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<h3>Job Description</h3>
Job Description
Our client, a world leader in diagnostics and life sciences, is looking for a "Systems Engineer” based out of Tucson, AZ. 
 
Job Duration: Long term Contract (Possibility Of Further Extension) 
Pay Rate: $39/hr on W2 
 
Company Benefits: Medical, Dental, Vision, Paid Sick leave, 401K 
 
As a member of our R&amp;D team, the Systems Engineer will drive requirements definition, risk management, and verification &amp; validation practices in projects, including defining requirements, designing system architectures, and implementing solutions to meet IVD standards. This individual will take ownership of project deliverables and facilitate the decision-making process with well-considered tradeoffs. 
 
Key Responsibilities 
<ul>
<li>Apply broad knowledge and skill-sets from Systems Engineering, focusing on the requirements engineering, risk management, and verification &amp; validation stages of the system lifecycle.Industry and Technology Analysis: Research and analyze industry trends, emerging technologies, and competitive products to identify opportunities for software differentiation and creative solutions. </li>
<li>Execute project deliverables specific to software requirements, risk analysis, configuration management, defect management, and verification and validation in the company-specific tool. </li>
</ul>
 
Qualifications: 
<ul>
<li>Bachelor's degree in Engineering, Biomedical Sciences, or related technical field with 4 years of experience (or a Master’s degree with 2 years of experience, or a PhD). </li>
<li>Demonstrated knowledge of systems engineering principles, specifically in requirements engineering, tradeoff analysis, risk management, configuration management, and verification and validation. </li>
<li>Experience working in a regulated environment, with familiarity with FDA, ISO, and other relevant regulatory standards for diagnostics products, especially regarding requirements, risk, and validation. Demonstrated interest in innovative technologies and understanding of the competitive landscape in IVD, with an eye for potential risks, critical requirements, and robust validation approaches. </li>
</ul>
 
Preferred Skills: 
<ul>
<li>Deep knowledge in requirements elicitation, risk analysis methodologies (e.g., FMEA), usability engineering, and V&amp;V test strategy development. </li>
<li>Assay Development: Familiarity with the assay development process and its associated requirements, risks, and validation needs. </li>
<li>Technical Tools: Prior experience in RETINA (Requirements &amp; Test Integration Application) and with LucidSpark/LucidChart. </li>
<li>Advanced Knowledge: Advanced understanding of software engineering, electronics, electro-mechanical systems, information technology, and basic chemistry, to better define requirements, assess risks, and plan validation across system components. </li>
</ul>
 
If interested, please send us your updated resume at 
<a href="mailto:hr@dawarconsulting.com" target="_blank">hr@dawarconsulting.com</a>/<a href="mailto:akansha@dawarconsulting.com" target="_blank">akansha@dawarconsulting.com</a>

Systems Engineer

<h3>Job Description</h3>
Job Description
Are you an innovative Field Service Engineer with a passion for cutting-edge technology? Join Sightpath Medical, the premier provider of mobile cataract and LASIK services in the U.S. You’ll have the unique opportunity to work with advanced ophthalmic equipment while supporting top surgeons in a fast-paced and rewarding environment. Whether you’re an entry-level candidate or bring years of experience, we offer knowledge, collaboration, and a shared commitment to excellence.
 
Why Sightpath Medical?
<ul>
<li>Comprehensive Training: Gain hands-on experience with the latest in ophthalmic laser technology. We provide all the training you need to excel in the field.</li>
<li>Independent Work Environment: You’ll have the autonomy to manage your work effectively while being part of an expert team.</li>
<li>Travel: You will have ownership of an assigned territory you will manage with a company provided vehicle and equipment. Every day is different. You will move from facility to facility providing expert service to our customers.</li>
<li>Work-life balance: With 8-10 case days per month, enjoy flexibility on non-case days when working from home or while traveling.</li>
<li>Medical benefits including health, dental, vision, short/long-term disability, and health savings account.</li>
<li>401(k) plan with employer contribution.</li>
<li>Health and Wellness Program to support your well-being.</li>
</ul>
 
What You’ll Do:
<ul>
<li>Technical Expertise: Install, de-install, calibrate, and operate transportable lasers and related equipment at customer sites.</li>
<li>Surgical Support: Ensure all equipment is programmed and calibrated to surgeon specifications prior to surgeries. You will also support the Surgeons during surgery to ensure customer satisfaction.</li>
<li>Preventative Maintenance: Perform routine maintenance and repairs to maximize equipment performance and minimize downtime.</li>
<li>Troubleshooting: Diagnose and resolve equipment issues efficiently, ensuring seamless surgical procedures.</li>
<li>Sterile Technique and Clinical: Adhere to sterile techniques during surgeries to ensure patient safety. Comprehensive training will be provided for all clinical aspects and requirements.</li>
<li>Manual Labor: Willing and able to assist with equipment setup and transport.</li>
<li>Other Duties: Flexibility to take on additional responsibilities as required.</li>
</ul>
 
