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1+ months

Product Engineer II - Surgical Robotics

Medtronic
North Haven, CT 06473
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Product Engineer II - Surgical Robotics

Location:

North Haven, Connecticut, United States

Requisition #:

220002WW

Post Date:

Mar 02, 2022


**Careers that Change Lives:**


You will join a world class team of mechanical, electrical, software and system engineers responsible for further development and enhancement of the globally launched Medtronics Robotic Assisted Surgery platform through commercial launch and production scale-up: https://www.medtronic.com/covidien/en-us/robotic-assisted-surgery/hugo-ras-system.html


**Impact patient outcomes. Come for a job, stay for a career.**


In the Surgical Robotics (SR) business, part of Medtronics Medical Surgical Portfolio, we believe patients around the world deserve access to quality care and improved outcomes. We strive to expand global access to care and reduce variability through robotic and analytics solutions.


**A Day in the Life**


This position will be based out of Medtronics campus in North Haven, CT and reports to the Consumables Lead - RD Sustaining.


The Sustaining Product Engineerwill work closely with the project management office, Medtronic engineers, and our contract manufacturing sites. You will be able to dive in deep technically, and lead design change initiatives on the consumable products used in Robotic Surgery. Outstanding written and verbal communication skills are critical to success in this role, as is the ability to thrive in a fast-paced environment.


**As a Product Engineer within RD Sustaining, you will:**


+ Have high aptitude for mechanical systems


+ Be the key central communications point for sustaining related project activity.

+ Track deliverables from internal and external teams against product design change requirements.

+ Anticipate, identify, and provide technical solutions to a wide range of difficult problems.

+ Mitigate production and manufacturing risks by identifying areas of opportunity and executing improvement projects.

+ Assess timeline impacts against project schedule.

+ Work with engineers to develop a deep understanding of the technological underpinnings of the system.

+ Conducts project management tasks documentation with design controls and risk analysis in accordance with established SOPs.

+ Incorporate required regulatory standards (FDA, ISO) in developmental and/or sustaining engineering projects including written protocols, test methods, assembly processes and the Design History File.

+ Contribute inventions, new designs and techniques regarded as advances in the medical and technical/scientific community.

+ Prepare reports, presentations and spreadsheets of an analytical and interpretative nature using statistical data analysis methods.


**Must Have: Minimum Requirements**


+ Bachelors degree required

+ Minimum of 2 years of relevant experience, or advanced degree with 0 years of experience


**Nice to Have**


+ Outstanding verbal and written communication skills

+ Strong leadership skills

+ Comfortable working in a fast paced, cross disciplinary environment

+ Ability to discuss technical details with engineering staff, the ideal candidate will have a strong engineering and product development background.

+ Ability to create and track a project budget and timeline

+ Able to work with minimal direction towards completing project tasks

+ Takes initiative in keeping current with technology developments in specialized area.

+ Effectively communicates and works cooperatively with others as part of a team.

+ Working knowledge of applicable FDA and ISO standards.

+ Thorough understanding of engineering practices, product safety and root cause analysis.

+ Knowledge of rapid prototyping, assembly tooling, injection molding, metal stamping / machining, design, and process methods.

+ Working knowledge of Design for Six Sigma, Failure Mode Effects Analysis, Statistical Analysis methods, and Design of Experiments.

+ Effective in written and oral communication; experienced in report writing and development of presentations.

+ Knowledge and experience with reusable medical device materials and biocompatibility testing.


+ Knowledge of medical product RD and clinical/regulatory process

+ Good understanding of structured product development (requirements-driven engineering, documentation, rigorous verification, etc.) Engineering verification test development and execution

+ Understanding and experience with system reliability testing and service.


**Working Conditions**


Standard office setting, manufacturing clean room, surgical lab, operating room, pilot lab, external research organizations, supplier visits. Travel (10%) and flex hours as needed.


Based in North Haven, CT USA


**About Medtronic**


Together, we can change healthcare worldwide. At Medtronic, we push the limits of what technology, therapies and services can do to help alleviate pain, restore health and extend life. We challenge ourselves and each other to make tomorrow better than yesterday. It is what makes this an exciting and rewarding place to be.


We want to accelerate and advance our ability to create meaningful innovations - but we will only succeed with the right people on our team. Lets work together to address universal healthcare needs and improve patients lives. Help us shape the future.


**Physical Job Requirements**


The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role. (ADA-United States of America)


**EEO**


It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.


This employer participates in the federal E-Verify program to confirm the identity and employment authorization of all newly hired employees. For further information about the E-Verify program, please click here: http://www.uscis.gov/e-verify/employees .
It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.

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Posted: 2022-03-08 Expires: 2022-06-13
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Product Engineer II - Surgical Robotics

Medtronic
North Haven, CT 06473

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