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<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 strong customer service is how you will build customer success.
Please note that this role is required to be based onsite in Piscataway, NJ when not traveling for customer visits. The estimated salary range depending on experience level is $80,000 - $100,000 base salary.
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, Catalog Products and Instruments

<h3>Job Description</h3>
Job Description
About Us: We are a dynamic and innovative medical device startup developing a point-of-care portable blood coagulation testing device. Our full-time team currently comprises a CEO/Biomedical Engineer and an Electrical Engineer.
Job Summary: We are seeking a talented and experienced Embedded Systems Engineer to join our team and lead the design and development of&nbsp;embedded computing systems, guiding our devices from prototypes to commercial readiness.&nbsp;The ideal candidate will have a Bachelor's or Master’s degree in Electrical Engineering, Computer Engineering, or a related field, with at least 5 years of experience (Ph.D. preferred). You will drive embedded hardware/software development for real-time systems, emphasizing proficiency in C, C++, and/or assembly language for hardware interfacing and optimization. Experience in hardware architectures, sensors, actuators, and communication protocols is crucial, alongside a knack for evaluating and selecting optimal components. Hands-on experience with embedded processors and display integration, as well as a strong grasp of design modification processes to enhance device durability, are also required. Proficiency in coding and optimizing for resource-constrained environments is a plus. As the first embedded engineer on our team, you will play a pivotal role in advancing our blood coagulation testing device from prototype to production. This role is critical to the success of our product and involves working on multiple federal grants and projects. You will be responsible for both hardware and software components, ensuring our device is efficient, reliable, and ready for market.
Startup Environment:&nbsp;Operating in a fast-paced startup, we value innovation, adaptability, and proactive mindsets. Ideal team members thrive under pressure, manage multiple projects, and adapt as company needs evolve. We are looking for individuals who are passionate about working in a startup setting and thrive in dynamic and challenging situations. We value individuals who are not just seeking a job but are driven by a genuine passion for creating impactful solutions and driving change in the medical device industry. If you are excited about the opportunity to make a meaningful impact and are ready to roll up your sleeves and tackle challenges head-on, we encourage you to apply.
Key Responsibilities:
<ol>
<li>Design &amp; build portable battery system for power supply.</li>
<li>Improve sample handling system design.</li>
<li>Implement an independent embedded processing system and streamlined user interface for straightforward operation.</li>
<li>Upgrade embedded processing system.</li>
<li>Develop efficient injection/fluid handling systems.</li>
<li>Identify and implement efficient computing by selecting and implementing embedded computers to run inside the medical device.</li>
<li>Ensure the embedded system replaces the laptop.</li>
<li>Integrate various hardware and software components together.</li>
<li>Enable battery operation of the device.</li>
<li>Design and develop sample handling systems and cartridges.</li>
<li>Lead end-to-end projects for multiple federal grants and develop innovative solutions.</li>
<li>Collaborate with other team members in taking device prototypes to market.</li>
<li>Participate in FDA-related activities and follow quality protocols.</li>
<li>Participate in grant writing or other fundraising activities as needed.</li>
<li>Perform other relevant tasks as needed for the company.</li>
</ol>
Minimum Qualifications:
<ul>
<li>Bachelors in Electrical Engineering, Computer Engineering, or a related field and minimum 5 years of experience.</li>
<li>Proven experience in embedded systems engineering, preferably in the medical device industry.</li>
<li>Knowledge of sensors and commercial medical devices.</li>
<li>Proficiency in C, C++, and/or assembly language for embedded software development.</li>
<li>Experience with battery systems, fluid handling systems, and embedded processing systems.</li>
<li>Familiarity with CAD design, particularly using software like SolidWorks.</li>
<li>Understanding of calibration techniques.</li>
<li>Familiarity with injection molding and 3D printing for rapid prototyping.</li>
<li>Ability to design devices for manufacturing at scale.</li>
<li>Knowledge of cybersecurity as it relates to medical devices.</li>
<li>Familiarity with rheology/acoustics topics is a plus.</li>
<li>Strong problem-solving and analytical skills.</li>
<li>Ability to learn new concepts proactively and break down work effectively.</li>
<li>Familiarity with Agile methodologies and efficient project management.</li>
<li>Demonstrated accountability, effective planning, and team leadership.</li>
<li>Innovative thinker with a track record of generating new ideas.</li>
<li>Strong written and verbal communication skills.</li>
</ul>
Preferred Qualifications:
<ul>
<li>Masters or Ph.D. in Electrical Engineering, Computer Engineering, or a related field.</li>
<li>Experience selecting and implementing embedded processors and displays.</li>
<li>Prior startup or medical device development experience</li>
<li>Experience in medical device regulatory compliance (FDA).</li>
</ul>
What We Offer:
<ul>
<li>Competitive salary</li>
<li>Health, dental, and vision insurance coverage</li>
<li>Generous paid time off</li>
<li>Professional development opportunities</li>
<li>Potential to receive stock options</li>
<li>Opportunities for growth within the company</li>
<li>Flexible work arrangements, including remote work options</li>
<li>Dynamic and innovative startup environment</li>
<li>Opportunity to make a meaningful impact in the medical device industry</li>
</ul>
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Embedded Systems Engineer for Medical Device Startup

