Senior System Engineering Manager

Working at Abbott
At Abbott, you can do work that matters, grow, and learn, care for yourself and your 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.

• Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.

• An excellent retirement savings plan with a 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 worldwide 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 the best place to work for diversity, working mothers, female executives, and scientists.

The Opportunity
This position works out of our Irving, TX location in the Core Diagnostics Business Unit.

As the Senior Systems Engineering Manager, you’ll have the chance to have direct oversight and accountability for our diagnostics analyzers as a total system.

We’re empowering smarter medical and economic decision-making to help transform the way people manage their health at all stages of life. Every day, more than 10 million tests are run on Abbott’s diagnostics instruments, providing lab results for millions of people. 

What You’ll Work On

• Direct accountability for the overall systems management related to on-market diagnostics products.

• Short-term operational/tactical responsibilities related to field and factory performance.

• Manage teams responsible for investigations and risk management as well as product performance monitoring.

• Makes decisions related to emerging product issues and elevates to senior management in a timely manner with recommendations.

• Responsible for the activities related to the development of a product or line of products, as well as the improvement of existing products and technology.

• Manages the design analysis on components and/or assemblies to develop process by ensuring designs are cost efficient, manufacturable, and reliable.

• Communicates with senior management to coordinate the interrelated design and assure project completion.

• Helps to formulate business plans to develop and implement products and strategies.

• Responsible for identifying and investigating emerging new product opportunities within a defined range of responsibility.

• Implements business plans and creatively solves product design, financial, marketing, or administrative problems.

• Responsible for maintaining knowledge of new trends and products in the appropriate markets.

• Responsible for development of staff and organizational engagement to achieve business and talent objectives.

Required Qualifications

• Minimum 4 years Supervisory/managerial experience.

• Minimum 7 years Progressively more medical device company experience or relevant systems experience in a clinic/hospital/university environment.

• Demonstrated understanding and familiarity with applicable FDA regulations, and other relevant clinical/regulatory requirements.

• Full understanding and experience with the software design and development in the regulated environment.  Demonstrated working knowledge of appropriate domestic/international regulatory standards, understanding of the data management in the clinical trial lifecycle, and familiarity with the software validation practices is also required. Academic or in-house courses in leadership, training, Total Quality Management (TQM), relational database programs, plus cardiac packing, are preferred.

• Experience working in a broade