Device Engineer Job at Arrow Electronics (Cedar Rapids)

Sr. Software Engineer (Medical Devices)

Location

United States , Raleigh, NC

Salary:

Not provided

Bytecubit Technologies

Expiration Date

Until further notice

Requirements

7+ years’ experience with SW development
SW development for Medical Devices
BS in Computer Science
C, C#, C++ skills
Microsoft.NET
SQL database
GUI application development
Windows 10
Cryptographic algorithm

Job Responsibility

Consultant will be responsible for design and development of embedded SW for medical device to support manufacturing of products
write SW requirements
provide design input for GUI system SW
design development and implementation of cybersecurity control methods for FDA NIST standards
testing, static analysis, profiling and debugging
take measurements using lab equipment tools
data processing for test protocols

Software Engineer - Platform Software, Device Drivers, System Bring-Up

Our team is responsible for driving technology leadership in the Juniper routing...

Location

India , Bangalore

Salary:

Not provided

Hewlett Packard Enterprise

Expiration Date

Until further notice

Requirements

BTech / MTech in CS/CE or related field with proven experience of 10+ years
Good understanding of hardware-level details for Optics, PCIe, SPI, I2C, Retimers, FPGA, CPLD, MDIO, Flash Driver
Proficiency with device drivers, system bring-up, FreeBSD/Linux internals
Understanding of Ethernet, OTN, SONET, etc. technologies
Strong technical, analytical, and problem-solving skills
Strong in C, C++ programming, OO analysis & design, data structures, and system debugging skills
Prior software development experience on networking products

Job Responsibility

Board bring-up related experience. 10G, 40G, 100G, 400G, 800G interface related platform software like interface drivers, etc.
Platform infrastructure-related software like Routing Engine Redundancy/High Availability, Chassis/line card, fabric, Optics, etc.
Timing software in PTP, SYNCE & Grand Master
You will be responsible for these product developments in the platform area in either JunOS or Junos evolved software architecture
In addition to the development activity, you are required to work closely with system and solution test teams to ensure products/solutions delivered are of the highest quality
You will be required to work closely with Juniper Technical Assistance Team for providing engineering assistance in supporting critical customer escalations for customer deployments

What we offer

Health & Wellbeing
Personal & Professional Development
Unconditional Inclusion

Fulltime

Staff Software Engineer - Devices interactions

Staff Software Engineer role focused on devices interactions, working on Ledger ...

Location

France , Paris

Salary:

Not provided

Ledger

Expiration Date

Until further notice

Requirements

Engineer profile with at least 8 years of experience in software development
Tech lead experience
Proficient with JavaScript and TypeScript
Strong background/interest in algorithm development and optimization
Excellent knowledge of React and hooks

Job Responsibility

Participate in modularization effort by contributing to Device Management Kit
Maintain and extend @ledgerhq/hw-transport-* libraries
Contribute to main Ledger's initiatives like 'Clear Sign all the things'
Contribute to 'My Ledger' section on Ledger Live application
Collaborate closely with other engineering teams like Firmware team
Help QA team automate testing approaches
Investigate bugs in blockchain edge cases

What we offer

Flexible work options - work from home up to 3 times per week
Health & Wellness support - Health and Life Insurance
Financial growth opportunities - employees can become shareholders
Commuter allowance
Learning & Development - comprehensive suite of training solutions

Fulltime

Software Engineer - Platform Software, Device Drivers, System Bring-Up

Our team is responsible for driving technology leadership in the Juniper routing...

Location

India , Bangalore

Salary:

Not provided

Hewlett Packard Enterprise

Expiration Date

Until further notice

Requirements

BTech / MTech in CS/CE or related field with proven experience of 10+ years
Good understanding of hardware-level details for Optics, PCIe, SPI, I2C, Retimers, FPGA, CPLD, MDIO, Flash Driver
Proficiency with device drivers, system bring-up, FreeBSD/Linux internals
Understanding of Ethernet, OTN, SONET, etc. technologies
Strong technical, analytical, and problem-solving skills
Strong in C, C++ programming, OO analysis & design, data structures, and system debugging skills
Prior software development experience on networking products

Job Responsibility

Board bring-up related experience
10G, 40G, 100G, 400G, 800G interface related platform software like interface drivers, etc.
Platform infrastructure-related software like Routing Engine Redundancy/High Availability, Chassis/line card, fabric, Optics, etc.
Timing software in PTP, SYNCE & Grand Master
Product developments in the platform area in either JunOS or Junos evolved software architecture
Work closely with system and solution test teams to ensure products/solutions delivered are of the highest quality
Work closely with Juniper Technical Assistance Team for providing engineering assistance in supporting critical customer escalations for customer deployments

What we offer

Health & Wellbeing
Personal & Professional Development
Unconditional Inclusion

Fulltime

Director Systems Engineering

As the Director Systems Engineering, Infusion Systems, you will lead the develop...

