Principal Design Assurance Quality Engineer

AtriCure, Inc. provides innovative technologies for the treatment of Afib and related conditions. Afib affects more than 33 million people worldwide. Electrophysiologists and cardiothoracic surgeons around the globe use AtriCure technologies for the treatment of Afib and reduction of Afib related complications. AtriCure's Isolator Synergy Ablation System is the first medical device to receive FDA approval for the treatment of persistent Afib. AtriCure's AtriClip Left Atrial Appendage Exclusion System products are the most widely sold LAA management devices worldwide. AtriCure's Hybrid AF Therapy is a minimally invasive procedure that provides a lasting solution for long-standing persistent Afib patients. AtriCure's cryoICE cryoSPHERE probe is cleared for temporary ablation of peripheral nerves to block pain, providing pain relief in cardiac and thoracic procedures. For more information, visit AtriCure.com or follow us on Twitter @AtriCure.

We foster a culture of inclusion by embracing diverse experiences and individuals where everyone's authentic self is welcome. We offer supporting programs and resources that provide enriching and equitable opportunities for each person to contribute professionally and personally.

POSITION SUMMARY : This position will

be part of one or more product development teams where they will responsible for contributing to the on-time development of high-quality products and optimization of core design control business processes.

ESSENTIAL FUNCTIONS OF THE POSITION :

On time quality delivery of assigned product development team deliverables

Ensure assigned design control procedures are compliant with FDA, GMP, ISO and other applicable standards and regulations

Optimize existing processes to maximize efficiencies and continue to identify, plan and execute continuous improvement activities

Drive continuous improvements through observation, measurement and root cause analysis / resolution

Develop new processes which support speed, cost reductions and quality improvements

Provide subject matter expertise for assigned processes to users as necessary

Responsible for cross functional collaboration with manufacturing operations, marketing, sales, regulatory and clinical functions

Provide coaching respective to investigative methods, risk mitigation techniques, Reliability analysis, design control, testing strategies and measurement system analysis (including Six Sigma, FTA, FMEA, HALT, etc.)

Provide guidance for development of manufacturing test / evaluation methods and process validation

Provides investigative support / leadership for product quality issues

Work with product development teams to help cascade requirements from VOC through manufacturing requirements and link to production controls\Work with product development teams on timely use of Risk Management activities including supporting and leading FMEAs and essential requirements analysis including standards review and evidence of conformity

Serve as technical resource for problem investigations to guide root cause analysis and corrective action development

Provide mentorship to junior level design assurance engineers in design control and product development

Ensure commitment to functional excellence and the ability to execute positive changes

ADDITIONAL ESSENTIAL FUNCTIONS OF THE POSITION :

Regular and predictable work performance

Ability to work under fast-paced conditions

Ability to make decisions and use good judgment

Ability to prioritize various duties and multitask as required

Ability to successfully work with others

Additional duties as assigned

BASIC QUALIFICATIONS :

Bachelor's degree in Engineering from an accredited college or university or demonstrated equivalent combination of education, training and experience

Minimum of 7 years of experience in an engineering role in the medical device industry

Experience in development of and linking product requirements from VOC through to design output and production controls

Experience with business process development

Experience in Reliability definition, testing and assessment

High level of knowledge / experience in statistical analysis techniques

High level of knowledge / experience in test method strategies, development and validation including GR&R

High level of knowledge / experience with risk management methodology using ISO 14971

High level of knowledge / experience of Design Controls and experience with FDA QSR 21 CFR Part 820 and ISO 13485

Ability to create and manage key internal and external partnerships

Excellent written and verbal communication skills

High level of attention to detail

Familiar with product safety and standards

Ability to demonstrate proficiency in issue resolution

Ability to multi-task and work with little direction

Ability to manage multiple priorities

Familiar with product safety standards

Ability to effectively mentor and coach others

Ability to travel 10%

PREFERRED QUALIFICATIONS :

10 years or more experience in an engineering role in Medical Devices

7 or more years' experience working with Product Development

Experience in processes related to Design Change Control, Design Reviews, Requirements Management

Certification in ASQ, Six Sigma / Design for Six Sigma

OTHER REQUIREMENTS :

Ability to regularly walk, sit, or stand as needed

Ability to occasionally bend and push / pull as needed

Ability to pass pre-employment drug screen and background check

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AtriCure has a variety of benefits available for US based employees and their families. Examples include Medical & Dental beginning day 1 of employment, 401K plus match, 20 days of paid Parental Leave, in addition to maternity leave, for new moms and dads, Volunteer Time off, Pet Insurance, and more. Corporate-based employees also have full access to our on-site fitness center and cafeteria. To see a complete list of our benefits, please visit our careers website : https : / / www.atricure.com / careers-atricure / benefits. AtriCure participates in the federal E-Verify program to confirm the identity of and employment authorization of all newly hired employees. For further information about the E-Verify program, please click here https : / / www.e-verify.gov / AtriCure is an Equal Employment Opportunity / Affirmative Action employer and provides Drug Free Workplaces. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national or ethnic origin, age, protected veteran status, status as an individual with disability, sexual orientation, gender identity or any other characteristic protected by federal, state, or local law(s).

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