Quality Control Manager jobs in Israel

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com. As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit. Job Function: Quality Job Sub Function: Quality Control Job Category: People Leader All Job Posting Locations: Kiryat-Ono, Tel Aviv District, Israel Job Description: About Surgery Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments. Are you passionate about improving and expanding the possibilities of surgery? Ready to join a team that’s reimagining how we heal? Our Surgery team will give you the chance to deliver surgical technologies and solutions to surgeons and healthcare professionals around the world. Your contributions will help effectively treat some of the world’s most prevalent conditions such as obesity, cardiovascular disease and cancer. Patients are waiting. Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech Join us in a key leadership role where quality, innovation, and operational excellence come together. As a QC Team Leader, you will lead the daily operations of our Quality Control laboratory, ensuring the timely and compliant testing of raw materials, in-process materials, and finished products while supporting manufacturing and product release activities. You will manage laboratory priorities, mentor and develop a team of analysts, drive investigations and troubleshooting efforts, and collaborate closely with Production, Quality Assurance, and R&D to ensure the highest quality standards are consistently achieved. ***This is a temporary role through early 2028. Key Responsibilities • Lead and coordinate day-to-day QC laboratory operations, including raw material testing activities. • Set laboratory priorities, allocate resources effectively, and support employee development and training. • Review analytical results, laboratory records, and compliance documentation to support product release. • Lead laboratory investigations, deviations, OOS/OOT events, and root cause analyses, ensuring timely closure and implementation of corrective actions. • Drive data trending, performance monitoring, and continuous improvement initiatives to enhance laboratory efficiency and compliance. • Support analytical method validation, verification, transfer, and implementation activities. • Ensure compliance with GMP, regulatory requirements, safety standards, and company quality procedures. • Troubleshoot analytical methods, laboratory equipment, and process-related issues, providing technical leadership and guidance to the team. • Collaborate cross-functionally with Manufacturing, QA, RA, and R&D to support operational and business objectives. • Maintain laboratory readiness for internal and external audits and inspections. Hands-On Leadership This role combines people leadership with strong technical involvement. While focused on managing laboratory operations, the QC Team Leader is expected to remain closely connected to laboratory activities and may occasionally perform hands-on testing, support investigations, and assist during periods of high workload. Qualifications & Requirements Education • Bachelor's degree in Chemistry, Life Sciences, Medical Laboratory Sciences, Biotechnology, or a related scientific discipline. Experience • 3–5 years of experience in a Quality Control laboratory environment. • Mandatory experience working in a GMP-regulated environment. • Previous leadership, supervisory, or team management experience – a significant advantage. • Experience with analytical laboratory techniques and laboratory equipment troubleshooting. • Experience in deviation investigations, root cause analysis, CAPA management, and data review. Skills & Competencies • Strong leadership, coaching, and team development capabilities. • Excellent analytical thinking and problem-solving skills. • Ability to prioritize multiple tasks and manage activities in a fast-paced environment. • Strong communication and cross-functional collaboration skills. • High attention to detail and commitment to quality and compliance. • Continuous improvement mindset with the ability to drive change and operational excellence. What You'll Bring A passion for quality, strong scientific and problem-solving skills, leadership experience in a QC laboratory environment, and a continuous-imvement mindset that inspires others, develops people, and drives results. Required Skills: Preferred Skills:

Job Description Summary The Regional Quality Excellence Manager will be part of the GE Vernova Hydro Power Central Quality organization and will drive the deployment, governance, and effectiveness of Root Cause Analysis (RCA), Continuous Improvement (CI), and Quality Excellence initiatives across Europe region. Reporting to the Global RCA Leader, this role serves as the regional focal point to strengthen problem-solving capabilities, improve quality performance, and drive sustainable corrective and preventive actions. The role is responsible for leading RCA and CI deployment, supporting QMS internal and certification audits, driving execution of the Zero-Defect Framework, and ensuring governance of Lessons Learned (LL), Customer Experience (CX), and Voice of Customer (VoC) processes across the region. Working closely with regional and global stakeholders, the role will improve quality