quality process engineer

Wasco Switches & Sensors

<div>Description:

 Job Summary:
The Quality Engineer applies technical and problem-solving skills to ensure products and processes meet quality requirements. This role supports corrective actions, risk management, and continuous improvement across the organization and supply chain.
Essential Functions:<ul><li>Process and Product Quality Support: Apply quality engineering principles to ensure product and process compliance with quality standards.</li><li> Internal Audit Program: Plan and conduct internal audits to the ISO9001 Quality Management Standard and Wasco&rsquo;s documented procedures.</li><li>Root Cause and Corrective Actions: Lead investigations into quality issues and develop corrective action plans.</li><li>Data Analysis and Risk Management: Analyze data, conduct risk assessments, and support FMEA and other preventive quality tools.</li><li>Supplier and Customer Support: Work with suppliers and customers to address quality requirements and resolve issues.</li><li>Continuous Improvement: Support initiatives that improve process capability, reduce defects, and enhance efficiency.</li></ul>
Requirements:

Education:
High School Diploma or equivalent required.
Bachelor's degree preferred.
Experience:
4 years in a full-time engineering or quality-related role required. (Experience in a manufacturing environment is preferred).
Skills and Abilities Summary:<ul><li>Technical Problem-Solving: Understands the necessary elements of an operator controllable process. Apply quality engineering methods and structured problem-solving to resolve complex quality issues.</li><li> Internal Auditing Expertise: Understanding of ISO9001 QMS Requirements and experience conducting process audits in a manufacturing environment, including Audit reporting and Corrective Action initiation.</li><li>Root Cause Analysis Expertise: Use tools such as 5 Whys, Fishbone, and FMEA to identify and prevent failures.</li><li>Data-Driven Approach: Collect, analyze, and interpret quality data to support decisions. Firm command of descriptive statistics, intermediate or above excel skills. Effectively applies SPC and MSA in a factory setting.</li><li>Cross-Functional Collaboration: Partner with manufacturing, engineering, and supply chain teams to ensure quality integration.</li><li>Standards Knowledge: Understand ISO 9001 and industry-specific standards to ensure compliance.</li></ul> 
Physical Requirements &amp; Work Environment:
This position may require the ability to lift 50 lbs. at chest level several times a day, good hand and eye coordination with demonstrated manual dexterity and fine motor skills for precision calibration and assembly of small parts, 20/20 or better corrected vision, and the ability to see the full spectrum of colors and track fine details visually to discover defects in parts or processes. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of the position.</div>

