The Role In this position, you will support and execute new product and process development activities across the full development lifecycle.
Working closely with cross-functional stakeholders, you will help translate design concepts into manufacturable, compliant medical devices while driving continuous improvement through engineering analysis and validation.
This is an excellent opportunity for an engineer who thrives on problem-solving, experimentation, and seeing designs move from the lab into production.
Your Profile Bachelor's degree in Mechanical, Biomedical, Chemical Engineering, or a related engineering discipline4+ years' experience in R&D or process development within medical devices or another regulated industry Familiarity with medical device quality systems and regulatory requirements (FDA, ISO)Experience with process validation activities (IQ, OQ, PQ) and verification & validation documentation Strong analytical skills with a hands-on, practical engineering approach Comfortable working with data, statistics, and technical reporting Effective communicator who works well within cross-functional teams Basic knowledge of tooling, design, and drafting principles Prospective Overview Considering your next move in the Med Tech sector?Do you bring solid experience in medical device development and enjoy working in a hands-on, technically focused role within a regulated environment?Our client, an established medical technology organisation, is currently recruiting an R&D Engineer to join their team in County Wexford.
This role offers the opportunity to work on innovative medical devices from concept through commercialisation, contributing directly to products that improve patient care on a global scale.
Interested?Apply nowIf your background aligns with the role, we'll be in touch shortly to discuss the opportunity in more detail before progressing your application.
#J-18808-Ljbffr