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<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.
Ceribell is looking for a Staff Embedded Linux Software Engineer who is passionate about biomedical applications and who has experience in the development of embedded Linux-based 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. 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, test, and maintain software features for Ceribell's EEG systems.</li>
<li>Work with cross-compilation toolchains, build systems (Yocto, Buildroot, or similar), bootloaders, and CI/CD pipelines.</li>
<li>Develop, integrate, and debug device drivers for various peripherals (I²C, SPI, UART, USB, PCIe, etc.).</li>
<li>Troubleshoot and resolve complex issues across the software/hardware boundary.</li>
<li>Understand user needs and translate them to the development of new and improved features.</li>
<li>Participate in code reviews, peer reviews, and risk management activities.</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 related field. Graduate degree preferred.</li>
<li>10+ years of experience in embedded software development of a commercial product. Medical device experience preferred.</li>
<li>3+ years of professional experience in embedded Linux software development, interfacing with peripherals, and configuring device drivers and associated toolchains, e.g. Ubuntu, Torizon, Yocto, Buildroot.</li>
<li>Experience with bootloaders (U-Boot, security-boot), and system startup.</li>
<li>Experience with GUI-based application development in e.g. Qt preferred.</li>
<li>Experience using Git for version control.</li>
<li>Proficient in C/C++.</li>
<li>Direct experience with development of WiFi connected/IoT devices preferred.</li>
<li>Strong analytical skills, detail-oriented and collaborative.</li>
</ul>
Compensation Range$175,000—$200,000 USD
A candidate's final salary offer will be based on their skills, education, work location and experience, and thus it may differ from the posted range. Compensation may also include bonuses consistent with Ceribell's corporate compensation plan. Note, the above description is not all-encompassing and Ceribell reserves the right to change or modify job duties and assignments at any time.
In addition to your base compensation, Ceribell offers the following:
<ul>
<li>Performance-based incentive compensation (varies by role)</li>
<li>Equity opportunities</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>
Application Deadline: Ongoing
Equal Opportunity Employer Ceribell is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth and related medical conditions), sexual orientation, gender identity or expression, national origin, age, marital status, disability, veteran status or any other characteristic protected by law. Any applicant with a disability who requires an accommodation during the application process should contact <a href="mailto:talent@ceribell.com" target="_blank">talent@ceribell.com</a> to request reasonable accommodation.
Privacy Statement For information on how Ceribell processes personal data of job applicants, please review our Privacy Policy.
Compliance Disclaimer If you believe this job posting is non-compliant, please submit a report to <a href="mailto:legal@ceribell.com" target="_blank">legal@ceribell.com</a>. Please note that we will not respond to inquiries unrelated to job posting compliance.

Staff Embedded Linux 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
 
See yourself as a MoFe Engineer at Sightpath Medical!!
In addition to learning the latest innovations in the ophthalmic industry, Sightpath Medical offers a challenging and rewarding environment where you'll work with smart, fun and energetic people.
 &nbsp;• Sightpath Medical is the premier cataract and LASIK mobile services provider in the U.S. &nbsp;• We provide an independent working atmosphere &nbsp;• We provide on the job training to help you become an expert in our area of expertise &nbsp;• Salary position with quarterly bonus eligibility &nbsp;• 401(k) plan &nbsp;• Medical Benefits including medical, dental, vision, health savings account, short term disability, long term disability &nbsp;• Health and Wellness Program &nbsp; &nbsp;Responsibilities: &nbsp;• Requires the ability to install/de-install and operate transportable lasers and related equipment on one business unit at&nbsp;&nbsp;&nbsp; customer sites. &nbsp;• Responsible for calibration and programming of equipment for surgeon's approval prior to surgery being performed. &nbsp;• Responsible for the operation of both lasers when they are both required. &nbsp;• Provide routine preventative maintenance and repairs on the laser systems to maximize usage and minimize downtime. &nbsp;• Ability to troubleshoot, remove and replace components of the laser and calibrate to vendor specifications. &nbsp;• Responsible for maintaining all company assets in good working order. &nbsp;• Adherence to company standard operating procedures that meet/exceed standard of care. &nbsp;• Ability to complete Annual and Semi-Annual Preventative Maintenance checks and services on all assigned equipment. Successfully completes all PM paperwork during &nbsp;and at the end of PM. &nbsp;• Understands and adheres to proper sterile technique. &nbsp;• Other duties as required &nbsp; &nbsp;Qualifications: &nbsp;• Degree in Laser Electro-optics, Biomedical Electronics, Electronics or military training equivalent. &nbsp;• Proficiency with basic electronics and associated test equipment. &nbsp;• Able to work a varied work schedule and travel. &nbsp;• Able to work in a team environment. &nbsp;• Valid Driver's License &nbsp;• Ability to pass company administered road test. &nbsp;• Ability to occasionally lift 50 lbs. &nbsp;• Ability to stand for extended periods of time. &nbsp;• Able to work a varied work schedule and travel. &nbsp;• Great customer service skills.
 
