מהנדס בדיקות Sr

ב-Medtronic תהיה לך אפשרות להתחיל קריירה לכל החיים של חקר וחדשנות, תוך סיוע בקידום גישה לשירותי בריאות ושוויון לכולם. ההובלה שלך תהיה מתוך מטרה, תוך שבירת מחסומים לחדשנות בעולם מחובר יותר ובעל חמלה גדולה יותר.

יום בחיים

Within Medtronic's global Neuroscience organization, Cranial and Spinal Technologies (CST) advances care for some of medicine's most complex neurological and spinal conditions. CST is a leader in surgical imaging and navigation, and its operating unit develops and delivers an integrated ecosystem of spinal implants, navigation and robotic guidance systems, advanced imaging and data-driven planning tools for complex spine and cranial procedures. Together, these technologies are intended to support surgeons and care teams in their work.

Test Engineering within CST is responsible for the independent design verification of medical device software and systems, ensuring that products meet user needs and our quality, reliability and regulatory standards before release. As a Senior Test Engineer in Caesarea, you will join a dedicated team focused on verifying the correctness and accuracy of the algorithms embedded in CST's products. You will develop test strategies, create and execute verification plans, protocols and reports, and produce traceable evidence for release. Working under limited direction, you will apply your technical expertise to solve complex problems, partner with software, systems and quality teams, and provide technical leadership and mentoring to other test engineers. This is a permanent, onsite role with travel of 10-20%.

Primary Responsibilities:

• Provide technical leadership and mentoring to other test engineers.
• Develop test strategies, plans, protocols and reports for verification of new or changed algorithms, software and hardware, from initial design through release, ensuring alignment with applicable regulatory, cybersecurity, privacy and quality system requirements (e.g., FDA, IEC 62304, ISO 13485, ISO 14971, HIPAA, GDPR, SOC 2, as relevant to the product).
• Lead and develop the schedules and equipment required for testing, including exam, tool, fixture and phantom design.
• Create, develop and maintain test software, and design, implement and execute automated testing and test automation frameworks to improve test efficiency, coverage and repeatability.
• Plan and execute algorithm correctness, accuracy, performance, robustness and regression testing, including comparison of algorithm outputs against reference methods and acceptance criteria, and assess results across the intended range of inputs and conditions.
• Perform system integration testing so that hardware and software components function correctly as an integrated system, separate algorithm effects from integration effects, and generate traceable release evidence.
• Participate in all phases of product development as needed, including reviewing requirements, design, usability, risk assessment and defects, and partner with R&T and cross-functional teams (systems, software and hardware engineering, regulatory affairs and quality) to review test methods, acceptance criteria and datasets early, including before regulatory pre-submission.
• Compile data and define changes required in test equipment, testing procedures, or new testing requirements; keep test equipment in good working order and calibrated; and set up test tracking, monitoring and data recording systems, including testing at outside test facilities.
• Troubleshoot, debug and support existing products, participate in defect tracking and analysis, identify and implement process improvements, and communicate findings, problems and solutions to project teams and stakeholders in compliance with the Quality System.
• Develop and establish new procedures, working practices, standards, and processes to build and mature the organization’s algorithm verification and testing capabilities.

Required Qualifications:

• Baccalaureate degree in Mechanical Engineering, Electrical Engineering, Computer Science, Biomedical Engineering, or a related engineering discipline.
• 4+ years of relevant experience with a Bachelor's degree, 2+ years with a Master's degree, or 0+ years with a PhD.
• Working knowledge of software design, development, debug and test practices.
• Working knowledge of statistical methods and quantitative analysis for evaluating algorithm correctness and accuracy, such as error metrics, tolerances, sample size and data analysis.
• Oral and written communication skills in English, and the ability to work in a team environment.
• Creative and innovative problem-solving skills, with the ability to work effectively in new and evolving technical areas where established methods, processes, or precedents may not yet exist.

Preferred Qualifications:

• Knowledge of applicable AAMI, ISO, FDA and EN standards.
• Experience developing or testing Software as a Medical Device (SaMD) or software within a medical device context, and an understanding of FDA Quality System Regulations (QSR).
• Experience with test automation, including GUI, integration and stress testing and designing and implementing test automation frameworks.
• Hands-on experience with system integration testing of complex hardware/software systems, across product types including embedded/firmware, capital equipment or connected systems.
• Experience testing algorithm correctness and accuracy (for example image processing, measurement, detection or registration algorithms), including defining reference methods and ground truth, selecting and managing test datasets, writing scripts (e.g., Python) to analyze algorithm outputs, and building reproducible, defensible test methods and regression tests.
• Familiarity with x-ray or medical imaging system testing, and experience with reliability demonstration of large capital equipment.
• Demonstrated ability to influence and lead cross-functional teams, to manage multiple tasks and priorities, and to work independently in a fast-paced, collaborative environment; experience with Agile and iterative development practices is a plus.
• Project management skills (planning, estimation, tracking and communication) and machine shop experience.

דרישות עבודה פיזיות

ההצהרות לעיל נועדו לתאר את האופי הכללי ואת הרמה של העבודה המבוצעת על ידי עובדים שהוקצו לתפקיד זה, אך הן אינן מהוות רשימה ממצה של כל תחומי האחריות והכישורים הנדרשים עבור תפקיד זה.

‌

‌

התראה לגבי הונאת גיוס

הובא לידיעתנו שקיימות הונאות דיוג שמתמקדות במחפשי עבודה. זכרו בבקשה את הדברים הבאים: 

הגישו מועמדות רק דרך הערוצים הרשמיים של Medtronic. כל התכתובת הלגיטימית של Medtronic בנוגע לגיוס עובדים מגיעה מפלטפורמות מאושרות של Medtronic וכתובות דוא"ל רשמיות עם הסיומת ‎@medtronic.com.

Medtronic לעולם לא תבקש תשלום או מידע אישי רגיש (כגון מספר חשבון בנק או פרטי ביטוח לאומי) בשלבים הראשונים של תהליך הגיוס. כל בקשה שכזו אינה לגיטימית. 

אם קיבלתם הודעה חשודה שטוענת שהיא מגיעה מ-Medtronic, אל תגיבו, אל תלחצו על קישורים ואל תפתחו קבצים מצורפים. 

אם יש לכם שאלות או חששות בנוגע לאותנטיות של תכתובת שלכאורה נעשתה על ידי Medtronic או מטעמה, צרו איתנו קשר מייד בכתובת AskHR@medtronic.com.

הטבות ופיצויים

Medtronic מציעה שכר תחרותי וחבילת הטבות גמישה
המחויבות לעובדים שלנו נמצאת בליבת הערכים שלנו. אנו מכירים בתרומתם. הם שותפים להצלחה שהם עוזרים ליצור.  אנו מציעים מגוון רחב של הטבות, משאבים ותוכניות תגמול תחרותיות שנועדו לתמוך בך בכל קריירה ובכל שלב בחיים.

‌

This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).