Research and Development Engineer (Contract)Location:Galway, IrelandContract Type:Contractor (Onsite or Hybrid – as required)Role Overview:A leading global organisation in the healthcare technology sector is currently seeking aResearch and Development Engineer (Contractor)to support aShelf-Life Extension projectfor a range of commercial medical products. This role is ideally suited to someone with a strong background inDesign Control,Design Verification, andtechnical documentation, along with a solid understanding ofmaterial science,product testing, andregulatory standards.Key Responsibilities:Contribute to the planning and execution of shelf-life extension strategies for existing medical products, ensuring alignment with quality and regulatory requirements.Develop and carry out Design Verification activities, including writing and executing protocols and compiling detailed reports.Analyse and interpret the impact of material ageing on product performance and safety.Determine appropriate sample sizes and selection criteria, applying sound statistical methods (including variable and attribute data analysis).Work extensively with technical documentation, including Bills of Materials (BOMs), Process Plans, design drawings, and specifications.Support regulatory submissions and design documentation updates in line with project changes.Collaborate with cross-functional teams to drive project deliverables and escalate technical challenges when necessary.Maintain a proactive and solutions-oriented approach to technical problem-solving.Qualifications and Experience:Degree in Engineering or a related technical field (Level 8 or higher); postgraduate qualification is an advantage.Experience in a regulated environment, preferably medical devices or a similarly structured industry.Strong working knowledge of Design Control processes, particularly in the context of product lifecycle extension.Proven track record with Design Verification —from protocol creation to report generation.Excellent technical writing and documentation skills.Familiarity with material properties, ageing studies, and related testing methodologies.Understanding of product specifications, test method validation, and statistical approaches to sample testing.Comfortable navigating complex technical documents such as BOMs, drawings, and process documentation.Working knowledge of risk management processes and regulatory standards (e.g., ISO 13485, FDA QSR).Ability to work independently while also contributing effectively within a multidisciplinary team environment.