production engineer

ai engineer

consultant, qa/qc

director of quality

implementation engineer

quality control engineer

Talent 360 ME

<div>
 🔍
 
 We&rsquo;re Hiring | Mid-Level Quality Control Engineer
 
 
 
 We are looking for a
 
 Mid-Level Quality Control Engineer
 
 to join our Quality Control team and help ensure the stability, performance, and usability of our web and mobile applications.
 
 
 
 Key Responsibilities:
 
 
 
 <ul>
 <li>
 Perform front-end &amp; back-end testing for new features and releases
 </li>
 <li>
 Execute UI, regression, performance, and API testing (web &amp; mobile &ndash; Android/iOS)
 </li>
 <li>
 Identify, document, and track bugs using Jira
 </li>
 <li>
 Write test cases aligned with Agile methodologies
 </li>
 <li>
 Collaborate closely with developers and designers
 </li>
 <li>
 Support clients when needed and mentor junior QA members
 
 
 
 </li>
 </ul>
 
 Requirements:
 
 
 
 <ul>
 <li>
 Bachelor&rsquo;s degree in Computer Science or a related field
 </li>
 <li>
 3&ndash;5 years of QA/testing experience (mobile &amp; web)
 </li>
 <li>
 Experience with Selenium/Appium, Jira, API &amp; performance testing (JMeter preferred)
 </li>
 <li>
 Strong understanding of Agile and CI/CD processes
 </li>
 </ul>
</div>

Quality Control Engineer (Tech. Industry)

EDECS

<div>
 
 
 Role Overview
 
 
 
 
 
 
 We are seeking a detail-oriented and experienced
 
 Senior QA/QC Engineer
 
 to ensure that all construction activities at the project site comply with approved specifications, drawings, method statements, and quality standards. The ideal candidate will be responsible for conducting inspections, managing inspection requests, maintaining quality records, and coordinating with site teams and consultants to ensure successful project delivery in line with contractual and quality requirements.
 
 
 
 
 
 
 Key Responsibilities
 
 
 
 
 
 
 
 Quality Control &amp; Inspection:
 
 
 
 Review project specifications, approved drawings, and method statements, and prepare the required inspection and testing checklists.
 
 
 Conduct daily site inspections and walkthroughs in accordance with approved Inspection and Test Plans (ITPs).
 
 
 Receive inspection requests and coordinate with the site team and supervision consultant to follow up on inspection results.
 
 
 Ensure that completed works conform to approved requirements and are ready for final inspection by the site supervision consultant.
 
 
 Monitor inspection statuses and follow up on corrective actions and resubmissions, ensuring all actions are completed before re-inspection.
 
 
 
 Drawing &amp; Documentation Control:
 
 
 
 Monitor and verify the revision status of drawings used on site by construction teams and subcontractors to ensure that superseded drawings are not implemented.
 
 
 Maintain all quality records as specified in Inspection and Test Plans and contract documents.
 
 
 Ensure that original copies of quality records are properly submitted to the Document &amp; Data Controller.
 
 
 
 Materials &amp; Storage Monitoring:
 
 
 
 Inspect material storage areas and take necessary actions to prevent damage or deterioration.
 
 
 Report any unacceptable practices to the Project Quality Manager and follow up on corrective and preventive actions.
 
 
 Training &amp; Coordination
 
 
 Ensure that technical activity training is conducted for site teams and subcontractors as required.
 
 
 Attend quality control meetings and contribute to continuous quality improvement initiatives on site.
 
 
 
 
 
 
 Requirements:
 
 
 
 
 
 
 
 Education:
 
 
 
 Bachelor&rsquo;s degree in civil engineering, Mechanical Engineering, Electrical Engineering, or a related discipline.
 
 
 
 Experience:
 
 
 
 Minimum of 4&ndash;5 years of proven QA/QC experience, preferably in construction or project-based environments.
 
 
 
 Skills:
 
 
 
 Strong knowledge of quality control procedures, inspection processes, and ITPs.
 
 
 Excellent coordination and communication skills.
 
 
 Strong attention to detail and problem-solving abilities.
 
 
 Computer Skills
 
 
 Proficiency in Microsoft Excel and other Microsoft Office applications.
 
 
 Experience with document control systems and reporting tools.
 