Quality Engineer

Transpo Group Middle East

Our client is a multidisciplinary, third-party approved engineering firm providing structural, MEP, inspection, testing, and certification services to the construction industry, delivering cost-effective and high-quality engineering solutions and they are looking to hire a Quality Assurance Engineer.Position Overview:We are seeking a proactive and detail-oriented Quality Assurance Engineer to ensure the effective implementation and maintenance of the Quality Management System (QMS). The role will focus on monitoring quality processes, ensuring compliance with international standards, supporting audits, and driving continuous improvement across testing, inspection, laboratory, or construction operations.Key Responsibilities:1. Quality Management System (QMS)<ul><li>Implement and maintain the Quality Management System in line with ISO 9001, ISO/IEC 17020, and ISO/IEC 17025 standards</li><li>Ensure all operational activities comply with approved procedures, standards, and regulatory requirements</li><li>Monitor and report on QMS performance and suggest improvements</li></ul>2. Quality Assurance &amp; Control<ul><li>Monitor site, laboratory, or inspection activities to ensure compliance with project specifications and international standards (ASTM, BS, AASHTO, etc.)</li><li>Review and verify inspection reports, test results, and technical documentation for accuracy and completeness</li><li>Ensure proper calibration and maintenance of testing and measuring equipment</li></ul>3. Audit &amp; Compliance<ul><li>Conduct internal audits and support external audits by certification bodies and authorities (e.g., EIAC, ENAS, ADNOC, etc.)</li><li>Identify non-conformities and ensure timely closure through corrective actions</li><li>Maintain audit records and compliance documentation</li></ul>4. Documentation &amp; Reporting<ul><li>Prepare, review, and control quality documentation including:</li><li>Method Statements</li><li>Inspection &amp; Test Plans (ITPs)</li><li>SOPs and procedures</li><li>Quality reports and logs</li><li>Ensure document control and version management are properly maintained</li></ul>5. Non-Conformance &amp; Continuous Improvement<ul><li>Raise and manage Non-Conformance Reports (NCRs)</li><li>Conduct Root Cause Analysis (RCA) and implement Corrective and Preventive Actions (CAPA)</li><li>Identify trends and recommend process improvements</li></ul>6. Coordination &amp; Support<ul><li>Coordinate with project teams, laboratory staff, inspectors, and external stakeholders</li><li>Provide technical guidance on quality requirements and standards</li><li>Support training and awareness initiatives related to quality processes</li></ul>Qualifications &amp; Requirements:<ul><li>Bachelor&rsquo;s Degree in Engineering (Civil, Mechanical, Industrial, or related field)</li><li>Minimum 5 years of experience in QA/QC within construction, testing laboratories, or inspection environments</li><li>Strong knowledge of: ISO 9001, ISO/IEC 17020, ISO/IEC 17025, International standards (ASTM, BS, AASHTO)</li><li>Experience in internal/external audits and QMS implementation</li><li>Familiarity with laboratory testing, inspection processes, or construction QA/QC</li></ul>Note: Only those with ISO 17020/17025 certification will be shortlisted for the role. Please do not submit your application if you do not have this.Application Question(s):<ul><li>Did you attach your original CV to your application?</li><li>Did you specify the projects you worked on in your CV?</li></ul>Education:<ul><li>Bachelor's (Preferred)</li></ul>Experience:<ul><li>QA/QC in construction: 5 years (Required)</li><li>internal/external audit: 5 years (Required)</li><li>QMS implementation: 5 years (Required)</li><li>ASTM, BS, AASHTO: 5 years (Preferred)</li></ul>License/Certification:<ul><li>ISO 17020 (Required)</li></ul>Work Location: In person

GE Aerospace

<div>
 
 Job Description Summary
 
 
 
 The GE Aerospace Quality Engineer in Pittsburgh will be responsible for key functional, business, and company objectives and report to the onsite Quality Leader. In this role, you will solve complex issues affecting the business, executing the long-term business plan and driving quality excellence in the organization. You will work with the larger sub-section team (including Global Quality), as well as a cross-functional team from other organizations.
 
 
 
 Job Description
 
 
 
 
 Essential Responsibilities:
 
 
 
 <ul>
 <li>
 Lead and support inspection and release-to-service processes in accordance with applicable regulatory requirements
 </li>
 <li>
 Provide oversight of inspection procedures to ensure inspection methods and techniques are performed accurately by inspection personnel.
 </li>
 <li>
 Drive quality excellence, regulatory compliance, and a strong safety and quality culture across the site
 </li>
 <li>
 Reduce risk in shop operations through robust inspection methods, documentation integrity, and strong control of materials and data
 </li>
 <li>
 Solve complex quality and compliance issues while supporting execution of the long-term business plan
 </li>
 <li>
 Maintain historical records in accordance with required retention timelines and practices.
 </li>
 <li>
 Ensure all applicable inspection and test equipment is checked, calibrated, repaired, or readjusted at required intervals to maintain correct calibration status.
 </li>
 <li>
 Serve as the secondary interface with regulatory agencies, (e.g. FAA, EASA, UK CAA)
 </li>
 <li>
 Ensure that all regulatory requirements are met.
 </li>
 <li>
 All Regulatory, Customer and Supplier audit requirements are satisfied.
 </li>
 <li>
 Introduce and manage the Safety Management System at the shop.
 </li>
 <li>
 Perform internal audits locally and at remote locations.
 </li>
 <li>
 Conduct Quality and Human Factor training for all staff.
 </li>
 <li>
 Conduct Root Cause Analysis and PFMEA when required.
 </li>
 <li>
 Own the proactive quality framework for reducing quality risk at the shop.
 </li>
 <li>
 Lead RCCA Execution for the shop facilitating best practice sharing with other GE Aerospace and OWS shops
 
