Senior Manager Engineering

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries.

     

JOB DESCRIPTION:

Senior Manager, Engineering

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 Westfield IN location, in the Structural Heart Medical Device Division.  Our business purpose is to restore health and improve quality of life by designing and providing device and management solutions for treating structural heart disease.

This position is responsible directly and through subordinate managers to oversee specific manufacturing and operations engineering activities.

What You’ll Work On

• Oversee manufacturing activities of multiple product lines operating on multiple shifts.

• Coach, manage and develop an immediate staff of managers and engineers.

• Develop and implement short and long term strategic plans to ensure systems are in place to meet business objectives.

• Develop, implement, train and monitor systems and procedures to ensure compliance to FDA, GMP and all other applicable agency regulations.

• Mentor engineering staff on root cause problem solving, data analysis, and other engineering disciplines as needed.

• Work with Continuous Improvement and other functions to develop effective processes capable of meeting quality, cost and supply chain objectives.

• Work cross-functionally with R&D, Quality, Clinical, Regulatory and other departments as needed to ensure effective new products transition into production.

• Develop and maintain solid relationships with all functions of the organization and possesses the ability resolve cross functional issues and appropriately influence these functions.

• Anticipate and resolve highest level issues and conflicts that could impact operations success.

• Ensure a safe work environment consistent with OSHA requirements and Abbott policies.

• Hire and retain a diverse, highly qualified staff and provides ongoing performance feedback.

• Set goals which align to department plans and manage the execution of goals through coaching and mentoring.

• Maintain a safe and professional work environment.

• Support all company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements.

• Comply with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, company policies, operating procedures, processes, and task assignments.

• Maintain positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.

Required Qualifications

• Bachelors’ degree in engineering; mechanical, electrical, biomed or industrial preferred.

• Minimum 12 years experience in engineering, manufacturing industry.

• Progressively responsible work experience in a high-volume, multi-product manufacturing environment, preferably in the medical device industry.

• Demonstrated proficiency and expertise in m