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Posted : Sunday, October 15, 2023 08:00 AM
*Company Description*
Evinex is a consulting firm based in Newport Beach, California.
This is a direct hire placement for a position with one of our prestigious global clients.
Why Join? The client is leading the industry in innovative technologies and requires a senior level person to help develop firmware for microcontroller-based systems.
This position will participate in development lifecycle activities including specification, design, debugging, test development, formal verification, failure analysis and sustaining engineering.
This position will also develop and maintain Windows desktop software application using C, C#, Embedded C, Python, and RF Embedded Software.
*Job Description* The Principal Engineer Firmware for Medical Devices contributes to efforts of the existing team that conducts research on optimal ways of encoding speech and music for cochlear implant recipients.
Develop firmware for microcontroller-based systems.
Participate in development lifecycle activities including specification, design, debugging, test development, formal verification, failure analysis and sustaining engineering.
Develop and maintain Windows desktop software application using the C# programming language This is a full-time employee (W2 FTE) position placed directly with the client, with full benefits.
Relocation assistance is available.
*Responsibilities and Duties* * Analog and digital circuits development * Power subsystems, both inductively coupled and long range RF power * Communication links operating at frequencies below 100mhz * Organic PCB technologies including related electrical performance issues * Developing firmware for implantable hearing solutions * Various aspects of designing Class III electronic medical technologies involving custom components and should be experienced with the regulatory requirements associated with the submission of such technologies to regulatory bodies (CE and FDA) * Digital signal processing technologies, custom component specification and design and verification of inductively powered systems * Ensure adherence of designs and processes to applicable industry standards and internal quality system standards.
* Working with Marketing, Project Management and other R&D groups to guide requirements and generate product specifications for a future generation platform * Obtain a system level view to drive tradeoff analysis during product development while considering features, schedules, cost, complexity, risk and usability.
* Conduct feasibility work on product / system components and features in the area of technical expertise.
Study and be able to propose suitable components, algorithms and solutions at the least in the area of expertise.
* Work with Electrical (RF, Board & IC), Firmware, Software and Mechanical teams during the product development and system integration phase.
* Work with R&T and other R&D groups to define architectures for future products and systems with a solid understanding of market needs.
* Maintain design history consistent with the submission requirements of regulatory agencies.
Directly applicable experience with electronic implantable hearing technologies and systems involving custom components *Education / Professional Experience Required* * 2+ year Class 3 Medical Device experience is a must including knowledge of relevant standards (IEC60601, EN 45502, etc.
).
* 2+ year experience working in a highly regulated environment with strict requirements for process, procedures and documentation and experience with formal regulatory procedures for Class III submissions to CE and FDA bodies.
* 10+ years of firmware design, implementation & testing * Master’s degree in Electrical Engineering or a related field *Knowledge / Skills / Abilities Required* * Strong hands-on technical ability in at least three of the following: Circuits, Embedded systems, DSP, RF, custom ics.
* Competent with the relevant tools in the area of expertise (MATLAB, Embedded tools, SPICE, VHDL, etc.
).
* Core competency in designing and testing inductively powered systems using custom RF components * Core competency in digital signal processing for audio * Competency in HDL design and verification * Experience with vendor and technology selection for Class III medical systems * Capable of working independently with high level input and limited guidance * Project Management skills are highly demonstrated Job Type: Full-time Pay: $125,000.
00 - $155,000.
00 per year Benefits: * 401(k) * 401(k) matching * Dental insurance * Flexible spending account * Health insurance * Health savings account * Life insurance * Paid time off * Parental leave * Relocation assistance * Retirement plan * Vision insurance Schedule: * Monday to Friday Education: * Bachelor's (Required) Experience: * Class 3 Medical Device: 2 years (Required) * Class III regulatory procedures for CE and FDA: 2 years (Required) * firmware: 10 years (Required) Work Location: Hybrid remote in Valencia, CA 91355
This is a direct hire placement for a position with one of our prestigious global clients.
