דרושים » אבטחת איכות QA » Global Suppliers Quality Manager

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3 ימים
Location: Merkaz
Job Type: Full Time
Required Global Suppliers Quality Manager
Job Description
The Global Suppliers Quality Manager is responsible for ensuring the quality and compliance of suppliers across multiple regions. This role involves developing and implementing supplier quality management strategies, conducting audits, improving supplier performance, and collaborating with cross-functional teams to ensure the highest standards in product and service quality. The position requires strong leadership, problem-solving skills, and the ability to drive continuous improvement in global supply chains.
Key Responsibilities
Supplier Quality Management
Manage the team of supplier's quality leaders/engineers globally.
Develop and implement global supplier quality standards, policies, tools and procedures.
Ensure compliance with industry regulations, company standards, and customer requirements.
Oversee supplier qualification and approval processes.
Lead supplier audits, assessments, and corrective action plans.
Establish and monitor key supplier quality performance metrics (KPIs) and scorecards
Lead suppliers PPAP, suppliers' quality manual and SOW.
Manage the suppliers' complaints.
Work with suppliers to develop corrective action plans and drive continuous improvement initiatives
Supplier Performance & Continuous Improvement
Drive supplier performance improvements through data analysis, root cause analysis and corrective and preventive actions.
Implement Lean, Six Sigma, or other quality improvement methodologies.
Work with suppliers to enhance quality control processes and reduce defects.
Collaborate with suppliers to improve manufacturing processes and product reliability.
Cross-Functional Collaboration
Partner with procurement, engineering, R&D and operations to align supplier quality with business objectives.
Support new product development (NPD) by ensuring supplier readiness and quality assurance via PPAP.
Act as the primary liaison between the company and suppliers regarding quality-related issues.
Compliance & Risk Management
Ensure suppliers adhere to global regulatory and quality standards (ISO 9001, REACH/ROSH, etc.).
Identify and mitigate risks in the supplier network.
Develop contingency plans for critical suppliers.
Reporting & Documentation
Maintain accurate supplier quality documentation, including audit reports, quality agreements, SOWs, PPAP and Complaint
Provide regular reports on supplier performance via supplier's scorecard to the supplier.
Provide Monthly report on global supplier's quality team activities and suppliers quality performance.
Requirements:
Bachelor's degree in engineering, Quality Management (master's degree preferred).
7+ years of experience in supplier quality management, preferably in a global manufacturing or supply chain environment.
Strong knowledge of quality management systems (QMS).
Proven ability to lead, influence, and motivate a high-performing team.
Experience with supplier audits, root cause analysis and corrective action plans (RCCA/8D).
Certifications such as Six Sigma, Certified Supplier Quality Professional (CSQP), or Lead Auditor (ISO 9001) are a plus.
Proficiency in quality tools (FMEA, SPC, 8D, PPAP, GR&R).
Willingness to travel to suppliers locally and globally as needed.
Personal Skills & Capabilities
Ability to work across different cultures and time zones.
Strong problem-solving, leadership, and communication skills.
Fast learning capabilities.
Data analysis skills and analytical abilities
Preferred Skills:
Knowledge in different manufacturing processes such as injection, extrusion, construction, electronics, assembly.
Knowledge of ERP/SAP and supplier management software.
This position is open to all candidates.
 
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4 ימים
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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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8182328
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16/06/2025
חברה חסויה
Location: Tel Aviv-Yafo
Job Type: Full Time
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 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 open to all candidates.
 
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8219067
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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 Labs is part of a life-saving mission.

About the job
We are looking for a Senior 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
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עדכון קורות החיים לפני שליחה
8220858
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15/06/2025
Location: Shlomi
Job Type: Full Time
Quality Engineering, Team Leader oversees projects, maintains processes and addresses quality issues by analyzing outcomes and collaborating with teams for effective resolutions. This position will continue the QA routine activities of a working WSS lab and QA duties for future business.