<h3>Job Description</h3>
Job DescriptionField Support Engineer, Pharmacy Automation Compensation: Salary + Bonus + Company Car
We're looking for a dedicated Field Support Engineer to join our team. In this role, you'll be the face of our company, providing world-class technical and customer support for our advanced pharmacy automation products. You'll travel regionally to service and maintain equipment in various pharmacy environments, ensuring our clients receive exceptional service and their systems run flawlessly. ????
Key Responsibilities
As a Field Support Engineer, you'll be responsible for a wide range of tasks, including:
<ul>
<li>Providing outstanding customer service by addressing inquiries and resolving issues in a professional, collaborative, and supportive manner.</li>
<li>Maintaining pharmacy automation equipment and performing preemptive maintenance to maximize uptime and ensure customer satisfaction.</li>
<li>Responding to service requests within specified SLA requirements for break/fix situations.</li>
<li>Working with regional and national service teams to diagnose and solve complex technical problems.</li>
<li>Assisting the Product Implementation Team with the installation of new automation systems.</li>
<li>Training customers on the operation and daily maintenance of our products.</li>
<li>Documenting all issues and resolution actions in Salesforce Field Service Lightning.</li>
<li>Providing valuable feedback to our management and engineering teams to help drive product improvements and efficiency.</li>
<li>Managing and organizing company-supplied tools and inventory.</li>
<li>Handling occasional weekend, holiday, and overtime coverage, as well as periodic overnight stays and travel outside the local region.</li>
<li>Maintaining a professional appearance and attitude while working independently with minimal supervision.</li>
</ul>
Work Environment and Physical Demands
This role requires a high level of physical activity and adaptability to different environments. You should be able to:
<ul>
<li>Work in both indoor and outdoor environments common to pharmacy settings.</li>
<li>Perform long-term standing and frequent walking.</li>
<li>Lift, carry, push, and pull up to 50 pounds frequently and up to 100 pounds occasionally.</li>
<li>Stand for up to 10-12 hours a day on occasion.</li>
<li>See, smell, hear, talk, climb ladders and step stools, balance, stoop, kneel, twist, crouch, crawl, reach, and grasp.</li>
<li>Drive a car for an average of four hours per day, with some shorter and longer drive times expected. Occasional air travel may also be required.</li>
</ul>
Reasonable accommodations will be made for individuals with disabilities to perform these essential job functions.
Requirements
Required Skills and Experience
<ul>
<li>Education/Experience: An Associate's degree in Electronics Engineering, Electronics Engineering Technology, Mechanical Engineering Technology, Robotics Engineering, or Biomedical Engineering Technology is preferred. Alternatively, you should have 3-5 years of experience in a field service role, or an equivalent combination of education and relevant experience servicing complex medical or business equipment.</li>
<li>Technical Knowledge:</li>
<ul>
<li>Proficient in Microsoft Operating Systems (including Windows 2000, XP, 7, 10, and 11) and Microsoft Office.</li>
<li>Extensive knowledge of basic computer networking, including the use of Windows tools to identify network and PC information, as well as the setup and use of routers and switches.</li>
<li>Familiarity with locating and editing configuration and XML files within a file structure.</li>
<li>Knowledge of ghosting and re-imaging processes.</li>
<li>SQL knowledge is a plus.</li>
<li>Strong mechanical aptitude with the ability to use standard hand tools for complex disassembly and reassembly.</li>
<li>Proficiency with digital multi-meters and voltage/amperage testers.</li>
</ul>
<li>Other Skills:</li>
<ul>
<li>Highly motivated to deliver superior customer care.</li>
<li>Willingness to extend beyond the typical workday when the situation requires it.</li>
<li>Strong organizational skills for managing tools and inventory.</li>
<li>Timely reporting of expenses through Concur.</li>
</ul>
</ul>
Benefits
Benefits
We provide the tools you need to succeed, including:
<ul>
<li>A fleet vehicle.</li>
<li>A corporate credit card for travel and expenses.</li>
<li>A company-issued laptop and phone.</li>
<li>A complete toolkit with standard and specialty tools.</li>
<li>A comprehensive suite of benefits.</li>
</ul>

