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Senior Mechanical Engineer

Job in Mason, Warren County, Ohio, 45040, USA
Listing for: AtriCure, Inc.
Full Time position
Listed on 2026-05-01
Job specializations:
  • Engineering
    Product Engineer, Mechanical Engineer, Biomedical Engineer, Medical Device Industry
Salary/Wage Range or Industry Benchmark: 100000 - 125000 USD Yearly USD 100000.00 125000.00 YEAR
Job Description & How to Apply Below

Position Summary

This position will contribute to the development of ablation products that treat atrial fibrillation, postoperative pain, and/or Left Atrial Appendage (LAA) Exclusion System products. Job performance requires application of technical abilities, command of physics and mechanical engineering, healthcare practices and procedures, and a solid understanding of product development methodologies. Deliverable outputs include analysis, design, evaluation, production transfer, and documentation of products that meet medical and regulatory guidelines.

The Senior Mechanical Engineer will play a technical leadership role in the context of multi‑disciplinary teams under the direction of a project manager.

Essential Functions
  • Work in a cooperative cross‑functional team environment to accomplish personal and team goals and objectives associated with development of innovative medical devices or innovative improvements to existing devices.
  • Support and lead the technical development efforts of medical device projects including requirements development, mechanical design, testing, analysis, verification, and validation.
  • Develop component and product technical specifications including the integration and consideration of applicable standards and regulations.
  • Support the product development life cycle including needs assessment, voice of the customer, technology development, detail design & manufacturing systems development, regulatory requirements, and product verification/validation.
  • Develop an understanding of Atri Cure devices with an eye for improvement and development projects.
  • Generate work plans and coordinate activities with product development teams.
  • Operate program management tools and documentation requirements of Medical Device Design Controls.
  • Perform analytical modeling / analysis of new technologies in support of achieving product performance requirements.
  • Communicate with external suppliers of components, subassemblies, and finished assemblies.
  • Generate and document intellectual property submissions.
  • Understand and practice GD&T and how to properly apply it to yield the desired fits between joining parts.
  • Expertise in computer communication tools, ability to manage design research & development activities through the product life cycle, computer aided engineering tools (Solid Works, FEA software), scheduling (Microsoft Project), project documentation, statistical analysis, and intellectual property generation.
  • Perform mechanical analysis including statics and dynamics, finite element modeling, and material properties.
  • Establish understanding of clinical procedures and techniques applicable to Atri Cure products.
  • Develop and validate test methods.
  • Have knowledge of manufacturing methods and capabilities including plastic injection molding, metal stamping, and metal machining, casting, stamping, forming, grinding, etc.
  • Lead tasks with minimal supervision or guidance.
  • Work independently applying comprehensive and diverse engineering principles and practices to broad assignments, including independently leading a moderate project.
  • Prioritize tasks and provide a timely schedule of completion.
Additional Essential Functions
  • 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 required in Engineering or demonstrated equivalent combination of education, training and experience.
  • 5+ years of experience in mechanical engineering in medical device product development or an equivalent field.
  • Must be confident, goal oriented, self‑motivated and a team player.
  • Must have strong and proven relationship‑building skills.
  • Proven track record of significant technical achievement, capability, and contribution to the success of the business.
  • Ability to lead project activity, mentor others, and lead company technical initiatives.
  • Experience developing inspection/testing requirements and techniques.
  • Data analysis, problem‑solving, troubleshooting and formal root‑cause analysis…
Position Requirements
10+ Years work experience
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