Why Join? The client is leading the industry in innovative technologies and requires a senior level person to help develop firmware for microcontroller-based systems.
This position will participate in development lifecycle activities including specification, design, debugging, test development, formal verification, failure analysis and sustaining engineering.
This position will also develop and maintain Windows desktop software application using C, C#, Embedded C, Python, and RF Embedded Software.
*Job Description* The Principal Engineer Firmware for Medical Devices contributes to efforts of the existing team that conducts research on optimal ways of encoding speech and music for cochlear implant recipients.
Develop firmware for microcontroller-based systems.
Participate in development lifecycle activities including specification, design, debugging, test development, formal verification, failure analysis and sustaining engineering.
Develop and maintain Windows desktop software application using the C# programming language This is a full-time employee (W2 FTE) position placed directly with the client, with full benefits.
Relocation assistance is available.
*Responsibilities and Duties* * Analog and digital circuits development * Power subsystems, both inductively coupled and long range RF power * Communication links operating at frequencies below 100mhz * Organic PCB technologies including related electrical performance issues * Developing firmware for implantable hearing solutions * Various aspects of designing Class III electronic medical technologies involving custom components and should be experienced with the regulatory requirements associated with the submission of such technologies to regulatory bodies (CE and FDA) * Digital signal processing technologies, custom component specification and design and verification of inductively powered systems * Ensure adherence of designs and processes to applicable industry standards and internal quality system standards.
* Working with Marketing, Project Management and other R&D groups to guide requirements and generate product specifications for a future generation platform * Obtain a system level view to drive tradeoff analysis during product development while considering features, schedules, cost, complexity, risk and usability.
* Conduct feasibility work on product / system components and features in the area of technical expertise.
Study and be able to propose suitable components, algorithms and solutions at the least in the area of expertise.
* Work with Electrical (RF, Board & IC), Firmware, Software and Mechanical teams during the product development and system integration phase.
* Work with R&T and other R&D groups to define architectures for future products and systems with a solid understanding of market needs.
* Maintain design history consistent with the submission requirements of regulatory agencies.
Directly applicable experience with electronic implantable hearing technologies and systems involving custom components *Education / Professional Experience Required* * 2+ year Class 3 Medical Device experience is a must including knowledge of relevant standards (IEC60601, EN 45502, etc.
).
* 2+ year experience working in a highly regulated environment with strict requirements for process, procedures and documentation and experience with formal regulatory procedures for Class III submissions to CE and FDA bodies.
* 10+ years of firmware design, implementation & testing * Master’s degree in Electrical Engineering or a related field *Knowledge / Skills / Abilities Required* * Strong hands-on technical ability in at least three of the following: Circuits, Embedded systems, DSP, RF, custom ics.
* Competent with the relevant tools in the area of expertise (MATLAB, Embedded tools, SPICE, VHDL, etc.
).
* Core competency in designing and testing inductively powered systems using custom RF components * Core competency in digital signal processing for audio * Competency in HDL design and verification * Experience with vendor and technology selection for Class III medical systems * Capable of working independently with high level input and limited guidance * Project Management skills are highly demonstrated Job Type: Full-time Pay: $125,000.
00 - $155,000.
00 per year Benefits: * 401(k) * 401(k) matching * Dental insurance * Flexible spending account * Health insurance * Health savings account * Life insurance * Paid time off * Parental leave * Relocation assistance * Retirement plan * Vision insurance Schedule: * Monday to Friday Education: * Bachelor's (Required) Experience: * Class 3 Medical Device: 2 years (Required) * Class III regulatory procedures for CE and FDA: 2 years (Required) * firmware: 10 years (Required) Work Location: Hybrid remote in Valencia, CA 91355
• Phone : NA
• Location : 28515 Westinghouse Place, Valencia, CA
• Post ID: 9003696238