Field Support Engineer, Pharmacy Automation

<h3>Job Description</h3>
Job DescriptionAbout Us Optopax is a Silicon Valley–based design and OEM manufacturing company delivering integrated AI imaging solutions—from concept through prototyping to production. We specialize in AI‑enabled camera modules, high‑precision optics across UV to LWIR, and custom embedded systems powering robotics, industrial vision, submersible imaging, biomedical devices, AR/VR optics, medical and optical computing. Join our small, global team headquartered in San Jose, CA on a mission to engineer and manufacture camera solutions that transform how machines see, through custom optics, sensor integration, and embedded imaging platforms. About the Role As a Senior or Manager‑level Optical Design Engineer (depending on experience), you’ll lead the development of advanced optical systems—taking ideas from simulation through validation and integration into Optopax’s end‑to‑end imaging platforms. You’ll drive innovation and help strengthen our capabilities in photonics, AI cameras, and embedded vision. We are open to remote candidates within the US with a preference for Bay Area candidates to work on-site alongside the Executive Management team in San Jose, CA.&nbsp; What You’ll Do
<ul>
<li>Lead design, simulation, tolerancing, and optimization of complex optical systems using tools such as Ansys Optics Studio (Zemax), Code V, LightTools, Lumerical, Quadoa, or equivalent.</li>
<li>Perform stray‑light, ray‑trace, wavefront, photon budget, and design for manufacturability (DFM) analyses (e.g., Monte‑Carlo tolerancing).</li>
<li>Translate customer specifications into detailed design requirements; collaborate across mechanical, electrical, firmware/software, and manufacturing teams for system integration and prototyping.</li>
<li>Guide validation of designs via lab testing, metrology, and performance measurement (e.g., MTF, distortion, SNR, wavefront).</li>
<li>Mentor and support junior optical engineers and cross‑functional partners, establishing design best practices and documentation.</li>
<li>Drive innovation through research into new optical technologies, materials, coatings, and manufacturing techniques, informing future product strategies.</li>
<li>Drive critical technical communications / negotiations with&nbsp; customers to ensure optical solutions align with performance, cost, and manufacturability goals.</li>
</ul>
What You’ll Bring Required
<ul>
<li>Master’s or PhD in Optical Engineering, Physics, or a related field.</li>
<li>Minimum 5+ years experience in optical design and engineering—ideally handling advanced, multi‑element systems.</li>
<li>High proficiency with optical design and simulation tools (e.g., Zemax, Code V and others).</li>
<li>Strong fundamentals in geometrical and physical optics design methodology, optical fabrication techniques, DFM, tolerancing, and metrology.</li>
<li>Experience in design documentation and cross-functional collaboration.</li>
</ul>
Preferred
<ul>
<li>Background in imaging systems for robotics, embedded cameras, LWIR, biomedical, AR/VR, sensors, or AI vision modules (reflecting Optopax’s core markets).</li>
<li>Exposure to prototyping processes including wafer‑level optics, active alignment, cleanroom assembly, or rapid prototyping workflows.</li>
<li>Familiarity with optical test stations or imaging qualification methods (a pillar of Optopax’s product offerings).</li>
<li>Experience in team leadership or mentoring, and process improvement with a proven track record of success</li>
<li>Programming or scripting skill (MATLAB, Python) for automation of analyses or data processing.</li>
</ul>

