quality systems engineer

Manufacturing Commercial Vehicles

<div>Company: MCV INDUSTRY ( egypt)- Job Purpose:Responsible for verifying and reviewing the quality systems applied to ensure their compatibility with required standards guided by the estimated cost and time setJob Duties and Responsibilities:<ul><li>Implement quality assurance standards, processes and control quality assurance standards</li><li>Evaluate production capabilities and recommends improvements</li><li>Assist in developing quality assurance policies and procedures</li><li>Maintain proper documentation and reports</li><li>Organize all audits activities, which include internal, suppliers, distributors and external audits</li><li>Participate in building and updating the quality management system (QMS),</li><li>Promote interest in quality improvement efforts by publicizing product results</li><li>Coordinate with line audits and technical department to ensure making the required corrective and preventive action and avoid non- compliance with the required product specifications and codes</li><li>Maintain quality records in accordance with the requirement of ISO 9001</li><li>Fulfill additional tasks as per job requirements and as directed by line managementMain KPI Key Performance indicators:
</li></ul><ul>
<li>Core Competencies<ul>
<li>Financial Management</li>
<li>Customer Excellence</li>
<li>Process Management</li>
<li>Growth &amp; Development</li></ul> 
</li>
<li>Functional Competencies<ul>
<li>Job Knowledge</li>
<li>Monitoring, Reporting and Trend Thinking</li>
<li>Technology and Cyber Security</li></ul> 
</li>
<li>Leadership Competencies<ul>
<li>Accountability &amp; Focusing on Business Results</li>
<li>Emotional Intelligence</li>
<li>Integrity &amp; Professional Behavior</li></ul></li> 
</ul>
Job Skills and Abilities:<ul><li> Excellent in English language</li><li> Very good communication skills</li><li> Very good computer skills</li><li> Ability to work under pressure</li><li> Multi task Engineer</li></ul>Qualifications:<ul><li> BSC in Mechanical Engineering Preferable (Power or Production)</li></ul>- 3 - 6 Years of Experience</div>

Quality Assurance Engineer

Parsons

<div>In a world of possibilities, pursue one with endless opportunities. Imagine Next! 

