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Supply Chain and Strategic Commodity Manager in Irvine, CA


Irvine, CA 92697
6w ago


$100K - $150K*


Supply Chain & Logistics


8 - 10 years

Job Description

Job Summary

The Supply Chain and Strategic Commodity Manager will develop, oversee and implement initiatives per the direction of executive staff to support Masimo's strategic vision. (S)he will provide strategic input into the development and execution of projects to enhance the company's operations.

Duties & Responsibilities

  • Create and manage strategic parts of category sourcing.
  • Develop long term commodity group execution strategy.
  • Develop and monitor supply chain analytics dashboard analytics.
  • Continually optimize supply chain with respect to price, inventory, supply continuity, terms and conditions;
  • Ensure adherence to internal standards and practices;
  • Identify means to improve efficiencies/speed of routine work; lead efforts to implement change;
  • Provides strategic leadership
  • Monitors on-going project(s) status.
  • Develops and deploys training materials,
See More

Valid through: 2020-3-4

About Masimo

Masimo is an American Irvine, California-based manufacturer of noninvasive patient monitoring technologies. The company is best known for its pulse oximetry and it sells more pulse oximeters to hospitals than any other company. Masimo was founded in 1989 by electrical engineer Joe Kiani, who was later joined by fellow engineer Mohamed Diab. Masimo invented measure-through motion and low perfusion pulse oximetry, known as Masimo SET (Signal Extraction Technology). Masimo has been recognized for its intellectual property and for being one of the most innovative companies in the medical device industry. The company went public in 2007 and is currently traded on the NASDAQ stock exchange under the symbol MASI. In 2011, Forbes named Masimo to its list of top 20 public companies under a billion dollars in revenue, based on earnings growth, sales growth, and return on equity. In 2012, Joe Kiani, founder, CEO and Chairman of the Board was named the Ernst & Young National Entrepreneur of the Year - 2012 Life Sciences Award Winner. Kiani was recognized for "revolutionizing the health care industry by taking risks to create and commercialize noninvasive patient monitoring devices, which include an array of sensors that lead to improved accuracy, a reduction in the overall number of false readings, and ultimately, reduced cost of care." Pulse oximetry uses two light emitting diodes (LEDs), one red and one infrared, to measure the absorption of light and translates that into the percentage of hemoglobin molecules that are bound with oxygen, which is called arterial oxygen saturation (SpO2). Conventional pulse oximetry assumes that arterial blood is the only blood moving (pulsating) in the measurement site. However, during patient motion, the venous blood also moves, which can cause conventional pulse oximetry to under-read SpO2 levels because it cannot distinguish between the arterial and venous blood. SET identifies the venous blood signal (which has a lower oxygen saturation level than arterial blood), isolates it, and uses adaptive filters to cancel the noise and extract the arterial signal in order to report accurate SpO2 and pulse rate. In addition, SET pulse oximetry provides perfusion index (PI) and pleth variability index (PVI). Multiple studies have shown that compared to non-SET pulse oximeters, SET increases the ability to detect life-threatening events and reduces false alarms during challenging conditions. Additional studies have also shown the impact of SET on patient outcomes, such as helping clinicians: In 2011, the American Academy of Pediatrics and the U.S. Department of Health and Human Services recommended mandatory screening for all newborns, using "motion-tolerant pulse oximeters that report functional oxygen saturation have been validated in low perfusion conditions". To make this recommendation, the CCHD workgroup relied on two independent studies that exclusively used SET pulse oximetry to assess newborns. In 2012, Masimo received FDA 510(k) clearance for devices and sensors with labeling for screening newborns for CCHD. It marked the first time the FDA cleared specific labeling indicating the use of pulse oximeters, in conjunction with a physical examination, to screen newborns for CCHD. In 2012, the National Health Service (NHS) Technology Adoption Centre in the United Kingdom advised hospitals to use Intraoperative Fluid Management Technologies as a way to improve patient outcomes, and included Masimos PVI among technologies available for helping clinicians manage fluid during surgeries. In 2013, the French Society for Anaesthesia and Intensive Care (SFAR) added PVI to its guidelines for optimal hemodynamic management of surgical patients.
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