Location

United States , Round Lake

Salary:

184000.00 - 253000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

Bachelor's or Master’s degree in Systems Engineering, Biomedical Engineering or a related field
Minimum of 10 years of experience in systems engineering, with a focus on medical fluid management devices (electromechanical pumps) in the medical device industry
Demonstrated experience leading, developing and managing engineering teams in a highly regulated environment
Strong technical skills, with a deep understanding of systems engineering principles and practices
Excellent communication and collaboration skills, with the ability to work effectively with cross-functional teams
Critical thinker, strong problem-solver, analytical
Proactive approach to project management, able to address potential risks and issues before they become critical
Organized, able to prioritize tasks effectively
Passionate about ensuring the safety and effectiveness of medical devices, and committed to delivering high-quality products that meet user needs
Customer focus, with a deep understanding of user needs and preferences, and a commitment to designing and developing products that meet these needs

Job Responsibility

Lead and develop global systems engineering teams based in Round Lake, IL, Bangalore, India, and Medina, NY
Create, effectively communicate, and deploy the strategy for the team that aligns with the overall systems organization strategic plan
Own capturing system use environments, workflows, user needs and use cases across all infusion systems platforms
Lead systems design validation across all platforms
Drive creation and verification of comprehensive system requirements for new and existing infusion systems pumps, administration sets, elastomerics, and accessories, ensuring they are complete, accurate, and aligned with user needs and business objectives
Collaborate to ensure alignment and traceability of requirements throughout the product development process
Implement and maintain a robust systems risk management framework to identify, analyze, and mitigate potential risks
Lead resource demand planning, allocation, and actuals
Recruit, mentor, and lead a multi-disciplinary engineering team, fostering a culture of innovation, collaboration, and continuous improvement
Conduct regular risk assessments and reviews ensuring compliance with medical device regulations and standards

What we offer

Support for parents
Continuing education/professional development
Employee health & well-being benefits
Paid time off
2 days a year to volunteer
Medical and dental coverage that starts on day one
Basic life, accident, short-term and long-term disability, and business travel accident insurance
Employee Stock Purchase Plan (ESPP)
401(k) Retirement Savings Plan (RSP) with company matching
Flexible Spending Accounts

Fulltime

Principal Supplier Quality Engineer

This position provides technical leadership for Supplier Quality Management proc...

Location

United States

Salary:

Not provided

Avanos

Expiration Date

Until further notice

Requirements

Personnel performing work affecting product quality shall be competent based on appropriate education, training, skills and experience.
B.S. in Engineering, Science, Business, or another relevant field
Minimum of 10 years of collective experience in a Research, Manufacturing, Quality and/or Regulatory Affairs function within a medical device, pharmaceutical, biologic, or other highly regulated industry.
Supplier Quality Engineering experience in the Medical Device industry
Strong understanding of Risk Management principles and techniques.
Knowledge of Statistical Techniques
Experience in root cause analysis and failure investigation tools
Working knowledge of the MDSAP Single Audit program including the regulations for US, Japan, Canada, Australia, and Brazil
Working knowledge of the key medical device compliance related standards such as ISO 13485, ISO 14971, ISO 19011, ISO 10993, etc.
Certification as CQA, CBA, MDA, or ISO 13485 Lead Auditor

Job Responsibility

Ensure conformance to industry practices, domestic and international regulatory requirements and established company procedures.
Provide global technical leadership in the development and implementation of quality and regulatory compliance strategies and best practices to ensure the manufacturing and distribution of products comply with applicable regulatory requirements.
Lead cross-functional collaboration with Procurement, R&D/Operations, Technical Quality, and Logistics teams to address quality issues at contract manufacturers and suppliers.
Establish and administer the supplier audit program for quality/regulatory compliance.
Maintain the Approved Supplier List (ASL).
Support the Global Supplier Review Board, including providing metrics for supplier assessments.
Actively engage with suppliers in the event of a supplier issue requiring corrective action or upcoming external audits.
Provide guidance as needed for corrective action required because of assessment findings.
Execute supplier audits in accordance with approved schedules.
Support documentation of supplier changes through the supplier notification, change management, QNC, or CAPA processes.