 
PM25
 
Compensation details: 65000-75000 Yearly Salary
 
PI56a4b0128b7c-25405-38089401

MoFe Engineer I

<h3>Job Description</h3>
Job Description
Company Description
MiRus is a privately held medical device company focusing on the design and manufacturing of cardiovascular, orthopedic, and spinal systems based on innovative designs making use of proprietary technologies. The company is experiencing rapid growth in the orthopedic and spinal areas while bringing new technologies to the cardiovascular space. The company provides opportunity for advancement and professional growth, as there is a high level of visibility to all roles within the organization with a high level of recognition for your contributions.
Job Description
The Cardiovascular Delivery System Engineer will work with the team to design, develop, and test the delivery system for our transcatheter valve replacement system. Work may include communication with surgeons and sales consultants, to gain an understanding of clinical issues and define design parameters.
Tasks will include working with cross-functional project teams through all phases of the product development process.
<ul>
<li>Assist in spec development, design conceptualization and concept prototyping</li>
<li>Source vendors for components and sub-assemblies</li>
<li>Create component and assembly drawings for manufacturing</li>
<li>Develop fixtures, tooling and processes for manufacturing of final product through a combination of in-house and out-of-house suppliers</li>
<li>Perform testing of prototypes for design evaluation</li>
<li>Assist in the development and execution of design verification and validation plans and activities, test plan formation and execution to support regulatory approval</li>
</ul>
Strong organizational skills to support all aspects of the project including scope definition, and contingency planning. Ability to prioritize tasks and manage a varied workload, exhibit strong written and verbal communication skills, and interface effectively with peers, cross-functional project teams, and management.
Qualifications
<ul>
<li>A minimum of a bachelor’s degree in Mechanical Engineering or Biomedical Engineering is required.</li>
<li>3+ years of relevant catheter design experience</li>
<li>Experience with 3-D CAD modeling and drafting, preferably SolidWorks.</li>
<li>Familiarity with injection molding design a plus</li>
<li>Knowledge of medical materials related to catheters (i.e. Polymers, Nitinol, Stainless Steels, Fluoropolymers, etc.).</li>
<li>Microsoft Office (Word, Excel, PowerPoint) proficiency.</li>
<li>Demonstrate a strong initiative and follow through in executing project responsibilities, overcoming obstacles, and balancing multiple priorities.</li>
<li>Must have the ability to effectively communicate concepts, ideas and knowledge to other team members, cross-functional teams, customers, and suppliers.</li>
<li>Experience with FDA Medical Device guidelines.</li>
<li>Comfortable working in a fast-paced start-up environment.</li>
</ul>
Location: Marietta, Georgia Employee Type: Full-time

