11 дней назад
Sr Engineer (Medical Devices)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Sr Engineer (Medical Devices): Developing and validating mechanical systems and disposables for vital organ therapy products with an accent on design integration, testing, manufacturing transfer, and regulatory compliance. Focus on creating verification methodologies, analyzing design verification data, managing platform-level testing, and resolving complex mechanical and cross-functional integration risks.
Location: Bangalore, Karnataka, India
Company
develops vital organ therapy products and digital solutions, with a long-standing focus on kidney care and dialysis.
What you will do
- Lead the evaluation and development of disposables and mechanical systems using mechanics, thermodynamics, hydraulics, heat transfer, and materials engineering.
- Integrate mechanical designs with electrical and consumable components while optimizing products for production, reliability, regulatory compliance, and cost.
- Develop mechanical system architectures, documentation, specifications, drawings, and design history file verification materials.
- Define and execute test plans, protocols, reports, methodologies, measurement systems, fixtures, and platform-level testing activities.
- Analyze design verification data and statistical measures to assess product performance, operational stability, and design variants.
- Coordinate engineering, manufacturing, purchasing, regulatory, marketing, external partners, and subsystem teams while coaching junior engineers and lab technicians.
Requirements
- Mechanical engineering expertise applicable to medical devices and disposable products.
- Experience with mechanical analysis, calculations, system and subsystem integration, and engineering first principles.
- Ability to create and validate verification protocols, test methods, measurement systems, and testing infrastructure.
- Experience interpreting design verification data and identifying design integration, manufacturing transfer, and product reliability risks.
- Ability to develop technical documentation and ensure compliance with safety, regulatory, user, and business requirements.
- Ability to work onsite in Bangalore, Karnataka, India.
Culture & Benefits
- Work focused on improving outcomes for patients and care teams worldwide.
- Contribute to innovations in kidney care, dialysis, and broader vital organ therapies.
- Collaborate across engineering, manufacturing, regulatory, purchasing, marketing, and external partner functions.
- provides reasonable accommodations for individuals with disabilities during the application and interview process.
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