דרושים » ייצור ותעשייה » Medical Device Operations Quality Assurance engineer לסטארט-אפ מצליח מהמבטיחים בארץ בתחום.

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לפני 5 שעות
Job Type: Full Time
A Medical device company,Innovative and successful, in Netanya area is looking for an Experienced Operations Quality Assurance Specialist to join the QA Operations group and support the variety of activities related to QA Operations, such as:

Lead QA Operations activities with regards to verifications/validations for an FDA reviewed complex, multidisciplinary, active investigational device.
Lead and perform the Engineering Change Order (ECO) process from risk analysis through protocol approval.
Verification, execution, and analysis of reports until FDA-ready.
Provide guidance to the R D and Engineering teams on IQ/OQ/PV activities.
Requirements:
B.A. or B.S. degree in a technical discipline, such as Engineering or Science.
3-5 years of relevant experience in the medical device industry.
Previous experience with medical device verification/validations, ECOs, medical device statistics
Working knowledge of medical device international standards.
Ability to work independently with minimal work direction and in a cross-functional team environment.
Fluent in English with excellent writing skills, effective written and verbal communication skills.
Excellent computer skills, including a working knowledge of Microsoft Office applications.
Strong time management abilities to ensure timely task completion.
Detail-oriented
This position is open to all candidates.
 
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הגשת מועמדות
עדכון קורות החיים לפני שליחה
8156039
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לפני 5 שעות
קבוצת נישה
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Job Type: Full Time and English Speakers
Join a leading Medical Device Company as a Director of Quality to be responsible for leading the Quality Management system in compliance with ISO 13485, 21 CFR Part 820, MDSAP and other applicable regulatory requirements. This role oversees quality across the product lifecycle, including design control, operations, and post-market activities.
Key Responsibilities:
Lead implementation and oversight of design control processes for new and modified devices.
Manage and ensure quality in operations: production, final product release, incoming inspection activities, process validation and supplier quality.
Manage configuration and doc control process.
Own and maintain the quality management system, including internal audits, CAPA, complaints, and management review.
Prepare for and lead external audits (e.g. notified bodies, FDA).
Requirements:
Bachelors degree in engineering, life sciences, or a related field (Masters preferred).
Minimum 10 years of experience in quality roles within the medical device industry.
Strong knowledge of ISO 13485, 21 CFR Part 820, and MDSAP requirements.
Proven leadership and team management experience.
Experience with quality in Operations.
Experience with internal/external audits and regulatory inspections. Certified lead auditor.
Experience in design control process.
Excellent problem-solving, communication, and cross-functional collaboration skills.
Fluent in English Hebrew
This position is open to all candidates.
 
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הגשת מועמדות
עדכון קורות החיים לפני שליחה
8182328
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4 ימים
חברה חסויה
Job Type: Full Time and Hybrid work
Key Responsibilities:
Coordinate Cross-Functional Teams: Collaborate with R D, design, procurement, and production teams to ensure smooth product launches.
Process Development: Develop and optimize manufacturing processes for new products using quality tools.
Documentation: Review and maintain process documentation, work instructions, and operator training materials.
Prototype Builds: Support PT builds and production ramp-up activities, ensuring product quality, yield, and cycle times meet expectations.
Issue Resolution: Identify and resolve production issues during development and transfer phases.
Compliance: Ensure compliance with quality and regulatory standards.
Continuous Improvement: Implement continuous improvement practices to enhance production efficiency and product quality.
Requirements:
Education:
CQE or B.sc in quality engineering.
Bachelors degree in mechanical, Electrical, Industrial Engineering, or a related field advantage.
Minimum 3 years of experience in NPI or manufacturing engineering, with a focus on transferring products from development to production.
Knowledge of manufacturing processes and materials and familiarity with quality systems and regulatory requirements.
ability to manage multiple projects simultaneously.
Strong problem-solving and analytical abilities (8D /A3 method)
Interpersonal and communication skills.
Familiarity with ISO 9001 and /or AS9100.
Certified internal auditor - advantage
Complete Control of MS Office with advanced Excel Skills
ERP / PLM knowledge.
Fluent Hebrew and English (Reading, Writing and Speaking)
Preferred Qualifications:
Experience in industries such as electronics and mechanics and multidi
This position is open to all candidates.
 