Cardio Vascular Delivery System Engineer

<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
We are seeking a detail-oriented Mechanical Engineer to drive product design and development for implantable drug delivery systems. The ideal candidate will have extensive experience in medical device design, a rigorous approach to design for manufacturability (DFM), expertise in geometric dimensioning and tolerancing (GD&amp;T), and a solid grounding in Good Manufacturing Practice (GMP). Familiarity with unique challenges and regulatory requirements for implantable devices, and a strong orientation toward application-specific tolerances is desired. 
Come Join Us!
You'll be part of a talented and dedicated team of engineers, scientists, and other professionals at Vivani Medical, an emerging biopharmaceutical company developing a pipeline of miniature, long-term drug implants with its proprietary NanoPortal™ platform technology for obesity/weight management and other chronic diseases.
Key Responsibilities
<ul>
<li>Drive the mechanical design of implantable drug delivery systems, from conceptualization through commercialization, with a focus on meeting demanding implantable device standards.</li>
<li>Apply design for manufacturability principles early in the design phase to ensure robust, scalable, and regulatory-compliant implantable products.</li>
<li>Ensure all designs are fully compliant with relevant GMP, FDA, and ISO requirements specific to long-term implantable medical devices.</li>
<li>Assign all tolerances and material selections with clear justification tied to the end-use environment (e.g., biocompatibility, sterilizability, in-body durability), and anchored in URS and clinical requirements.</li>
<li>Collaborate closely with cross-functional stakeholders (R&amp;D, manufacturing, regulatory, clinical) to capture and implement requirements unique to implantation, such as long-term reliability and risk management.</li>
<li>Participate actively in design reviews, Design History File (DHF) creation, risk analyses, and verification/validation activities, with emphasis on the unique aspects of implantable device safety and performance.</li>
<li>Support the transition from prototyping to scaled manufacturing, addressing material selection, assembly, and cleaning processes suitable for implantables.</li>
<li>Document design decisions thoroughly for full regulatory traceability and audit readiness.</li>
</ul>
Requirements
<ul>
<li>Bachelor’s degree in Mechanical Engineering (or related biomedical engineering field) </li>
<li>A minimum of 6 years of medical device experience.</li>
<li>Product design experience for implantable medical devices.</li>
<li>Experience with design, development, and manufacturing transfer of implantable drug delivery devices or other active implant systems.</li>
<li>A proven track record in meeting clinical and regulatory requirements.</li>
<li>Deep understanding of GMP and regulatory demands of implantable devices (including design history files, design controls, risk management).</li>
<li>High-level proficiency in design for manufacturability, specifically for products requiring robustness in vivo, sterilization compatibility, and miniaturization.</li>
<li>Strong command of GD&amp;T for precision assemblies, with hands-on experience assigning and reviewing tolerances </li>
<li>High proficiency with solid modeling and drawing software (SolidWorks, AutoCAD, or similar), and engineering documentation in a regulated environment.</li>
<li>Skillful at translating user needs into clear, actionable URS - including consideration of implant environment, mechanical stresses, and biocompatibility.</li>
<li>Effective communicator with a collaborative spirit who's also adept at dealing with shifting priorities (flexible). </li>
<li>The role requires 3 days in the office.</li>
<li>Legally authorized to work in the US</li>
</ul>
Salary range: $140-$175K
Benefits
<ul>
<li>Medical</li>
<li>Dental and Vision</li>
<li>Flexible Spending Account (FSA)</li>
<li>401K with Company Safe Harbor Match: 100% /up to 4%</li>
<li>Life Insurance</li>
<li>Long Term Disability</li>
<li>Home Office Stipend</li>
<li>Commuter benefits </li>
</ul>

