משרות והצעות עבודה

The opportunity: As an R&D Engineer, you will play a key role in the development of innovative medical devices for minimally invasive surgical and radiation oncology procedures. Working as part of a multidisciplinary R&D team, you will contribute to all stages of the product development lifecycle, from concept evaluation and design verification to validation and regulatory documentation. This is an exciting opportunity to combine hands-on engineering, technical problem-solving, and cross-functional collaboration while helping bring cutting-edge technologies to patients worldwide. In this position you will be asked to: • Contribute to the development of innovative medical devices throughout the entire product development lifecycle. • Design, execute, and document verification and validation activities to ensure product performance and quality. • Develop engineering solutions, evaluate design alternatives, and support technical risk management. • Collaborate with cross-functional teams, suppliers, manufacturers, and external development partners. • Prepare technical documentation in compliance with FDA Design Controls and support regulatory submissions. • Contribute to continuous product improvement, innovation, and intellectual property activities.

This is an independent, individual contributor role (no direct people management) for a highly skilled QA/RA professional. Responsibilities: • Maintain, implement, and continuously improve the company Quality Management System in accordance with applicable regulatory and quality requirements. • Manage document control, change control, eviations/nonconformances, CAPA, and complaints. • Lead or support internal audits, supplier audits, regulatory inspections, and external certification audits. • Support design and development activities to ensure appropriate implementation of design controls, risk management, verification and validation, and software lifecycle requirements. • Support Regulatory Affairs activities, including preparation and submission of regulatory documentation to applicable authorities. • Assess product, software, labeling, manufacturing, and process changes for potential quality and regulatory impact and ensure appropriate documentation and approvals. • Support post-market surveillance, complaint handling, and vigilance/reportability assessments. • Identify training requirements and support implementation and documentation of employee training related to the QMS and applicable regulatory requirements. • Support supplier qualification and ongoing supplier quality management, as applicable. Data Privacy and Information Security (an advantage): • Support compliance with applicable data privacy, data protection requirements, and privacy risk assessments, ensuring processes involving personal information adhere to company policies and legislation. Location: Haifa, Israel (Hybrid – 1 day WFH, 4 days on-site)

About the Role: The Scientific Director, Physics will lead the Physics R&D organization, reporting directly to the Global Head of Product Development. In this highly visible leadership role, you will lead a team of physicists working at the intersection of physics, biology, engineering, and clinical science. You will provide scientific direction, develop organizational capabilities, and help solve complex multidisciplinary challenges that drive innovation from early discovery through clinical application. What you will do •Lead, mentor, and develop a team of 10–15 physicists focused on product innovation, biophysics, modeling, and experimental physics •Serve as a key member of the Product Development Leadership Team, providing scientific leadership across product innovation initiatives •Partner closely with Product Innovation, Preclinical Research, Clinical, Medical Affairs, Publications, and other cross-functional teams to solve multidisciplinary scientific and technical challenges •Define and advance the scientific and modeling framework that supports product innovation, translational research, and clinical development •Apply deep scientific expertise to guide multiple initiatives spanning device physics, biology, and clinical applications •Build new organizational capabilities by developing internal talent and leveraging external scientific expertise when needed •Promote and model a hypothesis-driven scientific approach to problem solving and decision-making •Support scientific publications, patent development, regulatory submissions, and external research collaborations •Deliver internal and external scientific training on the physics of Tumor Treating Fields (TTFields), as needed

Location: North District, Israel (On site) Role Overview: A Business Development Manager, supporting strategic planning and fund raising for our portfolio bio-pharma & medtech companies. This is a hands-on, highly interpersonal role focused on human connections, technical and scientific understanding and relationship-building. Key Responsibilities: • Investor outreach & pipeline management: Build, track, and maintain a targeted global pipeline of venture capital funds, CVCs, and family offices actively investing in healthcare and deep-tech. Must have disciplined approach to tracking engagement & managing investors database. • Investor Engagement: Identify and engage target VCs and CVCs suited for each graduating company’s specific sector, facilitating warm introductions and guiding founders through syndicate building. • Strategic partnerships: Support strategic initiatives of portfolio companies with corporate biopharma and medtech partners • Relationship Management: maintain active, trust-based dialogue with key industry stakeholders. • Collateral material optimization: Work closely with portfolio companies on collateral development including investment decks, financial narratives, and commercial pitch presentations to support fund raising requirements. Coach the portfolio companies on investor management and presentation skills. • Syndicate Building: Actively build and manage co-investor syndicates, bringing institutional lead and follow-on investors into portfolio funding rounds.

