Principal Manufacturing Engineer

AtriCure, Inc.Cincinnati, OH
39dOnsite

About The Position

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. This Position is located in Mason/Cincinnati OH and will be onsite. Must be able to commute or relocate to Cincinnati OH for this position to be considered. 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.

Requirements

  • Bachelor's degree in Industrial Eng., Biomedical Engineering or Mechanical Eng. or equivalent is required
  • 15+ years (10 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 programs that foster the achievement of organizational objectives
  • Ability to translate broad strategies into specific objectives and action plans
  • Demonstrated possession of in-depth and current knowledge of industry best practices and the ability to implement the same
  • Experience in technical report writing and verbal and oral communication skills
  • Must be able to read blue prints and interpret technical specifications and illustrations
  • Comfortable driving multiple initiatives at a rapid pace, making thoughtful recommendations with available data
  • Active, high-energy communicator who drives a company vision/mission to align teams, critical resources, management, and stakeholders
  • Creative thinker with exceptional process, analytical, management and relationship skills
  • Problem solving/trouble shooting experience
  • Ability to travel 10%
  • Ability to regularly walk, sit, or stand as required
  • Ability to occasionally bend and push/pull
  • Ability to regularly lift up to 25 pounds
  • Ability to pass pre-employment drug screen and background check

Responsibilities

  • 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
  • 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

Benefits

  • 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
  • Corporate-based employees also have full access to our on-site fitness center and cafeteria

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What This Job Offers

Job Type

Full-time

Career Level

Mid Level

Industry

Miscellaneous Manufacturing

Number of Employees

1,001-5,000 employees

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