Process Engineer jobs in Israel

Process Engineering- מהנדס.ת תהליך - עפולה Job Description An English translation of the job description is provided immediately below the Hebrew version: האגיס®. קוטקס®. דיפנד®. קימברלי-קלארק פרופשנל® המותגים האייקונים שלנו בטוח כבר מוכרים לך - וכך גם לשאר העולם. למעשה, מיליוני א.נשים בעולם משתמשים במוצרי קימברלי-קלארק מדי יום. אנו יודעים שהמוצרים האלה של קימברלי-קלארק לא היו קיימים ללא א.נשים מוכשרים, כמוך. בקימברלי-קלארק תוכלי.י לעבוד עם הצוותים הטובים ביותר שמחויבים לחדשנות, צמיחה והשפעה. יותר מ-150 שנה כחברה מובילה ועדיין - ואנחנו תמיד מחפשים דרכים טובות יותר להמשיך ולצמוח – אז יש כאן דלת פתוחה להזדמנות, הכול כאן עבורך הכול מתחיל בך. תחומי אחריות עקריים: • הבטחת תפעול יעיל ועמידה ביעדי היצור: איכות בתהליך ובתוצאה, סנטרליין, יעילות, מקצועיות הצוותים בפתרון תקלות • ניהול שינויים ברמה יום יומית- עדכון וניהול סנטרליין, עדכון וניהול חילופי מוצר. • תיעוד תהליכים · • טיוב תהליכים – חילופי מוצר, טיפולים, שגרות עבודה וכיוצא בזה. • ניהול מקצועי של צוות אנשי התהליך –ליווי , הנחיה לימוד ומשוב. • אחריות ביצועית על הוצאה לפועל ושמירה על הנחיות SetUp. • הובלה והוצאה לפועל של תהליכי שינוי טכנולוגיים ותהליכיים חדשים. • אחראי על יצירה ושימור הקשרים להעברת יידע עם מפעלים אחרים או עם KCI בתחום הטכני. • מתן פתרון תהליכי, שירות וסיוע לאסט לידרים בכל שעות היממה. • אחריות על מעקב צריכות היתר ומציאת פתרונות לטיפול בהם. • במסגרת התפקיד יתכנו תחומי אחריות נוספים שיתווספו בהמשך. דרישות התפקיד: • מהנדס מכונות/ חומרים או כימיה - חובה • 2-3 שנות ניסיון בתעשייה כמהנדס תהליך/כמהנדס מכונות • שליטה באנגלית רמה גבוהה של דיבור, קריאה וכתיבה - חובה • שליטה ברמה גבוהה בתוכנות מחשב , עם דגש על תוכנות אופיס • משרה מלאה א'-ה' , יתכנו קריאות ועבודה בימי שישי. הטבות: אנו מאמינים שהעובדים שלנו הם הנכס הגדול ביותר שלנו, ואנו מחויבים לספק להם את המשאבים שהם צריכים כדי להצליח. אם אתם מחפשים קריירה מתגמלת בחברה שאכפת לה מהעובדים שלה, קימברלי-קלארק הוא המקום בשבילכם. • קליטה לחברה מהיום הראשון • סביבת עבודה תומכת ומתגמלת • סל רווחה - קבלת מוצרי החברה בחינם • חדר אוכל פעיל באתר להגשת מועמדות לחץ/י על כפתור הגשת מועמדות והשלם/י את הגשת המועמדות שלך. צוות הגיוס שלנו יבחן את הבקשה שלך ויהיה איתך בקשר אם נראה שאת/ה מתאים/ה לתפקיד זה. בינתיים, אנו מזמינים אותך להיכנס לאתר אתר הקריירה שלנו, שם תוכל/י למצוא מידע נוסף ומשרות נוספות. האותיות הקטנות: כדי שקימברלי-קלארק תמשיך לצמוח ולשגשג, עלינו להיות ארגון המיישם את הניסיון המגוון של חברי הצוות שלו למותגים שמשפרים את חייהם של אנשים ברחבי העולם. אנו פועלים באופן פעיל לבניית כוח עבודה מגוון המשקף את חוויות הצרכנים שלנו. כאשר את/ה מביא/ה את החשיבה המקורית שלך לקימברלי-קלארק, את/ה תורמ/ת להצלחה המתמשכת שלנו. אנו מחויבים להיות מעסיק שוויוני המאפשר לכל המועמדים המתאימים לקבל הזדמנות להעסקה ללא קשר לגזע, צבע, דת, מין, מוצא לאומי, מצב נכות, מעמד ותיק מוגן, נטייה מינית, זהות מגדרית, גיל, הריון, מידע גנטי, מעמד אזרחי או כל מאפיין אחר המוגן על פי חוק. ההצהרות הנ"ל נועדו לתאר את האופי הכללי ורמת העבודה המבוצעת על ידי עובדים המשויכים לסיווג זה. ההצהרות אינן מיועדות להיחשב כרשימה ממצה של כל החובות, האחריות והכישורים הנדרשים לתפקיד זה. Key Responsibilities • Ensure efficient manufacturing operations and achievement of production targets, including process and product quality, centerline compliance, operational efficiency, and effective troubleshooting capabilities across production teams. • Manage daily process changes, including updating and maintaining centerlines and overseeing product changeovers. • Develop, maintain, and update process documentation and work instructions. • Drive continuous process improvement initiatives, including optimization of product changeovers, maintenance activities, operational routines, and manufacturing procedures. • Provide professional leadership and guidance to Process Technicians and Process Specialists through coaching, training, mentoring, and performance feedback. • Ensure proper execution and compliance with approved setup instructions and standards. • Lead and implement new technological and process improvement initiatives across the manufacturing area. • Establish and maintain knowledge-sharing relationships with other Kimberly-Clark facilities and technical stakeholders to support best-practice adoption. • Provide process engineering expertise, technical support, and problem-solving assistance to Asset Leaders on a 24/7 basis, as required. • Monitor material overconsumption and process losses, identify root causes, and implement corrective actions. • Undertake additional responsibilities and projects as assigned to support business and operational needs. Qualifications & Requirements • Bachelor's degree in Mechanical Engineering, Materials Engineering, Chemical Engineering, or a related engineering discipline – required. • 2-3 