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Manufacturing Engineer ; Catheter

Job in Santa Clara, Santa Clara County, California, 95053, USA
Listing for: Cirtec Medical
Full Time position
Listed on 2026-07-20
Job specializations:
  • Engineering
    Manufacturing Engineer, Quality Engineering, Process Engineer, Lean Manufacturing / Six Sigma
  • Manufacturing / Production
    Manufacturing Engineer, Quality Engineering, Lean Manufacturing / Six Sigma
Salary/Wage Range or Industry Benchmark: 85000 - 105000 USD Yearly USD 85000.00 105000.00 YEAR
Job Description & How to Apply Below
Position: Manufacturing Engineer I (Catheter)

Description

About us:

For over three decades, Cirtec Medical has been a leading outsourcing partner for complex medical devices. We specialize in providing comprehensive solutions for Class II and III devices, from design and development to precision components and finished device assembly. Our expertise spans neuromodulation, implantable drug delivery, cardiac rhythm management, structural heart, mechanical circulatory support, and minimally invasive surgical systems.

Our dedicated teams prioritize growth, innovation, and collaboration. We actively seek opportunities for improvement to enhance our support for clients. If you embrace a growth mindset and thrive on challenges, you may be a perfect fit for our team!

Position Summary

We are actively looking for a Manufacturing Engineer I who can bring innovation and creative thinking to the team on catheter-based devices in a fast-paced medical contract manufacturing space. As a Manufacturing Engineer I, you will be primarily responsible for new product introduction. You will be working to mature the process to ensure new lines are ready for transfer, along with developing and implementing robust, cost effective manufacturing processes and methods.

You will provide day to day support of the catheter manufacturing floor operations from an engineering perspective. Manufacturing Engineers document processes and implement ideas and solutions to improve assembly, operations, and reduce costs, develop tooling/fixturing, and drive investigations tied to non-conformances.

Key Responsibilities
  • Improve manufacturing processes, methods and controls for cost reduction, quality improvements and efficiency for both sustained and new products.
  • Prepare engineering change orders and coordinates the deployment of changes including training operation team members.
  • Improve manufacturing process instructions, product flow, assembly methods, space allocation, product quality and safety performance for both sustained and new products.
  • Coordinate the manufacturing launch of new products including establishing yield targets, run rates, training needs, and evaluating results.
  • Develop and qualify various tools and equipment required for manufacturing processes.
  • Perform product and process analysis for cost reduction, quality improvement and improved efficiency.
  • Utilize tools associated with risk management (e.g., PFMEA) to identify potential risks and the associated corrective actions.
  • Support required equipment qualification and process validations (IQ, OQ and PQ).
  • Troubleshoot manufacturing processes when defects occur. Determine root cause and implement effective containment and countermeasures.
  • Disposition non-conforming products and develop re-work procedures.
  • Communicate with customers regarding process improvements and production changes.
  • Represent manufacturing on cross functional teams.
  • Participate in Kaizen events and drive continuous improvement efforts.
  • Attend and schedule project meetings to determine current and future process initiatives.
Must Have
  • BS in Mechanical / Biomedical / Industrial Engineering or in an equivalent engineering (STEM) discipline required.
  • Knowledge of manufacturing and assembly processes.
  • Prefer 2+ years of experience in medical device process development and/or manufacturing engineering with Class II or Class II medical devices.
  • Experience with new product introduction (NPI).
  • Solid knowledge of GMP and ISO/FDA regulations.
  • Must be able to review and interpret technical drawings and specifications.
  • Strong computer skills including the MS Office suite.
  • Must be able to read, write, and speak fluent English and must possess excellent communication skills, both written and oral.
  • Must have demonstrated organizational skills to manage multiple priorities and schedules.
Good to have
  • Experience with lean manufacturing techniques, value stream mapping, and continuous improvement methodologies.
  • Proficiency in Solid Works.
  • Experience working directly with catheters.
Salary Range

$85,000 - $105,000 based on skills and experience.

Cirtec Medical Corporation considers for employment and hires qualified candidates without regard to age, race, religion, color, sex, sexual orientation, gender identity, national origin, ancestry, protected veteran or disability status or any factor prohibited by law. Cirtec Medical Corporation and all of its related companies fully endorse equal opportunity for all. Cirtec Medical provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in the job application process.

We work to create a culture that is built on innovation, respect, transparency and communication, and hope you take pride in being a member of our team. It is Cirtec's goal to create a great work environment and to keep the company a great place to work. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.

Our benefits include Training and career development, Healthcare and…

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