 
 
 
 
 
 About EDECS:
 
 
 
 
 
 
 EDECS is a leading organization with over 30 years of experience in marine constructions, infrastructure, earthworks, and transportation projects in Egypt and Saudi Arabia, employing more than 2,000 employees. The organization delivers innovative, sustainable, and cost-effective solutions while maintaining the highest standards of quality, safety, and sustainability.
 
 
 EDECS has a strong presence in logistics projects, including high-speed and light-speed railways, railway stations, and commercial and administrative buildings, as well as extensive experience in earthworks, water irrigation, and yacht marinas. EDECS is a trusted partner committed to creating lasting positive impact within the communities it serves.
 
</div>

Senior Quality Control Engineer

SYSTRA

<div>
 SYSTRA is one of the world's leading engineering and consultancy groups specialising in public transport and sustainable mobility. With over 10,300 employees, SYSTRA's mission is to design safe and sustainable transport solutions to bring people together, develop social inclusion and facilitate access to employment, education and leisure throughout the world.
 
 
 For 65 years, the Group has been working alongside cities and regions to contribute to their development by creating, improving and modernising their infrastructure and transport systems, throughout the life cycle of their projects. SYSTRA is involved from the earliest stages of design through to the testing, deployment and maintenance phases. The company provides all its services in over 80 countries worldwide and generates 74% of its turnover internationally. With its new services, SYSTRA supports its clients and partners in their digital, ecological and energy transition, in order to invent the mobility of tomorrow.
 
 
 Context
 
 
 Blue Line Section 4 Led QAQC Engineer
 
 
 Missions/Main Duties
 
 
 Performs quality control inspection duties related to work activities including, but not limited to the following:
 
 
 <ul>
 <li>
 Review submissions from the Contractor and prepare comments
 </li>
 <li>
 Receives inspection notification from Contractor and ensures attendance as described in ITP
 </li>
 <li>
 Maintains frequent contact with Contractor&rsquo;s quality control staff in performing their duties.
 </li>
 <li>
 Performs observation, surveillance activities on selected Contractor project field activities and field supervision operations including health, safety and environmental controls.
 </li>
 <li>
 Prepares Site Observation Reports reflecting observations of potential non-compliance and issue QVN if Contractor fails to provide their NCR
 </li>
 <li>
 Liaises with Project Construction personnel for any significant quality matters. Maintains a daily diary and issues daily reports to the Senior QA / QC Engineer
 </li>
 <li>
 Issues Site Observation Reports (SOR) to Contractor as appropriate
 </li>
 <li>
 Monitors progress for close out evidence of NCRs, QVNs and SORs
 </li>
 <li>
 Monitors project safety programs, assuring Contractor adherence to its approved safety plans
 </li>
 <li>
 Witness and record result of planned inspections (IR) as notified by the Contractor and maintain photographic records
 </li>
 <li>
 Witness laboratory sampling and testing
 </li>
 <li>
 Witness material inspections (MIR)
 </li>
 <li>
 Recognize developing issues related to non-compliant work
 </li>
 <li>
 Maintains proactive relationship with Contractor&rsquo;s quality and supervisory staffs to facilitate any necessary corrective action by the Contractor in accordance with authorized procedures.
 
 
 </li>
 </ul>
 Profile/Skills
 
 
 <ul>
 <li>
 Experience on industry relevant projects for position, preferably with successive responsibility on large projects transportation or infrastructure projects.
 </li>
 <li>
 Accredited college degree in related industry activities (engineering or construction management) or equivalent related experience.
 </li>
 <li>
 Certifications of continued industry training and education related to the work such as specifications quality standards related to the heavy construction, rail or transportation industry.
 </li>
 <li>
 Preferred Internal Auditor skills
 </li>
 <li>
 English fluency in reading, writing and speech
 </li>
 <li>
 Proficient experience in key MS Desktop applications.
 </li>
 <li>
 Preferred prior experience on multi-phase projects
 
 
 </li>
 </ul>
 Systra is an equal opportunities company; this position is open to all applicants.
</div>

QA /QC Engineer – Lead Section (4)

Unilever

<div>
 
 About Unilever
 
 
 
 With 3.4 billion people in over 190 countries using our products every day, Unilever is a business that makes a real impact on the world. Work on brands that are loved and improve the lives of our consumers and the communities around us. We are driven by our purpose: to make sustainable living commonplace, and it is our belief that doing business the right way drives superior performance. At the heart of what we do is our people &ndash; we believe that when our people work with purpose, we will create a better business and a better world.
 