Who We’re Looking For:
<ul>
<li>Technical Degree: Degree in Laser Electro-optics, Biomedical Equipment Technology, Electronics, or a similar field; military training in related fields is also acceptable.</li>
<li>Hands-On Experience: Proficiency with basic electronics and test equipment. Experience with laser systems is a plus.</li>
<li>Adaptable and Travel-Ready: Comfortable with driving to various locations in assigned territory and staying overnight when needed. All travel expenses are covered (hotel stays, gas for company vehicle, and meal allowances while traveling).</li>
<li>Driving Record: Able to produce a valid driver's license and pass a Motor Vehicle Report (MVR)/ driving record.</li>
<li>Excellent Communicator: Able to build strong relationships quickly with surgeons and their teams.</li>
<li>Self-assured: Able to thrive in high-pressure environments with confidence and professionalism.</li>
<li>Organized and Detail-Oriented: Skilled at managing equipment and completing administrative tasks required to support assigned territory.</li>
<li>Physical Demands: Ability to lift up to 100 lbs. and stand for extended periods.</li>
</ul>
 
Relocation Assistance:
We offer relocation allowances for qualified candidates who may need to move to join our team.&nbsp;
 
Compensation Range:
<ul>
<li>$65,000 - $80,000 annually with bonus eligibility</li>
<li>Company credit card provided for company use including: hotel stays, gas for company vehicle, maintenance for vehicle, meal allowance (when an overnight stay is required for coverage purposes), etc.</li>
</ul>
SIGHTPATH is an equal opportunity employer. In accordance with applicable law, we prohibit discrimination based on race, color, religion, creed, gender, pregnancy or related medical conditions, age (40 and over), national origin or ancestry, physical or mental disability, genetic information or any other consideration protected by federal, state or local laws. Our commitment to equal opportunity employment applies to all persons involved in our operations and prohibits unlawful discrimination by any employee, including supervisors and coworkers.
 
