משרות והצעות עבודה

• Collaborate with senior leadership to understand the organization’s goals related to recruitment and employee welfare. • Lead end-to-end recruitment processes in Israel: sourcing, interviewing, and hiring new employees. • Maintain relationships with recruiting agencies and headhunters. • Manage employee onboarding processes to ensure a smooth and positive integration into the company. • Manage and support ongoing employee welfare and wellbeing activities, including employee experience, engagement initiatives, benefits coordination, and employee support throughout key stages of the employee lifecycle. • Maintain knowledge of recruitment trends, sourcing best practices, and relevant tools and platforms. Location: Sharon District, Israel (On-site)

• Overall responsibility for the Quality Management System, including ownership and leadership of QMS processes such as CAPA, Complaints, Document Control, Training, Internal and External Audits, and Supplier Quality • Lead, maintain, and continuously improve the QMS to ensure compliance with applicable regulatory and quality standards • Manage and develop QMS processes and procedures, ensuring effective implementation across the organization • Monitor and assess QMS performance, identify gaps and improvement opportunities, and drive corrective and preventive actions • Prepare and present QMS-related data and metrics for Management Review and quality forums • Lead internal audits and support external and regulatory audits • Provide professional guidance, training, and support to stakeholders on QMS-related topics

The CEO’s primary mandate will be to drive the company’s clinical development strategy, fundraising efforts, and overall business execution, while working closely with the Board, scientific leadership, and external partners. Key Responsibilities • Lead significant fundraising efforts, including venture capital rounds and strategic partnerships. • Lead the company’s transition from pre-clinical to early clinical development (Phase I–II). • Define and execute the clinical development and regulatory strategy in close collaboration with scientific and clinical teams. • Manage investor relations and serve as the primary interface with the Board of Directors. • Drive the overall business strategy, corporate development activities, and long-term value creation. • Represent the company with investors, partners, regulators, and key opinion leaders. Location: Center District - Israel

In this role, you’ll be a key partner to R&D, leading quality activities across new product development and design changes, while ensuring compliance with global regulatory standards. Lead design control activities throughout the product lifecycle (ISO 13485, 21 CFR 820). Review and approve design inputs/outputs, V&V protocols, and reports. Maintain and execute risk management activities (ISO 14971), including FMEAs. Support EO sterilization and packaging validation activities (ISO 11135 / ISO 11607). Support root cause investigations, CAPAs, and engineering changes. Ensure design documentation is support for global regulatory submissions. Work closely with R&D, Operations, and Regulatory in a fast-paced, collaborative environment. Support internal and external audits as needed.

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 Sales Manager will be responsible for communication with customers, presenting new technologies to our customers, providing excellent customer service, driving sales, conducting training sessions, Application support, and managing sales activities. Responsibilities: Presenting high end solutions for the Israeli food, pharmaceutical and other local industries. Lead the Israeli market sales operations, end-to-end (Pre-sale, sale and post-sale cycle). Manage the commercial activities, negotiation and closing deals. Establish and execute the yearly sales plan based on the go to market plan in Israel. Prepare quarterly and annual sales forecasts. Manage the day-to-day customers relations management grow our country's customer base and manage the accounts. Maintain strong relationships with the various stakeholders in the field. Identify and address customer challenges and needs and represent the voice of the customer within the company. Build and grow customer loyalty and customer satisfaction. Continually analyze competitive landscape and environment within assigned accounts to determine trends and provide customer feedback to the company leadership.

