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<h3>Job Description</h3>
Overview: Draper is an independent, nonprofit research and development company headquartered in Cambridge, MA. The 2,000+ employees of Draper tackle important national challenges with a promise of delivering successful and usable solutions. From military defense and space exploration to biomedical engineering, lives often depend on the solutions we provide. Our multidisciplinary teams of engineers and scientists work in a collaborative environment that inspires the cross-fertilization of ideas necessary for true innovation. For more information about Draper, visit <a href="http://www.draper.com" target="_blank">www.draper.com</a>. Job Description Summary: At Draper, we apply cutting edge science and engineering to solve our nation's most challenging problems in strategic systems, space systems, biotechnology, and electronic systems. Our Operations team plays a critical role in bringing these innovations from concept to reality. We are seeking an experienced NPI Manufacturing Engineer to join our Manufacturing Operations organization. This role will serve as the bridge between Production, Supply Chain, and Program teams, ensuring operational excellence from proposal through production and sustainment. WHAT YOU WILL DO: • Support Operation programs across the product lifecycle, with a focus on emerging programs. • Support Operations content in proposals, including cost, schedule, and manufacturing approaches, ensuring accuracy, compliance, and alignment with New Product Introduction (NPI) requirements. • Interface with Operations and assigned programs, driving execution. • Develop and maintain Operations program plans encompassing supply chain, quality, internal manufacturing, and production schedules. • Support Basis of Estimates (BOEs) for proposals and NPI programs. • Support production readiness by leading manufacturing planning, bid &amp; proposal inputs, and Production Readiness Reviews. • Partner with supply chain teams to confirm procurement plans, document make/buy decisions and establish complete supplier Statements of Work (SOW). • Evaluate supplier Manufacturing Readiness Package (MRP) to support make/buy decisions. • Drive continuous improvement into Operations activities, advancing efficiency, quality, and delivery performance. WHAT YOU'LL BRING: • Strong understanding of NPI and transition-to-production practices. • Ability to work cross-functionally (manufacturing, supply chain, engineering, quality) with competing priorities. • Experience developing and managing manufacturing plans, cost estimates, and schedules. • Knowledge of defense/aerospace hardware production is a plus. Job Description: Duties/Responsibilities • Use Computer Aided Design (CAD) programs to create product concepts. • Gather materials or resources needed to design the product. • Test the product for usability and safety. • Oversee the manufacturing and production process to set standards • Drive solutions to complex problems with limited direction - contribute to requirements development, propose ways forward, and adapt appropriately to changes in requirements. • Provide insight and suggest design or process modifications based on quantitative data or results. • Identify program/system-level technical risks and develop and execute mitigation strategies. • Actively mentor less experienced engineers and provide thoughtful, constructive feedback. Skills/Abilities • Curiosity-driven approach to solving complex, customer-driven problems as part of a multi-disciplinary team. • Collaborate and communicate effectively and openly with multi-disciplinary program team members, program leadership, and non-technical personnel. • Be a team player able to work in a fast-paced environment with the ability to balance multiple competing tasks and demands. Education Bachelor's or Master's degree in Mechanical Engineering or other relevant field. Experience 5-7 years experience in Product Engineering or related. Additional Job Description: Applicants selected for this position will be required to obtain and maintain a U.S. Security Clearance. Connect With Draper for Future Opportunities! If you don't find the right posting in our Career Opportunities, you may submit your resume for future consideration. Job Location - City: Cambridge Job Location - State: Massachusetts Job Location - Postal Code: 02139-3563 The US base salary range for this full-time position is $82,300.00 - $205,750.00 Our salary ranges are determined by role, level, and location. The range displayed on each job posting reflects the minimum and maximum target salaries for the position across all US locations. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. Union ranges will be in compliance with the collective bargaining agreement's approved rates by location and role. Your recruiter can share more about the specific salary range for your preferred location during the hiring process. Please note that the compensation details listed in US role postings reflect the base salary only, and does not include bonuses or benefits. Our work is very important to us, but so is our life outside of work. Draper supports many programs to improve work-life balance including workplace flexibility, employee clubs ranging from photography to yoga, health and finance workshops, off site social events and discounts to local museums and cultural activities. If this specific job opportunity and the chance to work at a nationally renowned R&amp;D innovation company appeals to you, apply now <a href="http://www.draper.com/careers" target="_blank">www.draper.com/careers</a>. Draper is committed to creating an inclusive environment. We understand the value of inclusivity and its impact on a high-performance culture. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, disability, age, sexual orientation, national origin, veteran status, or genetic information. Draper is committed to providing access, equal opportunity, and reasonable accommodation for individuals with disabilities in employment, its services, programs, and activities. To request reasonable accommodation, please contact [email&nbsp;protected].