PM25
 
Compensation details: 60000-75000 Yearly Salary
 
PI6e4e3125bf84-25405-38196172

Laser Engineer III

<h3>Job Description</h3>
Job Description
ABOUT ORGANOX:
OrganOx is an innovative, fast-paced, global medical device company with a mission to save lives by making every donated organ count. We are a commercial stage organ technology company, spun out of the University of Oxford in 2008, committed to improving transplantation outcomes throughout the world. The company’s first product, the OrganOx metra® normothermic machine perfusion (NMP) system for liver transplantation, has been used to support more than 5,000 liver transplant operations globally.
Position Summary
The Product Quality Engineering team at OrganOx is a technical quality engineering team responsible for monitoring, understanding, and improving product performance of the OrganOx Metra, a Class III medical device. The Product Quality Engineering team works closely with Product Sustaining Engineering and Contracted Suppliers to set in place quality control and management processes for externally built products and componentry, including sterilization and microbiology, supplier management, and contract manufacturing processes. 
The Product Quality Engineer will have strong hands-on technical skills with an ability to analyze product quality issues and work cross-functionally to solve problems related to product quality. 
The successful candidate is collaborative, has excellent communication and problem-solving skills, and is passionate about delivering world-class products that make healthcare more accessible, simpler, and safer. 
Listed below are the major responsibilities of the role and a brief description of some of the key tasks to be performed. This list is not totally exhaustive.
This is a flexible, on-site role in our Madison, NJ office.
Major Responsibilities 
Under direction from the Senior Product Quality Engineer and Senior Manager, Product Quality Engineering, the Product Quality Engineer may be responsible for the following: 
<ul>
<li>Lead root-cause investigations in response to customer complaints </li>
<li>Support hands-on analyses of returned products to identify root causes of failures</li>
</ul>
· Support development of investigation criteria and test methods to properly diagnose and root cause field failures 
<ul>
<li>Analyze and trend on product performance data to provide recommendations for product improvements </li>
<li>Raise Supplier Corrective Action Reports (SCARs) in response to product performance trends. Support timely closure of SCARs. </li>
<li>Work cross-functionally with other engineering teams and contracted suppliers to implement changes in manufacturing and inspection procedures to mitigate field failures. </li>
<li>Maintain good working relationships with suppliers to support root cause investigation and failure mitigation efforts </li>
</ul>
· Support CAPAs, Escalations, and engineering investigations in response to field quality issues. 
<ul>
<li>Participate in the development and review of engineering change orders that impact product quality activities </li>
<li>Perform DHR, Service History record, and PFMEA reviews in support of complaint investigations.</li>
<li>Adhere to the letter and spirit of OrganOx’s Code of Conduct and all other company policies.</li>
</ul>
Requirements
Skills and Experience
<ul>
<li>Experience investigating and resolving SCARS and CAPAs </li>
<li>Strong experience with statistical analysis of data; Experience with Minitab preferred </li>
<li>Experience with Six Sigma principles preferred</li>
<li>Excellent oral and written communication skills with the ability to communicate with audiences of varying technical skills</li>
<li>A strong ability to prepare written technical plans and reports in support of engineering changes, product or process validations, and failure investigations</li>
<li>Strong focus on meeting customer needs</li>
<li> Proven ability to work cross functional and within global teams, fostering a culture of high collaboration</li>
<li>Ability to be self-driven and solve complex problems independently. Committed to upholding OrganOx values in daily work and decision-making </li>
<li>Experience in driving a global quality mindset across teams and geographies</li>
<li>Demonstrated strong attention to detail and “do it right the first time” attitude</li>
</ul>
Qualifications 
<ul>
<li>Bachelor’s degree in an Engineering discipline (Electrical, Mechanical, Bio-Medical, etc.) or the equivalent work experience is required</li>
</ul>
· 1-4 years of related hands-on engineering experience in Medical Devices, Pharmaceuticals or other regulated industry is required
<ul>
<li>Excellent technical report writing skills are required</li>
<li>Strong Root Cause Analysis, Design of Experiments, and Test Method Development experience as related to complaint investigations is required</li>
<li>Strong experience with MS Office Products (Word, Excel, Visio, Project, PowerPoint, Outlook, etc.) is required</li>
<li>Prior experience performing complaint investigations preferred </li>
<li>A solid understanding of the FDA QSR Quality System Requirements, and the ability to apply the knowledge to comply with goals and objectives is highly preferred</li>
<li>Knowledge of electro-mechanical troubleshooting techniques is preferred</li>
<li>Familiarity with ISO14971 and associated Risk Management Processes is a plus</li>
<li>Six Sigma Green Belt or Black Belt Certification preferred </li>
<li>Ability to travel 10-20% (domestically and internationally)</li>
</ul>
#LI-Hybrid
A job description does not imply that the duties stated are the only ones to be performed by the job holder. Job holder will be required to follow any other job-related instruction as reasonably requested by their line manager or their designate. 
Benefits
The Pay Range for this position is $105,000 - $115,000 annually, with a 10% target annual bonus and benefits.
At OrganOx, We offer competitive compensation and comprehensive benefits available from day one, including health, dental, vision, disability coverage, and flexible spending accounts. Additionally, we offer a 401(k)-retirement plan with company matching after 90 days, paid time off, holidays, and additional leave benefits, as well as employee discounts and access to our onsite wellness facility. OrganOx supports work-life balance and provides opportunities for ongoing professional development.
We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender identity or expression, national origin, disability status, protected veteran status, genetic information, or any other characteristic protected by law.

Product Quality Engineer

<h3>Job Description</h3>
Job Description
Job Summary: The Quality Engineer will be responsible for assisting in the development, implementation, and maintenance of the quality system of the company including supporting all FDA and registrar inspections/audits. Candidates must be located within commuting distance to the Wilmington, MA or willing to relocate to be considered. Essential Duties and Responsibilities:
<ul>
<li>Contributes to design and process verification and validation activities including definition and qualification of test methods, acceptance criteria, and statistical principles. Assists in writing and reviewing protocols, reports, and operating procedures to support product and process development.</li>
<li>Supervises and performs risk management activities including creation and maintenance of risk management files by product and process as the key quality representative for those tasks.</li>
<li>Support design control new product introduction teams as the quality subject matter expert and provide review and approval of product Design History Files.</li>
<li>Act as the leader in bringing the culture of quality in medical device development.</li>
<li>Exercise independent judgment in evaluating complex processes, procedures and systems against written regulatory requirements and company procedures.</li>
<li>Collaborate with and guide cross-functional team members and stakeholders to ensure correct and efficient implementation of Design Controls and Quality System procedures.</li>
<li>Active participant in assigned Design and Phase Review meetings.</li>
<li>Drives improvements to the QMS including those resulting from quality events, audits, or regulatory changes to ensure compliance with FDA 21 CFR 820.</li>
<li>Assisting in the development of the company quality system to support medical device offerings and operations and ensure continual improvement in quality. This may include drafting and reviewing quality system documents as necessary, managing document change requests, and regularly reviewing procedures for appropriateness.</li>
<li>Assisting with quality system implementation including, but not limited to:
<ul>
<li>Maintaining and documenting supplier approvals and audits as needed.</li>
<li>Participating in internal audits and serving as subject matter expert during regulatory inspections and notified body audits.</li>
<li>Assisting with and documenting regular management reviews.</li>
<li>Drafting and executing IQs, OQs, and PQs, where applicable.</li>
<li>Initiating, investigating, and reviewing non-conformances as well as corrective and preventative actions, as assigned.</li>
<li>Assisting in product failure and root cause investigations.</li>
</ul>
</li>
<li>Generally assuring adherence to all company quality procedures</li>
<li>Other responsibilities as assigned.</li>
</ul>
 Qualifications:
<ul>
<li>Bachelor’s degree in mechanical engineering or biomedical engineering.</li>
<li>Six Sigma Certification – Green, Brown or Black belt preferred.</li>
<li>ASQ CQE preferred.</li>
</ul>
 Skills, Abilities, Competencies Required:
<ul>
<li>Excellent written and verbal communication skills.</li>
<li>Able to work accurately in a fast-paced, hectic, ever-changing environment with strong attention to detail.</li>
<li>Demonstrated ability to monitor own work to ensure quality, accuracy, and thoroughness.</li>
<li>Strong organizational, analytical, and time-management skills.</li>
<li>Able to self-motivate and work both independently and as part of a team.</li>
</ul>