Manage and mentor a growing V&V team, fostering a culture of quality, accountability, and continuous improvement. Define and lead the V&V strategy, master plans, and schedules aligned to product development cycles and regulatory requirements. Coordinate V&V activities with external testing laboratories and vendors to ensure high-quality and timely deliverables. Champion continuous improvement of V&V tools, methodologies, and infrastructure. Oversee and execute verification and validation activities, including protocol design, testing, and documentation for capital systems and disposable devices. Ensure robust test method development, validation, and equipment qualification in accordance with industry and regulatory standards. Drive readiness for regulatory submissions and audits through comprehensive V&V documentation and compliance. Partner closely with R&D, Quality Assurance, Regulatory Affairs, Clinical, and Manufacturing teams to ensure integrated and risk-based V&V planning. Actively participate in design reviews, risk assessments (per ISO 14971), and contribute to the development and maintenance of DHF and DMR. Ensure all V&V activities comply with applicable regulatory standards, including FDA, ISO 13485, ISO 14971, IEC 60601, and EU MDR.

ניהול והובלה של תהליכי גיוס מורכבים בעולם הביוטק: • הבנת המשרה לעומק ביחד עם הלקוח – גם בפן המקצועי וגם בהתאמה בין אישית לארגון. • פרסום המשרה בערוצים השונים וכתיבת פוסטים יצירתיים. • סורסינג תוך שימוש במגוון תוכנות וכלים (מערכת גיוס, לינקדאין, AI וכדומה). • ביצוע ראיונות טלפוניים ופרונטאליים. • ליווי תהליך הגיוס משלב פתיחת המשרה ועד לאיוש. • ניהול הקשר עם הלקוח ועם המועמדים לאורך כל תהליך הגיוס וגם לאחר מכן. *** העבודה מהבית, הגעה למשרד בחיפה יום בשבוע.

The Technical Project Manager – Responsible for full lifecycle management of R&D projects, including systems engineering, HW / SW and mechanical integration. Ensures projects meet technical, regulatory, and quality requirements, while coordinating execution, timelines, and resources across teams. The project manager interacts with all functions and levels throughout the company and outside the company, working in an international, multidisciplinary, and multi-project environment. The position reports to the Program Manager and requires ongoing communications with a team based in the US, Europe, and Israel. Responsibilities: • Lead the planning and implementation of R&D projects • Facilitate the definition of project scope, goals, and deliverables • Develop full-scale project plans, including timelines, tasks, and resource requirements • Monitor and report on project progress to all stakeholders. • Deep understanding of the technical details of the project • Provide technical leadership, lead problem-solving, and support the project team. • Ensure project deliverables meet the quality requirements Location: Sharon area (Hybrid)

The Clinical Operations Manager will be responsible for the planning, execution, and oversight of the compay's clinical studies and post marketing clinical activities, ensuring that studies are conducted in accordance with applicable regulatory requirements (FDA, ICH-GCP) and company standards. Key Responsibilities •Clinical Operations Leadership: Manage clinical operations, including study planning, site and investigator selection, managing negotiations with sites, study initiation and monitoring. In addition, clinical commercial activities, post-market clinical operations •CRO & Vendor Oversight: Select, contract, and supervise CROs, laboratories, and other clinical vendors to ensure quality and compliance. •Regulatory & Documentation Management: Lead the preparation, review, and maintenance of essential clinical documents — including study protocols, Investigator’s Brochures, informed consent forms, case report forms (CRFs), and clinical reports. •0Data Management: Oversee data collection, EDC systems, data review, and the generation of clinical summaries and metrics. •Site Management: Build and maintain strong relationships with investigators, site coordinators,). Ensure effective communication and timely issue resolution. •Monitoring Oversight: Review monitoring reports, track enrollment progress, and ensure timely follow-up on action items. •Compliance & Quality: Ensure all activities adhere to GCP, ICH, and FDA regulations as well as internal SOPs. •Reporting: Prepare progress reports, timelines, and risk assessments for internal management and regulatory stakeholders. •Collaboration: Partner with cross-functional teams (Regulatory Affairs, Clinical, QA, Operations, and R&D) to ensure alignment and readiness for submissions.

The role of Senior Physicist at the company involves designing the next generation of the product components, such as gradient coils and magnet systems, with a focus on creating affordable, lightweight, and reliable solutions. This requires a deep understanding of the underlying physics and a first-principles approach. As part of the early team in the company, you’ll have the opportunity to help define the company’s DNA, as well as your own career path.

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