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Sr. Process Development Engineer

Resonetics


Job Location:

Fridley, MN - USA

Yearly Salary: USD 105000 - 135000
Posted: 29 September 2026 (2 days ago)
Application Deadline: 27 December 2026
Vacancies: 1 Vacancy

Job Summary

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 Senior NPI/Process Development Engineer is a key member of a team developing and bringing to market Class 3 active implantable devices. The role requires collaboration and partnership with Active Implantable Design Engineers and core teams and is responsible for developing and validating the manufacturing processes and approaches to support readiness for commercial addition the NPI engineer also focuses on costs quality continuous improvement and high level of customer service.

Join Resonetics and be part of a team thats redefining medical device manufacturing. If youre passionate about innovation and thrive in a fast-paced environment wed 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.
  • Performs other related duties as assigned by management.
Required Qualifications
  • Bachelors degree in engineering or related field
  • 5 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 Demands
  • 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.
Compensation
  • The compensation for this role is competitive and will be based on experience and qualifications. The anticipated range is $105000$135000.
  • 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.

Required Experience:

Senior IC


About Company

We understand the fast-paced medical device development process and the importance of time-to-market. Let us help bring your breakthrough medical devices and diagnostics to market faster.

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