Quality Engineer

<h3>Job Description</h3>
Job Description
About Nudge
At Nudge, our mission is to develop the best technology for interfacing with the brain to improve people's lives. We're starting with an approach that we believe can help the most people the fastest, and also allow us to learn as much about the brain as possible: developing a non-invasive, ultrasound-based device that can stimulate and image the brain at high resolution and depth. This is a vertically integrated effort building cutting-edge hardware, software, and research capabilities to create products that can benefit millions — and eventually billions — of people.
We’ve brought together a team of the best, who believe hard things are worth doing. To succeed, we need to assemble world-class teams across everything we do. We hire people who are exceptional at their craft, do the real work, and execute relentlessly — people who expect the highest levels of both rigor and integrity from each other.
About the role
As an ultrasound engineer at Nudge, you will:
<ul>
<li>
Improve acoustic models of transducer arrays and subject-specific acoustic properties with feedback from benchtop and clinical testing
</li>
<li>
Evaluate the devices for both safety and performance considerations
</li>
<li>
Inform the design of next-generation devices through modeling and prototype testing
</li>
<li>
Develop software and algorithms for signal processing, beamforming, holography, and imaging
</li>
</ul>
About you
We are looking for engineers of all levels, but regardless of your career level, you should have:
<ul>
<li>
Strong engineering / physics first principles
</li>
<li>
Experience with ultrasound metrology
</li>
<li>
Experience with acoustic modeling software
</li>
<li>
Strong understanding of biomedical applications of ultrasound
</li>
<li>
PhD in a relevant engineering discipline
</li>
<li>
Demonstrated history of exceptional technical contribution
</li>
</ul>

