Electrical Engineer

Batesville, IN, US • Posted 13 hours ago • Updated 12 hours ago
Full Time
Part Time
On-site
USD $0-60/hr
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Fitment

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Job Details

Skills

  • Electrical Engineer
  • FDA
  • Medical device
  • NPI - New Product Introduction

Summary

Hi,



We are having an immediate requirement for the below mentioned role.



Job Title: Senior Electrical Engineer Medical Device Product Development

Work Model: Hybrid 3 days onsite / 2 days remote

Work Location: Batesville, Indiana,

Work Auth: All Visas accepted (No H1 and No Fake Profiles)



Note: Candidate must be available onsite for the first 1 2 weeks.

Job Summary

We are seeking an experienced Senior Electrical Engineer / Medical Device Product Development Engineer to support product development and electronic end-of-life initiatives for existing medical devices.

The ideal candidate will have strong experience with medical device design controls, electronic medical equipment, embedded firmware, verification and validation, and product development within a regulated medical device environment. The engineer will serve as a technical lead and collaborate with cross-functional teams, suppliers, Operations, and external partners to maintain and improve existing products.

Required Education

  • Bachelor's degree in Engineering, Technology, or a related technical field
  • Electrical Engineering degree strongly preferred

Required Experience

  • 5 10 years of experience in design and/or product development within the medical device industry
  • Experience with Medical Device Design Controls
  • Product development experience involving regulated medical devices
  • Experience developing and verifying electronic medical equipment with embedded firmware
  • Previous operational experience supporting New Product Development (NPD) preferred

Required Skills

  • Strong knowledge of Medical Device Design Controls
  • Ability to provide design-control guidance to engineering team members
  • Understanding of FDA 21 CFR 820.30
  • Knowledge of applicable ISO quality/design control requirements
  • Working knowledge of IEC 60601-1 for medical electrical equipment safety and essential performance
  • Experience with electronic hardware and embedded firmware development
  • Strong understanding of engineering principles, processes, and product development practices
  • Experience defining and supporting verification and product testing
  • Ability to review and improve existing product designs
  • Experience working with suppliers and external engineering partners
  • Familiarity with engineering/statistical tools such as:
    • Design of Experiments (DOE)
    • Statistical Process Control (SPC)
  • Strong troubleshooting and problem-solving skills
  • Ability to manage multiple priorities simultaneously
  • Strong written and verbal communication skills
  • Experience working in and supporting cross-functional teams
  • Understanding of business objectives and cost implications when developing engineering solutions

Key Responsibilities

  • Serve as the technical lead for electronic product development and end-of-life activities
  • Develop engineering solutions for issues associated with existing medical device designs
  • Coordinate with suppliers and external resources to implement updates to existing products
  • Support electronic component obsolescence and product lifecycle activities
  • Work with Operations and external contractors to improve existing technology and product capabilities
  • Provide technical guidance related to medical device design controls
  • Collaborate with cross-functional teams to deliver business and project requirements
  • Define and support verification testing required to confirm product design
  • Investigate technical issues and recommend improvements to existing products
  • Utilize engineering tools such as DOE and SPC to support problem resolution
  • Provide clear project and technical updates to management and engineering teams
  • Consider quality, regulatory, technical, business, and cost requirements when developing solutions

Work Environment

  • Hybrid schedule: 3 days onsite and 2 days remote
  • First 1 2 weeks onsite
  • Combination of office, laboratory, production, and warehouse environments
  • Periodic lifting of up to 35 lbs
  • May work around chemicals routinely used in production and laboratory environments
  • May occasionally be required to observe surgical procedures in an operating-room environment

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
  • Dice Id: 91099353
  • Position Id: OOJ - 1608-609-1790005996
  • Posted 13 hours ago

Company Info

About Xcelo Group Inc

At Xcelo, we do much more than software integration. We deliver superior IT Solutions through the successful integration of people, technology and efficient business systems. We employ only senior-level, trusted consultants and programmers with proven track records of success. Because we are a small, efficient business staffed by technology experts, we can offer customers nimble service, unprecedented project turn times, and increased flexibility when compared to larger competitors.

By maintaining a strategic business model that combines Global IT Service Centers in USA with IT experts located offshore, we improve productivity and maximize our client s cost savings, without compromising on product quality or delivery timelines. As a result, Xcelo customers receive face-to-face service, save time and money, and eliminate the need to hire extra personnel or train existing staff for highly technical projects.

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