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הגשת מועמדות
עדכון קורות החיים לפני שליחה
8214280
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חברה חסויה
Location: Tel Aviv-Yafo
Job Type: Full Time
We are seeking a highly motivated and experienced Production and Quality Engineer to join our dynamic team. This is a critical, cross-functional role focused on ensuring the sustained and scalable production of our innovative device, while maintaining the highest standards of product quality, process readiness, and production continuity.
As a Production and Quality Engineer, you will be instrumental in bridging the gap between design and manufacturing, owning key engineering tasks across mechanical, electrical, and system-level components. This includes vital responsibilities such as Bill of Materials (BOM) validation, robust test system support, and seamless interface with our contract manufacturers (CMs). You will also play a pivotal role in supporting crucial New Product Introduction (NPI) activities.
Key Responsibilities:
Production Engineering:
Maintain and update the production tree (BOM structure) for the device and all associated hardware and accessories.
Proactively ensure that all products can be manufactured with a minimum of two approved BOM alternatives, strategically mitigating single-point-of-failure risks.
Define, develop, and provide comprehensive support for production test systems, fixtures, and calibration protocols, while continuously improving production costs and efficiency.
Develop clear and precise production instructions to support manufacturing across all production sites.
Act as the primary interface with production partners, implementing manufacturing best practices and swiftly resolving production-related issues.
Quality Engineering:
Lead investigations and resolve production and field quality issues through rigorous root cause analysis and the implementation of effective corrective action plans (CAPAs).
Define, implement, and continuously monitor quality control protocols, test methods, and inspection guidelines to uphold product excellence.
Maintain traceability and comprehensive documentation for all production and Quality Assurance (QA) processes.
Engineering & Change Management:
Lead the efficient execution of Engineering Change Orders (ECOs) and maintain precise SKU/version management for all products.
Coordinate seamlessly with engineering, logistics, and suppliers to ensure the effective and timely rollout of all changes.
Provide essential support for the launch and configuration of accessory SKUs and bundles as required.
Production Risk Mitigation:
Proactively identify and address risks associated with single-source components, tools, materials, and other critical aspects of the production process.
Work collaboratively to define and qualify alternative components and production paths to ensure continuity.
Plan and manage the tooling roadmap to strategically support future production scalability.
Cross-Functional Support:
Collaborate closely with hardware engineering, supply chain, and logistics teams to ensure optimal production alignment and efficiency.
Provide robust support for internal and external operations projects.
Requirements:
5+ years of hands-on experience in production engineering, quality engineering.
Strong, proven understanding of Bill of Materials (BOMs), Engineering Change Orders (ECOs), production test processes, and successful collaboration with Contract Manufacturers (CMs).
Familiarity with established quality systems (e.g., ISO 9001, ISO 13485) and proficient in failure analysis techniques.
Demonstrated ability to manage complex cross-functional technical projects and communicate clearly and effectively with diverse stakeholders.
Fluent in English, with excellent organizational and meticulous documentation skills.
"Startup-ready" mindset: Comfortable working independently, managing multiple priorities, and thriving across disciplines in a fast-paced, dynamic environment.
Familiarity with medical 510K Class I or II - An advantage.
Hands-on experience with test fixtures, calibration tools, and factory bring-up - An advantage.
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8200145
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Location: Tel Aviv-Yafo
Job Type: Full Time
a fast-growing medical technology company transforming the fields of hematology and cell morphology analysis. As a team, we work to enable faster, earlier detection and diagnosis of blood-related diseases, so patients can start treatment sooner and have better outcomes. We are collaborative and global and every individual at is part of a life-saving mission.
About the job
We are looking for a Quality Assurance Compliance Specialist to join our compliance and RA team, which plays a central role in both pre-market and post-market activities. The team is responsible for regulatory activities, quality management system, and ensuring compliance with applicable standards, including those related to privacy.

The Quality Assurance Compliance Specialist will play an important role in the companys regulatory, quality and compliance activities, such as ensuring compliance with relevant quality standards (including ISO 13485:2016, 21 CFR 820, MDSAP and IVDR); supporting internal audits, corrective efforts and different quality projects; and defining quality procedures, protocols and tools.

