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1+ months

Senior R&D Engineer

Irvine, CA 92604
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Senior R&D Engineer


Irvine, California, United States

Requisition #:


Post Date:

Aug 11, 2020

**Senior RDEngineer**

**Careers That ChangeLives**

This position has the responsibility and authority to
provide engineering expertise and advanced project team leadership for the
design, development and optimization of complex products, processes, tooling
and/or equipment. Applies strong engineering principles to provide engineering
support for released product engineering. Responsible for post-launch product
design life cycle including design optimization, material and component design
changes, design failure root cause investigations, CAPAs, and documentation
activities. Exercises judgment within broadly defined practices and
parameters.Applies principles of
Customer Focused Quality in daily activities in order to meet and exceed
internal and external customer requirements.


The Restorative Therapies Group develops life-restoring
therapies and healthcare solutions that span the care continuum; integrating
technologies and applying clinical and economic evidence to increase patient
access, improve efficiency of procedures and deliver successful patient

**Cerebral Spinal Fluid(CSF) Management** business located at the new Brain Therapies headquarters
in Irvine, CA focuses on the hydrocephalus management therapies and critical
care technologies

**A Day in the Life**


Provides engineering support for the design of products,
processes, tooling and/or equipment. Develops and tests prototypes from
design specifications, defines processes to properly make and assemble the
product and optimizes process.

Project Management:

Leads complex engineering projects. Utilizes advanced team
leadership skills to effectively communicate, facilitate, and organize project
activities to maximize team productivity.Develops and manages project schedules to ensure deadlines are met.Creates project budgets and recommends
necessary resources.

Documentation and Systems:

Demonstrates an advanced understanding and application of
quality and documentation systems.Applies knowledge in order to expedite documentation required by


Optimizes product, process, tooling and/or equipment design
to produce cost-effective, quality results within design specifications.


Evaluates products and competitor products and

Presentations and Training:

Conducts presentations and explains complex technical
information to management, employees and visitors in a manner that is easily
understood.Provides technical training
ranging in complexity for other employees.


Readily identifies safety issues in the immediate work
environment and other work areas and recommends and implements solutions for

Continuous Learning:

Remains informed about current medical/technical
procedures, engineering and material trends by reviewing current literature for
technology application, and appropriate coursework.

All activities must be performed in compliance with the
Quality System.

Performs duties in compliance with environmental, health
and safety related site rules, policies or governmental regulations.

**Must Have: MinimumRequirements**

Bachelors degree in Engineering and 4+ years experience or
an advanced degree and 2+ years experience

**Nice to Have**

Medical device industry experience preferred

Demonstrated engineering field of expertise such as
mechanical, electrical, biomaterials, etc.

Demonstrated ability to effectively manage complex projects

Demonstrated ability to solve complex problems in creative
and effective ways

Demonstrated advanced team leadership skills

Demonstrated excellent interpersonal skills

Demonstrated excellent organizational skills

Demonstrated excellent verbal and written communication
skills including ability to effectively develop and present complex technical
information necessary for the company

Demonstrated excellent analytical skills

Familiarity with personal computer software including word
processing, spreadsheet, and statistical programs; computer aided drawing and
project scheduling software preferred

Demonstrated advanced understanding and application of Quality System requirements, including FDA
GMPs, and ISO 9000 and documentation procedures; ability to learn MPSM systems

**Travel requirement: 25%**

**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)
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.


Posted: 2020-08-13 Expires: 2020-10-19
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