Senior Mechanical Design Engineer (Medical Devices)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Location: Galway, County Galway, Ireland; hybrid role with an onsite requirement at the Parkmore, Galway site. Work is performed in R&D laboratories and manufacturing facilities, with travel to suppliers and design and manufacturing sites as required.
Salary: EUR 64,640–96,960 per year, with final salary based on relevant experience, skills, and qualifications. Eligible for the Incentive Plan short-term incentive.
Company
develops healthcare technologies through its Electrophysiology Therapies division to improve clinical outcomes and quality of life.
What you will do
- Act as design owner for released product engineering, planning and executing testing and analysis during product changes.
- Drive improvements in product performance, manufacturability, quality, cost, and supply continuity while maintaining design intent.
- Apply risk-based decision-making and DRM methodologies, complete Design Control deliverables, and translate VoX feedback into product requirements.
- Design, develop, analyze, troubleshoot, and provide technical support during product development and manufacturing.
- Lead root cause investigations, technology evaluations, product improvements, pre-clinical studies, and development of manufacturing methods, materials, machines, and processes.
- Define and perform verification and validation activities, coordinate suppliers and consultants, document results, and mentor junior engineers.
Requirements
- Bachelor's degree in Engineering at NFQ level 8 with 4+ years of experience in mechanical product development, or a Master's degree in Engineering with 2+ years of experience in mechanical product development.
Nice to have
- Experience in the medical device industry and high-volume manufacturing.
- Experience in complex mechanical system design and product risk management.
- Experience with issue investigation and CAPAs.
- Experience in 3D modelling, finite element analysis, and statistical design analysis.
- Experience in process and test method development and validation.
- DRM Greenbelt certification or above.
- Ability to work collaboratively with diverse cross-functional teams and interact professionally across organizational levels.
- Hands-on mentality, excellent verbal and written communication, and strong interpersonal skills.
- Ability to apply statistical methods and science-based decisions to design experiments and implement improvements.
- Ability to deliver quality technical work within project schedules in a fast-paced, deadline-driven environment.
Culture & Benefits
- Competitive salary and flexible benefits package.
- Short-term incentive eligibility through the Incentive Plan.
- Work across R&D laboratories, manufacturing facilities, suppliers, and global design and manufacturing sites.
- Cross-functional collaboration with program management, manufacturing, quality, suppliers, consultants, and global teams.
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