משרות והצעות עבודה

תחומי אחריות תכנון ופיתוח ציפויים • תכנון תיאורטי מתקדם של מבני שכבות אופטיות • פיתוח ציפויים מסוג AR, HR ופילטרים • עבודה עם טכנולוגיות מתקדמות כגון PVD, IBS, Magnetron Sputtering • שימוש בתוכנות ייעודיות לתכנון ואופטימיזציה • שיפור ביצועים ושחזוריות תהליכים העברת תהליכים לייצור • פיתוח תהליכים יציבים וברי שחזור • העברת תהליכים מפיתוח לייצור סדרתי • ייעול ושיפור תהליכי עבודה • הגדרת מתודולוגיות ונהלי עבודה אפיון ומדידות • מדידה ואפיון שכבות דקות • ניתוח ביצועים אופטיים והתאמה לדרישות מערכת • פתרון בעיות תהליכיות ואופטיות פיתוח תשתיות ציפוי • תכנון ג'יגים ומתקני עזר • שיפור אחידות ציפוי על רכיבים מורכבים • פיתוח פתרונות לציפוי גיאומטריות מאתגרות • הגדרת דרישות לציוד ציפוי ומדידה עבודה רוחבית • עבודה עם צוותי פיתוח, הנדסה וייצור • ממשקים טכנולוגיים עם לקוחות ושותפים הובלת התחום • הובלה מקצועית של תחום הציפויים האופטיים בארגון • הגדרת ארכיטקטורות ציפוי וגישות תכנון • פיתוח פתרונות מתקדמים למערכות אופטיות מדויקות מיקום - צפון הארץ (לא היברידי)

• Full responsibility for registration, renewal, and label expansion of crop protection products, including biologicals, microbials, biostimulants, and chemical formulations. • Develop and lead regulatory strategies for both the existing portfolio and products under development, aligned with business goals and target markets. • Prepare, manage, and submit regulatory dossiers, including safety, efficacy, quality, manufacturing, and CMC data. • Lead regulatory and field efficacy trials in collaboration with R&D teams, external consultants, CROs, and contractors, locally and internationally. • Serve as the primary interface with regulatory authorities in Israel and abroad, including correspondence management, responses to questions, and handling objections or data gaps. • Continuously monitor regulatory developments and assess their impact on the company’s products and pipeline. • Provide regulatory leadership throughout the product development lifecycle, from concept through commercialization (Regulatory by Design). • Deliver regulatory guidance to marketing and sales teams, including claims substantiation, labeling, and marketing materials. • Manage external consultants, service providers, and regulatory budgets. • Identify, assess, and mitigate regulatory risks, and lead corrective and preventive actions. • Build, lead, and manage the regulatory team, including staff and consultants located internationally. Location: Sharon District, Israel

A skilled Robotics Engineer to join our core control team at a cutting-edge startup developing autonomous robotic solutions for the agricultural sector. Recently acquired by a global corporation, the company offers a unique blend of innovative startup agility and international corporate stability. In this role, you will be a key player in enhancing our current autonomous platform and developing our next-generation robotic systems. This is an opportunity to work on complex, "Deep-Tech" challenges within a stable environment backed by a global corporation, while maintaining a creative startup spirit. Key Responsibilities: Design and implement control systems for motors and advanced drive systems. Execute closed-loop control on motors to ensure high-precision performance. Develop control algorithms and motion planning for multi-motor robotic systems. Program and maintain robotic software systems using Python and PLC (Codesys or equivalent). Collaborate closely with cross-functional design and development teams to ensure high-standard project delivery. Location: Northern Israel (Hybrid Model)

This role is responsible for ensuring compliance, quality, and operational excellence throughout the development and manufacturing of Class III medical devices. Responsibilities • Lead, mentor, and manage the QA team, including task prioritization and performance development • Maintain and continuously improve the Quality Management System in compliance with ISO 13485, EU MDR, and FDA QSR (21 CFR 820) • Support Operations activities, including manufacturing, validation, MRB, CAPA, and supplier quality • Oversee CAPA, nonconformances, deviations, complaints, risk management, document control, and training processes • Prepare, implement, and maintain quality plans and annual quality activities • Actively participate in and support internal, supplier, and regulatory audits, including preparation, execution, and follow-up • Support regulatory submissions and interactions as required • Ensure quality oversight of QMS modules • Collaborate cross-functionally with R&D, Regulatory Affairs, Operations, and Clinical teams • Promote a strong culture of quality, compliance, and continuous improvement

Looking for a dynamic and experienced Director of Sales Europe, to lead sales efforts across Europe, consistently delivering Annual Recurring Revenue (ARR) targets. You will collaborate closely with Customer Success, Marketing, and Product teams for a leading Israeli software company. Role Overview Your primary focus will be overseeing sales activities and negotiations, fostering new business opportunities, and scaling subscription-based growth through complex B2B software-hardware integration projects. Tasks that you might work on include, but are not limited to: Enterprise Growth: Be the driving force behind efforts to generate new Enterprise business opportunities, overseeing the entire B2B sales cycle. Customer Base Expansion: Strategically expand the customer base through effective relationship-building using a consultative sales approach. Client Engagement: Identify and comprehend the strengths and needs of the existing client pipeline, ensuring tailored solutions that meet their requirements. On-Site Visits: Plan and execute successful on-site visits with prospective customers, fostering trust and collaboration. Product Demos: Conduct compelling online product demonstrations that showcase the value of the company's software integration platform. Contract Negotiations: Lead contract negotiations to secure mutually beneficial agreements.

• 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

Experienced and visionary CEO to lead an early-stage pharmaceutical company developing an innovative drug product. This is a unique opportunity to shape the strategy, secure the funding, and lead the development of a high-potential therapeutic candidate. Key Responsibilities: • Define and execute the company’s strategic and operational plans, in alignment with the Board’s vision. • Lead the company’s fundraising efforts, including interactions with VCs, angel investors, and strategic partners. • Establish strategic collaborations and co-development agreements with pharma and biotech partners. • Oversee and manage all R&D activities, including budget, timeline, and milestone tracking. • Lead the non-clinical development of the company’s lead asset. • Develop and adjust the clinical and regulatory roadmap in collaboration with key experts and partners. This is a full-time, on-site position (not hybrid), based in the Northern District of Israel.

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