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Sr Product Development Engineer - Test Method Development

Job in Fridley, Anoka County, Minnesota, USA
Listing for: Resolution Medical, LLC
Full Time position
Listed on 2026-03-01
Job specializations:
  • Engineering
    Product Engineer, Mechanical Engineer
Salary/Wage Range or Industry Benchmark: 80000 - 100000 USD Yearly USD 80000.00 100000.00 YEAR
Job Description & How to Apply Below

Description

Description

Job Summary

Activities include product design and development, defining technical solutions to abstract problems, defining methods and processes, design modeling, tooling design/fabrication, equipment design/fabrication, personnel management, design verification and validation, and documentation. Manage the day-to-day execution of reliability tasks by teams and team members through monitoring progress, providing technical direction, and problem-solving solutions. Subject matter expert on test method development and design verification.

Primarily by driving the testing of device, assist in design and develop innovative products & manage the product design from concept to full production.

This position will lead in the execution of development projects as part of a multi-functional project team with an emphasis on the V&V activities.

Essential Functions

Product Development (~50% allocation):

  • Research, design and implement new products based on customer specifications
  • Understand the end use of products, determine fitness-for-use of materials, and effectively advancing the specification development of new and derivative products
  • Perform data analysis (statistical and practical) and develop appropriate action plans based upon such analysis
  • Prepare and present plans and schedules as Technical Project Lead
  • Serve as Technical leader, and cross-functional team member representing Product Development, for development projects (as assigned). Duties include task management, organize and facilitate technical team meetings, lead technical reviews, provide documentation and coordinate project activities
  • Perform as a technical resource to all departments with a thorough understanding of related disciplines
  • Communicate progress and decisions to customers, associates and functional managers
  • Assist management in improving systems for product development, standard operating procedures, safety, quality control and training
  • Identify opportunities for productivity and quality improvements
  • Perform product/process analysis for cost reduction, quality improvement, and improved efficiency
  • Perform research, design and development of product assembly methods including production equipment
  • Contribute to the development of project plans that meet the required customer and/or internal milestones, specifications, and product cost goals, within project budget and staff assignments
  • Support company finance, accounting, human resources, quality, regulatory, and clinical departments as necessary to ensure compliance with requirements
  • Follow company policies and procedures

Requirements, Verification, & Testing (~50% allocation)

  • Design and develop simulated use models for engineering confidence testing and DVT. Specify and develop tests for product testing determining acceptability of designs to requirements
  • Develop product requirement specifications based on customer needs and applicable guidelines (industrial and government guidelines and/or standards)
  • Strong preference for experience in common catheter standards (e.g. ISO
    10555) or common active implantable device standards (e.g. ISO
    14708)
  • Develop tooling and test equipment designs for product assembly and testing
Requirements Functional Knowledge
  • Good engineering techniques
  • Knowledge of human anatomy
  • Articulate and able to effectively communicate very technical subjects with peers and customers
  • Knowledge of machining and assembly practices, tools and fixturing is required. Knowledge of plastic and/or metal is preferred
Education, Experience, Required Skills
  • Bachelor’s degree in related field (equivalent work experience may be considered)
  • Five (5) + years of medical device industry experience as an individual contributor with a majority of time spent on requirements development, design verification, & test method development.
  • Strong strategic focus in the areas of Product and Process Development
  • Ability to handle and be trusted with confidential and/or sensitive information
  • Strong problem-solving skills to identify, gather, and analyze information develop solutions and resolve problems in a timely manner
  • Must have knowledge of machining and assembly practices, tools and fixturing…
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