 
 </li>
 </ul>
 
 Minimum Requirements
 
 
 
 <ul>
 <li>
 Bachelors degree (in Aeronautical or Mechanical Engineering preferred) from an accredited college or university and 3+ years of experience in Aviation and Production Quality Assurance (or a minimum high school diploma / GED with an additional 4+ years of experience in Aviation and Production Quality Assurance).
 </li>
 <li>
 1+ years of experience working with aviation regulatory agencies.
 
 
 </li>
 </ul>
 
 Desired Characteristics
 
 
 
 <ul>
 <li>
 Experience working with FAA FAR 145 procedures.
 </li>
 <li>
 Qualified Auditor with auditing experience within regulated aviation environments desired.
 </li>
 <li>
 Prior inspection / certifying staff experience in an MRO or Part 145 setting is highly preferred.
 </li>
 <li>
 Familiarity with inspection methods and techniques used in the station&rsquo;s area of expertise.
 
 
 </li>
 </ul>
 GE Aerospace offers a great work environment, professional development, challenging careers, and competitive compensation. GE Aerospace is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.
 
 
 GE Aerospace will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a drug screen (as applicable).
 
 
 
 Relocation Assistance Provided:
 
 Yes
 
 
</div>

Quality Engineer - Pittsburgh

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

Proterial

<div>Location:
Dammam, Eastern Region, Saudi Arabia
Job ID:
R0118133
Date Posted:
2026-04-12
Company Name:
HITACHI ENERGY LTD
Profession (Job Category):
Quality Management
Job Schedule:
Full time
Remote:
No
Job Description:
The opportunity 
 
Under the supervision of BU, GPP/HUB or Local QMS managers supports implementation and maintenance of Quality Management System (QMS) in their area of responsibility in accordance with the Business Unit&rsquo;s QMS, applicable standards and internal regulations. Organizes and conducts
 
internal audits and support certifications audits. Responsible for process definition with its acceptance criteria and provide relevant trainings and instructions to the teams within their area of responsibility about the processes. Participates in Quality Improvement Plan (QIP) and continuous improvement
 
activities.
How you&rsquo;ll make an impact 
 
<ul><li>Implements and ensure adherence to applicable QMS within their area of responsibility. When applicable managers and mentors the quality professionals under their responsibility.
</li><li>Provides leadership and technical expertise in Quality Management System solutions to the teams in their area of responsibility.
</li><li>Ensures all necessary training for QMS is available at the appropriate tools or platforms and the organization is aware and trained.
</li><li>Supports integrating the Voice of the Customer into the QMS framework through effective implementation of customer feedback processes, such as customer surveys, complaint resolution, and comprehensive analysis of customer feed-back data.
</li><li>Ensures the business process mapping (BPM) is available, released and showing the up-to-date process landscape of their scope in appropriate tool (e.g. Adonis).
</li><li>Ensures the document management system (DMS) holds all relevant QMS related documents as official, controlled documents.
</li><li>Prepares and assists regular internal audits with all business relevant functions/departments and processes. Preferably use the GQSA (global quality self-assessment) approach and Intelex tool to document internal audits.
</li><li>Prepares and assists external ISO 9001 audits with external certification bodies that are approved by Hitachi Energy.
</li><li>Contributes to maintenance of an effective quality governance framework within their area of responsibility. This includes assisting in the development and implementation of quality procedures and practices in accordance with established standards and regulations.
</li><li>Implements process performance metrics and indicators to assess process efficiency, while closely monitoring critical parameters.
</li><li>Collaborates with cross-functional teams to support identified continuous improvement initiatives &amp; supports execution of the BU Quality Improvement Plan (QIP) within their area of responsibility.
</li><li>You will be responsible for ensuring compliance with applicable external and internal regulations, procedures, and guidelines.
</li><li>Living Hitachi Energy core values of safety and integrity, which means taking responsibility for your own actions while caring for your colleagues and the business.
</li></ul>Your background 
 