Mechanical Engineer - Implantable Drug Delivery Systems

<h3>Job Description</h3>
Job Description
Cresilon® is a Brooklyn-based biotechnology company that develops, manufactures, and markets hemostatic medical devices utilizing the company’s proprietary hydrogel technology. The company’s plant-based technology has revolutionized the current standard by stopping traumatic and surgical bleeds in seconds without the need for extended manual pressure. The company's current and future product lines target veterinary, human trauma, and human surgical applications. Cresilon's mission is to save lives. Learn more about the company at <a href="http://www.cresilon.com" target="_blank">www.cresilon.com</a>.
Description: 
The Medical Device Engineer is responsible for leading the design and development activities of new products and improving existing products in compliance with all quality and regulatory requirements. S/he will be responsible for authoring technical documents for the development of medical devices and combination products according to relevant Design Control regulations and standards. The person in this position will also be responsible for providing project-specific support, including technical analysis and review of supplier documentation as required. The position has a scientific focus that includes formulation development, product performance characterization, and implementation including proto-type design and fabrication and data generation through designed experiments. 
The Medical Device Engineer is expected to aspire for excellence with a bias toward action, willing to roll up their sleeves, get hands-on, and do what’s necessary to move projects forward in a fast-paced environment. They are committed to designing and developing products that dominate the marketplace and improve healthcare by partnering with our customers to drive purposeful innovation, resulting in best-in-class products. The Medical Device Engineer will work with a multidisciplinary team of researchers. This is a multi-faceted job in a highly collaborative environment across multiple functions that will require flexibility as well as an ability to learn about and develop new technologies and explore new techniques in pursuit of product innovation and robustness.
Role level is contingent on experience, but this is not an entry level role.. This is a full-time, on-site position, located in Brooklyn, New York. 
Responsibilities
<ul>
<li>Create and lead experimentation for exploratory and/or product development research focusing on polymeric materials devices and their use.</li>
<li>Define new product functional requirements (design inputs/user needs) and evaluate the design's overall effectiveness, cost, reliability, and safety.</li>
<li>Lead cross-functional teams to develop new products, address design issues, and maintain existing designs.</li>
<li>Apply strong problem-solving skills to find solutions to complex problems.</li>
<li>Work independently to plan and schedule own activities necessary to meet project timelines.</li>
<li>Work cooperatively with, quality, manufacturing, regulatory, clinical, and marketing to ensure project success.</li>
<li>Lead the creation of design history file documentation through the new product development process.</li>
<li>Develop new implant and instrument designs utilizing Solidworks and modeling/detail design specifications.</li>
<li>Generate technical protocols/reports to support device safety and efficacy.</li>
<li>Invent/create concepts and designs and submit invention disclosures.</li>
<li>Ensure that all design activities adhere to FDA Quality System Regulations and ISO 13485 design control and risk management requirements. Lead material/design/process changes through a design control process, with well-documented research/analyses.</li>
<li>Author protocols and reports including development studies and design verification/validation activities.</li>
<li>Develop and execute test methods to aid in exploratory research, product development, and quality control; conduct chemical and mechanical property evaluation tests to assess the desirability of process or formulation changes.</li>
<li>Exercise technical judgment in the design, execution, and interpretation of experiments within the scope of project responsibilities and ensure the use of professional concepts to solve complex problems in creative and effective ways, in conformance with scientific methods and procedures.</li>
<li>Prepare samples as required for testing, or other evaluations and data analysis, including in voice-of-customer (VOC) labs.</li>
<li>Interface with customers, suppliers, and internal cross-functional team members to develop specifications and coordinate prototype fabrication.</li>
<li>Maintain a laboratory notebook and other technical documentation to required GLP/GMP guidelines.</li>
<li>Maintain active dialogue with Regulatory Affairs as subject matter expert on all product design elements/documentation pertaining to research towards FDA/regulated authority submissions,</li>
