Philips System Test Designer V & - Medical Devices India, Karnataka, Bengaluru 784237612
You are responsible for
Supporting product verification through the phases of the Medical Device lifecycle.
Providing technical support and leadership on a cross-functional team
Define, document, and continuously improve verification tests including conducting peer reviews and maintaining traceability to requirements
Perform verification tests and conduct analysis of the test results to ensure complete verification of the requirements
Identifying, analyzing and driving technical issues to resolution
Perform work with little to no supervision as department subject-matter expert
Participates in design reviews, including reviews of design verification plans, reports, and test artifacts.
Development and execution of validation test plans , test records and Test fixtures
Keeps abreast of new developments in all relevant technological domains.
Provides technical leadership to ensure overall product development success.
Keeps abreast of new developments in all relevant technological domains.
Contributes to technology roadmaps and other strategic related activities
Provides technical leadership to ensure overall product development success.
To succeed in this role, you should have the following skills and experience
Bachelor’s degree in Electronics/Computer Science/Electrical Engineering or related field, good to have a Master’s degree.
Total 5+ years’ experience with Minimum 3 years of experience in medical device or other similar industry
Demonstrated knowledge of global quality and regulatory environment for medical devices including FDA CFR 21 part 820.30 and IEC 60601-1-1 (CE mark), ISO 13485, and risk management requirements and development dependencies.
Solid understanding of medical device product development, preferably Design Control experience with Class-III/Class-3 medical devices (FDA CFR Title 21, 820.30)
Experience specific to product verification.
Solid understanding of System Verification and Validation test plan/protocols, executing V&V activities, generating, and analyzing test reports
Experience in designing and assessing compliance to national/international standards.
Strong technical writing/documentation skills for a regulated medical device design environment, including requirements definition
Proven ability to communicate in both verbal and written form to technical and non-technical customers, stakeholders, and various levels of management.
Possess strategic agility/vision: Sees ahead clearly; can anticipate future concerns.
Develops and maintains effective relationships and is capable of quickly earning trust and respect.
Ability to study and understanding of Schematics and PCBA
Board bring up experience.
Good Knowledge of EMI/EMC (IEC- 60601-1-2)artifacts and testing , ISO 14971 (Risk Management), IEC 62304 (Software Lifecycle).
Strong knowledge of embedded systems, real-time operating systems (RTOS), and microcontroller-based architectures.
Proficient in test development tools, scripting languages (Python, Shell, etc.), and test automation frameworks.
Experience with communication protocols (I2C, SPI, UART, CAN, BLE, etc.).
Experience with hardware-in-the-loop (HIL) and system simulation environments.
Experience with version control systems (Git) and requirements management tools.
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