Senior Engineer / Manager of Optical Design

<h3>Job Description</h3>
Job Description
About Us:&nbsp; We are a dynamic and innovative medical device startup developing a point-of-care portable blood coagulation testing device. Our full-time team currently comprises a CEO/Biomedical Engineer, and an Electrical Engineer.&nbsp;
Job Summary:&nbsp; We are seeking a talented and experienced Senior Software Engineer to join our team and lead the development and optimization of software workflows for our innovative acoustic tweezing technology-based medical devices. The ideal candidate will have a Master's degree in Computer Science, Software Engineering, or a related field, with a minimum of 5 years of experience. This role requires strong coding skills in Python and C/C++, proficiency in developing intuitive and visually engaging graphical user interfaces, and expertise in SQL for effective data management and database design. Experience with version control systems, particularly Git, is essential, along with the ability to understand and generate code from workflow diagrams. As the first and only software engineer on the team, you will play a pivotal role in shaping the software development efforts for our groundbreaking technology. This role is critical to the success of our product and involves working on multiple federal grants and projects.&nbsp;
Startup Environment:&nbsp; We operate in a fast-paced startup environment where innovation, adaptability, and a proactive mindset are key to success. We are looking for individuals who are passionate about working in a startup setting and thrive in dynamic and challenging situations. We value individuals who are not just seeking a job but are driven by a genuine passion for creating impactful solutions and driving change in the medical device industry. Our team members are expected to work well under pressure, juggle multiple projects, and be flexible in their roles as the needs of the company evolve. If you are excited about the opportunity to make a meaningful impact and are ready to roll up your sleeves and tackle challenges head-on, we encourage you to apply.&nbsp;
Key Responsibilities:&nbsp;
<ol>
<li>
Optimize and Enhance Existing Software:&nbsp;
</li>
</ol>
<ul>
<li>
Improve the efficiency of our existing software written in Python.&nbsp;
</li>
</ul>
<ul>
<li>
Increase processing speed for short-term operation on laptops.&nbsp;
</li>
</ul>
<ul>
<li>
Convert and optimize the software for embedded computing devices inside the medical device long-term.&nbsp;
</li>
</ul>
<ol>
<li>
Software Packaging and Security:&nbsp;
</li>
</ol>
<ul>
<li>
Secure the code to prevent reverse engineering.&nbsp;
</li>
</ul>
<ul>
<li>
Package the software into executable files for easy installation and deployment.&nbsp;
</li>
</ul>
<ol>
<li>
Connectivity and Data Management:&nbsp;
</li>
</ol>
<ul>
<li>
Ensure the software can connect to the internet.&nbsp;
</li>
</ul>
<ul>
<li>
Implement connectivity to an online database for long-term data management.&nbsp;
</li>
</ul>
<ul>
<li>
Incorporate Data Science, Machine Learning, and AI for handling large amounts of health data.&nbsp;
</li>
</ul>
<ol>
<li>
Health Data Security:&nbsp;
</li>
</ol>
<ul>
<li>
Ensure the highest level of security for software and health data management.&nbsp;
</li>
</ul>
<ol>
<li>
New Technique Development:&nbsp;
</li>
</ol>
<ul>
<li>
Convert and develop existing crude MATLAB codes and technology algorithms into efficient software for commercial use.&nbsp;
</li>
</ul>
<ul>
<li>
Create executable files with efficient large data handling capabilities.&nbsp;
</li>
</ul>
<ul>
<li>
Develop complex data processing software and manage large data analysis.&nbsp;
</li>
</ul>
<ul>
<li>
Develop a user-friendly interface for healthcare professionals.&nbsp;
</li>
</ul>
<ul>
<li>
Implement a remote kill switch for the software.&nbsp;