<li>Provide support to marketing and sales team, support the introduction of new technologies with the development of presentations, sales tools, formulations, and applications data</li>
<li>Communicate results to the scientific community via published papers. Present research at academic/industry symposia as an external representative of the company.</li>
<li>Manage part-time staff as a research leader and mentor for ongoing research projects.</li>
<li>Work with company leadership to evaluate existing research practices and contribute to a culture of ethical, high-quality research operations within the organization.</li>
<li>Provide other project or product support as needed in order to support Cresilon’s business objective.</li>
<li>Responsibilities may include other duties as assigned and as required.</li>
</ul>
Requirements
Required Qualifications
<ul>
<li>BS in Chemical Engineering, Polymer Engineering, Material Science, Biomedical Engineering, Mechanical Engineering, or related scientific discipline.</li>
<li>A minimum of 4+ years of product development experience is required. </li>
</ul>
<ul>
<li>A minimum of 2 years of hands-on experience in new product research and development in a cGMP-regulated industry is required (work experience in the Medical Device field is strongly preferred)</li>
</ul>
<ul>
<li>Adept experimentalist with hands-on experience in product development of medical devices and their safety/efficacy characterization in an R&amp;D environment.</li>
<li>Experience gathering user needs, translating them to technical inputs, and developing viable V&amp;V (Design Verification and Validation) plans.</li>
</ul>
<ul>
<li>Experience leading complex product development initiatives from concept through release.</li>
<li>Good working knowledge of anatomy and surgical procedures is required.</li>
<li>Demonstrated ability to solve difficult technical problems and deliver practical solutions that meet the application requirements is required. This includes strong analytical, problem-solving, and decision-making skills with the ability to be observant and to think creatively.</li>
<li>Demonstrated ability to design experiments and analyze data with appropriate quality and statistical methodologies.</li>
<li>Demonstrated ability to work independently as well as effectively be a strong team contributor and work cross-functionally to expedite the completion of critical project tasks </li>
<li>Ability to handle multiple project assignments of medium scope and complexity and able to prioritize and complete work with a sense of urgency in a timely manner.</li>
<li>Ability to lead directly and by influence, including strong problem-solving, conflict resolution, and analytical skills.</li>
<li>Requires strong leadership skills, excellent written and verbal communication and presentation skills.</li>
<li>Working knowledge of FDA requirements as per 21 CFR 820 </li>
<li>Proficiency in the use of Microsoft Excel, Microsoft Word, and Microsoft PowerPoint is required.</li>
<li>Legal authorization to work in the United States is required.</li>
</ul>
Preferred Qualifications
<ul>
<li>An advanced degree (MS or Ph.D.) is highly preferred.</li>
<li>Hands-on experience in product development with Class II and Class III medical devices.</li>
<li>Experience developing test methods and protocols/reports for safety and efficacy testing of implant and instrument designs.</li>
<li>Working knowledge of ISO 9001, ISO 13485:2003, and ISO 14971:2007.</li>
<li>Experience with IDE and PMA submissions. </li>
<li>Working knowledge of Good Documentation Practices (GDP), and Good Manufacturing Practices (cGMP) </li>
<li>Good understanding of statistical tools and validation/verification techniques.</li>
<li>Six-Sigma green belt or black belt certification </li>
</ul>
Cresilon is an equal-opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws. This policy applies to all employment practices within our organization, including hiring, recruiting, promotion, termination, layoff, recall, leave of absence, compensation, benefits, training, and apprenticeship. Cresilon makes hiring decisions based solely on qualifications, merit, and business needs at the time. 
Benefits
<ul>
<li>Competitive annual base salary range of $80,000 - $160,000, depending upon job level and qualifications</li>
<li>Paid Vacation, Sick, &amp; Holidays</li>
<li>Monthly MetroCard Reimbursement</li>
<li>401(k) &amp; Roth Retirement Savings Plan with company match up to 5%</li>
<li>Work/Life Employee Assistance Program</li>
<li>Company Paid Life and Short-Term Disability Coverage</li>
<li>Medical, Dental, and Vision Insurance, FSA: Dependent &amp; Healthcare, Commuter &amp; Parking Benefits, Long Term Disability Coverage</li>
</ul>

Research and Development Medical Device Engineer

<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.

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