maturity, operational excellence, customer satisfaction, and prevention of recurring issues through standardized methodologies, governance, and data-driven decision-making. Job Description Roles and Responsibilities Regional RCA & Continuous Improvement • Serve as the regional focal point for RCA and Continuous Improvement across Europe, ensuring alignment with global quality strategy and governance. • Lead deployment and consistent application of standard RCA methodologies, tools, and problem-solving practices across projects, functions, and operational sites. • Facilitate and support complex root cause investigations for major non-conformities, recurring failures, customer concerns, and critical quality events. • Drive sustainable corrective and preventive actions (CAPA) to reduce recurrence of quality issues and improve operational performance. • Monitor RCA effectiveness, closure of actions, and business impact through defined KPIs and governance mechanisms. Zero Defect Framework Execution • Support deployment and governance of the Hydro Zero Defect Framework across the region. • Ensure implementation of preventive quality methodologies, risk mitigation actions, and process discipline to drive defect prevention and right-first-time execution. • Monitor regional progress, maturity, and effectiveness of Zero-Defect initiatives and support continuous improvement actions. QMS Governance, Internal & Certification Audits • Support execution and governance of the Quality Management System (QMS) within the Europe region, ensuring alignment with internal standards and external regulatory requirements. • Coordinate and support QMS internal audits and certification audits (e.g., ISO 9001) across regional sites and functions. • Ensure timely closure of audit findings, corrective actions, and systemic improvements to strengthen process compliance and quality maturity. • Promote standardization and continuous improvement of quality processes, documentation, and governance practices. Lessons Learned (LL), Customer Experience (CX) & Voice of Customer (VoC) Governance • Drive regional governance and effective deployment of Lessons Learned (LL) processes to strengthen preventive actions and organizational learning. • Support Customer Experience (CX) initiatives by monitoring quality feedback, identifying recurring pain points, and driving improvement actions. • Ensure effective governance and utilization of Voice of Customer (VoC) inputs to improve quality performance, customer satisfaction, and business responsiveness. • Promote cross-functional sharing of best practices, recurring learnings, and systemic improvement opportunities. Quality Performance, Analytics & Reporting • Analyse quality trends, recurring failure patterns, customer feedback, and performance indicators to identify systemic quality drivers and improvement opportunities. • Support regional quality reviews and reporting related to RCA effectiveness, NCR trends, audit findings, customer feedback, and CI performance. • Utilize dashboards, quality metrics, and analytics to support data-driven decision-making and performance improvement. Stakeholder Collaboration & Capability Building • Partner with Quality, Engineering, Project Management, Sourcing, Manufacturing, and Regional Leadership teams to drive effective RCA, CI, and quality governance deployment. • Coach and mentor teams on structured problem-solving methodologies (e.g., 8D, 5 Why, Fishbone, A3, CAPA, Lean Six Sigma tools). • Strengthen regional RCA, audit, and CI capabilities while fostering a proactive quality and continuous improvement culture. Required Qualifications • Bachelor’s degree in Engineering, Quality, Manufacturing, Industrial Engineering, or a related discipline. • min 12+ years of experience in Quality, Root Cause Analysis, Continuous Improvement, Manufacturing, Engineering, Project Quality, or Operational Excellence environments. • Strong expertise in structured problem-solving methodologies (RCA, 8D, CAPA, 5 Why, Fishbone, FMEA, A3, etc.). • Strong knowledge of Quality Management Systems (QMS), ISO 9001, Non-Conformity Management, and Continuous Improvement methodologies. • Experience supporting or leading internal and certification audits within a regulated or industrial environment. • Strong analytical capability to identify trends, systemic issues, and recurring quality drivers using quality metrics and performance data. • Excellent stakeholder management, influencing, and cross-functional collaboration skills in a global environment. • Fluent English communication skills, both verbal and written. • Preferred certifications: Lean Six Sigma Green/Black Belt and/or ISO 9001:2015 Internal Auditor certification Desired Characteristics • Strong problem-solving, process-oriented, and continuous improvement mindset with ability to manage complex quality challenges. • Experience leading regional or cross-functional quality improvement programs. • Good understanding of Cost of Poor Quality (CoPQ), Lessons Learned, Zero Defect methodologies, Customer Experience (CX), and Voice of Customer (VoC) concepts. • Strong operational judgment with ability to influence stakeholders and drive accountability without direct authority. • Experience with quality analytics, dashboards, digital quality systems, and performance reporting. • Ability to work independently, manage multiple priorities, and operate effectively in a fast-paced, matrixed global environment. • Additional European language skills (French, German, Italian, Spanish) would be an advantage. Additional Information Relocation Assistance Provided: No #LI-Remote - This is a remote position