</li>
</ul>
<ul>
<li>
Apply all relevant requirements from existing software.&nbsp;
</li>
</ul>
<ol>
<li>
Parallel Processing and Language Conversion:&nbsp;
</li>
</ol>
<ul>
<li>
Implement efficient parallel processing techniques.&nbsp;
</li>
</ul>
<ul>
<li>
Convert existing Python code to C/C++ or another suitable low-level efficient language to run software optimally on embedded hardware.&nbsp;
</li>
</ul>
<ol>
<li>
Other Responsibilities:&nbsp;
</li>
</ol>
<ul>
<li>
Develop high-quality, efficient, and maintainable code.&nbsp;
</li>
</ul>
<ul>
<li>
Design intuitive and visually engaging user interfaces.&nbsp;
</li>
</ul>
<ul>
<li>
Proactively take on new responsibilities and suggest innovative ideas for product and company growth.&nbsp;
</li>
</ul>
<ul>
<li>
Participate in grant writing and fundraising activities.&nbsp;
</li>
</ul>
<ul>
<li>
Engage in FDA-related activities and adhere to quality protocols.&nbsp;
</li>
</ul>
<ul>
<li>
Perform other relevant software-related tasks as needed for the company.&nbsp;
</li>
</ul>
Minimum Qualifications:&nbsp;
<ul>
<li>
Master’s degree in Computer Science, Software Engineering, or a related field.&nbsp;
</li>
</ul>
<ul>
<li>
Minimum of 5 years of experience in software development.&nbsp;
</li>
</ul>
<ul>
<li>
Strong coding skills in Python, C, and C++ (JavaScript is a plus).&nbsp;
</li>
</ul>
<ul>
<li>
Proficiency in developing intuitive and visually engaging graphical user interfaces.&nbsp;
</li>
</ul>
<ul>
<li>
Proficiency in SQL for effective data management and database design.&nbsp;
</li>
</ul>
<ul>
<li>
Experience with version control systems, particularly Git.&nbsp;
</li>
</ul>
<ul>
<li>
Ability to understand and generate code from workflow diagrams.&nbsp;
</li>
</ul>
<ul>
<li>
Knowledge of integrating multiple devices and establishing centralized control.&nbsp;
</li>
</ul>
<ul>
<li>
Familiarity with IDEs, preferably PyCharm.&nbsp;
</li>
</ul>
<ul>
<li>
Excellent problem-solving skills and ability to work independently.&nbsp;
</li>
</ul>
<ul>
<li>
Strong written and verbal communication skills.&nbsp;
</li>
</ul>
Preferred Qualifications:&nbsp;
<ul>
<li>
Experience working in the medical device industry.&nbsp;
</li>
</ul>
<ul>
<li>
Familiarity with Agile development methodologies.&nbsp;
</li>
</ul>
<ul>
<li>
Knowledge of machine learning techniques and algorithms.&nbsp;
</li>
</ul>
<ul>
<li>
Experience with Docker and containerization technologies.&nbsp;
</li>
</ul>
<ul>
<li>
Familiarity with cloud platforms such as AWS or Azure.&nbsp;
</li>
</ul>
<ul>
<li>
Prior experience working in startups.&nbsp;
</li>
</ul>
<ul>
<li>
Experience with embedded systems and medical device software development.&nbsp;
</li>
</ul>
<ul>
<li>
Strong knowledge of data security, especially related to health data.&nbsp;
</li>
</ul>
<ul>
<li>
Knowledge of parallel processing and algorithm optimization.&nbsp;
</li>
</ul>
<ul>
<li>
Innovative mindset with a track record of proactive contributions.&nbsp;
</li>
</ul>
<ul>
<li>
Experience in grant writing and regulatory compliance (FDA).&nbsp;
</li>
</ul>
What We Offer:&nbsp;
<ul>
<li>
Competitive salary&nbsp;
</li>
</ul>
<ul>
<li>
Health, dental, and vision insurance coverage&nbsp;
</li>
</ul>
<ul>
<li>
Generous paid time off&nbsp;
</li>
</ul>
<ul>
<li>
Professional development opportunities&nbsp;
</li>
</ul>
<ul>
<li>
Potential to receive stock options&nbsp;
</li>
</ul>
<ul>
<li>
Opportunities for growth within the company&nbsp;
</li>
</ul>
<ul>
<li>
Flexible work arrangements, including remote work options&nbsp;
</li>
</ul>
<ul>
<li>
Dynamic and innovative startup environment&nbsp;
</li>
</ul>
<ul>
<li>
Opportunity to make a meaningful impact in the medical device industry&nbsp;
</li>
</ul>
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Senior Software Engineer for Medical Device Startup

