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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 apply biomedical engineering principles to execute the design controls for medical devices as a part of one or more new product development projects. Ensure product compliance to 21 CFR Part 820, ISO 13485:2016, ISO 14971:2007/2019, MDD 93/42/EEC and EU MDR 22017/745 and 746. This position collaborates with cross-functional teams including Product Development, Manufacturing Operations, Regulatory, Clinical and Marketing to maintain adherence to AtriCure’s QMS planning, execution and implementation activities for New Product Development. Lead the development and enforcement of AtriCure’s risk management activities to ensure patient and user safety through identification of risk-driven product requirements, generation of risk management report/benefit analyses, and participation in post-market product surveillance.

ESSENTIAL FUNCTIONS OF THE POSITION:

On time quality delivery of assigned product development team deliverables by adherence to internal QMS and design controls procedures in compliance with FDA, GMP, ISO and other applicable standards and regulations.
Responsible for cross functional collaboration with manufacturing operations, marketing, sales, regulatory and clinical functions
Responsible to generate and independently maintain project risk management files for new product development projects. These include risk management plans, hazard analysis, Application or Use FMEAs via failure mode effects analysis, risk mitigations and effectiveness checks, and Risk Management Reports using principles from ISO 14971.
Drive design assurance into product development through support of user needs/VOCs, product design requirements, design specifications, design verification and validation strategies, usability studies, process qualifications, design reviews and transfer.
Collaborate with Product development teams to define and cascade user needs/VOC to technical system and subsystem level design requirements through manufacturing requirements, develop rationales, establish traceability to detail designs and Design FMEAs
Provide expertise in development and implementation of C/R strategy, statistical support, inspection, sampling plans, test methods during Design Verification and Design Validation planning using a risk-based approach.
Provide coaching respective to investigative methods, risk mitigation techniques, DOE, statistical analysis, Reliability, and other related techniques (including Six Sigma, FTA, FMEA, HALT, etc.)
Participates or leads Technical Design Phase Reviews
Supports Manufacturing Operations with development of Validation Master Plans, Test Method Validations, Process FMEAs, and Process Validations (IQ, OQ and PQs).
Maintains product DHFs and DMRs.
Understanding of global standards and regulations including but not limited to FDA and ISO and Labeling, Packaging, Electrical (IEC 60601), Biocompatibility (ISO 10993) and Sterilization (Gamma, EO or other).
Own applicable corporate quality policies and drive updates based on new standards or regulations for compliance, and/or process improvements for efficient use of QMS.
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
Provides investigative support/leadership for product quality issues
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
Ability to mentor and coach others
Additional duties as assigned

BASIC QUALIFICATIONS:

Bachelor’s degree in Engineering required 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 with business process development
High level of knowledge in statistical analysis techniques
High level of experience in test method strategies, development and validation including GR&R
High level of experience with risk management methodology
Knowledge 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 travel 10%

PREFERRED QUALIFICATIONS:

9 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, 30 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).

You may access our global privacy policy here: https://www.atricure.com/privacy

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Staff Design Assurance Quality Engineer

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