Ultrasound Engineer

<h3>Job Description</h3>
Job DescriptionAbout GenScriptGenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy.GenScript is committed to striving towards its vision of being the most reliable biotech company in the world to make humans and nature healthier through biotechnology.About ProBioProBio proactively provides end-to-end CDMO service from drug discovery to commercialization with proactive strategies, professional solutions and efficient processes in cell and gene therapy, vaccine, biologics discovery and antibody protein drug to accelerate drug development for customers. ProBio's total cell and gene therapy solution covers CMC of plasmid and virus for IND filing as well as clinical manufacturing and commercial manufacturing.
Job Scope:
Every day, Genscript's Field Service Engineer helps our customers to tackle issues that enable scientists to make research easy. Through our work, we deliver insights and provide support that keep labs running smoothly and more efficiently. Join our team to be a part of this exciting work!
As a Field Service Engineer for Genscript, you will work at a variety of labs, so having an appetite for continuously learning about instruments and troubleshooting is key. The ability to help with solving customer problems and a dedication to deliver the customer service is how you will build customer success.
Please note that this role is based onsite in Piscataway, NJ when not traveling for customer visits. 
Responsibilities:
You will be responsible for supporting our customers with on-site installation, implementation, maintenance and repair of multiple solutions. Our products include hardware, software, and consumables.
<ul>
<li>Installs and optimizes hardware/software products at customer sites.</li>
<li>Respond to internal and external customer needs by providing testing, repair, installation, upgrade, and preventive maintenance activity on service experience with automation and liquid handling.</li>
<li>These devices contain a large amount of electro-mechanical, pneumatic, systems as well as computer hardware and software.</li>
<li>Diagnoses and resolves product performance problems.</li>
<li>Contact customers in a timely manner and schedules service efficiently Performs maintenance and repairs.</li>
<li>Ensures customer happiness by advising customers on preventive maintenance and configurations, which may impact product performance.</li>
<li>Connect with manager and sales team to ensure customer needs and expectations are clearly understood and met.</li>
<li>Provide promptly feedback to the manufacturing and R&amp;D team concerning performance anomalies encountered as required.</li>
<li>Proactively responds to potential equipment issues to prevent unplanned interruption of customers' business.</li>
<li>Responsive to customer requests for service and communicate proactively before, during and after service.</li>
<li>Document time and expenses in a timely manner as required as requested by manager.</li>
<li>Serves as an internal resource on technical issues and manages product customer concerns. Collaborates with teams such as Support, Sales, Marketing and R&amp;D to provide solutions to customers.</li>
</ul>
Qualifications:
<ul>
<li>Bachelor's or master's degree within the science field - e.g., mechanical or electrical is a plus.</li>
<li>2+ years of experience in a similar position. Hands on and troubleshooting experience.</li>
<li>Must have experience working with Automation and liquid handling.</li>
<li>Previous instrumentation maintenance, wire diagram, electromechanical, preventative maintenance, biomedical equipment or laboratory repair instrument repair experience is a plus.</li>
<li>Experience with the Genscript product is desired but not crucial.</li>
<li>Verbal and written communication is clear, respectful, and timely.</li>
<li>Travel: 50% travel per week in the field visiting customers</li>
<li>Able to work independently</li>
<li>Able to lift 40 lbs.</li>
</ul>
#LI-EB1
#GS
GenScript USA Inc/ProBio Inc. is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is the Company's policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law.
GenScript USA Inc./ProBio Inc. maintains a drug-free workplace.
Please note: Genscript USA Inc./ProBio Inc. will only contact candidates through verified application sources. GenScript/Probio does not request personal information from candidates through individual email or any other platform.

Field Service Engineer, CPBU

<h3>Job Description</h3>
Job Description
Signal Processing Engineer
About CoVar
CoVar is a small AI/ML R&amp;D software company in Durham, NC, that uses artificial intelligence to solve problems that matter. We develop AI/ML tools to help the DoD detect enemies and threats, help biomedical researchers find new cures for diseases, and help monitor machinery to prevent injuries and environmental catastrophes. We are passionate engineers, dedicated to pushing the bounds of what AI/ML can do in the real world.
About this position
You will help CoVar develop signal processing algorithms and software to solve real-world customer problems. You will develop novel and advanced algorithms for sense making and sensor decision making for applications in the RF domain to include detection, localization, classification, tracking and EW. You will design and implement simulations for these RF applications as well as evaluate results on real world data. You will have the opportunity to present your work to high-level customers in the DoD and in the industry. The position includes opportunities to publish novel work in both classified and unclassified settings.
Key Responsibilities
<ul>
<li>Algorithm Development: Design, implement, and optimize signal and array processing algorithms for RF applications, detection, localization, tracking, channel estimation, beamforming, and spectral analysis.</li>
<li>Data Analysis: Process and interpret RF datasets for signal detection, classification, tracking, parameter estimation, and pattern recognition.</li>
<li>Prototyping &amp; Testing: Develop simulation models (e.g., Python, MATLAB) and implement algorithms on real-time platforms such as FPGAs, GPUs, or SDRs (Software-Defined Radios).</li>
<li>RF System Integration: Collaborate with hardware engineers to integrate digital signal processing (DSP) algorithms into RF systems and ensure optimal end-to-end performance.</li>
<li>Performance Evaluation: Conduct laboratory and field testing to validate system performance under various operational conditions.</li>
<li>Research &amp; Innovation: Stay up to date with emerging RF technologies, advanced signal processing techniques, and industry best practices.</li>
<li>Documentation: Prepare technical reports and presentations for internal and external stakeholders. </li>
</ul>
Minimum qualifications
<ul>
<li>B.S., M.S., or Ph.D in Electrical Engineering, Computer Engineering, Applied Physics, Applied Mathematics, or a related field.</li>
<li>3+ years of experience in RF signal processing or a related discipline.</li>
<li>Strong proficiency in one or more of the following programming languages: Python, C/C++, or MATLAB.</li>
<li>Experience in the following areas:
<ul>
<li>RF signal processing, electronic warfare, optimization, array processing, machine learning, adaptive signal processing, AI/ML algorithm development, radar modeling, RF propagation</li>
</ul>
</li>
<li>Ability to work with cross-functional engineering teams and clearly communicate complex technical concepts.</li>
<li>Ability to work in Durham, NC (relocation assistance available)</li>
<li>Eligibility for US security clearance </li>
</ul>
Preferred qualifications
<ul>
<li>Experience with:
<ul>
<li>Radar signal processing in Department of Defense (DoD) specific applications including electronic warfare (EW) techniques such as electronic support measures, attack, protection, and cognitive EW.</li>
<li>AI/ML algorithm design in the areas of computer vision, reinforcement learning (RL), and natural language processing.</li>
<li>Spectrum monitoring and signal classification using machine learning techniques.</li>
<li>Translating the mission needs of DoD customers into an end-to-end technical solution.</li>
<li>Proposal development and proposal writing.</li>
</ul>
</li>
<li>Familiarity with FPGA or GPU acceleration for high-performance DSP.</li>
<li>Proficiency in C/C++ for embedded or real-time applications.</li>
<li>Active U.S. security clearance. </li>
</ul>
Benefits
<ul>
<li>Competitive salary, cash bonus, equity structure, and 401k with employer contributions</li>
<li>Excellent health care coverage, including dental and vision plans</li>
<li>Flexible work schedule</li>
<li>Tuition support</li>
</ul>
Visit us: <a href="http://www.covar.com" target="_blank">www.covar.com</a>