What we offer

comprehensive and competitive range of benefits
Total Rewards package
pay
health care benefits
retirement plans
work/life benefits
generous 401(k) employer match of 100% of each pretax dollar you contribute on the first 4% and 50% of the next 2% of pay contributed with immediate vesting
benefits on day 1
free onsite gym
onsite cafeteria

Principal Electrical Engineer

We are seeking a highly experienced and technically driven Principal Electrical ...

Location

United States , Plymouth

Salary:

Not provided

Blackrock Neurotech

Expiration Date

Until further notice

Requirements

B.S. in Electrical Engineering, Biomedical Engineering, or related field
10+ years of experience in electrical design for active implantable medical devices (AIMDs), such as neurostimulators, pacemakers, or cochlear implants
Proven track record designing low-noise analog front ends, stimulation circuits, power management, and wireless telemetry (RF and inductive coupling)
Deep knowledge of implant power and safety considerations
Familiarity with closed-loop control systems and physiological signal acquisition
Experience operating within a quality system supporting Class III systems
Proficient in analog/digital mixed-signal design tools (e.g., SPICE, Altium, Cadence)
Strong understanding of embedded systems interfaces (SPI, I²C, UART)
Experience with simulation, modeling, and reliability analysis (Monte Carlo, tolerance analysis)
Knowledge of relevant standards: ISO 14708, IEC 60601, ISO 14971, ISO 13485, FDA Class III design controls

Job Responsibility

Develop circuit-level designs for ultra-low-power analog front ends, stimulation drivers, power management, and telemetry interfaces
Define and maintain electrical requirements, design specifications, and interface documents
Lead the design of production test equipment and processes
Perform schematic capture, circuit simulation, component selection, and PCB layout guidance for implantable and external system electronics
Collaborate with firmware and algorithm teams to enable closed-loop control of stimulation based on sensed physiological signals
Drive prototype development, bench testing, and design characterization for implantable hardware
Provide technical leadership to multidisciplinary design teams and mentor junior engineers
Champion design best practices, design for reliability (DfR), and design for manufacturability (DfM)
Driving verification and validation (V&V) activities, including unit, integration, and system-level testing to ensure reliability and traceability
Lead design verification testing (DVT) and verification planning to ensure compliance with medical device standards and safety requirements

Fulltime

Senior Principal Software Quality Engineer

As a Senior Principal Software Quality Engineer at Baxter, you will play a criti...

Location

United States , Raleigh

Salary:

120000.00 - 165000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

B.S. in Engineering or other technical degree required, preferably Computer Science/Engineering or Electronics/Electrical Engineering
Software Quality experience is highly sought, especially in the medical device industry
Knowledge of AAMI 62304 standard is valuable
Minimum 8 years of experience in medical device or other regulated technical industry (e.g., aerospace, automotive, defense) in a design/development/quality role or in a role closely connected to design/development/quality is required
Proven ability to perform and influence in cross-functional team environments and utilize effective interpersonal skills
2+ years of Quality experience desired
Product Design experience may be considered in lieu of Quality Assurance experience
Software development experience in a regulated industry is desirable
Knowledge of software development lifecycle processes and standards required
Understanding of software development tools and methods for medical devices and/or other regulated industries desirable

Job Responsibility

Responsible for all Design Assurance functions as a core team member on new product development (NPD) teams, ensuring the team complies with all portions of Design Control and related Quality System elements
Prepare and manage all Design Assurance required deliverables as well as support the remainder of the team in developing a quality product that meets regulatory requirements
Responsible for ensuring product development activities related to verification and validation are fully compliant to the quality system procedures
Assist in identification and mitigation of product or process-related risks

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Health & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer
Medical and dental coverage that start on day one
Insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
Employee Stock Purchase Plan (ESPP)
401(k) Retirement Savings Plan (RSP)
Flexible Spending Accounts

Fulltime

Device Engineer

Arrow Electronics

Location:
United States of America , Cedar Rapids

Category:
IT - Software Development

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
March 21, 2026

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Arrow Electronics

Location:United States of America , Cedar Rapids

Category:IT - Software Development

Contract Type:Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:March 21, 2026

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