10 дней назад
Principal Eng, Mechanical (Medical Devices)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Principal Eng, Mechanical (Medical Devices): Developing and improving mechanical systems for Continuous Renal Replacement Therapy products with an accent on mechanical design, electromechanical integration, manufacturing, and verification testing. Focus on FEA, tolerance and fatigue analysis, prototype development, root-cause investigations, and transferring designs into production.
Location: Bangalore, Karnataka, India; onsite full-time
Company
develops vital organ therapy products and digital solutions, with a focus on kidney care and dialysis technologies.
What you will do
- Develop creative mechanical solutions for Continuous Renal Replacement Therapy products.
- Improve existing products and develop new functions and features for integration into established systems.
- Execute requirements, specifications, concept development, detailed design, prototyping, verification testing, and transfer to manufacturing.
- Perform structural, tolerance, load, fatigue-life, thermal, heat-transfer, FEA, and experimental analyses.
- Integrate mechanical design elements into electromechanical systems and create complete engineering and manufacturing documentation.
- Troubleshoot field and manufacturing issues, including root-cause investigations, change orders, NCRs, and CAPAs.
Requirements
- Bachelor’s degree in Mechanical Engineering or an equivalent field; a master’s degree is preferred.
- At least 5 years of experience in product development and production manufacturing.
- Extensive SolidWorks experience; familiarity with ProE/Creo is preferred.
- Experience with electromechanical systems, contract manufacturers, and component suppliers.
- Expertise in mechanical manufacturing processes, DFM/DFA, engineering drawings, geometric dimensioning and tolerancing, and FEA.
- Excellent written and verbal English communication skills, plus strong documentation, presentation, organization, and hands-on prototyping abilities.
Nice to have
- Experience in regulated industries, preferably medical devices.
- Familiarity with ISO 13485, IEC 60601, and ISO 14971.
- SolidWorks administrator experience.
Culture & Benefits
- Work on products intended to improve and sustain patients’ lives.
- Collaborate on multidisciplinary global hardware projects.
- Operate in a fast-paced environment with multiple projects and priorities.
- Reasonable accommodations are available throughout the application and interview process.
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