Signal Processing Engineer

<h3>Job Description</h3>
Job Description
Company Overview: Second Order Effects (SOE) is an engineering consulting firm that transforms uncertainty into fully functional hardware and software. We work on projects at all stages of development; we perform analysis, build prototypes, and take products to market. Our team solves high-impact problems across numerous industries, including automotive, aerospace, consumer electronics, industrial automation, biomedical, and green energy. Our designs control rocket engines, manage satellite communications, instrument fusion reactors, and are enjoyed by consumers around the world. The only thing we won't build is weapons.
Founded in 2016, Second Order Effects has 50+ employees (and counting!) in offices in El Segundo, California and Redmond, Washington. We've worked with &gt;130 clients on &gt; 300 projects as a partner, on retainer, or on demand.
How do we do this? We empower others, build the right thing, lead with curiosity, and own the outcome. Learn more at soeffects.com!
Job Overview: As a Lead Electrical Engineer, you'll help shape the design, architecture, and implementation of cutting-edge electrical systems across a diverse range of projects. Joining a growing organization, you'll have the opportunity to guide small teams, drive quality in electrical engineering deliverables, and ensure alignment between design decisions and project goals. This position is ideal for engineers ready to take on more leadership responsibility, mentor others, and contribute to process improvement—while still staying hands-on with hardware. What You Will Do: 
<ul>
<li>Provide technical leadership on project teams, aligning different disciplines towards shared solutions </li>
<li>Contribute to the design, architecture, prototyping, and validation of electrical systems </li>
<li>Mentor early-career engineers and interns by reviewing designs and providing feedback </li>
<li>Drive the project lifecycle from inception to customer success, ensuring alignment with customer needs</li>
<li>Support business development efforts by engaging in early-stage calls and reviewing cost and labor estimates</li>
</ul>
What You Will Need:
<ul>
<li>Bachelor's Degree in Electrical Engineering, Computer Engineering, Physics, Math, or a related field</li>
<li>3+ years of experience with end-to-end electronics design, including requirements generation, schematic design, board layout, design verification and acceptance testing</li>
<li>Experience leading small technical teams in the delivery of complex hardware design projects </li>
<li>Strong problem-solving skills and initiative to overcome technical and non-technical challenges</li>
<li>Strong communication skills to explain complex technical concepts to both technical and non-technical stakeholders</li>
<li>Expertise in mixed-signal design, power electronics, digital design, or electrical systems integration</li>
</ul>
What Would Be Useful:
<ul>
<li>Master's degree or graduate research experience in a relevant field</li>
<li>Experience in startup, tech, or consulting environments, managing multiple responsibilities simultaneously </li>
<li>Experience mentoring early-career engineers and/or engineering interns </li>
<li>Flexibility to pivot between projects and balance workload across teams </li>
<li>Passion for tackling diverse technical challenges across industries</li>
<li>Experience designing PCBs for high-reliability applications (e.g., aerospace, automotive, medical)</li>
</ul>
Benefits:
<ul>
<li>Compensation range of $129,480-$161,850 + equity incentive plan</li>
<li>Flexible work hours and work from home policy </li>
<li>100% employer-paid health insurance (Medical, Dental, Vision) for employees + 50% dependent coverage</li>
<li>Unlimited paid time off policy, 11x paid company holidays, 12x paid sick days</li>
<li>401(k) retirement account and employer matching (Safe Harbor 4%)</li>
<li>Generous paid parental leave</li>
<li>Relocation assistance available if 50+ miles away from the office</li>
<li>Electric Vehicle (EV) charging ports</li>
<li>Daily catered lunches, snacks, and accessible kitchen</li>
</ul>
Additional Requirements: 
<ul>
<li>Applicant must be willing to work 40 hours a week on-site in El Segundo, California, USA</li>
<li>Applicant must be eligible to work on export controlled projects</li>
<li>Job Type: Full-time (Salary)</li>
</ul>
Export Control Requirements:
<ul>
<li>To conform with U.S. Government export control regulations, including the Export Administration Regulations (EAR), you must be a U.S. citizen, lawful permanent resident of the U.S., protected individual as defined by 8 U.S.C. 1324b(a)(3), or eligible to obtain the required authorizations from the U.S. Department of State. Unfortunately, we are unable to provide sponsorship at this time.</li>
</ul>
If you don't meet 100% of the preferred skills and experience, we encourage you to still apply! Second Order Effects is proud to be an Equal Opportunity Employer; employment with SOE is governed on the basis of excellence and will not be influenced in any manner by race, color, religion, gender, national origin/ethnicity, veteran status, disability status, age, sexual orientation, gender identity, marital status, mental or physical disability, or any other legally protected status.

