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Confluent Medical Technologies

Contract manufacturer of Nitinol medical devices

Staff Surface Process Development Engineer

Process EngineeringConfirmed live in the last 24 hours
Full-timeFremont, CA, USA$103.9k - $173.1kIn-person

About the Job

Requirements

  • A bachelor's degree in Materials, Biomedical, or Chemical Engineering, or a related discipline, and at least 5 years of relevant engineering experience.
  • Proficiency in Microsoft Word and Excel.
  • Ability to read and interpret engineering drawings and technical specifications.
  • Ability to communicate clearly and efficiently in a highly technical environment.
  • Ability to work independently with limited direction.
  • Strong analytical and problem-solving skills.
  • Ability to take on new or unfamiliar technical challenges.
  • Ability to perform under pressure from multiple competing deadlines while maintaining cooperative and constructive working relationships.

Responsibilities

  • Work as part of the multifunctional Process Development Team on through-process development, optimization, validation, and manufacturing transfer of medical device production processes.
  • Develop and optimize surface processes, including microblasting, chemical etching, chemical polishing, electropolishing, cleaning, and surface quality standards.
  • Use statistical analysis and Design of Experiments (DOE) to characterize processes, identify key parameters, optimize performance, and support data-driven decisions.
  • Perform and support root cause investigations for process and product issues and drive appropriate corrective actions.
  • Analyze process and product data to identify trends, risks, and improvement opportunities.
  • Transfer developed processes to manufacturing sites, including documentation, training, validation support, and troubleshooting during implementation.
  • Collaborate with operators, technicians, engineers, quality, and manufacturing teams to ensure processes meet product and customer requirements.
  • Create and maintain work instructions, visual standards, engineering studies, drawings, and other manufacturing documentation.
  • Support process validation and continuous improvement using Lean, Six Sigma, and structured problem-solving principles.
  • Manage multiple technical priorities and independently drive assigned work to completion.

Desired Qualifications

  • Experience with Minitab or JMP.

About the Company

Confluent Medical Technologies

Contract manufacturer of Nitinol medical devices

Confluent Medical Technologies provides contract manufacturing and materials science services to medical device OEMs, supporting projects from early design and prototyping through full-scale production and commercialization. Its offerings span Nitinol components, high-precision polymer tubing, biomedical textiles, and complex catheter systems, all produced through a vertically integrated process that covers raw materials to finished devices. The company differentiates itself by owning the entire supply chain from Nitinol alloy to the final product and by expanding capabilities through acquisitions in catheters, textiles, and polymer components. Its goal is to help OEMs bring safe, high-quality interventional devices to market faster by delivering end-to-end manufacturing and materials science support.

Company size
1,001-5,000
Company stage
Debt Financing
Total funding
$590M
Headquarters
Scottsdale, AZ
Founded
1991

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