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Design Assurance Quality Engineer

Job in Mason, Warren County, Ohio, 45040, USA
Listing for: AtriCure, Inc.
Full Time position
Listed on 2025-12-22
Job specializations:
  • Engineering
    Quality Engineering, Electrical Engineering
Salary/Wage Range or Industry Benchmark: 80000 - 100000 USD Yearly USD 80000.00 100000.00 YEAR
Job Description & How to Apply Below

Atri Cure, 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 Atri Cure technologies for the treatment of Afib and reduction of Afib related complications. Atri Cure's Isolator Synergy Ablation System is the first medical device to receive FDA approval for the treatment of persistent Afib.

Atri Cure's Atri Clip Left Atrial Appendage Exclusion System products are the most widely sold LAA management devices worldwide. Atri Cure's Hybrid AF Therapy is a minimally invasive procedure that provides a lasting solution for long-standing persistent Afib patients. Atri Cure's cryo

ICE cryo

SPHERE probe is cleared for temporary ablation of peripheral nerves to block pain, providing pain relief in cardiac and thoracic procedures. For more information, visit  or follow us on Twitter @Atri Cure.

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 be 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
  • May include coaching and training respective to investigative methods, risk mitigation techniques and general safety (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
  • 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 3 years of experience in an engineering role in the medical device industry
  • Experience with quality system process development
  • Working knowledge in statistical analysis techniques including Reliability assessment
  • Experience in test method strategies, development and validation including GR&R
  • 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…
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