 
 At Unilever, your career will be a unique journey, grounded in our inclusive, collaborative, and flexible working environment. We don&rsquo;t believe in the &lsquo;one size fits all&rsquo; approach and instead we will equip you with the tools you need to shape your own future.
 
 
 
 Job Purpose
 
 
 
 Unilever is the place where you can bring your purpose to life with the work that you do &ndash; creating a better business and a better world. If you looking to break down the barrier between accountancy and management to support business objectives and corporate growth &amp; act as an advisor to leadership, supporting business decision making through a combination of analytical insights, strategic acumen, and commercial mindedness then this role is just for you!
 
 
 
 What Will Your Main Responsibilities Be
 
 
 
 <ul>
 <li>
 Supports deploying of UL Quality strategy, governance and goals through specific Quality projects and targets.
 </li>
 <li>
 Supports in enhancing and change mindset through trainings.
 </li>
 <li>
 Ensure HACCP plans for the site are designed and operated to assure product safety
 </li>
 <li>
 Supports ensuring compliance to product technology GMP requirements
 </li>
 <li>
 Supports in Quality management for resolution of quality / consumer safety issues
 </li>
 <li>
 Supports engineering studies to approve, evaluate or certify new or modified equipment capabilities (relative to quality attributes or performance) and identify specific design reviews for such aspects as hygienic design
 </li>
 <li>
 Supports ensuring that quality requirements / considerations are managed for VIP changes
 </li>
 <li>
 Supports changes to existing and new materials suppliers through activities that assure quality / hygienic control processes are in place and operating effectively, e.g. follow up on audit action plans
 </li>
 <li>
 Supports ensuring that quality / hygiene control plans are established for production site changes or production capacity increases
 </li>
 <li>
 Supports ensuring consumer safety and product quality in newly acquired Make sites by assessing compliance to UL Quality requirements and driving improvement plans to close gaps
 </li>
 <li>
 Supports Quality Management System deployment and continuous improvement through support to WCM Quality Pillar and Virtual Sites
 </li>
 <li>
 Supports resolving consumer/ customer product and package complaints and CRQS issues through analysis of care-line and CRQS audit information to identify improvements
 </li>
 <li>
 Supports Factory Management with the Quality efforts to raise visibility and set priorities for Quality improvement
 </li>
 <li>
 Determines quality improvement parameters by identifying statistical methods relevant to manufacturing processes.
 </li>
 <li>
 Establishes statistical confidence by identifying sample size and acceptable error; determining levels of confidence.
 </li>
 <li>
 Prepares reports by collecting, analyzing, and summarizing data; making recommendations.
 </li>
 <li>
 Analyze quality performance utilizing using statistical and analytical tools and methods.
 </li>
 <li>
 Implement methods to inspect, test and evaluate reliability, precision, reliability and accuracy of processes, products and production equipment.
 </li>
 <li>
 Develop and establish quality procedures and systems for inspecting plans, quality trends, statistical plan price estimates and technical quality proposal plans.
 </li>
 <li>
 Ensure process control documents adhere with set requirements.
 </li>
 <li>
 Ensure on time processing of non-conforming components.
 </li>
 <li>
 Assist disposition process by involving in failure analysis and suggest corrective actions as Material Review Board member.
 </li>
 <li>
 Coordinate with suppliers and customers relating to quality trends, performance and corrective action.
 </li>
 <li>
 Verify conformance and productivity of quality engineering system through supplier audits and surveys.
 </li>
 <li>
 Initiate programs to enhance supplier performance.
 </li>
 <li>
 Interact with product development committees to inspect and review engineering releases.
 </li>
 <li>
 Review all product quality aspects like planning, manufacturing methods and process specifications.
 </li>
 <li>
 Interact with manufacturing and engineering teams to optimize documentation related to quality and inspection checks.
 </li>
 <li>
 Report and supply subassemblies as well as finish goods following Device Master Record.
 </li>
 <li>
 Interact with Quality Control Packaging team to conduct Technician Training Program after evaluating Quality Inspections Techniques.
 </li>
 <li>
 Assist manufacturing scrap performance evaluation and management.
 
 
 </li>
 </ul>
 
 Experiences &amp; Qualifications
 
 
 
 WHAT YOU WILL NEED TO SUCCEED
 
 
 <ul>
 <li>
 Bachelor&rsquo;s degree in engineering.
 </li>
 <li>
 2 to 5 years of experience in Quality Control (QC) or Quality Assurance (QA).
 </li>
 <li>
 Experience working in the FMCG industry is a plus
 </li>
 <li>
 ISO 9001 certification is a plus
 
 
 </li>
 </ul>
 Unilever embraces diversity and encourages applicants from all walks of life! This means giving full and fair consideration to all applicants and continuing development of all employees regardless of age, disability, gender reassignment, race, religion or belief, sex, sexual orientation, marriage and civil partnership, and pregnancy and maternity.
 