Production Ops. Manufacturing Engineer

<h3>Job Description</h3>
Job DescriptionSalary: 
About us:
Founded in 2015 to develop the worlds first industrially scalable laser metal additive manufacturing solution, VulcanForms is reshaping how the world manufactures critical products. We build and operate advanced digital infrastructure that enables innovation, accelerates growth, and supports sustainability across aerospace, defense, medical, and other essential industries. Through our vertically integrated capabilities, including scalable additive manufacturing and precision machining, we deliver true end-to-end production at scale by combining cutting-edge technology with a foundation of proven industrial craftsmanship. Our team brings deep expertise in manufacturing, materials science, software, automation, and operations, united by a shared commitment to quality, curiosity, and accountability. We foster an inclusive culture where people take ownership, solve meaningful problems, and continuously learn, because we believe diverse perspectives lead to better outcomes.
VulcanForms Inc. seeks a for a Sr. Product Development Engineer for our Devens, MA location.
Job Purpose
As a Sr. Product Development Engineer at VulcanForms, your mission is to design and optimize our high-speed laser-powder-bed-fusion process and its digital workflow to deliver production-ready parts at scale. Youll collaborate across hardware, software, and operations teams to continuously improve print quality, system reliability, and workflow efficiency enabling transformative outcomes for our customers and the future of advanced manufacturing.
Key Responsibilities
<ul>
<li>Partner with hardware, software and operations teams to develop and implement integrated process from R&amp;D through pilot runs to full serial production achieving high manufacturing readiness levels.</li>
<li>Create and iterate LPBF process recipes and build configurations, including build files, post-process sequences, and machine integration to ensure consistent production of parts within the VulcanForms platform.</li>
<li>Translate user requirements into engineering specifications that guide end-to-end product and process development; collaborate with internal teams to optimize part designs for LPBF, balancing geometry, supports, tolerances and material performance.</li>
<li>Build and iterate parts, hardware, and tools to support First Article Inspection and production launches of products in medical, aerospace, consumer, defense, and other industries.</li>
<li>Serve as the technical interface with customers, program managers, and operations leaders communicating development status, sharing findings, troubleshooting issues, and aligning on production plans.</li>
<li>Own root cause analysis of print defects and drive corrective actions through rapid iteration and testing.</li>
<li>Develop application-specific process workflows that meet customer requirements for dimensional accuracy, mechanical performance and surface finish.</li>
<li>Collaborate with downstream process owners in machining, finishing, and other areas to implement DFM principles with a top-down approach.</li>
<li>Collaborate with operations and quality teams to establish standard operating procedures and quality control methods.</li>
<li>Create and maintain detailed documentation: build recipes, work instructions, inspection protocols, change logs and training materials ensuring repeatability, traceability and production compliance.</li>
</ul>
Qualifications
<ul>
<li>Bachelor's degree in Mechanical, Materials, Aerospace, Biomedical Engineering, or a related field; Masters or Ph.D. preferred.</li>
<li>Minimum of 2 years hands-on experience in product or applications development, preferably with a focus on LPBF or directed energy deposition (DED) processes.</li>
<li>Proficiency in 3D CAD software such as Siemens NX, Creo, or SolidWorks.</li>
<li>Solid understanding of GD&amp;T, tolerance analysis, and design for manufacturability (DFM) principles.</li>
<li>Familiarity with quality management systems and associated standards.</li>
<li>Strong interpersonal and communication skills with the ability to collaborate effectively across multidisciplinary teams.</li>
<li>Knowledge of subtractive manufacturing operations (e.g. milling, turning) and their design constraints is a plus.</li>
</ul>
Benefits
<ul>
<li>Medical, dental, vision, and life insurance are available to you starting on your first day of employment</li>
<li>Generous time off package, including vacation PTO, sick PTO, and 14 company-paid federal holidays</li>
<li>401(k) with company match and stock options</li>
</ul>
VulcanForms Inc. is committed to being an Equal Opportunity Employer, valuing employees with diverse, multi-cultural perspectives. We are dedicated to fostering an inclusive environment, empowering our team, and embracing diversity. We welcome all applicants and ensure fair and impartial treatment regardless of race, color, religion, sex, national origin, ancestry, citizenship status, age, legally protected physical or mental disability, protected veteran status, status in the U.S. uniformed services, sexual orientation, gender identity or expression, marital status, genetic information, or any other characteristic protected by applicable federal, state, or local law.

