan, and specified testing frequency for each property.
 </li>
 <li>
 Ensure that all laboratory equipment is maintained in good operating condition and that calibration certificates remain valid.
 </li>
 <li>
 Prepare and submit daily, weekly, and monthly testing reports and summaries for management review.
 </li>
 <li>
 Report any detected nonconformities immediately to the Production Shift Supervisor or Production Manager and actively participate in root cause analysis and corrective actions.
 </li>
 <li>
 Support the effective implementation and continual improvement of the Integrated Management System (ISO 9001, ISO 14001, and ISO 45001).
 </li>
 <li>
 Escalate any quality, safety, or environmental concerns to the Quality Manager or relevant manager.
 </li>
 <li>
 Contribute to achieving company objectives regarding quality, safety and environment.
 
 
 </li>
 </ul>
 
 Qualifications
 
 
 
 <ul>
 <li>
 Bachelor&rsquo;s degree in chemistry or chemical engineering with 3+ years of experience in a manufacturing laboratory environment, preferably in polyethylene or polypropylene production.
 </li>
 <li>
 Good command of English (spoken and written).
 </li>
 <li>
 Statistical Process Control (SPC) and Quality Management Systems.
 </li>
 <li>
 Proficiency in MS Excel, MS Word, Outlook, and ERP systems (e.g., Dynamics 365).
 </li>
 <li>
 Strong analytical, communication, and documentation skills.
 
 
 </li>
 </ul>
 
 Benefits
 
 
 
 <ul>
 <li>
 Competitive salary &amp; annual profit share.
 </li>
 <li>
 Medical &amp; Life insurance.
 </li>
 <li>
 Dynamic and Multinational company
 
 
 </li>
 </ul>
</div>

Lab Chemist

Explore 753+ Quality control supervisor in Cairo this December. Find roles across top companies and apply now to boost your career.