Job Description

Senior Electronic Engineer

Location

Munster Region, Ireland

Working Pattern

Predominantly onsite

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.