2 часа назад
Sr. Mechanical Engineer (MedTech)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Sr. Mechanical Engineer (MedTech): Designing and developing mechanical components for active implantable medical devices with an accent on reliability, manufacturability, testing, and regulatory-compliant design control. Focus on FEM analysis, mechanical modelling, verification planning, multidisciplinary integration, and leading technical development across the full product cycle.
Location: Barcelona, Spain; hybrid working modality
Company
develops graphene-based neuroelectronic interfaces and implantable neural solutions for treating brain disorders.
What you will do
- Lead the mechanical design, assembly, prototyping, integration, and testing of components for implantable electro-mechanical systems.
- Apply concept engineering, functional analysis, FEM analysis, mechanical modelling, sensitivity analysis, and stress analysis.
- Prepare device documentation, including BOMs, drawings, specifications, and test plans, in line with ISO 13485 and ISO 14971 design-control requirements.
- Define and execute verification methods for safety and mechanical performance, including bench, characterization, integration, and system testing.
- Coordinate outsourced mechanical design, assembly, testing, and manufacturing activities.
- Collaborate with Electronics, Systems, Quality, Regulatory, Clinical, and Project Management teams during design and stage reviews.
Requirements
- BSc or MSc in Mechanical Engineering and at least 5 years of MedTech experience with a proven full development cycle.
- Experience developing multidisciplinary medical devices and at least 2 years leading a technical mechanical engineering aspect of a project.
- Strong practical mechanical engineering experience for commercial production, including DFM, DFR, design-for-assembly, design-for-test, and pFMEA.
- Familiarity with electrical engineering, SolidWorks, PDM, manufacturing processes, and mechanical design methodologies.
- Ability to manage projects involving external subcontractors and manufacturers.
- Fluent English required; applications must be submitted in English.
Nice to have
- Experience with neuroscience and active implantable medical device development.
- Hands-on experience with machine shop tools.
- Experience applying ISO 13485 quality control and medical risk analysis in a regulated industry.
- Understanding of standards applicable to active implantable medical devices.
Culture & Benefits
- Collaborative environment focused on open communication, knowledge sharing, mutual respect, and diverse perspectives.
- Opportunity to work on healthcare technology intended to create meaningful societal impact.
- Exposure to state-of-the-art technologies and resources, with training support and access to Udemy.
- Competitive salary based on experience and skills, plus an internal flexible compensation scheme.
- Private health insurance, 23 vacation days per year, and Christmas week off.
- Hybrid working modality.
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