Cal Poly Intern Undergrad (Tech)
Location: Santa Rosa California
Description: Medtronic is employing Cal Poly Intern Undergrad (Tech) right now, this job will be placed in California. For complete informations about this job opportunity please give attention to these descriptions. Medtronic is an Equal Opportunity/Affirmative Action Employer
Position Description
We are considering students for Intern, co-op and FT pooprtunities. An Example Oppor! tunity:
Medtronic is the global leader in medical technology -- alleviating pain, restoring health, and extending life for people with chronic conditions around the world. Medtronic develops and manufactures a wide range of products and therapies with emphasis on providing a complete continuum of care to diagnose, prevent and monitor chronic conditions. Each year, Medtronic therapies help more than seven million people.
Our Summer Associate Program offers technical internships to top graduate and undergraduate engineering students. Even before you graduate, you will get a taste of our innovative, mission-driven culture, while gaining meaningful work experiences and improving lives. In addition to a challenging 10-12 week internship assignment or 6 month co-op, you'll have opportunities to support the sixth tenant of our Mission through volunteer activities, and experience our dynamic culture through a variety of networking, leadership, and social events. Position Responsibilities
The R&D Engineer in the ! Coronary Business Unit’s Science and Technology Engineering group develops new and innovative methods and devices for the treatment of unmet clinical needs.
R&D Engineer are to execute to the position requirements, to develop new technologies and devices used to treat cardiovascular diseases.
May have functional leadership responsibility for technicians by assigning tasks and conducting performance evaluations. Must have ability to work on teams and lead or take ownership of sub-projects activities and participate as extended team member. May be lead for sub-projects of limited scope.
May produce multiple results consistent with larger projects of partially defined situations within well defined timeline. May complete product design test reports of product testing and make decisions broad in scope. Must understand research and input required in order to arrive at best decision, participate in risk analysis activities and bring specific knowledge of a! defined portion of a device with limited procedural understanding
Must understand and apply conceptual ideas in a clinical setting, the possible effects of an implant within the body have a solid grasp of in vitro models and of products and how they work in vitro, attend pre-clinical evaluations and attend Anatomy and Physiology classes. May have attended clinical procedures e.g. cath lab or operating room procedure and can apply learning.
May submit invention disclosures of original ideas, produce creative solutions to problems, and actively participates in brainstorming activities. May create many hypotheses for a complex problem, build representative prototypes (physical-prototypes and virtual-computer models), devise and perform simplified tests to prove the hypotheses, explain and interpret the results to problem owner. Communicate written results in lab notebooks and peer reviewed reports, write reports and presentations of limited scope. May presents to peer! s and to other professionals within and outside of own department and a! ct as spokesperson for peers. Collaborate candidly within and outside of own department. Interact effectively with cross functional groups i.e. (Quality, Regulatory, Manufacturing, Clinical, Marketing, Finance)
Must work to project milestones or larger task level assignments, seek guidance and feedback periodically, and develop a sense of what and when assigned information needs to be reported. Must have a working knowledge of how ones own work and work of team produces project milestones and business objectives.
May write and execute test methods and process instructions, develop product documentation, and work to a defined set of design requirements. May write typical engineering documents, e.g. operator instructions, process instructions. May have limited working knowledge of regulatory indications, e.g., that application of ISO and FDA standards, and quality standards.
Basic Qualifications
The successful candidate must possess:
Minimum of! 2 years with BS degree, or a MS degree, mechanical engineering, biomedical engineering, materials science and engineering, or similar .
Confident in the use of engineering and scientific principles to solve complex technological issues.
Excellent communication skills.
Ability to perform well in cross-functional, highly dynamic development teams.
Desired/Preferred Qualifications
Physical Job Requirements
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If you were eligible to this job, please email us your resume, with salary requirements and a resume to Medtronic.
If you interested on this job just click on the Apply button, you will be redirected to the official website
This job starts available on: Tue, 15 Oct 2013 13:32:40 GMT