years of experience in a manufacturing environment as a Process Engineer or Mechanical Engineer. • Fluent English communication skills, including speaking, reading, and writing – required. • Strong computer skills, including advanced proficiency in Microsoft Office applications. • Full-time position, Sunday through Thursday. Availability for occasional on-call support and Friday work, as business needs require. What We Offer At Kimberly-Clark, we believe our people are our greatest asset. We are committed to providing employees with the resources, support, and opportunities they need to succeed and grow their careers. • Employment with Kimberly-Clark from day one • Supportive, collaborative, and rewarding work environment • On-site cafeteria • Opportunities for professional development and continuous learning • The chance to make a meaningful impact within a global industry-leading organization Primary Location: Afula, Israel Work Arrangement: On-site, Full-Time Kimberly-Clark is an Equal Opportunity Employer and values diversity, inclusion, and respect in the workplace. Primary Location Afula, Israel Additional Locations Worker Type Employee Worker Sub-Type Regular Time Type Full time

Description Eitan Medical is a fast-growing international medical device company that develops and manufactures innovative medical equipment. We are looking for a Process Engineer to join our Manufacturing Engineering team. Job Description: The Process Engineer will lead engineering changes and qualify manufacturing processes - on our production floor and at our subcontractors in Israel and abroad - while providing hands-on technical support to production. · Lead engineering changes (ECOs) end-to-end, from definition and impact assessment, through implementation on the production floor, to formal closure. · Plan and execute process verification and validation activities, including IQ/OQ/PQ protocols and reports. · Lead process qualification at subcontractors in Israel and abroad, including new and replaced equipment and production lines. · Support injection molding activities: DFM reviews with the molder, mold qualification and evaluation of samples. · Provide hands-on engineering support to production and final test lines, and define jigs, fixtures and process parameters. · Conduct technical investigations and root cause analysis as part of the NCMR process, and drive corrective actions to closure. · Develop, improve and optimize manufacturing and assembly processes, based on production and yield data. · Work closely with Production, Quality, Regulatory, R&D and Purchasing, and manage internal and external stakeholders. Direct Manager: Engineering Manager. Requirements Must Have: · B.Sc. in Engineering - mandatory; Mechanical Engineering - preferred. · 3-5 years of experience in Process Engineering, Manufacturing Engineering, or a similar production engineering role. · Proven experience leading engineering/process changes end-to-end, from definition through implementation and closure. · Experience with process verification, validation, or qualification activities. · Experience working with external suppliers and subcontractors. · Strong understanding of manufacturing and assembly processes, and proven hands-on experience supporting production. · Practical experience using measurement tools and equipment, and the ability to analyze data. · Strong problem-solving, investigation, and root cause analysis capabilities. · Fluent English - written and verbal, including technical writing Advantages: · Experience in the medical device industry. · Familiarity with FDA, ISO 13485, or other regulated manufacturing environments. · Experience with formal process validation protocols and reports (IQ/OQ/PQ). · Experience with manufacturing technologies such as injection molding, sheet metal & machining processes. · Experience working with, or qualifying processes at, overseas suppliers and subcontractors. · SolidWorks/PDM experience and the ability to read mechanical drawings. · Experience with eQMS systems. · Experience with Lean Manufacturing / Continuous Improvement methodologies. Computer Skills: · Proficiency in Microsoft Office applications, with a good level of Excel for data analysis. Personal Skills: · Strong technical and analytical capabilities. · Hands-on, practical, and solution-oriented approach. · Ability to lead cross-functional processes and drive stakeholders to deliver. · Excellent interpersonal and communication skills. · Self-motivated and independent. · Ability to manage multiple priorities and work effectively under pressure. · Team player with a proactive and continuous-improvement mindset.