 
 Unilever is an organisation committed to equity, inclusion and diversity to drive our business results and create a better future, every day, for our diverse employees, global consumers, partners, and communities. We believe a diverse workforce allows us to match our growth ambitions and drive inclusion across the business. At Unilever we are interested in every individual bringing their &lsquo;Whole Self&rsquo; to work and this includes you! Thus if you require any support or access requirements, we encourage you to advise us at the time of your application so that we can support you through your recruitment journey.
</div>

Quality Engineer

<div>
 SYSTRA is one of the world's leading engineering and consultancy groups specialising in public transport and sustainable mobility. With over 10,300 employees, SYSTRA's mission is to design safe and sustainable transport solutions to bring people together, develop social inclusion and facilitate access to employment, education and leisure throughout the world.
 
 
 For 65 years, the Group has been working alongside cities and regions to contribute to their development by creating, improving and modernising their infrastructure and transport systems, throughout the life cycle of their projects. SYSTRA is involved from the earliest stages of design through to the testing, deployment and maintenance phases. The company provides all its services in over 80 countries worldwide and generates 74% of its turnover internationally. With its new services, SYSTRA supports its clients and partners in their digital, ecological and energy transition, in order to invent the mobility of tomorrow.
 
 
 Context
 
 
 QA/QC Engineer-Lead- Section 3
 
 
 Missions/Main Duties
 
 
 Senior QC/QA Engineer experience should be including but not limited to: -
 
 
 <ul>
 <li>
 Technical office QC/QA documents review.
 </li>
 <li>
 All technical submittals (prequalification - Material Submittals - Method statements - ....................)
 </li>
 <li>
 Supervision all construction items and activities.
 
 
 </li>
 </ul>
 Profile/Skills
 
 
 <ul>
 <li>
 Senior QC/QA Engineer Skills should be including but not limited to: -
 </li>
 <ul>
 <li>
 Decision maker.
 </li>
 <li>
 Team work cooperation.
 </li>
 <li>
 Leadership skills.
 </li>
 <li>
 Ability to work under pressure and hard conditions.
 </li>
 <li>
 Availability to work at many places and smooth movement as per work requirement.
 
 </li>
 </ul>
 </ul>
 Systra is an equal opportunities company; this position is open to all applicants.
</div>

QA/QC Engineer-Lead- Section 3

Talaat Moustafa Group

<div>
 <ol>
 <li>
 Assess and review existing designs, structures, and systems to identify areas requiring alteration or improvement.
 </li>
 <li>
 Conduct site visits and inspections to gather data and evaluate the feasibility of proposed alterations.
 </li>
 <li>
 Develop and modify engineering designs, plans, and specifications for alterations, ensuring they meet project requirements and regulatory standards.
 </li>
 <li>
 Coordinate with architects, engineers, and other stakeholders to integrate alterations seamlessly into existing projects.
 </li>
 <li>
 Ensure that all alterations comply with industry standards, safety regulations, and quality benchmarks.
 </li>
 <li>
 Monitor and inspect work during and after implementation to confirm that alterations are executed to specification.
 </li>
 <li>
 Prepare and maintain detailed records of alterations, including design modifications, project progress, and any issues encountered.
 </li>
 <li>
 Implement innovative solutions to optimize the performance and functionality of altered systems or structures.
 </li>
 <li>
 Full inspections of villas, apartments, and shops that have completed modifications and finished works to ensure there are no violations
 </li>
 <li>
 Monitoring and documenting violations, taking measures to freeze any work in progress that is violating El Rehab and Cilia cities standards
 </li>
 <li>
 Supervising work progress related to public facilities and installations including design and implementation, in accordance with the city's master plan.
 </li>
 <li>
 Ensure that all procedures related swimming pools and elevators are met and aligned with construction approvals
 </li>
 <li>
 Communicate with the technical department and the traffic consultant in case of requesting any unregular modifications
 </li>
 <li>
 Ensure securing consulting report approved by the Engineers Syndicate
 </li>
 <li>
 Ensure securing certificate of supervision of the implementation from a syndicate of engineering
 </li>
 <li>
 Ensure securing and review architectural and structural engineering drawings from the same consultant for any additional work scope (swimming pool - rooftop annex)
 </li>
 <li>
 Ensure securing construction and mechanical drawings for elevators package (machine room, shaft foundations, etc.)
 </li>
 </ol>
 