SCOPE & RESPONSIBILITIES Quality Assurance • Manage ECOs: conduct risk assessments, update relevant DMR documents and carry out necessary IQ, OQ, PQ activities if required, finalization of implementation tasks. • Manage DCOs in the PLM system: write and update QA procedures to ensure compliance with quality standards and regulatory requirements. • Manage NCR and CAPA processes: lead, write and supervise the NCR and CAPA processes, ensuring timely and effective resolutions. • Manage QA production activities: provide quality support to production operations, addressing deviations and non-conformities to maintain high product quality. • Ensure timely resolution of quality issues: promptly address all identified or assigned quality issues to prevent delays and maintain efficient operations. • Participate in internal and external audits, such as FDA inspections and notified body audits based on ISO 13485, EU MDR, and MDSAP requirements. • Supplier Quality Management: manage supplier qualification and performance monitoring, including SCAR management, and support supplier audits. Regulatory Affairs • Prepare, coordinate, track, and follow up on submissions for medical devices across various international markets. • Prepare and manage EU MDR technical documentation submissions. • Oversee CER, PMS, and PMCF activities, including customer complaints, vigilance, and recall. • Participate in regulatory inspections and audits. • Prepare regulatory assessments for design changes. • Develop labeling according to applicable regulatory requirements. • Evaluate and communicate regulatory impact of ECOs and design changes across QA and RA domains.

The opportunity: Production & Validation Engineer is responsible for supporting and improving manufacturing operations within a regulated medical device environment. This role ensures that production processes are efficient, compliant and capable of consistently delivering high-quality medical products. The Production Engineer works closely with cross-functional teams including Quality, R&D, Regulatory, Maintenance, and Supply Chain. Responsibilities: 1. Manufacturing Process Support • Monitor daily production activities, troubleshoot issues, and provide timely technical support to maintain output and product quality. • Optimize manufacturing processes through root-cause analysis, cycle-time reduction, and waste elimination. • Develop and maintain work instructions and Test Instructions. • Collaborate closely with production and engineering teams Resolve process challenges within production facilities 2. Process Validation & Compliance – • Execute and document qualification/validation activities (IQ/OQ/PQ) per ISO 13485 and FDA 21 CFR 820 requirements. • Lead engineering investigation and Failure Analysis activities in Operation, on component, product or process level 3. Equipment & Tooling management • Validate new equipment, fixtures, and tooling. • Support preventive maintenance programs and collaborate with maintenance to ensure equipment uptime. • Perform equipment capability studies and implement improvements. • Lead engineering activity regarding design changes (ECO), NPI, test method and tooling design, monitoring and continuous improvement of manufacturing processes • Design new Jigs based on improvement recommendations. 4. Supports MRB processes in Operation, assisting with issues relating to CAPAs, complaints and manufacturing support

The Senior Design Quality Assurance Engineer is responsible for providing Design Quality leadership for new product development (NPD / NPI) of a Next-Generation (Gen2) medical device. In this role, you will partner directly with R&D, Clinical, Regulatory, and Operations to set quality direction, mentor engineering teams, and drive compliant, timely execution from concept to product release. Job Description: • Drive the design & execution of Production Release Process project for components & finished devices. • Lead and implement complex projects including quality improvement initiatives. • Sets direction for cross-functional teams and drives towards compliant and efficient solutions to complex problems. • Lead Process/Design Risk Analysis (focusing on both Product Risk and Production Risk). • Lead multiple product Design Control activities for new product development efforts. • Provide leadership in understanding of the quality regulations to other disciplines, providing guidance to R&D engineers and supporting their technical writing capability. • Lead multiple product Design Control activities for new product development efforts. • Support Process/Design Validation/Verification activities and approach. • Lead implementing limited cost of quality concepts, including cost of quality, data collection, & reporting. • Support Manufacturing Engineering in the creation of DMR, DHR, routes, and bills of material, print changes, and specifications for in-house / external manufacturing. Know and follow all laws and policies that apply to one's job, and maintain the highest levels of professionalism, ethics and compliance at all times. Location: Sharon District - Israel (On-site)

