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Research And Development Engineer Medical Device Jobs in Minnesota

Design contributor for components, sub, or finished medical device assemblies. * Support ... Master's degree in Biomedical Engineering * 0-1 year of experience in R&D engineering field ...

Design contributor for components, sub, or finished medical device assemblies. * Support ... Master's degree in Biomedical Engineering * 0-1 year of experience in R&D engineering field ...

Sr. R&D Engineer

Eden Prairie, MN · On-site

$100K - $130K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

As Senior R&D Engineer , you will take full ownership of the technical execution for internal and ... Medical Device Design Control and Risk Management: * Leveraging a high level of experience and ...

MN

$55 - $60/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Engineering & Scientific, Engineering Title: R&D Engineer Location: Plymouth, MN Duration: 12 ... Medical device experience Exposure to a variety of manufacturing processes used in medical devices ...

Senior R&D Engineer

Saint Paul, MN · On-site

$105K - $145K/yr

  • Medical

  • Retirement

As the Sr. R&D Engineer, you will be part of our EP product development team focused on delivering ... medical device industry. * Experience in or willingness to learn preclinical testing methods.

Senior R&D Engineer

Saint Paul, MN · On-site

$105K - $145K/yr

  • Medical

  • Retirement

As the Sr. R&D Engineer, you will be part of our EP product development team focused on delivering ... medical device industry. * Experience in or willingness to learn preclinical testing methods.

Senior R&D Engineer

Saint Paul, MN · On-site

$105K - $145K/yr

  • Medical

  • Retirement

As the Sr. R&D Engineer, you will be part of our EP product development team focused on delivering ... medical device industry. * Experience in or willingness to learn preclinical testing methods.

Senior R&D Engineer

Brooklyn Park, MN · On-site

$116 - $136/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

We are seeking an experiencedResearch and Development Engineerwith deep medical device development ... Lead R&D efforts in understanding the anatomical and physiological landscape a TAVR system ...

Medical Device Assembler I

Eden Prairie, MN · On-site

$18.25 - $22.50/hr

The Medical Device Assembler I is responsible for performing a variety of production tasks related ... Instructions (WI), Engineering Prints and Bills of Materials (BOM). Primary Duties ...

Showing results 41-60

Research And Development Engineer Medical Device information

What does a research and development engineer do in the medical device industry?

A Research and Development (R&D) Engineer in the medical device industry is responsible for designing, developing, and testing new medical devices and technologies. They work closely with cross-functional teams to ensure products meet regulatory standards, are safe for patient use, and address clinical needs. Their tasks may include prototyping, conducting experiments, analyzing data, and collaborating with manufacturing teams to bring products from concept to market. R&D Engineers also stay updated on technological advancements and regulatory changes to ensure innovation and compliance.

What are the key skills and qualifications needed to thrive as a research and development engineer in the medical device industry?

To excel as a Research and Development Engineer in Medical Devices, you need a solid background in biomedical engineering or a related field, strong problem-solving skills, and experience with product development cycles. Familiarity with CAD software, prototyping tools, regulatory standards like ISO 13485, and relevant certifications (such as Six Sigma) is highly valued. Excellent teamwork, creativity, and effective communication are crucial soft skills for collaborating across multidisciplinary teams and driving innovation. These competencies ensure the design and launch of safe, effective, and compliant medical devices that improve patient outcomes.

What are some common challenges faced by research and development engineers in the medical device industry?

Research and Development Engineers in the medical device industry often face challenges such as navigating complex regulatory requirements, managing tight project timelines while ensuring product safety and efficacy, and collaborating with cross-functional teams like quality assurance and clinical affairs. Additionally, adapting to rapid technological advancements and integrating feedback from clinicians and end-users into the design process can be demanding. These challenges require strong problem-solving skills, adaptability, and effective communication to deliver innovative and compliant medical devices.

What is the difference between Research And Development Engineer Medical Device vs Quality Assurance Engineer Medical Device?

AspectResearch And Development Engineer Medical DeviceQuality Assurance Engineer Medical Device
Primary FocusDesigning, developing, and testing new medical device productsEnsuring products meet quality standards and regulatory requirements
Required CredentialsEngineering degree, knowledge of product developmentEngineering or science degree, knowledge of quality systems
Work EnvironmentResearch labs, product development teamsManufacturing facilities, quality control departments
Industry UsageInvolved in innovation and product creationInvolved in compliance, validation, and process improvement

While both roles require engineering knowledge and are integral to the medical device industry, Research And Development Engineers focus on creating and testing new products, whereas Quality Assurance Engineers ensure these products meet safety and quality standards throughout production.

What job categories do people searching Research And Development Engineer Medical Device jobs in Minnesota look for?

The top searched job categories for Research And Development Engineer Medical Device jobs in Minnesota are:

What cities in Minnesota are hiring for Research And Development Engineer Medical Device jobs?

Cities in Minnesota with the most Research And Development Engineer Medical Device job openings:

Infographic showing various Research And Development Engineer Medical Device job openings in Minnesota as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 15% Part Time, and 7% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution.