<h3>Job Description</h3>
Job Description
Our client, a world leader in diagnostics and life sciences, is looking for a "Sr Systems Engineer” based out of Santa Clara, CA. 
 
Job Duration: Long Term Contract (Possibility Of Further Extension) 
Pay Rate: $60 - $80/hr on W2 DOE Company Benefits: Medical, Dental, Vision, Paid Sick leave, 401K 
We are seeking a Senior Systems Engineer to join our Systems Development Group supporting Next Generation Sequencing (NGS) product development. In this hands-on role, you will lead and contribute to all phases of the system development lifecycle including feasibility, integration, verification, and validation of end-to-end NGS solutions, while ensuring compliance with regulatory and quality standards. 
 
Key Responsibilities: 
<ul>
<li>Drive system design, integration, testing, and risk management activities for NGS platforms. </li>
<li>Develop and execute test cases, analyze performance data, and ensure requirements traceability. </li>
<li>Collaborate across functions to develop sample-to-answer workflows including sample extraction, library prep, and sequencing. </li>
<li>Contribute to design history files and maintain documentation aligned with quality systems. </li>
<li>Support troubleshooting, backlog review, and continuous improvement initiatives. </li>
</ul>
 
Qualifications: 
<ul>
<li>Bachelor’s degree in Biology, Chemistry, Biomedical Engineering, Systems Engineering, or related field; advanced degree preferred. </li>
<li>4+ years of hands-on experience in NGS workflows (e.g., nucleic acid extraction, library prep). </li>
<li>Strong troubleshooting skills; familiarity with statistical analysis tools (e.g., Python, JMP). </li>
<li>Experience with automation, imaging data, and regulated product development (preferred). </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>

Senior Systems Engineer

<h3>Job Description</h3>
Job Description
Position Summary: The Kenjya-Trusant Group is looking for a System Engineer to support our Maryland Customer for cross domain solutions. Essential Job Functions: 
<ul>
<li>Applies systems engineering principles throughout the systems life cycle phases: Concept, Development, Production, Utilization, Support, and Retirement. Interacts with the Government regarding Systems Engineering technical considerations and for associated problems, issues or conflicts.</li>
<li>Communicates with other program personnel, government overseers, and senior executives. Responsibility for the technical integrity, quality, and completeness of work performed and deliverables associated with one or more of the 25 process areas defined by ISO/IEC15288.</li>
<ul>
<li>Technical Process Area - Stakeholder Requirements Definition, Requirements Analysis, Architectural Design, Implementation, Integration, Verification, Transition, Validation, Operation, Maintenance, and Disposal.</li>
<li>Project Process Area - Project Planning, Project Assessment and Control, Decision Management, Risk Management, Configuration Management, Information Management, and Measurement.</li>
<li>Enterprise (Organizational Project-Enabling) Process Area -Project Portfolio Management, Infrastructure Management, Lifecycle Model Management, Human Resource Management, and Quality Management.</li>
<li>Agreement Process Area - Acquisition and Supply.</li>
</ul>
<li>Assist in developing a new or innovative approach to a technical or engineering issue.</li>
<li>Assist in conducting an evaluation to determine its suitability for project implementation.</li>
<li>Supervise or coordinate the work of other contractor engineers or technicians on a project.</li>
</ul>
Minimum Required Qualifications:
<ul>
<li>Due to the nature of this position and the information employees will be able to access; US Citizenship is required.</li>
</ul>
<ul>
<li>A Bachelor's degree in a Qualified Engineering Field or related discipline from an accredited college or university plus ten (10) years of systems engineering experience OR a High School Diploma or GED plus fourteen (14) years of general systems engineering experience (any process area) OR a Master's degree in a Qualified Engineering Field a related discipline from an accredited college or university plus eight (8) years of systems engineering experience OR a PhD in a Qualified Engineering Field or a related discipline from an accredited college or university plus eight (8) years of systems engineering experience.
<ul>
<li>Qualified engineering fields include: Aeronautics, Biomedical, Chemical, Civil, Computer, Electrical, Environmental, Mechanical, Nuclear, Software, Systems, and Engineering Management.</li>
<li>Related disciplines include: Chemistry, Computer Science, Information Systems, Mathematics, and Physics.</li>
</ul>
</li>
</ul>
<ul>
<li>Required Security Clearance: TS/SCI w/ Poly.</li>
</ul>
Desired/Preferred Skills:
<ul>
<li>Testing and Linux Systems administration experience is a plus.</li>
</ul>
Pay Range: There are a host of factors that can influence final salary including, but not limited to, geographic location, Federal Government contract labor categories and contract wage rates, relevant prior work experience, specific skills and competencies, education, and certifications. The proposed salary range for this position is: $135,000 - $265,000
Employment Type: Full-time, Exempt THE KENJYA-TRUSANT GROUP, LLC is a Service-Disabled Veteran-Owned Small Business that was established in 2015 as a merger between The Kenjya Group, Inc. and Trusant Technologies, LLC. Our mission is to implement, support and protect the nation's advanced technology systems, business processes and high-technology facilities. Working with the Department of Defense, Department of Homeland Security, the Intelligence Community, state and local governments, and commercial clients, Kenjya-Trusant provides cyber protection, information technology, engineering, construction management and acquisition support services. THE KENJYA-TRUSANT GROUP, LLC is an Equal Opportunity/Affirmative Action Employer that does not unlawfully discriminate in any of its programs or activities on the basis of race, color, religion, sex, age, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other basis prohibited by applicable law. We strive to create a diverse, inclusive and respectful work culture that values all.