What youll be doing
Provide ongoing support for the companys quality management activities, including SDLC, PMS, product investigation, operations, training management, supplier management, and document control
Maintain the companys quality management system (QMS)
Evaluate and address quality assessment related to customer complaints
Prepare and maintain technical documentation in compliance with standards such as ISO 13485, 21 CFR 820, and IVDR
Collaborate with cross-functional teams, including R&D, product development, and technical support on quality-related activities
Perform privacy-related tasks, such as evaluating suppliers for privacy compliance and reviewing data processing agreements (DPAs)
Analyze post-market surveillance data to support company initiatives
Prepare teams for internal and external audits
Requirements:
Bachelor's degree in industrial engineering, biotechnology engineering, life science/exact science, or law
At least 5 years of experience working with the QMS of a medical device company, including development, implementation, or compliance with standards such as ISO 13485 and FDA regulations
Understanding of QA processes and methodologies (ISO 13485:2016, 21 CFR 820 or similar)
Understanding of privacy requirements such as HIPAA, GDPR and ISO27799
Ability to collaborate effectively with cross-functional teams to achieve quality objectives
A motivated, collaborative, and proactive approach to work
Team orientation
Excellent communication skills (both written and verbal)
Strong attention to detail
Ability to lead and implement processes
English proficiency
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8170674
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חברה חסויה
Location: Tel Aviv-Yafo
Job Type: Full Time
a fast-growing medical technology company transforming the fields of hematology and cell morphology analysis. As a team, we work to enable faster, earlier detection and diagnosis of blood-related diseases, so patients can start treatment sooner and have better outcomes. We are collaborative and global and every individual at is part of a life-saving mission.

About the job
We are looking for a compliance analyst to join our compliance and RA team, which plays a central role in both pre-market and post-market activities. The team is responsible for regulatory activities, quality management system, and ensuring compliance with applicable standards, including those related to privacy.

The analyst will play an important role in the companys regulatory, quality and compliance activities, such as ensuring compliance with relevant quality standards (including ISO 13485:2016, 21 CFR 820, MDSAP and IVDR); supporting internal audits, corrective efforts and different quality projects; and defining quality procedures, protocols and tools.

What youll be doing
Provide ongoing support for the companys quality management activities, including SDLC, PMS, product investigation, operations, training management, supplier management, and document control
Maintain the companys quality management system (QMS)
Evaluate and address quality assessment related to customer complaints
Prepare and maintain technical documentation in compliance with standards such as ISO 13485, 21 CFR 820, and IVDR
Collaborate with cross-functional teams, including R&D, product development, and technical support on quality-related activities
Perform privacy-related tasks, such as evaluating suppliers for privacy compliance and reviewing data processing agreements (DPAs)
Analyze post-market surveillance data to support company initiatives
Prepare teams for internal and external audits
Requirements:
Bachelor's degree in industrial engineering, biotechnology engineering, life science/exact science, or law
At least three years of experience working with the QMS of a medical device company, including development, implementation, or compliance with standards such as ISO 13485 and FDA regulations
Understanding of QA processes and methodologies (ISO 13485:2016, 21 CFR 820 or similar)
Understanding of privacy requirements such as HIPAA, GDPR and ISO27799
Ability to collaborate effectively with cross-functional teams to achieve quality objectives
A motivated, collaborative, and proactive approach to work
Team orientation
Excellent communication skills (both written and verbal)
Strong attention to detail
Ability to lead and implement processes
English proficiency
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8170342
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6 ימים
חברה חסויה