Principal Process Development Engineer - IPG

Resonetics

Fridley, MN

Full-time

Medical, Dental, Vision, Life

Posted 5 days ago


Resonetics rating

7.1

Company rating: 7.1 out of 10

Based on 28 frontline employees who took The Breakroom Quiz


Job description

Overview

Resonetics is a global leader in advanced engineering, prototyping, product development, and micro manufacturing, driving innovation in the medical device industry. With rapid expansion across all our locations, we continue to push the boundaries of technology while fostering a dynamic, employee-centered culture. Our commitment to excellence and continuous improvement makes Resonetics an exciting place for professionals passionate about shaping the future of micro-manufacturing and being part of something bigger.

The Principal NPI/Process Development Engineer position leads the development, improvements and implementation of optimal cost-effective designs and associated processes that meet the high rigor of product requirements and exceptional quality standards. This role will work specifically with active implantable products.

Join Resonetics and be part of a team that's redefining medical device manufacturing. If you're passionate about innovation and thrive in a fast-paced environment, we'd love to hear from you.

Responsibilities
  • Works independently to drive project completion by developing the processes used to manufacture component, sub-assemblies, and FG devices.
  • Provides leadership and mentors less experienced engineers and technicians.
  • Acts as the liaison between development and operations.
  • Advocates for the process to ensure they are repeatable and can capably produce product that meets the design requirements.
  • Prepares and presents detailed plans necessary to complete assigned projects.
  • Develops schedule milestones, coordinates resources, facility and equipment for assigned projects.
  • Assists in improving the system of production controls, standard operating procedures, safety, quality control and training.
  • Prepares and maintains detailed layouts of buildings and equipment.
  • Coordinates the manufacturing launch of new/revised products including establishing goals, training team members and evaluating results.
  • Designs, develops and tests as well as sources various tools, machinery and equipment for recommended manufacturing methods while providing ROI analysis.
  • Performs product/process analysis for production and quality metrics.
  • Write engineering change orders to process changes to manufacturing documents, drawing, and Bill of Materials.
  • Support company finance, accounting, human resources, quality, regulatory, and clinical departments as necessary to ensure compliance with requirements.
  • Recommend, support and implement improvements, modifications, or additions that will improve work processes.
  • Take the lead in analyzing the need for new process development and to meet company needs including specifying, ordering, installing and validating new equipment or processes.
  • Prepares justification for capital expenditures.
  • Aid in production transfers from R&D to manufacturing.
  • Propose potential new manufacturing technologies, including automation and new equipment.
  • Contribute to the definition, development and implementation of LEAN manufacturing initiatives.
Required QualificationsEducation, Experience, Required Skills
  • Bachelor's degree in engineering or related field
  • 10+ years related experience in medical device industry with a heavy focus on product or process development of Active Implantable Devices. Strongly preferred experience in Neuromodulation Devices (IPGs or Leads). Experience with pacemakers, cardiac monitors, brain computer interface, etc. also considered.
  • Extensive experience with process validations for laser welding, header attachment, and internal moisture (bake) and Test Method Validation for Helium Leak Testing.
  • Demonstrated ability to independently develop medical device manufacturing processes from concept to production.
  • Experience with medical device Design For Manufacturing, design control, quality systems and product development phases.
  • Demonstrated ability to implement change in a way that positively impacts overall department and company performance.
  • Must be able to handle multiple projects simultaneously.
  • Must excel at working in a team environment with a high level of people/interpersonal skills and demonstrated ability to cross functionally drive results.
  • Experience using influence to affect project and organizational success.
  • Experience with programs including SolidWorks and/or Mastercam.
  • MS Office Proficiency.
  • Ability to handle and be trusted with confidential and/or sensitive information.
Physical Requirements
  • Prolonged periods of sitting at a desk and working on a computer.
  • Must be able to lift up to 25 pounds at times.
  • Must have excellent hand-eye coordination.
  • Ability to differentiate between colored wires, tabs, and electronic components.
  • Must wear gown, gloves, and ear protection if applicable.
Summary of Benefits
  • Group health & welfare benefits: Options for Medical, Dental and Vision insurance, Health Savings Account (requires participation in eligible medical plan), and Flexible Spending Accounts.
  • Company-paid benefits: Employee Life Insurance & Accidental Death & Dismemberment (AD&D), Long Term Disability (LTD), Kavira (requires participation in medical plan).
  • Voluntary, employee-paid benefits: Employee Supplemental Life & AD&D, Spouse and Dependent Life & AD&D, Short Term Disability (STD), Accident, Critical Illness, and Hospital Indemnity, Employee Assistance Program.
  • Flexible Time Off Program
  • Paid Parental Leave
  • Paid Holidays
  • Benefits and incentive compensation may be subject to generally applicable eligibility, waiting period, contribution, and other requirements and conditions.
Compensation
  • The typical base pay range for this role is between $135,000-185,000/year. Compensation may vary based on individual job-related knowledge, skills, expertise, and experience. This position is eligible for a discretionary annual incentive program driven by organization and individual performance.
  • Our company policy is that we are unable to provide visa sponsorship. Candidates must already be legally authorized to work in the United States without the need for sponsorship now or in the future.
Employment Type: FULL_TIME

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