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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 Source: Abbott Laboratories companyAbbott
Santa Clara, CA, United States
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 Source: AbbottCampbell
Title: Principal R&D Engineer, Preclinical
Location : This position is based in our Campbell, California offices. This position is on-site & full-time with some travel.
Why Imperative Care?
Do you want to make a real impact on patients? Imperative Care is changing the way stroke is treated. As part of our team, you’d be developing breakthroughs that will revolutionize the future of stroke care. Every day, the technologies that we develop at Imperative Care directly impact human lives. Our focus is on the needs of the patient, and they come first in everything we do.
What You’ll Do
You will be responsible for contributing to all pre-clinical related research, design and testing to further the conceptualization, design, development, and manufacturability of product/s in accordance with the company’s Quality System and customer requirements.
You will be responsible for designing and managing all aspects of physician evaluations, in-vitro bench and simulated use testing, and in-vivo studies, and will partner with Marketing representatives to create marketing collateral via bench and in-vitro testing.
+ Design and manage in-vitro (in-house and external) and in-vivo testing: study design and model selection (including model design/development as needed)
+ Coordinate, design and manage internal and external resources, as well as generation of protocols, and reports, in addition to overseeing the testing lab
+ Collaborate with project teams to prepare and conduct physician evaluation sessions, including method/test sequence development, model design and selection, and data collection
+ Significant interaction with customers, study centers, etc, coordinate study schedules, seeking and providing input into our processes
+ Work directly with customer representatives to determine needs in simulated use/in-vitro testing, product design, user interface, and possible integration of product with other medical systems or products
What You’ll Bring
+ BS in Engineering or related discipline and 12+ years of related experience; or MS in Engineering with 8+ years of related experience; or equivalent combination of education and work experience in the medical device or related regulated industry.
+ 5+ years previous experience in medical device pre-clinical engineering related activities strongly preferred (participating in conducting animal studies, in-vitro testing, etc.)
+ Prior experience working with physicians in OR setting strongly preferred
+ Knowledge of and exposure to product testing and data collection
+ Extensive experience working under quality systems designed to meet governmental regulations such as FDA QSR, ISO 13485, and the MDD
+ Extensive experience in full R&D product life cycle
Employee Benefits include a stake in our collective success with stock options, competitive salaries, a 401k plan, health benefits, generous PTO, and a parental leave program.
Salary Range: $176,000-191,000
Please note that the salary information is a general guideline only. Imperative Care considers factors such as scope and responsibilities of the position, candidate's work experience, education/training, key skills, and internal equity, as well as location, market and business considerations when extending an offer.
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