System Engineer, Level 4 (SF)

<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 Overview:
We are seeking a detail-oriented and highly skilled Medical Device Software Quality Engineer to join our Quality Assurance team. The engineer will be responsible for championing quality assurance throughout the software development lifecycle, ensuring that all processes adhere to high standards and corporate requirements. The successful candidate will play a key role in ensuring the quality, safety, and compliance of software used in medical devices. You will work closely with software engineers, product managers, and regulatory teams to define and execute quality processes and activities that meet industry standards and regulatory requirements, including FDA Design Controls CFR 820.30, IEC 62304 – Software in a Medical Device, IEC 82304 – Software as a Medical Device, IEC 14971 – Risk Management, ISO 13485 – Quality Management Systems, 2017/745 – European Union Medical Device Regulation (EU MDR) and various FDA guidance Pre-market submission guidelines, and General Principles of Software Validation. This role will also assist on maintaining quality systems, supporting Corrective and Preventive Actions (CAPA), Non-conformance Reports (NCR), complaints, audits, and overall Quality Management System (QMS) functions.
What you'll do:
<ul>
<li>Act as a champion of Quality Assurance throughout the software development lifecycle, ensuring adherence to high standards and corporate requirements.</li>
<li>Develop and implement quality assurance processes for medical device software development, ensuring compliance with FDA, ISO 13485, IEC 62304, and other relevant standards.</li>
<li>Collaborate with software engineers, hardware engineers, and cross-functional teams to review design specifications, requirements, and software documentation for compliance with quality standards.</li>
<li>Conduct software risk assessments and contribute to risk management activities, including hazard analysis, FMEA (Failure Modes and Effects Analysis), and software safety analysis.</li>
<li>Develop and execute software verification and validation (V&amp;V) plans to ensure software functionality, performance, and safety meet required standards.</li>
<li>Lead software quality audits and reviews, ensuring adherence to quality systems, processes, and regulatory requirements.</li>
<li>Ensure proper documentation and traceability of quality activities, including test plans, test cases, defect reports, and validation protocols.</li>
<li>Support the preparation and review of regulatory submissions, such as 510(k) filings or CE marking applications, ensuring the software quality processes are adequately documented.</li>
<li>Troubleshoot and manage software-related quality issues, working closely with development teams to resolve defects and improve software reliability.</li>
<li>Participate in design control activities to ensure software quality throughout the product lifecycle, including planning, development, testing, and post-market surveillance.</li>
<li>Assist in the training and development of team members on software quality standards, best practices, and regulatory requirements.</li>
<li>Stay up-to-date with industry standards, regulatory changes, and emerging trends in medical device software quality management.</li>
</ul>
What We're Looking For: 
<ul>
<li>Bachelor's degree in Computer Science, Biomedical Engineering, Electrical Engineering, Quality Engineering, or a related technical field (Master's preferred), or equivalent experience.</li>
<li>Minimum of 8 years of software quality engineering, experience in planning, creating and executing test cases particularly in medical device development with a Bachelor's degree; or 6 years and a Master's degree; or a PhD with 3 years experience.</li>
<li>Strong knowledge of medical device regulations and standards, including FDA 21 CFR Part 820, ISO 13485, IEC 62304, and ISO 14971.</li>
<li>Experience in software verification and validation processes for embedded software and medical device software systems.</li>
<li>Strong understanding of software development life cycle (SDLC) and best practices for quality assurance and control.</li>
<li>Familiarity with programing language, software test tools, automated testing, and defect management systems.</li>
<li>Excellent problem-solving, analytical, and troubleshooting skills.</li>
<li>Strong attention to detail with a commitment to delivering high-quality, compliant products.</li>
<li>Excellent written and verbal communication skills, with the ability to work collaboratively in a cross-functional team environment.</li>
<li>Strong interpersonal skills including the ability to build authentic relationships, constructively challenge conventional thinking, engender trust, cooperate as a team leader or team member, share information and deliver results with a team.</li>
<li>Experience with risk management practices, including risk analysis and mitigation strategies.</li>
<li>Must be able to handle multiple tasks/projects and manage priorities accordingly.</li>
</ul>
Preferred Skills and Experience:
<ul>
<li>Experience with software quality systems for Class II or III medical devices.</li>
<li>Familiarity with AI/ML based medical device software quality management.</li>
<li>Familiarity with FDA software validation, design controls, and regulatory submission requirements (510(k), PMA).</li>
<li>Experience with software tools such as JIRA, TestRail, or similar defect tracking and test management platforms.</li>
<li>Experience with agile development methodologies and software development tools.</li>
<li>Certification in quality management or software quality (e.g., ASQ, CMMI) is a plus.</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$147,000—$165,000 USD

Staff Software Quality Engineer

<h3>Job Description</h3>
Job DescriptionSalary: 
About Proscia
Pathology is at the center of medicine and is undergoing a profound transformation as the final frontier of digitization in healthcare. We started Proscia to accelerate pathologys transition from microscope to images, and to use that AI to change the way we think about cancer. We cant change medicine alone. Thats why were looking for curious thinkers. Big dreamers. Developers, evangelists, pathologists, and scientists. Exceptional talent to help us use the great power of AI for good and advance humankind.
 
