Senior Electronic Engineer

Senior Electronic Engineer

Location: Munster Region, Ireland

Working Pattern: Predominantly onsite

Overview

A leading medical technology organisation in the Munster region is seeking an experienced Senior Electronic Engineer to play a key role in the design and development of advanced electro mechanical medical devices.

The position spans the full product lifecycle, from early stage technology development through to commercialisation, within a highly regulated and quality driven environment. The role sits within a growing multidisciplinary engineering team delivering high impact healthcare products used at scale.

Key Responsibilities

• Lead and deliver electrical and electronic design activities for electro mechanical medical devices
• Design electronic assemblies and printed circuit board assemblies to support new product development and lifecycle requirements
• Collaborate closely with mechanical, software, systems, and quality engineering teams to ensure alignment with project schedules and budgets
• Ensure electrical designs comply with applicable regulatory and safety standards including UL, IEC, and FDA requirements
• Plan, design, and execute testing for EMI, EMC, safety, and manufacturability
• Perform failure analysis and structured root cause investigations at system and component level
• Create, review, and maintain technical documentation including specifications, test protocols, and test reports
• Participate in and contribute to technical design reviews to ensure robust, safe, and compliant electrical designs
• Support and mentor junior engineers, contributing to knowledge sharing and team capability development

Experience and Qualifications

• Level 8 degree in Electronic Engineering or equivalent practical experience
• Five to seven years industry experience in a similar electronic engineering role
• Strong experience in analogue, digital, and mixed signal circuit design
• Previous experience in the medical device sector is a strong advantage
• Good knowledge of product design controls, EMC testing, and regulated documentation practices
• Experience working in a regulated engineering environment with robust quality and compliance requirements
• Strong problem solving skills, high attention to detail, and ability to work effectively in cross functional teams

Additional Information

This opportunity suits an engineer who enjoys hands on technical delivery, ownership of design outcomes, and close collaboration across engineering disciplines in a regulated MedTech environment. Due to the nature of the work, a strong onsite presence is required to support development, testing, and cross functional integration.