Lead Electrical Engineer

<h3>Job Description</h3>
Job Description
Company Overview: Second Order Effects (SOE) is an engineering consulting firm that transforms uncertainty into fully functional hardware and software. We work on projects at all stages of development; we perform analysis, build prototypes, and take products to market. Our team solves high-impact problems across numerous industries, including automotive, aerospace, consumer electronics, industrial automation, biomedical, and green energy. Our designs control rocket engines, manage satellite communications, instrument fusion reactors, and are enjoyed by consumers around the world. The only thing we won't build is weapons.
Founded in 2016, Second Order Effects has 50+ employees (and counting!) in offices in El Segundo, California and Redmond, Washington. We've worked with &gt;130 clients on &gt; 300 projects as a partner, on retainer, or on demand.
How do we do this? We empower others, build the right thing, lead with curiosity, and own the outcome. Learn more at soeffects.com!
Job Overview: We are seeking a creative Senior Systems Engineer to join our firm and take on the pivotal role of a high-fidelity translator. In this position, you will operate at the critical front-end of our product development lifecycle, bridging the gap between client vision and engineering execution. You will act as the technical lead across multiple projects and will transform clients' ambitious business objectives into creative, coherent architectures and concrete requirements. The ideal candidate is a T-shaped professional with deep expertise in electrical engineering, a passion for systems thinking, and who thrives on seeing their direct impact on mission-critical projects. What You Will Do: 
<ul>
<li>Act as the primary technical interface for customers from initial qualification through architectural design review, leveraging consultative problem-solving strategies to capture a client's true underlying needs</li>
<li>Translate high level client goals into high-level system architectures that balance technical, cost, and schedule constraints</li>
<li>Define clear, concise, and verifiable requirements that form the technical baseline for the engineering team. A key outcome is a successfully negotiated and agreed-upon scope that creates mutual value for both the client and the firm</li>
<li>Support the growth of early-career engineers by providing mentorship, cultivating systems thinking, helping them develop more robust problem-solving strategies, and fostering a collaborative, constructive feedback centered environment that raises the bar for quality and execution across the company</li>
<li>Tackle complex, early-stage challenges by identifying technical risks, developing mitigation strategies, and ensuring proposed engineering solutions are robust and buildable</li>
<li>Bridge client vision and internal engineering execution to ensure seamless handovers from the architectural concept into the detailed design and implementation phases</li>
</ul>
What You Will Need:
<ul>
<li>Bachelor's degree in Electrical Engineering, Physics, Mathematics, or a related field.</li>
<li>5+ years of experience in a systems engineering or hardware development role, preferably in the aerospace, medical, industrial, or consumer electronics industries.</li>
<li>Demonstrated ability to apply systems engineering principles and analyze complex problems to create and define system architectures, interfaces, and requirements for new, hardware-centric products.</li>
<li>Proven expertise to apply advanced concepts within a specific domain of electrical engineering (e.g., power electronics, analog/digital design, embedded systems, RF) and analyze their use in solving complex, real-world design challenges.</li>
<li>Demonstrated ability to apply written and verbal communication skills to technical communication</li>
</ul>
What Would Be Useful:
<ul>
<li>Exceptional client-facing communication skills, including experience facilitating technical workshops, leading requirements negotiations, and translating complex technical information for non-technical stakeholders</li>
</ul>
Benefits:
<ul>
<li>Compensation range of $151,100-$183,400 + equity incentive plan</li>
<li>Flexible work hours and work from home policy </li>
<li>100% employer-paid health insurance (Medical, Dental, Vision) for employees + 50% dependent coverage</li>
<li>Unlimited paid time off policy, 11x paid company holidays, 12x paid sick days</li>
<li>401(k) retirement account and employer matching (Safe Harbor 4%)</li>
<li>Generous paid parental leave</li>
<li>Relocation assistance available if 50+ miles away from the office</li>
<li>Electric Vehicle (EV) charging ports</li>
<li>Daily catered lunches, snacks, and accessible kitchen</li>
</ul>
Additional Requirements: 
<ul>
<li>Applicant must be willing to work 40 hours a week on-site in El Segundo, California, USA</li>
<li>Applicant must be eligible to work on export controlled projects</li>
<li>Job Type: Full-time (Salary)</li>
</ul>
Export Control Requirements:
<ul>
<li>To conform with U.S. Government export control regulations, including the Export Administration Regulations (EAR), you must be a U.S. citizen, lawful permanent resident of the U.S., protected individual as defined by 8 U.S.C. 1324b(a)(3), or eligible to obtain the required authorizations from the U.S. Department of State. Unfortunately, we are unable to provide sponsorship at this time.</li>
</ul>
If you don't meet 100% of the preferred skills and experience, we encourage you to still apply! Second Order Effects is proud to be an Equal Opportunity Employer; employment with SOE is governed on the basis of excellence and will not be influenced in any manner by race, color, religion, gender, national origin/ethnicity, veteran status, disability status, age, sexual orientation, gender identity, marital status, mental or physical disability, or any other legally protected status.

