Senior Design and Development (D&D) Specialist - São José do Rio Preto - SP ( Presencial)
- Presencial
- São José do Rio Preto, SP, BR São José do Rio Preto, SP, BR
- De segunda à sexta, das 8h às 17h48min com 1h de almoço
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Operacional
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Efetivo – CLT
Descrição e Responsabilidades
Join our team as a Senior D&D ( Design & Development) Specialist! We're seeking a hands-on innovator to spearhead the development of cutting-edge catheter-based products for treating Implantable devices for structural heart disease.
If you're an innovative D&D Specialist ready to lead transformative projects in medical device development, we want to hear from you! Solidworks, plastics, metals, prototyping, injection molding, and medical disposables design expertise is a plus.
About Us:
Be part of the forward-thinking advanced D&D division within an innovative company.
Job Responsibilities:
- Drive the design, prototyping, and development of pioneering solutions for minimally-invasive valve replacement, ensuring alignment with customer requirements and industry standards.
- Craft comprehensive design control requirements, encompassing CAD models, detailed specifications, verification/validation plans, and adherence to FDA/ISO guidelines.
- Foster seamless collaboration across departments—Marketing, Quality, Regulatory, and Manufacturing—to meet project deadlines effectively.
- Oversee external partners engaged in concept development, prototype fabrication, and device testing, ensuring seamless partnerships.
- Manage supplier relationships, guiding material selection, tool design, and manufacturing processes for components and assemblies.
- Cultivate intellectual property by generating and documenting innovative ideas while interacting with physicians to enhance product functionality.
- Uphold procedural standards and mentor junior engineers to foster growth within the team.
Requisitos
Requirements:
- Engineering degree (Mechanical or Biomedical preferred).
- 5+ years of Heart Valve R&D experience; 10+ years in medical, aerospace, automotive, or regulated fields.
- Proficiency in 3D modeling (Solidworks), with a strong grasp of drafting practices and manufacturing techniques.
- Ability to ideate, design, prototype, and validate complex mechanical devices.
- Expertise in FDA/MDR design control, varied manufacturing methods, and materials specific to medical device design.
- Familiarity with simulation techniques (CFD, FEA) and a strong mechanical aptitude.
- Excellent communication, collaboration, and organizational skills to thrive in cross-functional environments.
Benefícios
Código: 106571
Data de Cadastro: 2025-03-13
Data de Atualização: 2025-03-13
- Código: 106571
- Data de Cadastro: 2025-03-13
- Data de Atualização: 2025-03-13