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Catheter Process Development Engineer II

Fridley, Minnesota

Postularse
ID de la oferta 58909 Área funcional Investigación y desarrollo Tiempo completo/tiempo parcial Tiempo completo Nivel de experiencia Profesionales

Catheter Process Development Engineer II

[title]
Catheter Process Development Engineer II
Permanent 

About Heraeus

Making displays foldable? Helping hearts beat with medical innovations? Or breathing new life into precious metals? As a family-owned global technology group we help our customers to always being one step ahead.


About Heraeus Medevio

Together we improve lives. At Heraeus Medevio, we bring lifesaving and life-changing medical devices to market through partnerships with medical device manufacturing companies. Backed by Heraeus Group, we are committed to the growth of our teams and organization by providing an open space for open minds.

To reach our vision of improving 100 million lives every year, we foster a culture of curiosity that thrives on challenge, continuous learning, growth, and the opportunity to try new things. With sites in the United States, European Union, and Asia, and over 2,200 employees worldwide, together, we will meet tomorrow's challenges today.

Position Summary

The Catheter Process Development Engineer II will develop, optimize, and commercialize robust manufacturing processes for catheter assemblies and similar interventional medical components. As an Engineer II, you will be working within a cross-functional product development team, driving process innovation, ensuring design‑for‑manufacturability, and executing the required engineering deliverables to support successful design transfer and commercial release. The ideal candidate brings hands‑on problem‑solving ability, strong analytical, and experience with catheter or vascular‑access device manufacturing technologies.

We are open to hiring at an Engineer II or Engineer III level. This position will be based out of Fridley, MN with travel to the White Bear Lake, MN site to support project needs.

What You’ll Do Every Day:

  • Lead and support the development, characterization, and validation of manufacturing processes for medical devices and components throughout the product development lifecycle, with a likely focus on catheter related projects
  • Apply structured problem‑solving and critical thinking to define process strategies, resolve complex technical challenges, and make data‑driven decisions.
  • Utilize engineering tools such as DOE, pFMEA/PFMEA, DFM principles, capability studies, and statistical analysis to characterize and improve processes.
  • Develop clear, well‑supported documentation including process validation protocols (IQ/OQ/PQ), engineering studies, technical rationales, risk documentation, and process development reports.
  • Own process development workstreams, including timeline management, technical execution, communication of status, and risk mitigation.
  • Work hands‑on with production technicians and operators to diagnose issues, improve yields, and implement sustainable production solutions.
  • Contribute to the selection and qualification of equipment, tooling, fixtures, and automation solutions to support manufacturing scale‑up.
  • Mentor junior engineers and interns; cultivate a culture of constructive feedback, collaboration, and continuous improvement.
  • Support cross‑functional teams including Quality, Manufacturing, Supply Chain, and Regulatory in preparing for commercialization and design transfer.
  • Other duties may be assigned as required.

What We’re Looking For:

  • Bachelor degree in Engineering or related field required; master’s degree in engineering or related technical field preferred.
  • Minimum 2 years of relevant experience required, 5 years of experience required for Engineer III; 1 year of relevant work experience may be substituted for a graduate degree and 3 years for a doctorate degree.
  • Demonstrated knowledge of process development engineering and catheter‑specific manufacturing equipment (braiding, reflow, tipping), materials (e.g., Pebax, nylon, PTFE liners and coatings), or bonding technologies.
  • Proficiency in statistical analysis and data‑driven decision making.
  • Experience with process validation, IQ/OQ/PQ execution, and engineering deliverables required for medical device development.
  • Ability to manage and communicate technical workstreams, provide technical leadership, and collaborate across functions.
  • Strong communication skills, with the ability to convey complex concepts to diverse audiences including management, operators, and customers.
  • Demonstrated leadership and commitment to continuous improvement.

Medevio is committed to providing competitive total compensation and benefits packages. The expected hiring range for this position is between $79,000 and $115,000 based upon a full-time schedule. This is a good faith estimate on the applicable range. Base salaries are determined by taking a variety of factors in account, including, but not limited to, candidate qualifications, geographic locations, market conditions and internal equity. This position is bonus eligible, with a target bonus of 10%. Our total compensation package includes eligibility for comprehensive medical, dental, and vision coverage, a 401(k) plan with company match, education reimbursement, paid parental leave and paid time off.


ReqID: 58909
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