At Parsons, you can imagine a career where you thrive, work with exceptional people, and be yourself. Guided by our leadership vision of valuing people, embracing agility, and fostering growth, we cultivate an innovative culture that empowers you to achieve your full potential. Unleash your talent and redefine what&rsquo;s possible. 
Job Description:
Parsons is seeking a Quality Engineer to perform high-level quality activities on complex projects and functional programs. You will ensure that all products and services delivered are in strict accordance with customer requirements and Parsons&rsquo; global quality standards. This role requires regular interaction with project management, design, procurement, and construction teams to drive operational excellence.
What You Will Be Doing<ul><li>
System Support &amp; Optimization: Provide Quality Systems support using ISO 9001 as the foundation for process development, data reporting, and training.</li><li>
Audit Management: Plan and execute internal quality audits across offices and job sites. You will document findings to ensure compliance with contract requirements, codes, and specifications (Design, Procurement, Construction, etc.).</li><li>
Corrective Actions: Effectively document, follow up on, and close internal and external corrective actions. Analyze non-conformance trends to identify program-wide performance issues.</li><li>
Technical Reviews: Conduct quality engineering reviews of design documentation, vendor manuals, and technical deliverables to verify compliance with industry codes and regulatory commitments.</li><li>
Supply Chain Quality: Assist in qualification audits of suppliers and subcontractors to ensure they meet Parsons&rsquo; and the Client&rsquo;s rigorous quality expectations.</li><li>
Safety Integration: Promote safety awareness and participate in safety field audits and assessments to ensure a holistic approach to project risk.</li></ul>
Education &amp; Experience<ul><li>
Degree: Bachelor&rsquo;s Degree in Engineering, Business, Quality, or a related field.</li><li>
Experience: Typically 6+ years of related experience in the field of Quality.</li><li>
Certifications (Required/Preferred): * Lead Auditor certification (ISO 9001 or equivalent).<ul><li>
ASQ Certification (CMQ/OE, CQA, or CQE) is highly preferred.</li><li>
Specialized certifications (NQA-1, AWS Welding Inspector, NDT) are a plus.</li></ul></li><li>
Industry Knowledge: Working knowledge of infrastructure, aviation, or large-scale transportation projects</li></ul>
Skills &amp; Competencies<ul><li>
Systems Expertise: Deep knowledge of ISO 9000, ASME, ANSI, and ASTM standards.</li><li>
Analytical Skills: Proficiency in analyzing business metrics (ROI, cost per unit) and performing statistical process control.</li><li>
Communication: Ability to conduct management-level presentations and interface effectively with diverse professional groups.</li><li>
Software Proficiency: Expert knowledge of Microsoft Office (Word, Excel, PowerPoint, Access) and Visio.</li><li>
Attention to Detail: Strong risk assessment, problem-solving, and project planning skills are essential.</li></ul>
Parsons equally employs representation at all job levels no matter the race, color, religion, sex (including pregnancy), national origin, age, disability or genetic information.
We truly invest and care about our employee&rsquo;s wellbeing and provide endless growth opportunities as the sky is the limit, so aim for the stars! Imagine next and join the Parsons quest&mdash;APPLY TODAY!<div>
Parsons is aware of fraudulent recruitment practices. To learn more about recruitment fraud and how to report it, please refer to https://www.parsons.com/fraudulent-recruitment/.</div></div>
 <div><div><div>COMPETITIVE BENEFIT OFFERINGS</div></div><div><div><div> 
Financial Wellness</div><div> 
We care about your financial wellbeing. Parsons offers competitive pay and retirement plans to help you build wealth for the future while giving you the flexibility to diversify your investments.</div></div><div><div>
Work Life Harmony</div><div> 
Balance in life is important and time away from the office is imperative to allow you to refresh and focus your attention on the things that matter to you. Parsons supports your time away by providing paid time off and paid flexible holidays.</div></div><div><div>
Career Development</div><div> 
We are committed to fostering the personal and professional growth of our employees. Develop and advance yourself though our comprehensive training, educational and mentorship programs.</div></div><div><div> 
Veteran Support</div><div> 
We provide Industry leading benefits to support veterans and active-duty members to provide security for you and your family by offering robust leave and benefits; including paid active-duty military leave and paid time off when transitioning back to civilian life.</div></div><div><div>
Mind &amp; Body</div><div> 
At Parsons we inspire healthier habits, heathier minds, and a healthier you through our wellness program. Participate in our weekly Meditation Mondays and Wellness Wednesdays. Wellness, at Parsons, is more than just your annual checkup.</div></div><div><div>
Health</div><div> 
Health is not a one size fits all. At Parsons, we offer a robust Employee Assistance Program as well as comprehensive medical, dental and vision plans through large, national carriers with the choice of regional PPO, HDHP, or HMO networks.</div></div></div></div>

Quality Engineer (Saudi National)

