R & D Engineer II

at  STEM Recruitment Partners

R&D ENGINEER II- LIMERICK

STEM Recruitment Partners are working with an established medical device company, based in Limerick, who are seeking an R&D Engineer II to join their R&D operations. This is a permanent role, working on an exciting next-generation project. Competitive salary and benefits, plus the option to work on a hybrid model. As a Research & Development Engineer, you will play a crucial role in the design, development, and implementation of innovative medical devices. Your responsibilities will include project management, design evaluation, risk analysis, and collaboration with cross-functional teams to achieve project milestones and enhance product performance. Job Responsibilities

• Design and Development:
• Lead design development activities, including prototyping, test method design, and design evaluation.
• Conduct design reviews and prepare comprehensive reports to support decision-making processes.
• Manage the transfer of designs to production in a timely and efficient manner.
• Product Testing and Evaluation:
• Perform product testing and evaluation, generating detailed test reports to facilitate design selection.
• Conduct product performance evaluations and contribute to innovation through patent filings and disclosures.
• Project Management:
• Serve as project lead for assigned research & development projects, ensuring execution in accordance with project plans.
• Collaborate with cross-functional teams to drive project tasks and achieve timely completion of milestones.
• Risk Analysis and Compliance:
• Conduct product and project risk analysis, implementing risk management strategies as necessary.
• Ensure compliance with quality, regulatory, and company policies throughout the development process.
• Communication and Collaboration:
• Maintain regular communication with cross-functional teams, senior management, and business unit leaders.
• Educate oneself on relevant medical areas to align project goals with patient needs.

Job Requirements

• A bachelor’s degree in Biomedical, Mechanical Engineering or a related field is required.
• Minimum of 3 years of relevant experience, demonstrating strong project planning and execution skills.
• Proficiency in mechanical design, Solidworks /Pro Engineer CAD, and medical device quality regulations (ISO13485, FDA CFR 820, EU Medical Device Regulation 2017/745).
• Excellent communication, problem-solving, and interpersonal skills.
• Highly motivated individual with a passion for excellence and the ability to thrive in a fast-paced environment.
• Willingness to travel on company business as needed.

• Design and Development:
• Lead design development activities, including prototyping, test method design, and design evaluation.
• Conduct design reviews and prepare comprehensive reports to support decision-making processes.
• Manage the transfer of designs to production in a timely and efficient manner.
• Product Testing and Evaluation:
• Perform product testing and evaluation, generating detailed test reports to facilitate design selection.
• Conduct product performance evaluations and contribute to innovation through patent filings and disclosures.
• Project Management:
• Serve as project lead for assigned research & development projects, ensuring execution in accordance with project plans.
• Collaborate with cross-functional teams to drive project tasks and achieve timely completion of milestones.
• Risk Analysis and Compliance:
• Conduct product and project risk analysis, implementing risk management strategies as necessary.
• Ensure compliance with quality, regulatory, and company policies throughout the development process.
• Communication and Collaboration:
• Maintain regular communication with cross-functional teams, senior management, and business unit leaders.
• Educate oneself on relevant medical areas to align project goals with patient needs