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GE

Design Engineer for Medical Devices

Getinge
United Statesfull_timeVerifiedPosted 14 May 2025
💰 $117,840/yr($78,560/yr – $117,840/yr)

About the role

 

 

With a passion for life

 

Join our diverse teams of passionate people and a career that allows you to develop both personally and professionally. At Getinge we exist to make life-saving technology accessible for more people. To make a true difference for our customers – and to save more lives, we need team players, forward thinkers, and game changers.

Are you looking for an inspiring career? You just found it.

 

 

Healthmark, A Getinge company was founded in 1969 and employs over 300 people and is a growing company. We strive to provide customers with quality products and support services in a timely and effective manner. 

 

We are looking for a strong candidate who can design, develop, analyze, and standardize new and existing products and processes, with specific focus on medical devices and complex instruments.

 

Shift: Full Time, M-F, 8:30am-5:00pm

*Must be willing to relocate to MI*

 

WHAT YOU'LL DO:

  • Participates in, and at times, leads projects involving the design, fabrication, validation, and manufacture of medical devices and other healthcare-related instruments, including subassemblies, systems, or processes.
  • Analyzes, develops, and recommends design approaches required to meet design and production requirements for new, modified, or enhanced instruments.
  • Provide technical support to other Healthmark functional areas, including Business Development, Quality, R&D, and Manufacturing.
  • Compiles and evaluates design and test data, prepares technical specifications, and determines appropriate limits and variables for product/material specifications.
  • In-step with Quality, Design Engineer analyzes product requirements and other technical specifications to determine if product is performing to requirements; this includes performing risk analysis activities.
  • Achieve best practices that meet medical device industry standard, including design control and documentation.
  • Responsible for implementing and maintaining the effectiveness of the Healthmark QMS.

 

 SKILLS & REQUIREMENTS:

  • Bachelor’s or Master’s degree in Scientific or Engineering Field, preferably Mechanical, Chemical, or Biomedical.
  • Proficiency in technical documentation and oral and written communication skills
  • 2+ years in medical or automotive design and/or systems engineering, experience with risk management/FMEA a benefit.
  • Familiar with regulatory requirements for the medical device industry, particularly working experience in design control.
  • Capable of effectively interfacing with cross-functional team members in achieving common goals.
  • Attention to detail and high level of accuracy.
  • Good organizational skills and the ability to handle multiple projects at once.
  • Able to lift up to 20 lbs. unassisted.
  • Ability to sit or stand for long periods of time.
  • Hot or cold environment depending on weather/time of year.
  • Ability to travel as needed
  • Medical Device industry experience is preferred.

 

EQUIPMENT USED:

  • Use of Computer, CAD program, Scale, CNC Machine, Label Printer, Copier, Crimping Robot, Water Distiller, Water Robot,

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Company

Getinge

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