Mechanical Engineer

INBRAIN Neuroelectronics

Barcelona, Spain

YOUR MISSION

As a Mechanical Engineer at INBRAIN you will be contributing to the Design, development, and test of mechanical systems. These mechanical systems are part of a complex CNS neuromodulation implant and its peripheral equipment. This active medical device will be released in EU, requiring CE mark according to the MDR, and in the USA, requiring FDA approval. As a Mechanical Engineer you will investigate, create concepts, design, develop and test mechanical components, assemblies, and systems.

Main responsabilities

Lead the design, assembly, prototyping and test mechanical components that are part of an implantable CNS neuromodulation system, in direct collaboration with the electronics, systems, quality and regulatory teams.
Work with clinicians, users, and other team members to define and evolve requirements and guidelines for the design of mechanical components.
Design for reliability, manufacture and test, including concept engineering, functional analysis, FEM analysis, and mechanical modelling.
Deliver detailed documentation of the device design (BOM, drawings, Specifications, test plan,…) compliant with ISO 13485 and ISO14971design control requirements.
Support and collaborate with external partners in the outsourced design, assembly and test of mechanical components that are part of an implantable CNS neuromodulation system
Qualify, validate and create maintenance plans for lab tools and equipment.
Define test plans and methods to verify safety and mechanical performance of the device, in compliance with applicable standards and in collaboration with other teams.
Design and build and perform, experimental and product system setups necessary to perform bench tests, characterization testing, integration, system testing.
Identify sub-contractors who can be used to provide mechanical development and prototype build services to INBRAIN, and manage projects assigned to such 3rd parties.
Create test plans to verify our mechanical designs from the product requirements.
Generate intellectual property.
Understand DFR/DFM/DFT (Design for Reliability, Design for Manufacturing and Design for Test), including concept engineering, modelling, analysis, sensitivity, and stress analysis.
Work intensively with Quality, Regulatory, Clinical and Project Management on the formal product development procedure, perform or collaborate in design and stage reviews.
Follow change request processes.
Initiate and contribute to design, technical and milestone reviews.

YOUR PROFILE

BS or MS in Mechanical Engineering with at least 5 years of work experience in a relevant industrial setting (regulated environment, MedTech is a strong plus) with a proven experience executing a full development cycle. Experience in developing multidisciplinary medical device is a plus.
Minimum of 2 years of leading technical oriented team.
Demonstrated skills in the areas required to perform this job: Mechanical CAD design, Selection of medical-grade materials and components, safety and performance testing., Requirements based Design,
Ability to manage projects mandated to external sub-contractor and manufacturing.
Strong hands-on skills, experience with workshop tools. Desirable machining knowledge.
Fun, loving, people person. Motivated to make the world a better place.
Fast learner, self-motivated and pro-active individual able to work in the fast-moving environment of a dynamic start-up company.
A system-thinking attitude identify areas of potential improvement and develop plans to address these; Team oriented, a sparring partner to colleagues in other disciplines.
Preferred to have solid experience in neuroscience with a strong interest in gaining a further understanding of this field.
Preferred to have solid experience in (MDR) Medical Device Regulation, ISO 13485 Quality environments, ISO 14971 Risk Analysis and IEC 60601
Fluency in English required (English is the company language). Fluency in Spanish is a plus.

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