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com. As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit. Job Function: Quality Job Sub Function: Quality Control Job Category: People Leader All Job Posting Locations: Kiryat-Ono, Tel Aviv District, Israel Job Description: About Surgery Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments. Are you passionate about improving and expanding the possibilities of surgery? Ready to join a team that’s reimagining how we heal? Our Surgery team will give you the chance to deliver surgical technologies and solutions to surgeons and healthcare professionals around the world. Your contributions will help effectively treat some of the world’s most prevalent conditions such as obesity, cardiovascular disease and cancer. Patients are waiting. Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech Join us in a key leadership role where quality, innovation, and operational excellence come together. As a QC Team Leader, you will lead the daily operations of our Quality Control laboratory, ensuring the timely and compliant testing of raw materials, in-process materials, and finished products while supporting manufacturing and product release activities. You will manage laboratory priorities, mentor and develop a team of analysts, drive investigations and troubleshooting efforts, and collaborate closely with Production, Quality Assurance, and R&D to ensure the highest quality standards are consistently achieved. ***This is a temporary role through early 2028. Key Responsibilities • Lead and coordinate day-to-day QC laboratory operations, including raw material testing activities. • Set laboratory priorities, allocate resources effectively, and support employee development and training. • Review analytical results, laboratory records, and compliance documentation to support product release. • Lead laboratory investigations, deviations, OOS/OOT events, and root cause analyses, ensuring timely closure and implementation of corrective actions. • Drive data trending, performance monitoring, and continuous improvement initiatives to enhance laboratory efficiency and compliance. • Support analytical method validation, verification, transfer, and implementation activities. • Ensure compliance with GMP, regulatory requirements, safety standards, and company quality procedures. • Troubleshoot analytical methods, laboratory equipment, and process-related issues, providing technical leadership and guidance to the team. • Collaborate cross-functionally with Manufacturing, QA, RA, and R&D to support operational and business objectives. • Maintain laboratory readiness for internal and external audits and inspections. Hands-On Leadership This role combines people leadership with strong technical involvement. While focused on managing laboratory operations, the QC Team Leader is expected to remain closely connected to laboratory activities and may occasionally perform hands-on testing, support investigations, and assist during periods of high workload. Qualifications & Requirements Education • Bachelor's degree in Chemistry, Life Sciences, Medical Laboratory Sciences, Biotechnology, or a related scientific discipline. Experience • 3–5 years of experience in a Quality Control laboratory environment. • Mandatory experience working in a GMP-regulated environment. • Previous leadership, supervisory, or team management experience – a significant advantage. • Experience with analytical laboratory techniques and laboratory equipment troubleshooting. • Experience in deviation investigations, root cause analysis, CAPA management, and data review. Skills & Competencies • Strong leadership, coaching, and team development capabilities. • Excellent analytical thinking and problem-solving skills. • Ability to prioritize multiple tasks and manage activities in a fast-paced environment. • Strong communication and cross-functional collaboration skills. • High attention to detail and commitment to quality and compliance. • Continuous improvement mindset with the ability to drive change and operational excellence. What You'll Bring A passion for quality, strong scientific and problem-solving skills, leadership experience in a QC laboratory environment, and a continuous-imvement mindset that inspires others, develops people, and drives results. Required Skills: Preferred Skills:

