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Principal Manufacturing Engineer

3 months ago

Mason, United States AtriCure Full time

Principal Manufacturing Engineer Mason, OH, USA Req #2159 Thursday, July 11, 2024 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: A Principal Manufacturing Engineer is a high level, experienced manufacturing/process engineer and is accountable for developing and maintaining capable and stable manufacturing processes to meet product quality standards/requirements. The role is responsible for process development and improvement, and tooling and fixture development and improvement both internally at AtriCure, and externally at key suppliers. A principal manufacturing engineer may also be involved in development of process analytics for preemptive defect control, process documentation and process layout & material logistic flow. ESSENTIAL FUNCTIONS OF THE POSITION: Experienced member of the manufacturing engineering team responsible for the qualification, implementation and support of manufacturing processes and equipment Is considered a subject matter expert in at least 2 major areas of manufacturing engineering Ensures continuous improvement in process, cost, quality and production Responsible for leading/mentoring members of the Manufacturing/Process Engineering Teams Supports and drives a DFM focused culture within the PD teams and the operations organization Supports and drives a continuous improvement culture within the PD teams and the operations organization Key liaison with external suppliers. Expertise in machining, molding and extrusion tooling and processes ADDITIONAL ESSENTIAL FUNCTIONS OF THE POSITION: Regular and predictable worksite attendance 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 Industrial Eng., Biomedical Engineering or Mechanical Eng. or equivalent is required 20+ years (15 years + Masters) of experience: Experience in development of new manufacturing processes and the tooling/equipment required to implement the processes Knowledge base in Lean Processes and Continuous Improvement Experience in Design for Manufacturability Experience with medical device design and manufacture Previous class II or class III Medical Device manufacturing experience Possess a strong knowledge of manufacturing processes and capabilities. Provide guidance in process and supplier selection when necessary. Self-motivated with strong time management skills Demonstrated ability to develop business, operational and financial strategies, plans and