מיקוד התפקיד: מנהל.ת האיכות אחראי.ת על יישום ותמיכה במגוון תהליכי איכות, במטרה להבטיח שהמוצרים עומדים בדרישות הלקוחות ובתקני האיכות של התעשייה. תחומי אחריות מרכזיים: ניהול מערכת האיכות (ISO 9001) - ניהול מערכת האיכות של החברה, כולל תוכנית מבדקים פנימיים, סקירות איכות חודשיות, וסקר הנהלה שנתי בהתאם לדרישות התקן — כולל היערכות לגרסת 2026. ניהול נתוני איכות ואי-התאמות - ריכוז ומעקב אחר נתוני אי-התאמה ברמת המוצר והרכיב, וניהול פעילויות מתקנות עד לסגירתן. אבטחת איכות ספקים - הגדרת דרישות איכות מול ספקים בשיתוף התפעול, ביצוע מבדקי איכות ותהליך, וניהול דיווח וטיפול באי-התאמות ספקים, בדגש מיוחד על מעגלים מודפסים (PCB). ביקורת קבלה - מעקב ושיפור מתמיד של תהליכי ביקורת הקבלה, בהתאם לניהול סיכונים ומשאבים זמינים. הובלת חקרי כשל - הובלת חקרי כשל למוצרים החוזרים מלקוחות לפי מתודולוגיית 8D, תוך שיתוף צוותי תפעול ופיתוח לפי הצורך. שיתופי פעולה פנים-ארגוניים - עבודה שוטפת מול צוותי התפעול והפיתוח לאורך מחזור חיי המוצר, ותמיכה בתוכניות הדרכה והסמכה מקצועיות.

I'm seeking an experienced commercial leader to drive global business growth, develop new international markets, and build long-term relationships with strategic industrial customers worldwide. This is a true Individual Contributor role with no direct people management responsibilities. The successful candidate will personally lead business development, strategic customer relationships, and complex international sales processes. The company delivers highly engineered, customer-specific solutions rather than off-the-shelf products. Success in this role requires a consultative, solution-selling approach and the ability to work closely with engineering teams to develop tailored solutions for global industrial customers. Key Responsibilities: Business Development & Growth - • Identify new markets, applications, industry segments, and strategic customers. • Develop and implement Go-to-Market and market penetration strategies. • Analyze market trends, competitors, and emerging technologies. • Identify customer challenges and translate them into business opportunities. • Collaborate with R&D to shape product and technology direction based on market needs. Strategic Sales - • Personally lead complex international sales processes with global industrial customers. • Drive customer acquisition and sustainable revenue growth. • Lead commercial and technical negotiations for customer-specific engineered solutions. • Build and manage an international sales pipeline and forecasting process. • Close strategic, high-value agreements with global customers. Customer & Cross-Functional Collaboration - • Build long-term relationships with executive, commercial, and engineering stakeholders at global industrial organizations. • Serve as the commercial interface between customers and internal engineering teams. • Work closely with R&D, Operations, Quality, and Finance. • Represent the company at international customer meetings and industry events. Location: North District, Israel (Hybrid)

