4 - 8 years
15 - 25 Lacs
Posted:14 hours ago|
Platform:
Work from Office
Full Time
• Lead the end-to-end system design of respiratory therapy devices, including hardware, firmware, and software integration.
• Define system-level requirements and specifications in collaboration with cross-functional teams.
• Evaluate the technical, regulatory, and safety implications of engineering and design change requests to ensure system integrity and compliance throughout the product lifecycle.
• Identify and define Critical to Safety (CTS) and Critical to Quality (CTQ) parameters during design and development.
• Support verification and validation (V&V) activities across system and subsystem levels.
• Maintain and update traceability matrices for system requirements, risks, and testing.
• Ensure adequate traceability from design inputs to verification outputs and risk mitigations.
• Apply strong understanding of safety risk management, including: o DFMEAo Product risk analysiso Risk mitigations
• Ensure compliance with ISO 14971 and other relevant risk management standards.
• Demonstrated knowledge of global regulatory frameworks including: o FDA 21 CFR Part 820.30o ISO 13485o IEC 60601 serieso ISO 14971
• Maintain documentation for Design History File (DHF), traceability matrices, and risk files.
• Experience with requirement management tools (e.g., IBM DOORS) and lifecycle management platforms (e.g., Windchill).
• Collaborate with mechanical, electrical, software, quality, and regulatory teams throughout the product lifecycle.Lead and participate in design reviews, risk assessments, and Phase Gate Reviews.
• Lead and participate in design reviews, risk assessments, and Phase Gate Reviews.
Education & Skills preferred:
• Degree preferred, MTech / BE/ BTECH in Biomedical Engineering, Electrical Engineering, Mechanical Engineering, Systems Engineering, or related field.
• 3-5 years of experience in medical device product development, and overall 5-10 years of experience.
• Experience with ventilator
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