Company Overview KLA is a global leader in diversified electronics for the semiconductor manufacturing ecosystem. Virtually every electronic device in the world is produced using our technologies. No laptop, smartphone, wearable device, voice-controlled gadget, flexible screen, VR device or smart car would have made it into your hands without us. KLA invents systems and solutions for the manufacturing of wafers and reticles, integrated circuits, packaging, printed circuit boards and flat panel displays. The innovative ideas and devices that are advancing humanity all begin with inspiration, research and development. KLA focuses more than average on innovation and we invest 15% of sales back into R&D. Our expert teams of physicists, engineers, data scientists and problem-solvers work together with the world’s leading technology providers to accelerate the delivery of tomorrow’s electronic devices. Life here is exciting and our teams thrive on tackling really hard problems. There is never a dull moment with us. Job Description/Preferred Qualifications • The Customer Acceptance (CA) team plays a critical role in driving customer success. The team is responsible for the full qualification and on-time delivery of KLA tools to leading semiconductor customers worldwide, including Intel, Samsung, TSMC, and others. Key Responsibilities • Lead and execute tool qualification in accordance with customer specifications and acceptance criteria • Perform comprehensive data analysis and manage large, complex datasets to support qualification decisions • Proactively identify, troubleshoot, and resolve HW, application, and quality issues • Drive execution within predefined schedules, ensuring alignment with customer expectations and delivery commitments Minimum Qualifications Qualifications & Skills • BA/ BSc in Statistics/Information Systems, Practical Engineer in Electronics or a related field • Strong proficiency in Excel; experience with JMP and Python – an advantage • High level of English proficiency (written and verbal) • Shown ability to work with and analyze large datasets • Fast learner with a strong analytical mindset • Team player with strong collaboration skills • Ability to work under pressure and meet tight deadline We offer a competitive, family friendly total rewards package. We design our programs to reflect our commitment to an inclusive environment, while ensuring we provide benefits that meet the diverse needs of our employees. KLA is proud to be an equal opportunity employer Be aware of potentially fraudulent job postings or suspicious recruiting activity by persons that are currently posing as KLA employees. KLA never asks for any financial compensation to be considered for an interview, to become an employee, or for equipment. Further, KLA does not work with any recruiters or third parties who charge such fees either directly or on behalf of KLA. Please ensure that you have searched KLA’s Careers website for legitimate job postings. KLA follows a recruiting process that involves multiple interviews in person or on video conferencing with our hiring managers. If you are concerned that a communication, an interview, an offer of employment, or that an employee is not legitimate, please send an email to [email protected] to confirm the person you are communicating with is an employee. We take your privacy very seriously and confidentially handle your information.

Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact. A Day in the Life Join our engineering team as a Senior Process Engineer and help drive meaningful improvements across our manufacturing operations. In this role, you will identify opportunities to enhance efficiency, quality, and safety while working closely with cross-functional teams to solve problems and optimize processes. This is an exciting opportunity for a motivated engineer who enjoys hands-on impact, continuous improvement, and contributing to a high-performing environment. If you are looking for a role where your ideas can make a real difference, we encourage you to apply. This position is on-site working based at Medtronic Yokneam, You will report to the engineering manager and collaborate regularly with teams across production, quality, maintenance, and operations. Some travel may be required to support other sites, project work, or training initiatives. The role offers the chance to work in a fast-paced environment with strong opportunities for learning, development, and career growth. Responsibilities may include the following and other duties may be assigned: • Responsible for all manufacturing processes on production floor, pFMEA, Equipment URS, Working instructions, test methods, Support production training, Define Packaging instructions. Project management skills, Responsible for timelines, Scop of work, Budget • Design and develop jigs, fixtures, and other manufacturing support tools for medical device assembly and testing. Designs manufacturing processes, procedures and production layouts for assemblies, equipment installation, processing, machining and material handling. Designs arrangement of machines within plant facilities to ensure most efficient and productive layout • Designs sequence of operations and specifies procedures for the fabrication of tools and equipment and other functions that affect product performance. Develops manufacturing processes that are applicable to statistical process control, and may develop those techniques • Provides guidance to engineering regarding design concepts and specification requirements to best utilize equipment and manufacturing techniques. Ensures processes and procedures are following regulations. Monitors documentation maintenance throughout all phases of product lifecycle • Drives a continuous improvement mindset by engraining and improving the MPS (Medtronic Performance System) methodologies in the day-to-day. Main contact with Operations Innovation and region improvement team. Execute Improvement in Yokneam Operations KPIs (Yields, Scrap, Quality, Safety, OEE) • Acts as a partner with mainly production and Quality operations and other functions in Operations and R&D sustain team. Required Knowledge and Experience: • B.Sc. degree in Mechanical Engineering or another relevant manufacturing-focused engineering field • Minimum of 5 years of experience in manufacturing engineering within the medical device, pharmaceutical, or process industries – a significant advantage • Strong problem-solving and execution abilities • Written and verbal communication skills in English - Must • Proactive approach including Interface management to delivers value; Full responsibility for the delivery of outputs, including supporting documentation; a "Big-picture" mindset, including influence and communication skills. Preferred Qualifications: • Certifications such as Six Sigma/Green belt or Lead Auditor (ISO 13485) are a plus • Sold work skills- advantage • Graduate of a management course. Physical Job Requirements The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.  ‌ ‌ Recruitment Fraud Alert We are aware of phishing scams targeting job seekers. Please keep the following in mind: Apply only through official Medtronic channels. All legitimate Medtronic recruiting communications come from approved Medtronic platforms and official @medtronic.com email addresses. Medtronic will never ask for payment or sensitive personal information (such as bank account or Social Security details) during early stages of the hiring process. Any such requests are not legitimate. If you receive a suspicious message claiming to be from Medtronic, do not respond, click links, or open attachments. If you have any questions, concerns regarding the authenticity of a communication alleged to have been made by or on behalf of Medtronic, please contact us immediately at [email protected]. Benefits & Compensation Medtronic offers a competitive Salary and flexible Benefits Package A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage. This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).

Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact. A Day in the Life Join our engineering team as a Process Engineer and help drive meaningful improvements across our manufacturing operations. In this role, you will lead opportunities to enhance efficiency, quality, and safety while working closely with cross-functional teams to solve problems and optimize processes. This is an exciting opportunity for a motivated engineer who enjoys hands-on impact, continuous improvement, and contributing to a high-performing environment. If you are looking for a role where your ideas can make a real difference, we encourage you to apply. This position is on-site working based at Medtronic Yokneam. You will report to the engineering manager and collaborate regularly with teams across production, quality, maintenance, and operations. Some travel may be required to support other sites, project work, or training initiatives. The role offers the chance to work in a fast-paced environment with strong opportunities for learning, development, and career growth. Primary Responsibilities • Responsible for all manufacturing processes on production floor, pFMEA, Equipment URS, Working instructions, test methods, Support production training, Define Packaging instructions; Ensures processes and procedures are following regulations; Monitors documentation maintenance throughout all phases of product lifecycle. • Project management skills, Responsible for timelines, Scop of work, Budget. • Implement jigs, fixtures, and other manufacturing support tools for medical device assembly and testing. • Improve manufacturing processes, procedures and production layouts for assemblies, equipment installation, processing, machining and material handling; Review arrangement of machines within plant facilities to ensure most efficient and productive layout. • Designs sequence of operations and specifies procedures for the fabrication of tools and equipment and other functions that affect product performance. • Support manufacturing processes that are applicable to statistical process control, and may develop those techniques; Issue specification requirements to best utilize equipment and manufacturing techniques. • Drives a continuous improvement mindset by engraining and improving the MPS (Medtronic Performance System) methodologies in the day-to-day; Execute Improvement in Yokneam Operations KPIs (Yields, Scrap, Quality, Safety, OEE). • Acts as a partner with mainly production and Quality operations and other functions in Operations and R&D sustain team. Required Qualifications • B.Sc. degree in Mechanical Engineering or another relevant manufacturing-focused engineering field. • Minimum of 3 years of experience in manufacturing engineering within the medical device, pharmaceutical, or process industries. • Written and verbal communication skills in English. • Strong problem-solving and execution abilities. • Proactive approach; Full responsibility for the delivery of outputs, including supporting documentation; a "Big-picture" mindset. including influence and communication skills. Preferred Qualifications • Certifications such as Six Sigma/Green belt or Lead Auditor (ISO 13485). • Sold work skills. Physical Job Requirements The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.  ‌ ‌ Recruitment Fraud Alert We are aware of phishing scams targeting job seekers. Please keep the following in mind: Apply only through official Medtronic channels. All legitimate Medtronic recruiting communications come from approved Medtronic platforms and official @medtronic.com email addresses. Medtronic will never ask for payment or sensitive personal information (such as bank account or Social Security details) during early stages of the hiring process. Any such requests are not legitimate. If you receive a suspicious message claiming to be from Medtronic, do not respond, click links, or open attachments. If you have any questions, concerns regarding the authenticity of a communication alleged to have been made by or on behalf of Medtronic, please contact us immediately at [email protected]. Benefits & Compensation Medtronic offers a competitive Salary and flexible Benefits Package A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage. ‌ This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).