 
</div>

Alteration Engineer

GE HealthCare

<div>
 
 Job Description Summary
 
 
 
 Engineering associated with the manufacturing process. Impacts departmental operations and responsible for planning/execution. The role has some autonomy but is focused on execution of activities within an operating discipline covered by standard functional practices and procedures. Some judgment may be required but this is typically with guidance.
 
 
 
 Job Description
 
 
 
 
 This Job is responsible for:
 
 
 
 
 Design Transfer
 
 
 
 <ul>
 <li>
 Lead the design transfer activities of product specifications to manufacturing by working with global design owners and local partners.
 </li>
 <li>
 Review the design specifications feasibility in terms of assembly and test, make sure that production constrains are respected.
 </li>
 <li>
 Define and validate production and test processes including production instructions and reports.
 </li>
 <li>
 Coordination of manufacturing releases
 </li>
 <li>
 Lead the manufacturing documentation development and release
 
 
 </li>
 </ul>
 
 Manufacturing Process Set Up, Validation And Continuous Improvement
 
 
 
 <ul>
 <li>
 Drive improved product quality by identifying manufacturing issues, developing cost-effective solutions, and overseeing successful implementation into production.
 </li>
 <li>
 Work with contract manufacturing supplier&rsquo;s production associates to resolve manufacturing and quality problems related to methods, processes, tooling, equipment and product design.
 </li>
 <li>
 Monitor and optimize contract manufacturing supplier&rsquo;s workstations designs and manufacturing cycle time
 </li>
 <li>
 Actively support lean, continuous improvement and design for manufacturing initiatives.
 </li>
 <li>
 Monitor and improve productivity, while ensuring all customer commitments are met in a timely, quality and cost-conscious manner
 </li>
 <li>
 Maintain (calibration and verification support) and troubleshoot production equipment
 </li>
 <li>
 Define, validate and control production process including tooling and equipment. Work with local and global suppliers to purchase and maintain them.
 </li>
 <li>
 Validate design specifications and shop floor application of new product, tools, or equipment.
 </li>
 <li>
 Specify and expedite planned maintenance routines on all production equipment and systems.
 </li>
 <li>
 Work closely with regulatory affairs department to support the compliance with all local regulations.
 </li>
 <li>
 Define and support local parts purchases and validation process according to GE HealthCare quality procedures.
 </li>
 <li>
 Design the production layout and assure the conformity to EHS policy and to local regulations.
 </li>
 <li>
 Act as a materials change coordinator or/and manufacturing process leader: be the contact point for design or process change communications and lead the implementation of changes in cooperation with supplier quality engineer (SQE)
 </li>
 <li>
 Provide guidance and expertise to manufacturing engineer
 
 
 </li>
 </ul>
 
 Quality Control
 
 
 
 <ul>
 <li>
 Responsible for determining processes requiring validation, development of plans and analysis criteria, execution and final analysis.
 </li>
 <li>
 Ensuring regulatory compliance through Validation &amp; Verification.
 </li>
 <li>
 Lead quality metrics follow up and control in production and drives process quality improvements and simplification
 </li>
 <li>
 Assure that corrective action is taken to resolve observed safety concerns in all areas.
 </li>
 <li>
 Support and follow up contract manufacturing supplier&rsquo;s CAPA cases management.
 </li>
 <li>
 Support SQE &amp; follow up for contract manufacturing supplier&rsquo;s SCAR&rsquo;s
 </li>
 <li>
 Ensure compliance to GE HealthCare quality procedures and local regulations.
 
 
 </li>
 </ul>
 
 Minimum Requirements
 
 
 
 <ul>
 <li>
 B.S. Degree in Mechanical, Electrical, Industrial Engineering or related technical degree
 </li>
 <li>
 7 years of experience in production, engineering
 </li>
 <li>
 Good analytical and planning skills
 </li>
 <li>
 Excellent English (Writing &amp; Communicating)
 
 
 </li>
 </ul>
 
 
 
 Additional Information
 
 
 
 
 
 
 Relocation Assistance Provided:
 
 Yes
 
 
</div>

Manufacturing Engineer

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