Senior R&D Engineer
AbbottAbout the role
JOB DESCRIPTION:
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
In Abbott’s Electrophysiology (EP) business, we’re advancing the treatment of heart disease through breakthrough medical technologies in atrial fibrillation, allowing people to restore their health and get on with their lives.
We are seeking a high caliber, experienced R&D Engineer to provide technical expertise through the planning and execution of high-profile, product quality improvement and product cost reduction projects related to electrophysiology catheters.
What You’ll Work On
Provides technical leadership for multiple product design and manufacturing quality improvement and product cost reduction projects related to electrophysiology catheters
Establish design and process requirements for electrophysiology catheter components
Run empirical and experimental analysis utilizing various analytical design tools to support design improvements and cost reduction efforts
Prepare technical reports, analysis, recommendations, and presentations reflecting the status and results of technical studies in progress
Partner with Project Management, Design Assurance, and other functional peers to execute key projects and deliver significant multi-year savings
Research various cost-effective, alternative approaches to current designs and processes
Directs support personnel and coordinates project activities
Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors
Plan, schedule, and coordinate R&D-related project tasks and activities
Test method and fixture development
Reviews and provides functional approval for project and quality system documentation.
Support all Divisional initiatives as identified by divisional 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.
Required Qualifications
Bachelors Degree in a related field - preferably in Mechanical or Biomedical Engineering
Equivalent combination of education and work experience
Medical device development and/or other highly regulated industry
Preferred Qualifications
Masters Degree in a related field - preferably in Mechanical or Biomedical Engineering
Design, manufacturing or process development experience related to one or more of the following technologies: high precision machining, injection molding, stamping, rolling, die cutting, polymer extrusions & bonds, soldering, welding, coatings and component specifications
Demonstrated success in executing design and process changes to on-market products in a regulated environment
Project leadership and management skills
Strong verbal and written communications with ability to effectively communicate at multiple
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