Join NVIDIA's outstanding team and contribute to our legacy of innovation in the Senior Product Quality role! At NVIDIA, we are dedicated to pushing the boundaries of pioneering technology. The Senior Product Quality Engineer will provide leadership and management for the Networking system product quality within the organization. Establish, maintain, and optimize an effective quality management methods and target to achieve high quality performance. As part of our team, you will work on networking IC products and ensure their readiness for production stage. Leading and mentoring root cause analysis for issues related to design, manufacturing or customers. Enhance and improve products performance by proactive risk assessment and other prevention methods. This is an outstanding opportunity to be part of a company that is crafting the future of AI and computing. What You'll Be Doing • Integrated Circuits (IC) quality manager will coordinate and lead the quality function and sustain the quality philosophy for the organization. • Establish, maintain and optimize an effective quality management system. • Build and implement a quality plan to achieve the levels of quality established through organizational goals, customer expectations, and related partners. • Improve products by working towards problem-solving tools, prevention methods, quality-at-the-source and continual improvement techniques. • Maintain and improve product build development, verification and validation processes, to allow high quality of interconnects and systems products throughout the entire product life cycle. What We Need to See • Bachelor’s degree or master’s degree or equivalent experience in electrical engineering or material science. Other technical degrees will be considered • Experience: 5+ years preferred in leadership and manufacturing • Knowledge in semiconductor design and process • Strong interpersonal and project management skills • Strong problem-solving skills and analytical ability, processes oriented Ways to Stand Out from the Crowd • Integrator experience in the semiconductor industry • Experience in Silicon Photonics develop and manufacturing • Leadership capabilities

Description The Senior Quality Assurance Manager is responsible for leading all quality, compliance, reliability, testing, and qualification activities across the Foil Division. The role ensures compliance with customer, regulatory, military, and corporate requirements while driving operational excellence, continuous improvement, and customer satisfaction. As a key business partner to Operations, Engineering, R&D, Supply Chain, and Commercial teams, this leader will oversee the Quality Management System, Calibration Laboratory activities, Reliability & Testing Laboratory operations, product qualification activities, and audit readiness across the organization. Please note: This position is focused on Quality Assurance within a manufacturing environment and is not related to Software QA or software testing roles. Key Responsibilities Quality Leadership & Compliance • Lead and manage all Quality Assurance and Quality Control activities across the Foil Division in accordance with local QMS and corporate quality procedures. • Maintain and continuously improve the Quality Management System (QMS) in VFR in accordance with AS9100, MIL-STD-790 and CECC. • Serve as the focal point for certifications, regulatory compliance, customer audits, and quality system assessments. • Ensure ongoing readiness for customers, certification, regulatory, and military audits. • Develop quality strategy, KPIs, and continuous improvement initiatives. Reliability Laboratory & Product Qualification • Lead the Reliability & Testing Laboratory, ensuring resources, capabilities, equipment readiness, and testing performance support business and customer needs. • Lead Maintenance Activities of existing product qualifications (QPL, CECC). • Oversee product qualification, validation, reliability testing, and compliance with customer and industry specifications (MIL-PRF, NASA & ESA, automotive, etc.) • Manage laboratory priorities, personnel, and continuous improvement programs. • Support internal development programs and external customer testing activities. Metrology & Calibration Management • Own the site calibration and metrology systems, ensuring compliance and traceability of measurement and test equipment. • Oversee calibration programs, measurement system effectiveness, and related compliance requirements. Customer & Supplier Quality • Lead customer quality improvement initiatives, complaint resolution (FA , root cause investigations, and corrective actions). • Oversee supplier qualification, supplier performance, audits, and change management processes. • Act as the primary quality representative to customers and external stakeholders. Operational & Organizational Leadership • Drive process improvements that enhance product quality, reliability, efficiency, and customer satisfaction. • Lead, develop, and mentor quality managers, engineers, technicians, and inspectors. • Manage departmental priorities, budgets, resources, and strategic plans. • Collaborate closely with Operations, Engineering, R&D, Supply Chain, and Commercial teams to support business growth and operational excellence. Requirements Education • B.Sc. or M.Sc. in Engineering, Materials Science, Physics, Electronics, Quality Engineering, or a related field. • Quality certifications such as CQE, CQM, Lead Auditor, or equivalent are an advantage. Experience • 8+ years of proven quality leadership experience in a highly regulated manufacturing environment. • Background in aerospace, defense, electronics, precision manufacturing, automotive, medical equipment industries is preferred. • Experience with reliability testing, testing laboratory operations, qualification programs, and metrology systems is an advantage.

We Are Teva We’re Teva, a leading innovative biopharmaceutical company, enabled by a world-class generics business. Whether it’s innovating in the fields of neuroscience and immunology or delivering high-quality medicine worldwide, we’re dedicated to addressing patients’ needs now and in the future. Here, you will be part of a high-performing, inclusive culture that values fresh thinking and collaboration. You'll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together. Our Team, Your Impact The Director, Site Quality Control is responsible for leading and managing all QC laboratory operations at the Kfar Saba site, ensuring testing, release, and analytical activities comply with global regulations, compendial standards, and Teva Quality policies. This role leads a key QC function at one of Teva’s flagship production sites, ensuring compliant supply of high‑quality medicines while shaping global quality outcomes. How You’ll Spend Your Day • Lead all QC laboratory units including Raw Materials QC, Finished Goods QC, , Stability, Analytical Development support and laboratories logistics • Develop QC strategy aligned with site priorities, supply needs, and compliance expectations. • Oversee QC deviations, OOS/OOT investigations, and laboratory CAPAs, ensuring timely closure and robust root cause analysis. • Ensure timely release of RM and FG, manage analytical bottlenecks, backlog reduction, and lab capacity planning. • Ensure audit/inspection readiness and represent QC during regulatory inspections. • Drive QC process optimization, automation, and efficiency improvements. • Partner with QA, MS&T, Engineering, Supply Chain, and R&D on investigations, analytics, and tech transfers. • Lead QC support for new product launches, validation batches, and market supply escalations. • Lead TLMS deployments in all laboratories Your Skills and Experience • Bachelor’s or Master’s degree in Chemistry, Life Sciences, Pharmacy, or related scientific discipline. • 12+ years of progressive QC experience in the pharmaceutical industry. • Significant leadership experience managing QC laboratories in a regulated GMP environment. • Strong understanding of analytical chemistry, microbiology, methods, and compendial standards. • Experience interacting with health authorities (FDA, EMA, EDQM). Also Good to Have • Strong leadership, communication, and stakeholder‑management skills. • Data‑driven decision‑making with focus on performance and reliability. • Excellent problem‑solving and root‑cause analysis abilities. • High resilience and ownership mindset. • Ability to manage multiple priorities in a dynamic, regulated environment. How We’ll Take Care of You At Teva, better health starts from within, and that includes you. From day one, you’ll be supported with benefits designed to help you thrive in and out of work. This includes generous annual leave, reward plans, flexible working schedules (dependent on role), access to tailored health support, and meaningful ways to give back to the community.  When it comes to your career, you’ll be encouraged to explore, evolve, and shape your path. Twist, our one-stop shop for career development platform, gives you access to a wide range of possibilities, from learning programs and short-term projects to opportunities for internal growth. Here, you’ll be part of a culture that empowers you to reach your goals and prioritize your wellbeing every step of the way.  Reports To Sr Director, Site Quality Head – Kfar Saba Already Working @TEVA? Make sure to apply through our internal career site on Twist—your one-stop shop for career development Teva’s Equal Employment Opportunity Commitment Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.