Glaukos Corporation
Overview
We are seeking a highly skilled and visionary
Principal Electrical Engineer
to lead the design, simulation, and development of complex electrical systems for our next-generation
corneal cross-linking system . This role requires deep technical expertise in
circuit design, simulation, PCB development, and system integration , paired with leadership in
architecting solutions, mentoring teams, and ensuring compliance with medical device regulations . What You7ll Do: The Principal Engineer will serve as an individual contributor, driving innovation, setting design strategy, and ensuring robust, reliable, and safe designs that meet both
clinical needs
and
regulatory requirements . Technical Leadership Support the
electrical system architecture
and ensure seamless integration with mechanical, optical, and software subsystems. Act as the
technical subject matter expert
in circuit design, simulation, and verification by applying a systematic approach. Technical lead
for all electrical design needs of the system development. Ensure adherence to
FDA design control requirements
(21 CFR Part 820) and compliance with applicable medical device standards ( IEC 60601-1, IEC 60601-1-2 ). Mentor, coach, and provide technical guidance to
junior, senior engineers and technicians . Circuit Design & Simulation Lead the design of
complex analog, digital, mixed-signal, RF, and power circuits
for medical device applications. Perform advanced
circuit simulations
(DC, AC, transient, Monte Carlo, noise, signal integrity, power integrity, EMC/EMI modeling). Conduct
worst-case, tolerance, and reliability analysis
to anticipate failures and ensure long-term product robustness. Drive
thermal and power distribution modeling
to inform PCB layout strategies. Correlate
simulation results with experimental data , refining models and designs for accuracy. PCB Design & Development Oversee
schematic capture and PCB layout
using
Altium Designer
and other industry tools. Create and approve
schematic symbols, footprints, and component libraries . Ensure PCB layouts meet
signal integrity, noise immunity, EMC/EMI, creepage/clearance, and thermal requirements . Lead component selection for
critical and electromechanical parts . Design Verification & Validation Author and oversee
design verification and validation protocols , ensuring compliance with product requirements. Lead the definition of
system test plans
and manage their release ECO's in the
EDMS (Electronic Document Management System) . Direct
bench testing
of PCBs using oscilloscopes, spectrum analyzers, and other advanced instrumentation. Ensure
traceability
between requirements, design outputs, and verification results per regulatory guidelines. System Integration & Collaboration Collaborate with
embedded software teams
to define hardware/software interface requirements. Drive issue resolution during
system integration and clinical evaluation phases . What We Offer Opportunity to lead the development of
cutting-edge medical technology
that directly improves patient outcomes. A collaborative and
innovative-driven environment
where your technical expertise drives product success. Growth opportunities into
technical fellow or engineering leadership tracks . How You\u2019ll Get There: Bachelors degree in
electrical engineering or related field
(Masters or Ph.D. preferred). Experience : 10+ years
of experience in
electrical design and product development , with a strong track record in
medical devices or other regulated industries . Expert-level knowledge in
analog, digital, mixed-signal, and power circuit design , validated by advanced
circuit simulation and modeling expertise . Hands-on experience with
EDA and simulation tools
(PSpice, LTspice, MATLAB/Simulink, Altium Designer, Allegro PCB, ORCAD). Proven experience in
signal integrity, power integrity, EMC/EMI, and thermal simulations . Strong background in
motor control circuits, sensors, and communication interfaces
(I2C, SPI, UART, CAN, Wi-Fi, BLE). Experience defining and executing
design verification and validation protocols
under
FDA design control
requirements. Familiarity with
IEC 60601-1, IEC 60601-1-2 , and other applicable safety/EMC standards.
#J-18808-Ljbffr
We are seeking a highly skilled and visionary
Principal Electrical Engineer
to lead the design, simulation, and development of complex electrical systems for our next-generation
corneal cross-linking system . This role requires deep technical expertise in
circuit design, simulation, PCB development, and system integration , paired with leadership in
architecting solutions, mentoring teams, and ensuring compliance with medical device regulations . What You7ll Do: The Principal Engineer will serve as an individual contributor, driving innovation, setting design strategy, and ensuring robust, reliable, and safe designs that meet both
clinical needs
and
regulatory requirements . Technical Leadership Support the
electrical system architecture
and ensure seamless integration with mechanical, optical, and software subsystems. Act as the
technical subject matter expert
in circuit design, simulation, and verification by applying a systematic approach. Technical lead
for all electrical design needs of the system development. Ensure adherence to
FDA design control requirements
(21 CFR Part 820) and compliance with applicable medical device standards ( IEC 60601-1, IEC 60601-1-2 ). Mentor, coach, and provide technical guidance to
junior, senior engineers and technicians . Circuit Design & Simulation Lead the design of
complex analog, digital, mixed-signal, RF, and power circuits
for medical device applications. Perform advanced
circuit simulations
(DC, AC, transient, Monte Carlo, noise, signal integrity, power integrity, EMC/EMI modeling). Conduct
worst-case, tolerance, and reliability analysis
to anticipate failures and ensure long-term product robustness. Drive
thermal and power distribution modeling
to inform PCB layout strategies. Correlate
simulation results with experimental data , refining models and designs for accuracy. PCB Design & Development Oversee
schematic capture and PCB layout
using
Altium Designer
and other industry tools. Create and approve
schematic symbols, footprints, and component libraries . Ensure PCB layouts meet
signal integrity, noise immunity, EMC/EMI, creepage/clearance, and thermal requirements . Lead component selection for
critical and electromechanical parts . Design Verification & Validation Author and oversee
design verification and validation protocols , ensuring compliance with product requirements. Lead the definition of
system test plans
and manage their release ECO's in the
EDMS (Electronic Document Management System) . Direct
bench testing
of PCBs using oscilloscopes, spectrum analyzers, and other advanced instrumentation. Ensure
traceability
between requirements, design outputs, and verification results per regulatory guidelines. System Integration & Collaboration Collaborate with
embedded software teams
to define hardware/software interface requirements. Drive issue resolution during
system integration and clinical evaluation phases . What We Offer Opportunity to lead the development of
cutting-edge medical technology
that directly improves patient outcomes. A collaborative and
innovative-driven environment
where your technical expertise drives product success. Growth opportunities into
technical fellow or engineering leadership tracks . How You\u2019ll Get There: Bachelors degree in
electrical engineering or related field
(Masters or Ph.D. preferred). Experience : 10+ years
of experience in
electrical design and product development , with a strong track record in
medical devices or other regulated industries . Expert-level knowledge in
analog, digital, mixed-signal, and power circuit design , validated by advanced
circuit simulation and modeling expertise . Hands-on experience with
EDA and simulation tools
(PSpice, LTspice, MATLAB/Simulink, Altium Designer, Allegro PCB, ORCAD). Proven experience in
signal integrity, power integrity, EMC/EMI, and thermal simulations . Strong background in
motor control circuits, sensors, and communication interfaces
(I2C, SPI, UART, CAN, Wi-Fi, BLE). Experience defining and executing
design verification and validation protocols
under
FDA design control
requirements. Familiarity with
IEC 60601-1, IEC 60601-1-2 , and other applicable safety/EMC standards.
#J-18808-Ljbffr