Staff Systems Engineer
AbbottAbout the role
JOB DESCRIPTION:
Working at Abbott
At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You’ll also have access to:
Career development with an international company where you can grow the career you dream of.
Free medical coverage for employees* via the Health Investment Plan (HIP) PPO
An excellent retirement savings plan with high employer contribution
Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree.
A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.
A company that is recognized as one of the best big companies to work for, as well as a best place to work for diversity, working mothers, female executives, and scientists.
The Opportunity
We are recruiting a Staff Systems Engineer to join our Abbott Heart Failure team in Pleasanton, CA, where we are focused on helping people with heart failure manage their health and ultimately change and save lives. The engineer will be primarily working on the CardioMEMS HF portfolio, which remotely monitors changes in pulmonary artery (PA) pressure, an early indicator of the onset of worsening heart failure, to aid physicians in preventing worsening heart failure, lower heart failure mortality rates, and improve quality of life for our heart failure patients. The role is responsible for driving the systems engineering for a wide range of CardioMEMS products including implantable sensors, external reader systems used by clinicians and patients, mobile application software, and cloud-based web applications. This person will help to drive and lead the development of new programs and next generation products, focusing on assessing risk and influencing requirements, design, and testing as a result of risk management.
What you will do:
Conduct and drive risk management activities within R&D, including various types of FMEA documentation. Conduct and lead risk brainstorming sessions.
Develop comprehensive understanding of existing and planned system and detailed designs in order to document and drive risk control measures and mitigators.
Identify, implement, educate, and share improved tools and methods for risk documentation. Influence style and language used in risk documentation to ensure systematic and thorough risk coverage.
Participate in product definition, system architecture, requirements writing, requirements management, requirements analysis, System V&V, and design control documentation, from design conception to launch.
Participate and drive systems level decision making, accounting for and prioritizing critical needs, risks, and requirements and assessing against various options and solutions.
Lead the planning of system engineering tasks, especially risk management tasks, including timelines, budgets, and prioritization.
Perform system level characterization of devices through development to refine requirements and finalize the design for System V&V. Collect, organize, analyze, document, and present results.
Plan, execute, and/or lead System V&V testing, data analysis, and documentation.
Communicate effectively to cross-functional teams and senior management.
Comply with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments.
Required Qualifications:
Bachler’s Degree in Engineering (Mechanical, Computer, Electrical, or Software), Computer Science, or related discipline
8+ years of in a similar position, including systems engineering and integration experience (integrating all system components - electrical, mechanical, software), system architecture, requirement/user nee
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