R&D Engineer II

Boston Scientific Gruppe; Galway; On-site; EUR 65,000 - 90,000; Full time

Job summary

Boston Scientific is seeking a highly motivated R&D Engineer II on a permanent basis to join our Galway team. You will contribute to the design, development, verification, regulatory readiness and commercial launch of innovative coronary intervention technologies across global healthcare markets.

The role works with cross-functional teams including Project Management, Quality, Regulatory, Clinical and Manufacturing to ensure timely delivery of project objectives and successful commercialisation.

Qualifications

• Develop and commercialise next-generation minimally invasive medical devices.
• Work within a multidisciplinary New Product Development organisation.
• Contribute to design control outputs in line with PDP/TDP methodologies.

Responsibilities

• Participate in project teams for product design, development and testing.
• Provide technical guidance and effective communication in an international organisation.
• Coordinate design verification, validation and regulatory testing activities.

Job description

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Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance

At Boston Scientific, we'll give you the opportunity to harness all that's within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we'll help you in advancing your skills and career. Here, you'll be supported in progressing - whatever your ambitions.

Advancing possibilities for a brighter tomorrow

Boston Scientific is seeking a highly motivated R&D Engineer II on a permanent basis to join our Galway team.

Job Purpose:

Responsible for supporting the development and commercialisation of next-generation minimally invasive medical devices for the treatment of coronary artery disease. Working as part of a multidisciplinary New Product Development (NPD) organisation, the R&D Engineer II will contribute to the design, development, verification, regulatory readiness, and commercial launch of innovative coronary intervention technologies across global healthcare markets.

The R&D Engineer II is responsible for providing technical support and design solutions throughout the product development lifecycle, including development verification, performance assessment, design evaluation, regulatory testing, and remediation activities. Under limited supervision, the individual contributes to and delivers design control outputs in accordance with TDP (Technology Development Project) and PDP (Product Development Project) methodologies. The role also partners closely with cross-functional teams including Project Management, Design Assurance / Quality, Regulatory, Clinical, Manufacturing, Marketing, and Sterilisation/Biocompatibility functions to ensure timely delivery of project objectives and successful commercialisation of new technologies. In addition, the engineer may support scientific communication, educational activities, and development of technical materials that promote understanding and appropriate use of Boston Scientific products.

Key Responsibilities:

• Participate and contribute to project teams, which typically includes the following activities: product design and development, product design troubleshooting and investigation support, report preparation. Provide technical guidancewithin a team and be aneffective communicatorwithin a multidisciplinary and international organisation.
• Work cross-functionally with project management, quality, manufacturing, regulatory, clinical, marketing, biocompatibility, sterility and other functions as required to ensure successful execution of development, verification, validation, regulatory and commercialisation activities.
• Designs and coordinates design verification and validation testing. Summarizes, analyses, draws conclusions from and documents test results.
• Work independently to plan and schedule own activities necessary to meet timelines.Uses initiativeto scope and execute tasks and activities by seeking out available data and expertise.
• Demonstrate strong working knowledge of design control through generation ofhigh-quality deliverables. Responsible for generation of design related documentation including prints, BOM's and specifications and driving their approval through documentation control processes.
• Develop, evaluate and optimise bench-top and simulated-use models used to assess device deliverability and performance, supporting design decision-making and comparative product evaluations.