• Participates in, and at times, lead 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

• 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
• Bachelor's or Master's degree in Scientific or Engineering Field, preferably Mechanical, Chemical, or Biomedical

If you are a highly motivated individual with a passion for design and systems engineering, we encourage you to apply for this exciting opportunity.