Required Skills

Hardware Design Analog Circuit Design Component Selection Power Supply Design

Work Authorization

  • Citizen

Preferred Employment

  • Full Time

Employment Type

  • Direct Hire

education qualification

  • UG :- - Not Required

  • PG :- - Not Required

Other Information

  • No of position :- ( 1 )

  • Post :- 18th Jul 2022

JOB DETAIL

SUMMARY OF POSITION

The candidate will be a key technical contributor in the product development of variety of electromechanical and electronic medical devices at MEIC. 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 designing, developing, prototyping, and testing of electronic and electromechanical systems and sub systems. The candidate will be required to provide reliable solutions using the latest computer automated engineering (CAE) tools for simulation and prototyping of both analog and digital circuits including test bench development.

ESSENTIAL DUTIES AND RESPONSIBILITIES

  • Have good understanding & knowledge about Digital and Analog  Circuit 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 and do Risk,  Failure analysis and obsolescence management 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 (SOP's), 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

EXPERIENCE

  • 10+ years of 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.

KNOWLEDGE, SKILL, AND ABILITY

  • Action Oriented
  • Dealing with Ambiguity
  • Approachability
  • Boss Relationships
  • Composure
  • Creativity
  • Timely Decision Making
  • Decision Quality
  • Functional/Technical Skills
  • Informing
  • Intellectual Horsepower
  • Learning On The Fly
  • Listening
  • Organizing
  • Perseverance
  • Presentation Skills
  • Priority Setting
  • Problem Solving

Company Information