Interact Engineering LLC

OVERVIEW The Quality Engineer will support the aseptic manufacturing and quality systems for sterile drug products packaged in glass vials and prefilled syringes. This role ensures compliance with applicable regulatory requirements including US FDA 21 CFR Parts 210, 211, 820, EU GMP Annex 1, and ISO 13485.The position is responsible for the Quality support functions associated with the manufacturing and packaging of aseptic fill products like Syringes, vials and Cartridges. The position is responsible for the timely assessment of Quality documents associated with the production and packaging of aseptic fill products. This position will also manage projects associated with process, documentation and other improvements necessary in the Quality arena.This role is 100% on site in Whippany, NJ.ESSENTIAL FUNCTIONS Key Responsibilities:1. Quality Systems &amp; Complianceo Ensure compliance with cGMP, Quality System Regulations (QSR), and ISO 13485 requirements in aseptic manufacturing and packaging.o Support the implementation and continuous improvement of quality systems: CAPA, deviations, change control, risk management, and supplier qualification.o Author, review, and approve SOPs, protocols, batch records, and validation documents.o Maintain compliance with FDA 21 CFR Part 210/211 (drug manufacturing), Part 820 (device QSR), and EU Annex 1 sterile manufacturing requirements.2. Aseptic Manufacturing Oversighto Provide on-floor quality support for aseptic filling operations of glass vials and prefilled syringes.o Perform aseptic technique observation, media fill support, and personnel qualification oversight.o Review and assess cleanroom classification, environmental monitoring, and process simulations.o Verify compliance of gowning, cleaning, and disinfection practices per EU Annex 1 and FDA expectations.3. Process &amp; Equipment Supporto Support validation and qualification of aseptic filling lines, isolators, RABS, cleanrooms, utilities, and associated equipment.o Participate in FAT, SAT, IQ/OQ/PQ and technical transfers for sterile manufacturing lines.o Ensure equipment, packaging, and container-closure systems for glass vials and prefilled syringes meet USP &lt;1207&gt; container closure integrity testing (CCIT) requirements.o Conduct risk assessments (FMEA, HACCP, risk-based approach per ICH Q9/Q10).4. Investigations &amp; Continuous Improvemento Lead and support root cause investigations for deviations, OOS/OOT, and complaints related to aseptic operations and packaging.o Develop and track CAPAs to ensure timely and effective implementation.o Monitor process performance and quality trends to identify opportunities for improvement.o Drive implementation of quality by design (QbD) and continuous improvement initiatives in aseptic processes.5. Documentation &amp; Regulatory Supporto Ensure accurate, complete, and contemporaneous documentation in compliance with data integrity principles (ALCOA+).o Support preparation for regulatory inspections (FDA, EMA, Notified Body, MHRA, etc.).o Assist in responding to inspection findings and regulatory queries.o Prepare quality reports, metrics, and risk assessments for management review.6. Continuous Improvement:o Drive continuous improvement initiatives through lean manufacturing principles and Six Sigma methodologies.o Lead quality improvement projects, collaborating with teams to enhance product quality, reduce waste, and improve operational efficiency.POSITION QUALIFICATIONS EDUCATION/EXPERIENCE:&middot; Bachelor&rsquo;s or master&rsquo;s degree in pharmacy, Microbiology, Biotechnology, Chemical Engineering, or related Life Sciences/Engineering field.&middot; 5+ years of experience in aseptic pharmaceutical or medical device manufacturing, with direct involvement in glass vial and/or prefilled syringe filling operations.&middot; Strong understanding of cGMP, FDA 21 CFR Parts 210/211/820, EU Annex 1, ISO 13485.&middot; Experience with validation, aseptic process simulations, cleanroom classification, and CCIT.&middot; Prior exposure to combination product regulations is highly desirable.Skills &amp; Competencies:o Strong knowledge of aseptic techniques, sterile barrier systems, and contamination control strategies.o Familiarity with quality risk management, statistical data analysis, and process capability tools.o Excellent technical writing and communication skills.o Strong problem-solving and root cause analysis skills.o Ability to work in a dynamic, fast paced, and highly regulated environment.Physical Requirements:o Primarily site-based with routine presence in classified cleanroom environments.o Ability to stand for up to 8 hours per day.Frequent sitting, standing, walking, reading written documents and use of computer monitor screen, talking, writing, listeningo May require gowning certification for Grade A/B aseptic areas.o Occasional travel for supplier audits, training, or regulatory inspections.Pay: $45.00 per hourWork Location: In person

