Job Description

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 115,000 colleagues serve people in more than 160 countries.

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.

MAIN PURPOSE OF THE ROLE

Working under general supervision, is responsible for providing engineering support to device manufacturing operations. Develops and implements efficient, cost-effective process improvements. Work requires the application of theoretical principles and creative/analytical techniques typically acquired in a recognized four-year or more academic course of study. Applies engineering and scientific principles to the evaluation and solution of technical problems. Exercises an appropriate level of technical judgment in planning, organizing, performing and coordinating product development engineering assignments. Performs engineering studies. Stays abreast of and communicates technical advancements to colleagues and associates. Identifies and routinely uses the most effective, cost efficient and best practices to execute processes; continually evaluates their effectiveness and appropriateness.

MAIN RESPONSIBILITIES

• Hands on experience with prototyping, including design iteration, build, test and transition to manufacturing
• Preferred experience supporting intravascular lithotripsy (IVL) and/or catheter based systems, including development, troubleshooting or manufacturing support
• Provides engineering support for existing operations
• May perform dimensioning and tolerance evaluations of components, drawings and tooling
• May perform electrical analysis of failed components or devices for troubleshooting and corrective action purposes
• Oversees device configuration control and modifies the configuration as required
• Writes Engineering Test Reports (ETR’s), memos, Engineering Change Papers, creates travelers, and develops written operator procedures
• Performs process validations on equipment and processes as required.
• Resolves and/or facilities the resolution of problems including identifying causes to prevent re-occurrence
• Support all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements.
• Complies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments. Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.

QUALIFICATIONS

Education

Education Level

Major/Field of Study or Equivalent

Bachelors Degree (± 16 years)

Electrical/mechanical engineering, material science, or related engineering field.

An equivalent combination of education and work experience

Experience/Background

Experience Details

Minimum 3 years of relevant/related exp.

Relevant design and manufacturing work experience as related to medical devices.

Demonstrated ability to analyze and evaluate technologically complex devices. Experience working in a broader enterprise/cross-division business unit model preferred. Ability to work in a highly matrixed and geographically diverse business environment. Ability to work within a team and as an individual contributor in a fast-paced, changing environment. Ability to leverage and/or engage others to accomplish projects. • Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization. Multitasks, prioritizes and meets deadlines in timely manner. Strong organizational and follow-up skills, as well as attention to detail. Ability to travel approximately 5%, including internationally.

The base pay for this position is

$50,700.00 – $101,300.00

In specific locations, the pay range may vary from the range posted.

JOB FAMILY:

Product Development

DIVISION:

AVD Vascular

LOCATION:

United States > Minnesota > St. Paul : 1225 Old Highway 8 NW

ADDITIONAL LOCATIONS:

WORK SHIFT:

Standard

TRAVEL:

Yes, 10 % of the Time

MEDICAL SURVEILLANCE:

Not Applicable

SIGNIFICANT WORK ACTIVITIES:

Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Keyboard use (greater or equal to 50% of the workday)Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO_English.pdfEEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf