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 109,000 colleagues serve people in more than 160 countries.
A healthy heart is essential to good health.
That’s why we’re committed to advancing treatments for people with cardiovascular disease.
As a global leader in Cardiac Rhythm Technologies, our breakthrough medical technologies help restore people’s health so they can get back to living their best lives, faster.
We focus on innovative technologies that can improve the way doctors treat people with heart arrhythmias, or irregular heartbeats.
This position will be located in our Sylmar , CA office.
SUMMARY 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.
WHAT YOU’LL DO
Provides engineering support for existing operations
Design parts to meet specific design goals and 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, memos, Engineering Change Papers, creates travelers, and develops written operator procedures
Performs process validations on equipment, test methods and/or processes as required.
Work with internal departments and outside vendors to obtain prototype parts
CREO or other CAD experience required
Ability to work within a team and as an individual contributor in a fast-paced, changing environment.
Support design reviews and Plan, coordinate, and execute activity in support of project goals
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.
EDUCATION AND EXPERIENCE YOU’LL BRING
Education
Major/Field of Study Or Bachelors Degree (± 16 years)
Mechanical or Biomedical engineering, or related engineering field.
Or
An equivalent combination of education and work experience
Master Degree or PHD Preferred
– Mechanical or Biomedical engineering
Experience/Background
Minimum 1 year 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.
Experience with machine tool and/or molding concepts preferred.
Experience within an operations focused environment preferred.
Exposure to a variety of manufacturing processes and designing for manufacturability preferred
Ability to work within a team and as an individual contributor in a fast-paced, changing environment.
Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization.
WHAT WE OFFER
At Abbott, you can have a good job that can grow into a great career.
We offer:
A fast-paced work environment where your safety is our priority (Include for Manufacturing roles only)
Production areas that are clean, well-lit and temperature-controlled (Include for Manufacturing roles only)
Training and career development, with onboarding programs for new employees and tuition assistance
Financial security through competitive compensation, incentives and retirement plans
Health care and well-being programs including medical, dental, vision, wellness and occupational health programs
Paid time off
401(k) retirement savings with a generous company match
The stability of a company with a record of strong financial performance and history of being actively involved in local communities
Learn more about our benefits that add real value to your life to help you live fully:
Follow your career aspirations to Abbott for diverse opportunities with a company that provides the growth and strength to build your future.
Abbott is an Equal Opportunity Employer, committed to employee diversity.
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