Position Overview: This executive role requires a growth-oriented, systemic and hands-on leader to build and scale the company’s global operating model during a significant Scale-Up phase. As a key member of the executive team, the role bridges business growth strategy with operational execution, with responsibility for manufacturing, global supply chain, quality, V&V, NPI and operational infrastructure. The role is focused not only on managing an existing operation, but on building and stabilizing a scalable operating system, connecting Operations, NPI, Engineering, Supply Chain and global customers. Key Responsibilities: • Strategic Leadership & Operating Model: Designing and building the future operating model; translating business growth plans into scalable operational capabilities while managing CAPEX/OPEX and operational risks. • Manufacturing Scale-Up & Industrialization: Expanding production capacity and transitioning from low-volume to increasing levels of serial production; leading NPI, DFM and DFA in close collaboration with R&D and Engineering. • Make vs. Buy & External Manufacturing: Leading strategic Make vs. Buy decisions; managing Contract Manufacturers / EMS and defining the balance between internal and external capabilities. • Global Supply Chain: Leading end-to-end planning, procurement, suppliers, logistics and inventory; building resilient global supply chains and ensuring high OTD for global customers. • Quality & Operational Excellence: Driving Lean Manufacturing, Continuous Improvement and KPI-based performance management; leading production validation, quality improvement and CAPA processes. • Organization Building: Designing the future Operations organization and building a strong management layer across Manufacturing, Supply Chain and Quality. Location: Lower Galilee (On site) Reporting to: CEO

נמצאים בצומת דרכים בקריירה ולא בטוחים מה הצעד הבא? אם אתם רוצים לקחת שליטה על הקריירה שלכם, אבל מרגישים שאתם זקוקים לכיוון, לאסטרטגיה ולמבט מקצועי – תוכנית הייעוץ האישית שלי נועדה בדיוק בשבילכם. אני מציעה תוכנית ייעוץ קריירה אישית, המבוססת על יותר מ-25 שנות ניסיון בגיוס, משאבי אנוש וליווי מועמדים. התהליך מתקיים במספר מפגשים ממוקדים, בזום או במשרד שלי בחיפה, ומטרתו לסייע לכם לבנות תוכנית פעולה ברורה ואפקטיבית להמשך הדרך. מה כולל התהליך? ✔ מיפוי קריירה והגדרת כיווני פעולה סקירת הניסיון שצברתם, זיהוי החוזקות שלכם והגדרת התפקידים והתעשיות שכדאי לכוון אליהם. ✔ דיוק הפרופיל המקצועי שיפור פרופיל ה-LinkedIn וקורות החיים, כך שישקפו בצורה מיטבית את הניסיון והערך שאתם מביאים. ✔ בניית אסטרטגיית חיפוש זיהוי ערוצי החיפוש הרלוונטיים ביותר עבורכם ובניית תוכנית פעולה ממוקדת. מה תרוויחו? 💡 בהירות לגבי הכיוון המקצועי הבא שלכם. 💡 תוכנית פעולה מסודרת ומותאמת אישית. 💡 כלים פרקטיים לניהול עצמאי של תהליך חיפוש העבודה. 💡 ביטחון רב יותר בקבלת החלטות מקצועיות. למי השירות מתאים? המיקוד המרכזי שלי הוא באנשי מקצוע ומנהלים מעולמות ה-Biotech, Medical Devices, Pharma וה-AgTech, שבהם נדרש ידע מעמיק בשוק, בתפקידים ובמסלולי הקריירה. עם זאת, במקרים המתאימים, השירות יכול להתאים גם לאנשי מקצוע מתחומים נוספים. חשוב לדעת: זהו שירות ייעוץ אישי בתשלום. מטרת התהליך היא להעניק לכם כלים, כיוון ואסטרטגיה לניהול הקריירה שלכם. השירות אינו כולל חיפוש משרות אקטיבי, פנייה למעסיקים מטעמי או התחייבות להשמה. 📥 רוצה להתחיל? מלא/י את פרטיך בטופס למטה וצרפ/י קורות חיים. מבטיחה לחזור אליך בהקדם לתיאום פגישה.