Senior Systems Engineer

<h3>Job Description</h3>
Job Description
About Ceribell
Ceribell is a medical technology company focused on transforming the diagnosis and management of patients with serious neurological conditions. The Ceribell System is a novel, point-of-care electroencephalography ("EEG") platform specifically designed to address the unmet needs of patients in the acute care setting, and is being used in hundreds of community hospitals, large academic facilities and major IDN's across the country. Our entire team is driven by a shared commitment to transforming the landscape of critical care through our rapid seizure detection technology, come join the movement!
Position Description
Ceribell is looking for a Senior Firmware Engineer / Senior Embedded Engineer who is passionate about biomedical applications and who has experience in the development of embedded or IoT products. The successful candidate will join the R&amp;D team and will play a key role in the development of the next generation of Ceribell's life saving technologies. Our firmware development stack is based around a STMicroelectronics STM32 ARM Cortex microcontroller and we use FreeRTOS, the IAR Embedded Workbench, and the TouchGFX framework. You must be able to work collaboratively as part of a cross-functional R&amp;D team, but you must also be able to take individual ownership for development, testing, and documentation of your projects.
What you'll achieve 
<ul>
<li>Develop and test firmware features for Ceribell's EEG systems</li>
<li>Understand user needs and translate them to the development of new and improved features</li>
<li>Contribute to GUI development using frameworks such as Qt, TouchGFX, LVGL, or custom OpenGL-based stacks</li>
<li>Participate in code reviews, peer reviews, and risk management activities</li>
<li>Create and revise technical documentation</li>
<li>Provide input on firmware and hardware architecture for new and existing products</li>
</ul>
What you'll need to be successful
<ul>
<li>Bachelor's Degree in electrical engineering, computer science, biomedical engineering or</li>
<li>related field. Graduate degree preferred</li>
<li>5+ years of experience in firmware development of a commercial product</li>
<li>Proficient in C/C++ and experienced with firmware development on ARM based systems</li>
<li>Hands-on experience developing GUIs for embedded devices using Qt, TouchGFX, LVGL, or other embedded graphics frameworks</li>
<li>Direct experience with development of WiFi connected / IoT devices preferred</li>
<li>Strong analytical skills, detail-oriented and collaborative</li>
</ul>
In addition to your base compensation, Ceribell offers the following:
<ul>
<li>Annual Bonus + Equity Opportunity</li>
<li>100% Employer paid Health Benefits for Employees</li>
<li>50% - 70% Employer paid Health, Dental &amp; Vision for dependents (depending on plan selection)</li>
<li>100% paid Life and Long-Term Disability Insurance </li>
<li>401(k) with a generous company match</li>
<li>Employee Stock Purchase Plan (ESPP) with a discount</li>
<li>Monthly cell phone stipend</li>
<li>Flexible paid time off</li>
<li>11 Paid Holidays + 5 Company Wellness Days</li>
<li>Excellent parental leave policy</li>
<li>Fantastic culture with tremendous career advancement opportunities</li>
<li>Joining a mission-minded organization!</li>
</ul>
Compensation Range$130,000—$165,000 USD

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