Senior Electronic Engineer
Senior Electronic Engineer
LocationMunster Region, Ireland
Working PatternPredominantly 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 ResponsibilitiesLead 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 requirementsCollaborate 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 QualificationsLevel 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.