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Sr Hardware Engineer

8.00 to 13.00 Years   Hyderabad   01 Dec, 2021
Job LocationHyderabad
EducationNot Mentioned
SalaryNot Disclosed
IndustryMedical / Healthcare
Functional AreaGeneral / Other Software,Hardware / Telecom Equipment Design
EmploymentTypeFull-time

Job Description

Careers that Change LivesThe Senior Hardware Engineer, based in Hyderabad, India, is responsible for various Hardware Design and Development activities during the development lifecycle of complex electro-mechanical medical devicesA Day in the LifeThe Senior Hardware Engineer will be a key technical contributor in the product development of variety of electromechanical medical devices. The candidate will be an integral member of a talented and diverse product development team which will not only be creating innovative products and taking them from early concept through commercialization but will also be responsible for back end maintenance of products post launch. This candidate will participate in design, prototyping, and testing of electromechanical systems and sub systems.The individual will report to the Engineer Manager and be a part of a project team that may consist of on and offsite resources and will work closely with cross functional team members.Must Have/Job Respobsibilities

  • Remidiation of Medtronic legacy products to comply with latest regulatory standards such IEC/FDA/MDR by reveiwing DHF and Technical files
  • Have good understanding & knowledge about Digital and Analog Board Level Designs
  • Should have demonstrated practical expertise in designing circuits involving microcontrollers, digital signal processors
  • Must have conceptual and practical experience in Digital and Analog Communications
  • Knowledge with PCB layout and firmware design processes including requirements management, documentation and verification testing.
  • Perform Risk and Failure analysis of electronic components and hardware
  • Knowledge of standard engineering laboratory procedures.
  • Knowledge of Restriction of Hazardous Substances Directive or RoHS
  • Good understanding of EMC design techniques and standards (IEC60601) & demonstrated practical experience in providing solutions for EMC & safety.
  • Ability to apply appropriate standards, processes, policies, procedures, practices and tools throughout the product/system development lifecycle, including Standard Operating Procedures (SOPs), and applicable medical device development protocols under FDA Quality Systems Regulations, CE Marking, and ISO Quality Systems
  • Ability to carry out engineering calculations and analysis.
  • Ability to write engineering documents, test protocols, laboratory notebook entries and reports.
  • Ability to perform component engineering design and changes.
  • Ability to operate laboratory instruments.
  • Actively participate in product transfer to production, including sustaining engineering
  • Effective oral and written communication skills
Minimum Qualifications & Specialized Knowledge required
  • ME/MTech/BE/BTech in Electronics & Communication Engineering, Electrical Engineering or relevant field, with 8 to 13 years related experience
  • Experience in development of complex medical products from concept to commercialization desired under FDA Quality System Regulations, CE Marking and ISO Quality Systems is desirable.
About MedtronicTogether, we can change healthcare worldwide. At Medtronic, we push the limits of what technology, therapies and services can do to help alleviate pain, restore health and extend life. We challenge ourselves and each other to make tomorrow better than yesterday. It is what makes this an exciting and rewarding place to be. We want to accelerate and advance our ability to create meaningful innovations - but we will only succeed with the right people on our team. Let s work together to address universal healthcare needs and improve patients lives.Help us shape the future. Whatever your specialty or ambitions, you can make a difference at Medtronic - both in the lives of others and your career. Join us in our commitment to take healthcare Further, Together.Additional Information
  • Posting Date: Nov 16, 2021
  • Travel: No
, Careers that Change LivesThe Senior Hardware Engineer, based in Hyderabad, India, is responsible for various Hardware Design and Development activities during the development lifecycle of complex electro-mechanical medical devicesA Day in the LifeThe Senior Hardware Engineer will be a key technical contributor in the product development of variety of electromechanical medical devices. The candidate will be an integral member of a talented and diverse product development team which will not only be creating innovative products and taking them from early concept through commercialization but will also be responsible for back end maintenance of products post launch. This candidate will participate in design, prototyping, and testing of electromechanical systems and sub systems.The individual will report to the Engineer Manager and be a part of a project team that may consist of on and offsite resources and will work closely with cross functional team members.Must Have/Job Respobsibilities
  • Remidiation of Medtronic legacy products to comply with latest regulatory standards such IEC/FDA/MDR by reveiwing DHF and Technical files
  • Have good understanding & knowledge about Digital and Analog Board Level Designs
  • Should have demonstrated practical expertise in designing circuits involving microcontrollers, digital signal processors
  • Must have conceptual and practical experience in Digital and Analog Communications
  • Knowledge with PCB layout and firmware design processes including requirements management, documentation and verification testing.
  • Perform Risk and Failure analysis of electronic components and hardware
  • Knowledge of standard engineering laboratory procedures.
  • Knowledge of Restriction of Hazardous Substances Directive or RoHS
  • Good understanding of EMC design techniques and standards (IEC60601) & demonstrated practical experience in providing solutions for EMC & safety.
  • Ability to apply appropriate standards, processes, policies, procedures, practices and tools throughout the product/system development lifecycle, including Standard Operating Procedures (SOPs), and applicable medical device development protocols under FDA Quality Systems Regulations, CE Marking, and ISO Quality Systems
  • Ability to carry out engineering calculations and analysis.
  • Ability to write engineering documents, test protocols, laboratory notebook entries and reports.
  • Ability to perform component engineering design and changes.
  • Ability to operate laboratory instruments.
  • Actively participate in product transfer to production, including sustaining engineering
  • Effective oral and written communication skills
Minimum Qualifications & Specialized Knowledge required
  • ME/MTech/BE/BTech in Electronics & Communication Engineering, Electrical Engineering or relevant field, with 8 to 13 years related experience
  • Experience in development of complex medical products from concept to commercialization desired under FDA Quality System Regulations, CE Marking and ISO Quality Systems is desirable.
About MedtronicTogether, we can change healthcare worldwide. At Medtronic, we push the limits of what technology, therapies and services can do to help alleviate pain, restore health and extend life. We challenge ourselves and each other to make tomorrow better than yesterday. It is what makes this an exciting and rewarding place to be. We want to accelerate and advance our ability to create meaningful innovations - but we will only succeed with the right people on our team. Let s work together to address universal healthcare needs and improve patients lives.Help us shape the future. Whatever your specialty or ambitions, you can make a difference at Medtronic - both in the lives of others and your career. Join us in our commitment to take healthcare Further, Together.Additional Information
  • Posting Date: Nov 16, 2021
  • Travel: No
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Keyskills :
networkingcomputer hardwaretroubleshootinglanoperating systemstransfer to productionstandard operating proceduresce markingboard levelquality systemhardware designquality systems

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