Quality Engineer

Global Engineering Services

Job description: Quality Management &amp; ISO Documentation Engineer Timings: 9:00 PM &ndash; 6:00 AM (Monday to Friday)- Night ShiftOverall Purpose of the Role:Responsible for maintaining the Quality Management System (QMS), writing procedures and processes to support the QMS development. Undertake audits across all areas of the business as well as across the supply chain. Provide training and champion the Quality Management System. Work under general supervision, reviewed at project milestones and/or on completion by Senior Management.Key Responsibilities: General and Task Management Implement the Quality Management System throughout the company, including any business accreditations Maintain the Quality Manuals and Quality Procedures and ensure contents are -appropriate for business Organize and manage the plant internal audit system and the corrective action reporting system Conduct Quality Systems audits and assist in training/guidance to other auditors Participate in external Quality System audits Coordinate the review of Quality procedures associated with plant continuous improvement initiatives Plan Standard Operating practices required under the overriding Quality procedures Maintain the Standard Operating Procedure content and coordinate the issuing of these documents Support other functional areas of the business including procurement, business services and design Collate quality data for monitoring targets Assist with training of quality awareness Report on Key Performance Indicators (KPIs) in order to adhere to process and prevent occurrence of any non-conformity relating to product, process or system Promote the use of customer preferred techniques for continuous improvement such as Six-Sigma, Poka-Yoke (Error Proofing), and Measurement System Analysis Undertake special projects as required Contribute to continuous improvement activities Quality control of work by appropriate reviews Support and lead process improvement activities Write reports and present progress at project meetings and to clients Achieve goals within budget Plan projects or subtasks so they may be tracked and presented Attend various meetings and action/communicate instructions Undertake continuous training and development Perform root cause analysis and resolve problems Independently determine approach and assigned tasksPeople Management Lead and/or support trainee engineers Train people within own work groupRelationship Management Liaise with cross functional team to implement an effective, documented process that defines product Quality requirements, best practice and training materials to support continuous improvement initiatives Liaise and communicate with other departments, customers, suppliers and other service providers Liaise with customers, joint ventures and supply chain partners Communicate efficiently throughout the shop floor and with own and customer&rsquo;s managementSelf-Management<ul><li>Comply with the Health, Safety and Environmental Policies</li><li>Assertive, resilient and welcomes change</li><li>Engages interest and participation of others and has a collaborative approach to working with others</li><li>Proactively contributes to the team</li><li>Actively committed to team development</li><li>Shows moral courage, openness and honesty in all dealings</li></ul>Skills &amp; Attributes:<ul><li>Knowledge of quality systems</li><li>Strong knowledge of Advanced Product Quality Planning (APQP), Production Part Approval Process (PPAP), Failure Mode and Effect Analysis (FMEA), Statistical Process Control (SPC)</li><li>Lean Manufacturing knowledge</li><li>Knowledge of ISO9001, ISO13485 and AS9100</li><li>Understanding of ISO14001 and Health and Safety Practices</li><li>Knowledge of measurement</li><li>Understanding of engineering drawings and manufacturing processes</li><li>Ability to work in a diverse and dynamic environment</li><li>Good communication and interpersonal skills</li><li>Negotiation skills</li><li>Ability to present data effectively</li><li>Problem-solving skills</li><li>Team working skills</li><li>Analytical skills</li><li>Understanding of cost and financial impacts</li><li>Ability to work on own initiative</li></ul>Qualifications and Experience Levels:<ul><li>Relevant business/commercial or manufacturing/engineering degree preferred,</li><li>Membership of an industry-related Professional Body would be advantageous</li><li>Previous experience in a high-mix-low- volume manufacturing environment, preferably medical and aerospace</li><li>Experience of working in Quality Assurance</li><li>Six Sigma/Lean Manufacturing skills</li><li>Experience of dealing with customers and suppliers</li></ul>Work Location: In person