Essential Duties and Responsibilities
Contribute to the development and implementation of quality management programs focusing on continual improvement across various processes.
Create processes to better evaluate, track and trend audit outputs and identify risks/issues and evaluate impact on global quality systems and initiate actions, as needed.
Coordinate communication between internal teams.
Regularly analyze data trends, drive improvements and meet customer expectations through efficient reporting and communication.
Reviews, revises, and creates operating procedures to ensure compliance with all related external requirements, internal procedures or instructions, and the West Quality Manual.
Ability to lead meetings with relevant teams, employees and contractors as necessary to manage changes.
Establishes monthly KPIs and metrics to Quality Leadership.
Drive continuous quality improvement projects across the enterprise for increased compliance and to create efficient use of company resources.
Leading personnel responsible for calibration activities monitoring, calibration reports approvals. Responsible for calibration specifications approval and for reviewing and approving calibration deviations.
Lead the sites device sterilization methods establishment, validation, maintenance and routine controls as the site sterilization SME by verifying that the sterilization methods validation is done according to the applicable standards and regulations. Verify the sterilization methods and risk-based approach are routinely maintained. Address sterilization issues and provide solutions to sterilization challenges. Be a part of the West Global Sterilization Council and provide support to other West CM and Medical device sites with Sterilization issues. Be key focal point with the West IL sterilization service providers related to sterilization matters.
Independently performs supplier audits and corporate facility audits.

