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<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
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: 72000-80000 Yearly Salary
 
PIf207ad4cd74b-25405-38089399

Laser Engineer III

<h3>Job Description</h3>
Job DescriptionDEKA R&amp;D has an immediate opening for a Product Complaints Engineer - Team Lead to work in a dynamic Medical Device Research and Development environment.&nbsp; The position reports to the Product Complaints Manager.&nbsp; This is a high visibility role with a significant direct impact in the Quality Management System. How you will make an impact:
<ul>
<li>Will lead a small team of Product Complaints Engineers focused on one or more of DEKA’s innovative, life-changing medical devices.</li>
<li>Responsible for reviewing complaints related to potential device-related issues.&nbsp;</li>
<li>Perform product complaint evaluations with minimal direction, utilizing experience and product knowledge.</li>
<li>Ensure that complaint documentation follows Good Documentation Practices; meets QMS requirements; and complies with U.S. Food and Drug Administration (FDA) regulations / other regulatory requirements.</li>
<li>Identify and make sound decisions regarding medical device reporting to regulatory agencies.</li>
<li>Interface with Third Party Manufacturers, health care professionals, internal customers, and regulatory agencies.</li>
<li>Participate in audits and CAPA investigations as they relate to complaint handling.</li>
<li>Work with the forensic investigation team to align product investigations related to complaints.</li>
<li>Track complaint processes to identify areas of improvement.</li>
<li>Author procedures and work instructions.</li>
<li>Establish and maintain a product training program.</li>
<li>Contribute independently while also collaborating with other team members and departments.</li>
<li>Maintain positive and cooperative communication with co-workers, customers, contractors, and vendors.</li>
<li>Perform other related duties as assigned under management supervision.</li>
</ul>
Skills needed to be successful:
<ul>
<li>4-year engineering degree, preferably in biomedical engineering, and 3+ year(s) relevant experience in a cGMP environment supporting complaint handling investigations, medical device reporting, or product analysis; OR 2-year degree and 5+ year(s) relevant experience in a cGMP environment supporting complaint handling investigations, medical device reporting, or product analysis.</li>
<li>Knowledge of FDA requirements for Quality Systems, pharmaceutical products, and Medical Device Reporting regulations (21 CFR 803, 820 and 211) is preferred.</li>
<li>Experience with SalesForce is preferred.</li>
<li>Strong motivation to see individual tasks through to completion, and to help as needed to achieve team goals.</li>
<li>Exceptional time management skills with the ability to prioritize multiple projects and ensure compliance with regulations and standard operating procedures.</li>
<li>Good problem-solving and proficient computer skills are required.</li>
<li>Solid written/verbal communication and organizational skills, as well as attention to detail.</li>
<li>Sound technical writing skills.</li>
<li>Ability to work well independently and on cross-functional teams in a fast-paced, changing environment.</li>
</ul>
About DEKA: One hour from the beach, Boston, and the mountains, the historic Amoskeag Millyard once housed the largest textile mills in the world. It is now home to DEKA Research &amp; Development, where we are taking the same innovation and cutting-edge technology into the modern age. Behind DEKA’s brick walls sits a team of professionals who strive to make a difference every day through thoughtful engineering, design, and manufacturing. Here at DEKA, some of the most innovative and life-changing products of our time are created, and new ideas are always welcome and explored.
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hXL4U7u4pQ

Product Complaints Engineer - Team Lead

<h3>Job Description</h3>
Job Description
About Ceribell
Ceribell is a medical technology company focused on transforming the diagnosis and management of patients with serious neurological conditions. The Ceribell System is a novel, point-of-care electroencephalography ("EEG") platform specifically designed to address the unmet needs of patients in the acute care setting, and is being used in hundreds of community hospitals, large academic facilities and major IDN's across the country. Our entire team is driven by a shared commitment to transforming the landscape of critical care through our rapid seizure detection technology, come join the movement!
Position Description
Ceribell is looking for a Senior Firmware Engineer / Senior Embedded Engineer who is passionate about biomedical applications and who has experience in the development of embedded or IoT products. The successful candidate will join the R&amp;D team and will play a key role in the development of the next generation of Ceribell's life saving technologies. Our firmware development stack is based around a STMicroelectronics STM32 ARM Cortex microcontroller and we use FreeRTOS, the IAR Embedded Workbench, and the TouchGFX framework. You must be able to work collaboratively as part of a cross-functional R&amp;D team, but you must also be able to take individual ownership for development, testing, and documentation of your projects.
What you'll achieve 
<ul>
<li>Develop and test firmware features for Ceribell's EEG systems</li>
<li>Understand user needs and translate them to the development of new and improved features</li>
<li>Contribute to GUI development using frameworks such as Qt, TouchGFX, LVGL, or custom OpenGL-based stacks</li>
<li>Participate in code reviews, peer reviews, and risk management activities</li>
<li>Create and revise technical documentation</li>
<li>Provide input on firmware and hardware architecture for new and existing products</li>
</ul>
What you'll need to be successful
<ul>
<li>Bachelor's Degree in electrical engineering, computer science, biomedical engineering or</li>
<li>related field. Graduate degree preferred</li>
<li>5+ years of experience in firmware development of a commercial product</li>
<li>Proficient in C/C++ and experienced with firmware development on ARM based systems</li>
<li>Hands-on experience developing GUIs for embedded devices using Qt, TouchGFX, LVGL, or other embedded graphics frameworks</li>
<li>Direct experience with development of WiFi connected / IoT devices preferred</li>
<li>Strong analytical skills, detail-oriented and collaborative</li>
</ul>
Compensation Range$130,000—$165,000 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.

Senior Firmware Engineer

<h3>Job Description</h3>
Job DescriptionAbout GenScriptGenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy.GenScript is committed to striving towards its vision of being the most reliable biotech company in the world to make humans and nature healthier through biotechnology.About ProBioProBio proactively provides end-to-end CDMO service from drug discovery to commercialization with proactive strategies, professional solutions and efficient processes in cell and gene therapy, vaccine, biologics discovery and antibody protein drug to accelerate drug development for customers. ProBio's total cell and gene therapy solution covers CMC of plasmid and virus for IND filing as well as clinical manufacturing and commercial manufacturing.
Job Scope:
Every day, Genscript's Field Service Engineer helps our customers to tackle issues that enable scientists to make research easy. Through our work, we deliver insights and provide support that keep labs running smoothly and more efficiently. Join our team to be a part of this exciting work!
As a Field Service Engineer for Genscript, you will work at a variety of labs, so having an appetite for continuously learning about instruments and troubleshooting is key. The ability to help with solving customer problems and a dedication to deliver 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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zZiskXxuZn

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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WVXkHF8KFK

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>

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