<ul><li>Bachelor&rsquo;s Degree in Engineering &amp; preferably Electrical or Mechanical.
</li><li>2-3 years of experience in Quality Management (QMS).
</li><li>Internal Auditor Certification is preferable.
</li><li>Lean 6Sigma, Yellow Belt (Quality) is preferable.
</li><li>Lean 6Sigma, Green Belt (Q&amp;CI) is preferable.
</li><li>Experienced representing the interests and requirements of the business.
</li><li>Ability to generate new ideas and challenge status quo.
</li><li>Proficiency in both spoken and written English and Arabic language is required.
</li></ul><h2 class="jobSectionHeader">Qualified individuals with a disability may request a reasonable accommodation if you are unable or limited in your ability to use or access the Hitachi Energy career site as a result of your disability. You may request reasonable accommodations by completing a general inquiry form on our website. Please include your contact information and specific details about your required accommodation to support you during the job application process.
</h2><h2 class="jobSectionHeader">This is solely for job seekers with disabilities requiring accessibility assistance or an accommodation in the job application process. Messages left for other purposes will not receive a response.</h2></div>

LEONI

<div><div><h2 class="jobSectionHeader">Company Description</h2>
LEONI is a global provider of products, solutions and services for energy and data management in the automotive industry. The group of companies has around 86,000 employees in 21 countries and generated consolidated sales of EUR 3.9 billion in 2025.
The value chain ranges from standardized cables and special and data cables to highly complex wiring systems and related components, from development to production. As an innovation partner with distinctive development and systems expertise, we support our customers on the path to increasingly sustainable and connected mobility concepts from autonomous driving to alternative drives as well as charging systems.</div><div><h2 class="jobSectionHeader">
Job Description</h2><ul><li>
Supervises the Operations Quality area of responsibility in line with defined objectives and KPIs</li><li>
Identifies improvement opportunities, provides consulting, and contributes to enhancing service delivery</li><li>
Ensures adherence to standards, governance, and effective process execution</li><li>
Leads and manages direct reports within the area of responsibility</li><li>
Plans and coordinates team activities to cover all operational stages and respond to all incoming requests</li><li>
Defines team members&rsquo; objectives, tasks, and responsibilities, providing clear instructions, monitoring, and performance evaluation</li><li>
Identifies training and development needs, supports professional growth, and implements initiatives for performance improvement, organizational flexibility, diversity, succession planning, coaching, change management, and personal development</li></ul></div><div><h2 class="jobSectionHeader">
Qualifications and Experience</h2><ul><li>
Bachelor&rsquo;s degree in engineering.</li><li>
(0-2) years of relevant experience, preferably in the Operations Quality field</li><li>
Full professional proficiency in English language</li><li>
Strong communication and interpersonal skills, with the ability to engage effectively across multiple stakeholders.</li><li>
Excellent problem‑solving capabilities, supported by strong analytical and critical‑thinking skills.</li></ul></div><div><h2 class="jobSectionHeader">
Interested?</h2></div></div>
 <div>Nadine Nasreldeen
Email Address:wegca_recruiting.egypt@leoni.com</div>

Operations Quality Engineer

<div>
 &lt;![CDATA[ The Manufacturing Engineer position can occur in Process, Production or Technology.
 
 
 The Manufacturing Engineer - Process is responsible for providing innovative and cost effective processes and solutions required to manufacture products. This includes the design and development of new and improved manufacturing techniques, processes and procedures. He/she develops, maintains, and continuously improves manufacturing processes and techniques using LEAN. He/she develops standards and establishes implementation plans, including training plans for shop floor personnel, and production metrics. He/she collaborates with Engineering and Manufacturing Technology to ensure that processes are created and developed for new products and that return-on-experience is captured for existing processes.
 