Location: Netanya
Job Type: Full Time
we are a global pioneer of RADAR systems for active military protection, counter-drone applications, critical infrastructure protection, and border surveillance. We are seeking for a skilled and dedicated Quality Engineer to oversee quality assurance processes for products in the development phase. The ideal candidate will have a strong technical background and experience in ensuring compliance with industry standards while driving continuous improvement in product quality.
Key Responsibilities:
Develop and implement comprehensive quality plans and strategies to ensure products meet specified standards throughout the development lifecycle.
Define and monitor Key Performance Indicators (KPIs) and Key Goal Indicators (KGIs) to measure product quality.
Create and maintain essential quality documentation, including test cases, test plans, validation records, and other quality-related reports.
Lead quality-related aspects during key phases of the development lifecycle, such as SRR, PDR, CDR, TRR, and PRR.
Identify areas for process improvement and collaborate with development teams to enhance product quality and reliability.
Assess potential risks and implement mitigation strategies to ensure product integrity and compliance.
Work closely with developers, designers, project managers, and other stakeholders to integrate quality assurance into all stages of product development.
Investigate the root causes of defects or quality issues and implement corrective and preventive measures to avoid recurrence.
Ensure that products comply with relevant industry standards, regulations, and certifications, particularly AS9100.
Oversee global configuration management processes during the development cycle, including chairing Change Control Board (CCB) meetings.
Conduct Failure Mode and Effects Analysis (FMEA) and implement recommendations to reduce risks and improve product reliability.
Execute comprehensive quality tests during the development cycle and approve validation and verification processes to confirm compliance and performance.
Comprehensive expertise in safety systems throughout the development lifecycle.
Requirements:
Experience
Proven experience of at least 3 years as a quality engineer in product development of complex hardware-based systems regulated under AS9100 standard requirements.
Knowledge of quality control tools and methodologies like Six Sigma, FMEA (Failure Mode and Effects Analysis), and SPC (Statistical Process Control)
Proven experience in NPI methodologies
Basic project management skills to plan and execute quality assurance activities within project timelines.
Education
Bachelors Degree (as a minimum) in Engineering (Electronics / Mechanics / Electronics / Mechanics / Another related field)
CQE advantage
Other skills
Effective communication and collaboration skills to work with design engineers, manufacturing teams, and other stakeholders.
Attention to detail, critical thinking, and a commitment to quality and safety.
Strong documentation skills for creating test plans, test reports, and quality records.
Additional Skills
Familiarity with advanced quality assurance tools and the latest industry best practices.
Ability to work in a dynamic and multidisciplinary team environment.
This position offers an opportunity to contribute to the development of cutting-edge technologies while ensuring the highest quality standards are maintained. If you are passionate about quality engineering and have the skills and experience we are looking for, we encourage you to apply.
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8211053
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25/05/2025
חברה חסויה
Location: Tel Aviv-Yafo
Job Type: Full Time
Gauzy (NASDAQ: GAUZ) is a world-leading material science company, focused on the research, development, manufacturing, and marketing of vision and light control technologies that support safe, sustainable, comfortable, and agile user experiences across various industries. We are seeking an experienced Quality Assurance Manager to lead our quality initiatives and ensure compliance with global standards. This role is integral to maintaining our high manufacturing standards, driving continuous improvement, and collaborating with cross-functional teams to enhance product quality and performance. Joining Gauzy means becoming part of a cutting-edge, fast-growing company that values innovation, excellence, and teamwork in shaping the future of smart materials. *** Please send a copy of your CV in English.

