Careers

Join the ReDS™ Revolution

At Sensible Medical, we believe that our technology is a game changer in a wide range of applications, and is evolving into the next generation monitoring system for Heart Failure patients across the continuum of care.

We invite you to join our team of brilliant professionals and make a difference in the care of HF patients.

Israel:  
Position Title:R&D Engineer
 

Sensible Medical Innovations has set out to develop a new standard of care in lung fluid management. Sensible developed the ReDS™ medical radar technology that stems from defense “see through wall” application. The technology is well positioned to be a game changer in a wide range of applications and become the next generation monitoring and imaging modality.

We are located in Kfar Neter industrial park (next to “Poleg” Netanya).

Core Responsibilities

  • Research core technology and develop novel medical applications.
  • Develop algorithm, signal analysis, and HW accordingly.
  • Design and execute research in medical settings .
  • Analysis of data obtained at bench tests and clinical studies.
  • Development and documentation of bench tests protocols and reports.
  • Collaborate and Communicate with R&D, Clinical and Operations teams.
  • The position is in the CTO team.

Education/Skills Requirements

  • BSc / Msc in Physics/ Electrical/ Bio-Medical engineering from the Technion / Weizmann Institute / Tel Aviv University / Ben Gurion University, with an average grade of 85 and above. Please add your final grades sheet.
  • Preference for hardware / algorithms experience.
  • Ability to work in a dynamic environment.
  • High interpersonal ability.

CV please send to neta.d@sensible-medical.com

LocationKfar Neter, Netanyia, Israel

➔ Send your resume
Position Title:הנדסאי/טכנאי אלקטרוניקה/מכונות לתפקיד ייצור
 

לסנסיבל מדיקל, סטרטאפ בתחום המכשור הרפואי הממוקם באזור התעשיה כפר נטר, דרוש/ה הנדסאי/טכנאי למחלקת הייצור למשרה מלאה:

תכולת התפקיד:

  • הרכבה מכנית וחשמלית של מערכת מאוסף תתי-מערכות.
  • בדיקות ראשוניות דרג א/ב למערכת בשעת ההרכבה.
  • בדיקות סופיות (ATP) לפי נהלי עבודה יעודיים באנגלית.
  • השלמת מסמכי מעקב תהליך למוצר באנגלית.
  • פתרון תקלות הרכבה ראשוניות ותיעודן.

דרישות התפקיד:

  • הנדסאי/טכנאי אלקטרוניקה או מכונות (עדיפות לאלקטרוניקה).
  • נסיון בבדיקות סופיות (ATP)
  • עדיפות לניסיון בחברת מדיקל וניסיון עם מערכות ERP
  • יתרון בניסיון תחת תנאי GMP ו-ISO13485
  • יתרון לנסיון בתפ”י/העברה מפיתוח לייצור.
  • היכרות טובה עם אקסל, וורד, אאוטלוק.
  • סדר וארגון
  • ראש גדול , אחראי
  • יכולת טובה כתיבה, קריאה והבנה של אנגלית – חובה!

**המשרה מיועדת לנשים וגברים כאחד

CV please send to neta.d@sensible-medical.com

LocationKfar Neter, Netanyia, Israel

➔ Send your resume
Position Title:VP Regulatory Affairs
 

We are seeking for VP Regulatory Affairs
Sensible Medical Innovations has set out to develop a new standard of care in lung fluid management. Sensible developed the ReDS™ medical technology that stems from defense “see through wall” application. The technology is well positioned to be a game changer in a wide range of applications and become the next generation monitoring and imaging modality.
Seeking candidate with proven track record of successful submissions and the ability to define and execute a comprehensive regulatory strategy. Reports to the company CEO.

Responsibilities

  • Establishing a dialog with the regulatory authorities (e.g. FDA, Notified body) to discuss the regulatory plan and assure efficient and productive process.
  • Strategy planning for new products/new models (clarifying classifications, relevant global regulations and following implications to the business).
  • Working with R&D to assure adherence to the agreed upon regulatory path, and to resolve emerging conflicts with regulatory requirements
  • Projecting regulatory requirements,
  • Assuring implementation and long term compliance with the requirements,
  • Assuring Risk management along the product full lifecycle,
  • Assuring the alignment b/w V&V planning and regulatory requirements, as well as the quality of execution.
  • Assuring the conductance of clinical evaluation
  • Providing regulatory inputs to the manufacturing process
  • Leading the regulatory aspects of labeling and marketing materials
  • Concluding the above into inclusive submissions, and defend the submissions externally.
  • Leading regulatory aspects of product changes along product lifecycle
  • Leading the regulatory aspects of post marketing activities (e.g. vigilance reporting)
  • Carrying management responsibilities as appropriate.

Education/Skills and Experience Requirements

  • MS/PhD in Life/Health Sciences/Biomedical Engineering.
  • Holding the Regulatory Affairs Certification (RAC). – Advantage
  • A proven leader with a minimum of 10+ years’ experience in the biomedical industry.
  • Must have experience with global regulatory agencies and ability to advise on regulatory strategy in the US and Europe.
  • Experience from a company that sells – Advantage
  • Able to drive strategic thinking and plans for successful regulatory outcomes.
  • Excellent Professional writing skills.
  • Experience in interfacing with regulatory authorities, including successful track record of submissions of class II devices in the EU and in the USA
  • Strong planning, organizational and leadership skills.
  • Dynamic individual with strong interpersonal skills and the ability to skillfully and appropriately manage, develop and mentor personnel in a matrix environment.
  • Results oriented. Strong initiative, accountability and willingness to take ownership and drive projects to completion.
  • Detail-oriented

CV please send to neta.d@sensible-medical.com

LocationKfar Neter, Netanyia, Israel

➔ Send your resume