Quality Management & ISO Documentation Engineer

Capgemini

<div><div><div><div>At Capgemini Engineering, the world leader in engineering services, we bring together a global team of engineers, scientists, and architects to help the world&rsquo;s most innovative companies unleash their potential. From autonomous cars to life-saving robots, our digital and software technology experts think outside the box as they provide unique R&amp;D and engineering services across all industries. Join us for a career full of opportunities. Where you can make a difference. Where no two days are the same.
<div><div><div><h2 class="jobSectionHeader">About the Role You're Considering</h2>
</div><div>This role involves the development and application of engineering practice and knowledge in the definition and execution of quality management systems (QMS) for product and process quality, ensure and validate compliance to standards, homologation of products and processes and registration to the competent authorities. It also involves management and audit of Occupational Health and Safety Management Systems (OHSMS) and environmental systems and their risk assessments.</div>
</div><div><div><h2 class="jobSectionHeader">What You Bring:</h2>
</div><div><ul><li>Must be a US Citizen</li>
<li>Bachelor&rsquo;s degree in Engineering, Quality, or a related technical field</li>
<li>5&ndash;10 years of experience in quality engineering, supplier quality, or a closely related role</li>
<li>Strong working knowledge of quality management systems and industry standards</li>
<li>Hands‑on experience with root cause analysis and structured problem‑solving techniques</li>
<li>Proven ability to write and maintain quality procedures and work instructions</li>
<li>Strong analytical thinking with attention to detail</li>
<li>Clear, confident communication skills and the ability to collaborate across teams</li>
</ul>Preferred Requirements
<ul><li>Aerospace experience</li>
<li>Experience with SAP or any favorable QMS</li>
<li>Comfortable with handling and managing data, data analysis and data dispatch</li>
<li>Previous experience with supplier management for quality defects</li>
<li>Experience managing quality issue databases</li>
</ul>Growth &amp; Development
This role offers meaningful opportunities to grow both technically and professionally while increasing visibility and influence across the organization.
As a Quality Engineer, you&rsquo;ll:
<ul><li>Build deep expertise in quality systems, root cause analysis, and supplier quality management</li>
<li>Expand ownership from individual quality issues to broader, cross‑functional initiatives</li>
<li>Strengthen leadership skills by influencing suppliers, mentoring peers, and guiding best practices</li>
<li>Play an active role in shaping quality metrics, documentation standards, and continuous improvement efforts</li> 
</ul></div></div></div>The base compensation range for this role in the posted location is: $68,911.00 - $181,673.00.
Capgemini provides compensation range information in accordance with applicable national, state, provincial, and local pay transparency laws. The base compensation range listed for this position reflects the minimum and maximum target compensation Capgemini, in good faith, believes it may pay for the role at the time of this posting. This range may be subject to change as permitted by law.
The actual compensation offered to any candidate may fall outside of the posted range and will be determined based on multiple factors legally permitted in the applicable jurisdiction.
These may include, but are not limited to: Geographic location, Education and qualifications, Certifications and licenses, Relevant experience and skills, Seniority and performance, Market and business consideration, Internal pay equity.
It is not typical for candidates to be hired at or near the top of the posted compensation range.
In addition to base salary, this role may be eligible for additional compensation such as variable incentives, bonuses, or commissions, depending on the position and applicable laws. 
Capgemini offers a comprehensive, non-negotiable benefits package to all regular, full-time employees. In the U.S. and Canada, available benefits are determined by local policy and eligibility and may include:
<ul><li>Paid time off based on employee grade (A-F), defined by policy: Vacation: 12-25 days, depending on grade, Company paid holidays, Personal Days, Sick Leave</li>
</ul><ul><li>Medical, dental, and vision coverage (or provincial healthcare coordination in Canada)</li>
<li>Retirement savings plans (e.g., 401(k) in the U.S., RRSP in Canada)</li>
<li>Life and disability insurance</li>
<li>Employee assistance programs</li>
<li>Other benefits as provided by local policy and eligibility</li>
</ul>Important Notice: Compensation (including bonuses, commissions, or other forms of incentive pay) is not considered earned, vested, or payable until it becomes due under the terms of applicable plans or agreements and is subject to Capgemini&rsquo;s discretion, consistent with applicable laws. The Company reserves the right to amend or withdraw compensation programs at any time, within the limits of applicable legislation. 
Disclaimers
Capgemini is an Equal Opportunity Employer encouraging inclusion in the workplace. Capgemini also participates in the Partnership Accreditation in Indigenous Relations (PAIR) program which supports meaningful engagement with Indigenous communities across Canada by promoting fairness, accessibility, inclusion and respect. We value the rich cultural heritage and contributions of Indigenous Peoples and actively work to create a welcoming and respectful environment. All qualified applicants will receive consideration for employment without regard to race, national origin, gender identity/expression, age, religion, disability, sexual orientation, genetics, veteran status, marital status or any other characteristic protected by law.
This is a general description of the Duties, Responsibilities and Qualifications required for this position. Physical, mental, sensory or environmental demands may be referenced in an attempt to communicate the manner in which this position traditionally is performed. Whenever necessary to provide individuals with disabilities an equal employment opportunity, Capgemini will consider reasonable accommodations that might involve varying job requirements and/or changing the way this job is performed, provided that such accommodation does not pose an undue hardship. Capgemini is committed to providing reasonable accommodation during our recruitment process. If you need assistance or accommodation, please reach out to your recruiting contact.
Please be aware that Capgemini may capture your image (video or screenshot) during the interview process and that image may be used for verification, including during the hiring and onboarding process.
Click the following link for more information on your rights as an Applicant in the United States. http://www.capgemini.com/resources/equal-employment-opportunity-is-the-law 
Capgemini is a global business and technology transformation partner, helping organizations to accelerate their dual transition to a digital and sustainable world, while creating tangible impact for enterprises and society. It is a responsible and diverse group of 340,000 team members in more than 50 countries. With its strong over 55-year heritage, Capgemini is trusted by its clients to unlock the value of technology to address the entire breadth of their business needs. It delivers end-to-end services and solutions leveraging strengths from strategy and design to engineering, all fueled by its market leading capabilities in AI, generative AI, cloud and data, combined with its deep industry expertise and partner ecosystem.</div></div></div></div>