Travel Requirements:
20%: Up to 52 business days per year.
Requirements:
Education:
Bachelor's Degree In Engineering or Science required and
Master's Degree In Engineering or Science preferred.
Work Experience:
Minimum 5 years Experience in regulated Quality Assurance / Document/Configuration Control (or a formal education equivalent) required and
Experience with Medical Device Product Development Life Cycle Activities, Verification / Validation Activities, Risk Management, DHF Activities preferred and
Experience with quality systems such as ISO 9001, ISO 15378 and ISO 13485, 21 CFR 820 preferred and
Experience Leading Internal / External Audits, MasterControl, SAP and Share Point preferred and
Experience with customer interface and meeting customer expectations preferred.
Preferred Knowledge, Skills and Abilities:
Ability to work independently, multi-task and thrive in fast-paced environment.
Excellent written and verbal communication skills.
Proficient in statistical software, Windows OS, Microsoft Office Suite including Word, Excel, and Power Point.
Proven knowledge and understanding of the Food and Drug Administration (FDA) 21 CFR 820 and International Organization for Standardization (ISO) ISO 13485.
Familiarity with root cause analysis tools.
Working knowledge of MasterControl and SAP.
Support and contribute in Lean Sigma programs and activities towards delivery of the set target.
Ability to make and implement decisions based on experience and facts as well as provide direction to peers or less experienced team members.
Able to be aware of all relevant SOPs as per Company policy and Quality Manual.
Able to comply with the companys safety policy at all times.
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
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16/06/2025
חברה חסויה
Location: Tel Aviv-Yafo
Job Type: Full Time
We are looking for Quality Manager with a 5 years experience.
This position will be responsible for overseeing the quality within the company, focusing on the development, implementation, and monitoring of quality methodologies and processes.
The role will be hands-on, including internal quality control, supplier audits, development of quality documentation, and management of multidisciplinary processes within the company.
The Quality Manager will work closely with our development & engineers, production, and regulatory teams to ensure compliance with rigorous quality standards.
Key Responsibilities:
Developing Quality Methodology: Develop and implement comprehensive quality methodologies, focusing on multi-disciplinary products (including hardware, electronics, mmechanics and software).
Hands-on Role: Perform independent quality control, design, and manage continuous quality improvement processes.
USO Certification and Quality Control: Ensure compliance with international quality certifications and standards, such as ISO, and specific defense standards (e.g., MIL-STD).
Supplier Audits: Conduct quality audits for suppliers in the hardware and electronics domains, analyze results, and provide recommendations for improvement.
Organizing Proposals and Processes: Define processes for organizing proposals and ensure quality requirements are met during supplier engagement.
Quality Documentation: Create and update technical documents, quality reports, specifications, and standard operating procedures.
Collaboration with Development and Production Teams: Coordinate with development, engineering, production, and regulatory teams to ensure compliance with quality standards.
Failure investigations, PFMEA management, MRB committees, and more.
Requirements:
Education: Bachelors degree in Electronics Engineering, Industrial Engineering, Systems Engineering, or a relevant engineering field.
Professional Experience: At least 5 years of experience in a similar role, particularly in companies developing multi-disciplinary products (hardware, software, and electronics).
Experience in a multidisciplinary manufacturing company Must
Experience in defense Sector in a similar job- Must.
Experience working with strict quality standards and certifications, including defense-specific standards such as MIL-STD, AS9100, or similar.
Quality Certifications: Certifications in quality management (ISO 9001) are a plus.
Project Management Skills: Ability to manage quality-related projects, organize processes, and handle technological challenges.
Technological Skills: Experience with quality management systems, ERP and tools related to hardware and electronics.
Personal Skills: Analytical thinking, problem-solving abilities, ability to work under pressure, and excellent communication skills with internal teams and suppliers.
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
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Location: Shlomi
Job Type: Full Time
We are looking for a Quality Engineering, Team Leader.
Essential Duties and Responsibilities
Contribute to the development and implementation of quality management programs focusing on continual improvement across various processes.
Create processes to better evaluate, track and trend audit outputs and identify risks/issues and evaluate impact on global quality systems and initiate actions, as needed.
Coordinate communication between internal teams.
Regularly analyze data trends, drive improvements and meet customer expectations through efficient reporting and communication.
Reviews, revises, and creates operating procedures to ensure compliance with all related external requirements, internal procedures or instructions, and the Manual.
Ability to lead meetings with relevant teams, employees and contractors as necessary to manage changes.
Establishes monthly KPIs and metrics to Quality Leadership.
Drive continuous quality improvement projects across the enterprise for increased compliance and to create efficient use of company resources.
Leading personnel responsible for calibration activities monitoring, calibration reports approvals. Responsible for calibration specifications approval and for reviewing and approving calibration deviations.
Lead the sites device sterilization methods establishment, validation, maintenance and routine controls as the site sterilization SME by verifying that the sterilization methods validation is done according to the applicable standards and regulations. Verify the sterilization methods and risk-based approach are routinely maintained. Address sterilization issues and provide solutions to sterilization challenges.
Requirements:
Bachelor's Degree In Engineering or Science required and
Master's Degree In Engineering or Science preferred
Work Experience:
Minimum 5 years Experience in regulated Quality Assurance / Document/Configuration Control (or a formal education equivalent) required and
Experience with Medical Device Product Development Life Cycle Activities, Verification / Validation Activities, Risk Management, DHF Activities preferred and
Experience with quality systems such as ISO 9001, ISO 15378 and ISO 13485, 21 CFR 820 preferred and
Experience Leading Internal / External Audits, MasterControl, SAP and Share Point preferred and
Experience with customer interface and meeting customer expectations preferred
Preferred Knowledge, Skills and Abilities
Ability to work independently, multi-task and thrive in fast-paced environment.
Excellent written and verbal communication skills
Proficient in statistical software, Windows OS, Microsoft Office Suite including Word, Excel, and Power Point
Proven knowledge and understanding of the Food and Drug Administration (FDA) 21 CFR 820 and International Organization for Standardization (ISO) ISO 13485.
Familiarity with root cause analysis tools
Working knowledge of MasterControl and SAP
Support and contribute in Lean Sigma programs and activities towards delivery of the set target
Ability to make and implement decisions based on experience and facts as well as provide direction to peers or less experienced team members
Able to be aware of all relevant SOPs as per Company policy and Quality Manual
Able to comply with the companys safety policy at all times.
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
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22/06/2025
חברה חסויה
Location: Netanya
Job Type: Full Time
DRS RADA is a global leader in cutting-edge radar solutions for active military protection, counter-drone systems, critical infrastructure security, and border surveillance. Our mission is to deliver reliable, innovative technologies that safeguard lives and assets. Role Summary: As the Quality Program Manager, you will spearhead the quality assurance strategy across R&D, Product, and Operations, ensuring our systems meet the highest standards of reliability, compliance, and performance. You will lead Quality team, define scalable processes, and drive a culture of continuous improvement in a fast-paced, Agile environment. Key Responsibilities: Strategic Quality Leadership
* Develop and execute the Quality Plan, aligning with program milestones and business objectives.
* Establish KPIs, metrics, and risk-based QA methodologies to monitor product reliability and process adherence.
* Lead internal/external audits and ensure compliance with defense industry regulations. Cross-Functional Collaboration
* Partner with R&D, Product, and Delivery teams to embed QA early in the development lifecycle (SDLC).
* Drive Agile/Scrum QA practices, including CI/CD pipelines, automated testing, and failure analysis.
* Mentor QA teams and engineers, fostering technical growth and accountability. Process Excellence & Innovation
* Design and optimize QA processes for hardware/software integration (e.g., radar systems, embedded software).
* Leverage statistical analysis(e.g., Weibull, MTBF) to predict and improve system reliability.
* Implement corrective/preventive actions (CAPA) based on field data and test results.
Requirements:
Qualifications Education: BSc/McS in Electrical Engineering, Computer Science, Quality Assurance, or related field. Experience:
*  7+ years in QA leadership, preferably in defence, aerospace, or mission-critical systems.
*  Proven track record in QA, reliability engineering, and risk management.
*  Familiarity with radar/RF systems or embedded systems (advantage). Skills:
*  Expertise in quality standards (e.g., AS9100 ,MIL-STD-810).
*  Strong data-driven decision-making and root-cause analysis.
*  Exceptional stakeholder management and cross-team leadership. Why Join DRS RADA?
* Impact cutting-edge defense technologies that protect global security.
* Collaborate with top-tier engineers in a dynamic, innovation-driven environment.
* Competitive compensation, professional development, and mission-driven culture. At DRS RADA , we believe that strong relationships – built on trust, collaboration, and shared purpose – are the foundation of groundbreaking innovation and mission success.
This position is open to all candidates.
 