At Proscia, we push the limits of medicine and technology, solving problems the world has never solved before. We build software used by thousands of scientists and pathologists, who work on the front lines of fighting big enemies, like cancer, for patients around the globe. To accelerate our vision, Proscia has raised over $100M in capital from world-class healthcare and technology investors.
 
About this Position
As an AI Systems Integration Engineer on the AI R&amp;D team, you will bridge the gap between web applications, model APIs, and scalable infrastructure. Your work will ensure smooth, reliable, and efficient interaction between users and the AI systems embedded in our digital pathology platform, enabling data-driven precision medicine at scale.
 
What Youll Do
Working at a startup like Proscia means wearing many hats, but when you come to work you can expect to focus on the following:
 
<ul>
<li>Design and implement robust interfaces between vision and language AI models, front-end applications, and backend services.</li>
<li>Develop and maintain APIs, SDKs, and wrappers to enable seamless integration of AI features into production environments.</li>
<li>Align data pipelines, inference workflows, and feedback loops for real-time and batch AI use cases.</li>
<li>Collaborate closely with DevOps, AI engineers, and product managers to coordinate system architecture and deployment strategies.</li>
<li>Write clean, maintainable code that connects diverse software components, from inference services to UI layers.</li>
<li>Ensure reliability and scalability of model-serving infrastructure on AWS and Kubernetes.</li>
<li>Support rapid prototyping and iteration of AI features by building flexible integration layers.</li>
<li>Create tools and utilities that simplify interaction with AI services for internal and external developers. </li>
</ul>
What Were Seeking
Were looking for people who are smart, nice, &amp; get stuff done. Proscia is a high-growth company, and we want entrepreneurial doers that thrive in a challenging environment, that are ready to build the plane while flying it. Proscia's next AI Systems Integration Engineer will have:
 
<ul>
<li>Bachelors degree in Computer Science, Biomedical Engineering, or a related technical field.</li>
<li>3+ years of experience working at the intersection of software engineering and AI/ML systems.</li>
<li>Demonstrated AI fluency, with real-world experience using tools such as ChatGPT to enhance productivity and problem-solving.</li>
<li>Proficiency in Python and experience building APIs, client libraries, and backend services.</li>
<li>Familiarity with deploying ML models in production, including considerations for latency, scalability, and monitoring.</li>
<li>Experience developing front-end or middleware logic that consumes inference results and enables user feedback.</li>
<li>Solid understanding of containerization (Docker) and orchestration (Kubernetes) in cloud environments.</li>
<li>Ability to work across cross-functional teams and translate between ML, product, and engineering requirements.</li>
<li>Strong debugging and integration skillscomfortable working with partially defined interfaces and evolving systems. </li>
</ul>
Nice to Have
<ul>
<li>Familiarity with modern web development technologies..</li>
<li>Experience with medical or histology image data.</li>
<li>Background in developing regulated medical software.</li>
<li>Advanced degree (masters/PhD) in CS, Biomedical Engineering, or related field. </li>
</ul>
Beyond Just Work
As a company in healthcare, we want our people to be happy and healthy, in and out of the office. In addition to competitive pay, we ensure everyone on our team is supported with savings, schedule, and insurance options that promote long-term health and personal growth.
Our office environment is designed for creativity and agility: with walls as notepads and couches for collaboration. Were located in the heart of Philadelphia, with views of the city so you can spend your time focusing on what matters most.
 
At Proscia, we dont just accept differences we celebrate them, we support them, and we thrive on them for the benefit of our employees, our products, and our community. Proscia is proud to be an equal opportunity workplace.
 
Compensation: Competitive and based on experience. We welcome candidates from a broad range of backgrounds,from those with foundational AI engineering experience ready to grow, to senior engineers seeking to architect transformative solutions.
 remote work

AI Systems Integration 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>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 Redmond, Washington, 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.

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