Quality Engineer (Onsite: Kinston, NC)

Talent 360

<div>Company: Dunes Constructions 
Location: Sheikh Zayed City 
Employment Type: Full Time
Job Description: 
Dunes Constructions is seeking a QS Engineer (Quantity Surveyor) to join our team in Sheikh Zayed. The candidate will be responsible for managing all quantity surveying and cost control activities, ensuring projects are delivered within budget and in line with contractual requirements.
Key Responsibilities:<ul><li>
Prepare BOQs, quantity take-offs, and cost estimates.
</li><li>Review drawings and specifications to identify project requirements.
</li><li>Monitor project costs and prepare cost reports.
</li><li>Prepare and review subcontractors&rsquo; invoices and variations.
</li><li>Evaluate and negotiate subcontractor quotations.
</li><li>Follow up on payments, variations, and claims.
</li><li>Coordinate with the technical office and site team to ensure accurate quantities and cost control.</li></ul> 

Requirements 
Requirements:<ul><li>
Bachelor&rsquo;s degree in Civil Engineering.
</li><li>2&ndash;3 years of experience in Quantity Surveying.
</li><li>Strong knowledge of BOQs, cost estimation, and contracts.
</li><li>Proficiency in Excel and AutoCAD (Primavera is a plus).
</li><li>Strong analytical and negotiation skills.</li></ul></div>

QS Engineer

Talent 360 ME

<div>
 
 Company:
 
 Dunes Constructions
 
 
 
 Location:
 
 Sheikh Zayed City
 
 
 
 Employment Type:
 
 Full Time
 
 
 
 Job Description:
 
 
 
 Dunes Constructions is seeking a
 
 QS Engineer (Quantity Surveyor)
 
 to join our team in Sheikh Zayed. The candidate will be responsible for managing all quantity surveying and cost control activities, ensuring projects are delivered within budget and in line with contractual requirements.
 
 
 
 Key Responsibilities:
 
 
 
 <ul>
 <li>
 Prepare BOQs, quantity take-offs, and cost estimates.
 </li>
 <li>
 Review drawings and specifications to identify project requirements.
 </li>
 <li>
 Monitor project costs and prepare cost reports.
 </li>
 <li>
 Prepare and review subcontractors' invoices and variations.
 </li>
 <li>
 Evaluate and negotiate subcontractor quotations.
 </li>
 <li>
 Follow up on payments, variations, and claims.
 </li>
 <li>
 Coordinate with the technical office and site team to ensure accurate quantities and cost control
 
 
 </li>
 </ul>
 
 Requirements
 
 
 
 
 Requirements:
 
 
 
 <ul>
 <li>
 Bachelor's degree in Civil Engineering.
 </li>
 <li>
 2-3 years of experience in Quantity Surveying.
 </li>
 <li>
 Strong knowledge of BOQs, cost estimation, and contracts.
 </li>
 <li>
 Proficiency in Excel and AutoCAD (Primavera is a plus).
 </li>
 <li>
 Strong analytical and negotiation skills
 </li>
 </ul>
</div>

Search 10000+ Quality systems engineer jobs near you this May. New roles added regularly across leading industries. Apply today.

10000 quality systems engineer jobs Near Me

Quality Assurance Engineer

Quality Engineer (Saudi National)

Quality Engineer

Quality Management & ISO Documentation Engineer

Quality Engineer (Onsite: Kinston, NC)

QS Engineer

QS Engineer