• Responsible for creating a constrained weekly/monthly production schedule (MPS) and ensuring raw material availability • Planning and freeze period management of production activities (Rescheduling, Reworks, Outsourced WIPS). • Maintain material inventories within OCA Finish goods goal, while minimizing excess, obsolete and expired products; develop overall inventory projections for specific products • Enables meeting inventory targets. • Align a three month committed production schedules with value stream managers in terms of resources, shifts, equipment, earned hours and shutdowns. • Communicate and escalate low finish goods inventory report ownership & updates • Resolve any manufacturing conflicts for site/ portfolio. Manage impact and communication of manufacturing driven change management • Provide Production Planning input into S&OP process. Provide transparency of risks and opportunity. Participate in S&OP forums as applicable. • Lead/support required compliance process activities for Change Control, Deviations, Events & CAPA’s and assess respective supply impact • Provide specific input to the End-to-End Supply Chain configuration process and ensure planning master data (safety stock, lead times) in the ERP system are up to date • Ensure participation in new product launch meetings and new product forecasts as a business partner. • Execute planning activities derived from products phase-in phase-out. • Meeting all operational KPIs – Inventory, DOH, customer backorder and OTD. • Support quarterly Finance budgeting process for Inventory and earned hours • Support the Repair Centers where applicable Other Essential Duties as required.

The opportunity: In this role, you will be hands-on managing the production team (including team leaders) and its day-to-day activities. You will collaborate with various departments, including Engineering, Quality, Finance, Supply Chain and R&D. Responsibility: • Responsible for all manufacturing aspects while ensuring quality requirements and work according to the working instructions • Managing the execution of the production plan and personal. • Responsible for manufacturing technician training • Evaluate, improve and document all manufacturing processes • Work closely with Quality and Engineering teams to review and approve operating, set up, and inspection instructions and verification documents • Serve as a subject matter expert for all production process flow design, process root cause investigations, and ongoing yield improvement as part of process and production excellence • Create, improve and maintain Work Instructions, procedures and processes in relation to manufacturing plan determine optimal utilization of manufacturing workers and equipment to meet manufacturing goals Location: Sharon District, Israel (On-site)

Position Overview: As the Senior R&D Team Lead, you will lead a talented research and development team, taking direct responsibility for the evolution of a core non-invasive sensing technology. This is a high-impact, multi-disciplinary role overseeing the design, development, and testing of an advanced sensing device. The position blends strategic team management with hands-on technical guidance, ensuring rigorous evaluation and testing of both individual components and complete systems using advanced lab equipment. In this position, you will work closely with executive leadership and report directly to the company’s leadership. Key Responsibilities: • Team Leadership & Management: Lead, mentor, and manage the R&D team, fostering a culture of innovation, excellence, and collaboration. • End-to-End Product Development: Oversee the complete design, development, and testing lifecycle of our multi-disciplinary non-invasive sensing device. • Advanced Lab Testing: Lead R&D efforts in the Israel lab and work with the lab in London and execute hands-on testing, verification, and characterization of the device and its high-frequency RF components using advanced lab equipment (e.g VNA). • Technical Integration: Ensure seamless hardware-software (HW/SW) integration, managing the intersections of RF systems, advanced signal processing, and embedded systems. • Project Execution: Own project timelines, resource allocation, and technical deliverables, ensuring complex projects are delivered on schedule. • ⁠Strategic Collaboration: Act as a counterpart and expert to manage and support the company’s collaboration with leading scientists. • Holistic Approach: Report directly to the company’s leadership, providing technical insights, progress updates, and strategic recommendations for the product roadmap.

General position. Here you can submit your CV that will enter our database. We will reach out to you as soon as a position opens. • שליחת קורות חיים למשרה זו מהווה אישור לשמירתם במאגר המידע של סטפ אפ קריירה, לצורך טיפול במשרה זו ו/או משרות נוספות. בכל שלב תוכל.י לבקש עיון או מחיקה

General position. Here you can submit your CV that will enter our database. We will reach out to you as soon as a position opens. * שליחת קורות חיים למשרה זו מהווה אישור לשמירתם במאגר המידע של סטפ אפ קריירה, לצורך טיפול במשרה זו ו/או משרות נוספות. בכל שלב תוכל.י לבקש עיון או מחיקה