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Engineer III, Product

ICU Medical, Inc. · Salt Lake City, UTtoday

BS-level Product Development roles on Crosslinked list a median of $117k (202 that show pay). This posting does not list pay.

Sustain and improve medical device products, including plastic injection molded components and assemblies

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Worth knowing

Why it is interesting. Hands-on with plastic injection molding and process control in a regulated medical device environment.

Might not be for you. Largely sedentary office role focused on sustaining existing products, not greenfield R&D.

Generalist BS acceptable Realistic requirements

Adjacent materials roleUnderstanding of ... plastic injection molding, part assembly, fixturing, testing, and process control techniques

H-1B filings

ICU Medical, Inc. filed 12 H-1B labor applications for scientist and engineer roles from Jan to Dec 2025.

Most common titles: Engineer III, Product, Senior Engineer, Quality, Principal Engineer, Mechanical. Median filed pay: $108K a year.

From U.S. Department of Labor disclosure data. A filing is a record of past hiring, not a promise about this role, so confirm sponsorship with the employer. Titles and filed pay ·Every employer's filings

Seniority
Mid-level
Work
On-site
Type
Full-time
Degree
BS
Experience
4+ yrs
Industry
Medical devices
Role
Product Development

Role details

Position Summary

The Product Sustaining Engineer III is responsible for supporting product improvements through adherence to established design control processes, good engineering and documentation practices. The key responsibility of this position is to exercise judgement and take action while adhering to defined procedures during project support & improvements.

The Product Sustaining Engineering III will complete advanced engineering projects with input and guidance from senior engineers and managers. Gains exposure to some of the complex tasks within the job function.

Essential Duties & Responsibilities

  • Support initiatives for continuous process and product improvements
  • Work to improve performance of manufacturing systems, e.g. yield, cycle-time, quality requirements, maintenance’s needs
  • Support project timelines and milestones and bring them to completion on time and within budget
  • Assist in completion of CAPA tasks and deliverables (Corrective and Preventive)
  • Identify and qualify “end-of-life” components.
  • Represent Sustaining Engineering to identify possible product modifications to improve manufacturability and impact on production processes.
  • Initiate and manage projects with adherence to program management guidelines
  • Coordinate efforts with the Materials Group to assess vendors and provide materials technical information
  • Conducts independent analysis and develops solutions to problems.
  • Develops approaches and designs where precedent usually exists.
  • Performs developmental and/or test work that relies heavily on a comprehensive knowledge of theory and design.
  • Writes detailed design specifications.
  • Assists in training new/current employees with respect to documentation, use of equipment, laboratory techniques and department procedures.
  • Delivers communications tailored to the needs of the receiver (managers, peers, customers) with appropriate frequency to maximize its utility and promote cross-functional collaboration.
  • Work on special projects as they arise

Knowledge, Skills & Qualifications

  • Understanding of strength of materials, automation, plastic injection molding, part assembly, fixturing, testing, and process control techniques
  • Knowledge of Solidworks to interpret part dimensions, sectional views, conduct mates, build assemblies.
  • Six-Sigma Methodology (DOE, Process Capability, Gage R&R, etc.) - use of Minitab Software for analysis
  • Knowledge of the Medical Device Industry and familiarity with FDA QSR Regulations is a plus
  • Competent in your domain. Familiar with other areas of domain expertise within the team.
  • Has a basic understanding of best practices. Has a basic to intermediate understanding of engineering discipline
  • Have awareness of the broader product strategy and contribute to it
  • Ability to receive general project direction and solicit input from more experienced engineers.
  • Requires the ability to independently make decisions that impact the attainment of project

Minimum Qualifications

  • Must be at least 18 years of age

Minimum Qualifications, Education & Experience

  • Must be at least 18 years of age
  • Bachelor of Science degree from an accredited college or university in Mechanical Engineering or a related field. Master's Degree preferred.
  • 4+ years of experience in Medical Device Product Development or related field

Work Environment

  • This is largely a sedentary role.
  • This job operates in a professional office environment and routinely uses standard office equipment.
  • Typically requires travel less than 5% of the time

Related roles

Common questions

Does ICU Medical, Inc. sponsor H-1B visas?

ICU Medical, Inc. has filed H-1B petitions with the US Department of Labor in past years, but this specific posting does not explicitly mention sponsorship for the Engineer III, Product role. Confirm with the employer before applying if visa support is required.

Where is the Engineer III, Product role at ICU Medical, Inc. based?

This role is based in Salt Lake City, UT.

What degree is required for the Engineer III, Product role at ICU Medical, Inc.?

This role requires a BS.

How many years of experience does this Engineer III, Product role require?

The posting calls for at least 4 years of relevant experience.

What techniques or methods are required for this Engineer III, Product role?

DOE, Process Capability, Gage R&R.