 
 The Manufacturing Engineer &ndash; Production performs the lead role in the implementation of manufacturing processes and techniques - and the implementation of LEAN and use of Six Sigma tools. He/she is the owner of their respective manufacturing processes and standards and enforces implementation by training shop floor personnel, implementing and monitoring metrics, and oversight. He/she is responsible to solve complex manufacturing problems and take an active role in troubleshooting quality and production yield related issues within manufacturing. The Manufacturing Engineer - Technology is responsible for finding, investigating, and/or creating new, next generation, innovative and cost effective technology solutions required to manufacture existing and new products. This includes the creation and development of a manufacturing technology roadmap for new and existing product technologies. For new technologies, he/she takes processes from the concept phase all the way to successful implementation.
 
 
 
 For Manufacturing Engineer - Production
 
 
 
 <ul>
 <li>
 Lean Six Sigma.
 </li>
 <li>
 Responsible for the implementation of key elements of Lean, such as: standardized work instructions, line balancing, layout and work sequence (routing) optimization, training development matrix, Value Stream Mapping, Kaizen/5S workouts, pull processes, TPM (total preventive maintenance), cell design, and quick changeover/batch-size optimization.
 </li>
 <li>
 Processes.
 </li>
 <li>
 Implement process improvements to achieve manufacturing excellence in areas such as process yield (e.g. First Pass Yield, Rolled Throughput Yield), cycle time reduction and productivity.
 </li>
 <li>
 Provide shop floor feedback on product design and manufacturability issues to Engineering and DFMs (e.g. through the use of Engineering Change Requests - ECRs).
 </li>
 <li>
 Review and sign-off on Engineering Change Orders that impact Inventory - including product life cycle issues, obsolescence, etc.
 </li>
 <li>
 Creates, implements, and monitors key performance indicators and metrics on manufacturing process capability and product quality.
 </li>
 <li>
 Monitoring and reducing process costs.
 </li>
 <li>
 Quality.
 </li>
 <li>
 Responsible to assist with investigation, root cause analysis and corrective action implementation for manufacturing quality issues.
 
 
 </li>
 </ul>
 
 For Manufacturing Engineer - Technology
 
 
 
 <ul>
 <li>
 Lean Six Sigma.
 </li>
 <li>
 Responsible to ensure that new processes are established using Lean concepts, such as: standardized work instructions, line balancing, layout and work sequence (routing) optimization, training development matrix, Value Stream Mapping, Kaizen/5S workouts, pull processes, TPM (total preventive maintenance), cell design, and quick changeover/batch-size optimization.
 </li>
 <li>
 Also responsible for driving continuous improvement projects on manufacturing processes.
 </li>
 <li>
 Processes.
 </li>
 <li>
 Evaluates and benchmarks best-in-class manufacturing techniques for Schlumberger and OEM products.
 </li>
 <li>
 Establishes pilot testing and scale up plan for manufacturing technology implementation.
 </li>
 <li>
 Works with Manufacturing and Engineering M&eacute;tiers and other stakeholders during prove-out testing of processes. * Supports the Manufacturing Engineer (DFM) on any specific technology issues/constraints for NPD and RR projects.
 </li>
 <li>
 Coordinates with Manufacturing M&eacute;tiers and other resources across the company to share and leverage best practices.
 </li>
 <li>
 Quality.
 </li>
 <li>
 Responsible for ensuring that manufacturing technology solutions achieve the required quality levels, reliability and consistency.
 
 
 </li>
 </ul>
 ]], &gt;
</div>

Manufacturing Engineer

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

10000 quality process engineer jobs Near Me

Quality Engineer

Quality Engineer

Quality Engineer - Pittsburgh

Quality Engineer

Quality Engineer

Operations Quality Engineer

Manufacturing Engineer