Responsibilities:

* Drive quality performance and continuous improvement across the organization.
* Develop and implement product quality assurance strategies across all development phases.
* Define QA compliance objectives and ensure adherence to international standards (ISO 9001, VDA 6.3, IATF 16949).
* Establish quality control methods, documentation, and risk management practices (FMEA, APQP, PPAP, SPC, MSA).
* Investigate root causes of deviations with R&D and production teams, ensuring corrective actions.
* Oversee supplier evaluations, internal audits, and customer compliance audits.
* Train and supervise technical staff in quality processes, testing, and reporting.
* Serve as the product safety representative and liaise with global quality teams.
* Prepare for and manage internal, customer, and certification audits.
* Willingness to travel internationally when required.
Requirements:
* Minimum of 5 years of quality assurance experience in production processes within a manufacturing company
* Experience in implementing and managing quality assurance metrics
* Familiarity with ISO 9001:2015 regulations, automotive industry standards (IATF 16949, VDA 6.3), CAPA, and automotive core tools (e.g., FMEA, APQP, PPAP, SPC, MSA)
* Excellent problem-solving, interpersonal communication, and project management skills (8D, Ishikawa, 5W)
* Ability to lead cross-functional organizational processes
* Certified 1st and 2nd party auditor for IATF 16949; VDA 6.3 auditor certification preferred
* Strong technical skills
* Proficiency in Microsoft Office tools, particularly Excel
* High proficiency in written and spoken English **This position is hybrid: 4 days from the office and 1 day from home**
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8092785
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28/05/2025
חברה חסויה
Location: Netanya
Job Type: Full Time
Required Quality Engineer
Department: QA
Reporting to: Operation QA Team leader
General Description:
Quality Engineer is responsible for identifying, analyzing, and correcting failures in products and processes. This role involves close collaboration with Development, Engineering, Production, and Customer service teams to ensure product and service quality.
Responsibilities:
FRACAS Management
Conduct failure analysis for products and processes.
Recommend and implement corrective actions to resolve identified failure modes.
Develop and implement quality control processes for continuous improvement.
Collaborate with cross-functional teams (e.g., design, manufacturing, quality) to understand the issues.
Prepare failure analysis reports and present findings to management.
Follow up on the effectiveness of corrective actions and make adjustments as necessary.
Participate in internal and external Quality audits.
Support the approval processes for new products.
Maintain detailed reports of failure investigations, findings, and corrective actions taken.
Identify opportunities for process or design improvements based on failure trends.
Analyzing Quality trends: Quality Yield , KPIs , CoPQ (Costs of Poor Quality), Customers Rating, RMA, ,Quarterly data analysis for QBR
Investigate and analyze product failures, identifying root causes using techniques such as root cause analysis (RCA), fault tree analysis (FTA), or failure mode and effect analysis (FMEA).
Requirements:
Education Quality / Electronic / Industrial / Mechanical practical engineer or engineer
3-5 years experience QA Engineer in failure analysis management or a similar role.
Knowledge of manufacturing processes (Mechanical, Electronics and Electro-mechanics) and of failure analysis methodologies (such as FMEA, RCA).
Ability to analyze data and draw conclusions.
Strong communication skills to interface with production, product development, program managers, project managers, engineering and supply chain.
Experienced with ERP and PLM systems
Excellent communication skills and ability to work in a team.
Proficiency in data analysis software and quality control tools.
Experience in developing multidisciplinary products an advantage
Hands-on approach with a strong understanding of practical application of failure analysis methods.
Passion for improving product quality and contributing to overall business success.
Languages: Hebrew high level, English- high level. Knowledge of other languages is advantage.
Knowledges: AS9100D is advantage
IPC-610 / IPC-620 , CQE , Internal & External auditor course is advantage
Additional Skills:
Problem-solving ability and creative thinking.
Attention to detail and ability to work under pressure.
Willingness to continuously learn and stay updated with new technologies.
High level understanding of cross organization processes
Assertiveness skills.
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8197344
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תודה על שיתוף הפעולה
מודים לך שלקחת חלק בשיפור התוכן שלנו :)
6 ימים
חברה חסויה
Location: Netanya
Job Type: Full Time
we are a global pioneer of RADAR systems for active military protection, counter-drone applications, critical infrastructure protection, and border surveillance. We are looking for a motivated and experienced Supplier Quality Engineer to join our team!
As a Supplier Quality Engineer, you will be responsible for managing supplier programs for manufacturing and ensuring that quality programs follow regulatory requirements.
Supplier Quality Engineer duties and responsibilities
Driving supplier quality performance, including new product development and product quality improvement
Providing leadership and management for the supplier quality department
Ensuring the supplier meets all regulatory and company requirements.
Performing quality system audits
Establishing quality control objectives & Maintaining supplier quality records
Promoting initiatives to improve quality.
Requirements:
Minimum of a bachelors degree in a related field (Mechanic / Quality)
Relevant education in quality CQE/CQM- advantage
Familiarity with mechanics production standards and special processes, paint and coating
Strong problem-solving skills
Minimum of 3 years of experience in a similar role
Strong technical skills
Knowledge and experience reading drawings
Excellent verbal and written communication skills
Excellent analytical skills
Ability to work well in a team environment.
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8211012
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תודה על שיתוף הפעולה
מודים לך שלקחת חלק בשיפור התוכן שלנו :)
6 ימים
Location: Netanya
Job Type: Full Time
we are a global pioneer of RADAR systems for active military protection, counter-drone applications, critical infrastructure protection, and border surveillance. We are looking for a motivated and experienced Global Supplier Quality Engineer to join our team!
As a Global Supplier Quality Engineer, you will be responsible for managing supplier programs for manufacturing and ensuring that quality programs follow regulatory requirements.
Supplier Quality Engineer duties and responsibilities:
Driving supplier quality performance, including new product development and product quality improvement
Providing leadership and management for the supplier quality department
Ensuring the supplier meets all regulatory and company requirements.
Performing quality system audits
Establishing quality control objectives & Maintaining supplier quality records
Promoting initiatives to improve quality.
Requirements:
Supplier Quality Engineer requirements and qualifications:
Minimum of a bachelors degree in a related field
Relevant education in quality CQE/CQM- advantage
Strong problem-solving skills
Minimum of 3 years of experience in a similar role
Strong technical skills
Knowledge and experience reading drawings
Excellent verbal and written communication skills
Excellent analytical skills
Ability to work well in a team environment.
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8211077
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