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22/06/2025
חברה חסויה
Location: Tel Aviv-Yafo
Job Type: Full Time
We are seeking an experienced VP, Verification to lead the Verification Group for Engineering group. The ideal candidate will oversee the testing strategy, planning, and execution of new and existing features to ensure product quality and performance. This role involves managing a group of 50 employees, including group managers and team leaders, collaborating closely with product management and development teams, and ensuring that features are tested thoroughly and efficiently throughout the product lifecycle.

Key Responsibilities:

Lead the methodology to test a scalable, high-performance data platform
Develop complex validation tools in the storage domain: Traffic generation, fault injection and running random loads in scale
Lead a large team: Manage and mentor group manager and team leaders of automation engineers responsible for feature progression testing across products.
Test Strategy Development: Define and implement test strategies, methodologies, and best practices for feature progression testing on storage systems.
Collaboration: Work closely with product management, development, and DevOps teams to ensure test coverage and align QA efforts with product roadmaps and release cycles.
Automation Strategy: Drive the adoption of automation in testing processes, identifying areas for automation and working with the team to implement frameworks.
Reporting and Metrics: Track and report on progress, coverage, defect rates, and other quality metrics to stakeholders.
Risk Management: Identify potential quality risks and implement proactive measures to mitigate issues during testing.
Continuous Improvement: Promote continuous process improvements to enhance testing efficiency, quality, and coverage.
Requirements:
Education: Bachelor's degree in Computer Science, Information Systems, Engineering, or a related field.
Experience: 5+ years in a leadership role, managing or leading QA groups /10+ years of experience in QA on various products .
Technical Skills:
Strong knowledge of storage products (NAS, object storage, etc.) and related technologies.
Experience with test automation tools and frameworks (e.g., Jenkins, Python, etc.).
Familiarity with CI/CD pipelines, build systems, and version control (e.g., Git).
Analytical Skills: Ability to analyze complex systems and define comprehensive validation strategies.
Communication: Excellent verbal and written communication skills for cross-functional collaboration.
Leadership: Proven ability to lead, motivate, and develop high-performing teams.
This position is open to all candidates.
 
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8225415
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2 ימים
חברה חסויה
Location: Haifa
Job Type: More than one
We are looking for a VP Global QA.
The job holders duties and responsibilities include any of the following:
Act as Quality Management Representative
Responsible for the quality management system
Lead the Quality Assurance team
Lead the company to meet its annual quality goals
Lead quality data analysis
Update company management on quality performance and policy implementation
Define and maintain quality aspects processes for relevant quality related activities
Lead and ensure company compliance with quality standards and certifications as required
Lead and prepare the company for internal and external auditing authorities as required
Support company teams with QA requirements and processes
Act as the person responsible for regulatory compliance (PRRC)
Requirements:
Experience of at least 10 years in a similar role in the Medical Device industry
BSC in Engineering or Sciences
Work experience with multi-disciplinary Systems
Regulatory experience with CE and FDA standards
Strong level of English (read, write and verbal skills)
Advantages:
Formal Auditing Conductance training
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8243250
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25/05/2025
חברה חסויה
Location: Tirat Carmel
Job Type: Full Time
The job holder’s duties and responsibilities include any of the following:
* Act as Insightec Quality Management Representative
* Responsible for the Insightec quality management system
* Lead the Quality Assurance team
* Lead the company to meet its annual quality goals
* Lead quality data analysis
* Update company management on quality performance and policy implementation
* Define and maintain quality aspects processes for relevant quality related Insightec activities
* Lead and ensure company compliance with quality standards and certifications as required
* Lead and prepare the company for internal and external auditing authorities as required
* Support company teams with QA requirements and processes
* Act as the person responsible for regulatory compliance (PRRC)

Advantages::

* Formal Auditing Conductance training
Requirements:
* Experience of at least 10 years in a similar role in the Medical Device industry
* BSC in Engineering or Sciences
* Work experience with multi-disciplinary Systems
* Regulatory experience with CE and FDA standards
* Strong level of English (read, write and verbal skills)
This position is open to all candidates.
 
Show more...
הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8181189
סגור
שירות זה פתוח ללקוחות VIP בלבד