Sr. Product Development 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
 
PIe2aa30ea658b-25405-38196172

Laser Engineer III

<h3>Job Description</h3>
Job Description
Calyxo, Inc. is a medical device company headquartered in Pleasanton, California, USA. The company was founded in 2016 to address the profound need for improved kidney stone treatment. Kidney stone disease is a common, painful condition that consumes vast amounts of healthcare resources each year. Our team is led by executives and investors with a proven track record of commercializing paradigm-shifting devices to meet unmet needs within urology.
Are you ready to change the future of kidney stone treatment? We are seeking high achievers who want to be part of a dynamic team working in a fun, diverse atmosphere.
Summary:
This position is responsible for providing clinical insights to support evidence generation through bench and animal model testing. The ideal candidate will also contribute to enhancing procedural excellence and refining current Calyxo commercial product offerings. Additionally, this role will assist in defining customer requirements and participate in physician evaluations during in-vitro bench testing, simulated-use studies, and in-vivo testing as needed for new product development.
In This Role, You Will:
<ul>
<li>Become an expert on the clinical application of Calyxo Inc's products, kidney stone disease state and treatment, and the competitive landscape.</li>
<li>Develop in vitro and in vivo kidney models for evidence generation, technique optimization, training, and new product evaluation. Research literature as needed to gather anatomical data necessary to develop appropriate in-vitro models.</li>
<li>Support the development and execution of test methods for evaluating and comparing the performance of devices (Company's and competitive products) for marketing analysis and collateral, evidence generation, concept selection, design optimization, design verification &amp; validation.</li>
<li>Contribute to the development of customer input requirements and support associated design validation testing plans, protocols, and test execution.</li>
<li>Support design and manage in-vitro, ex-vivo, and in-vivo product testing: study design, model design/development, and selection.</li>
<li>Collaborate with development teams to prepare and conduct physician evaluation sessions, including method/test sequence development, model design/selection, and data collection.</li>
<li>Ensure procedural excellence with Calyxo Inc products by combining engineering product knowledge, understanding of the complaints data, and in-field analysis of product performance.</li>
<li>Establish best practices for procedural techniques for field and customer training and to provide insights for new product development.</li>
<li>Evaluate and analyze procedural data including case videos, physician questionnaires, and complaints data.</li>
<li>Lead cross-functional alignment with Marketing, R&amp;D and Professional Education to incorporate procedural best practices learnings into training materials.</li>
<li>Collaborate with Marketing and R&amp;D to define clinical performance goals and perform risk assessments. Validate performance of the device relative to those goals.</li>
<li>Proctor cases evaluating advanced techniques. Create plans and systems to collect data from these initiatives.</li>
</ul>
Who You Will Report To:
<ul>
<li>See Organizational Chart</li>
</ul>
Requirements:
<ul>
<li>BS in Engineering or related discipline with 5+ years related experience in the medical device industry; MS with 3+ years experience or Ph.D. . Biomedical Engineering degree is a plus.</li>
<li>2 years previous experience in medical device clinical engineering-related activities strongly preferred (participating in conducting animal studies, in-vitro testing, etc).</li>
<li>Strong background in hypothesis development and experimental testing, ideally within an academic or research setting</li>
<li>Prior experience interfacing directly with physicians in a surgical setting is strongly preferred.</li>
<li>Knowledge of and exposure to product testing and data collection required.</li>
<li>Experience in endourological procedures, techniques, devices, and pre-clinical testing is preferred.</li>
<li>Ability to travel 40%</li>
<li>Excellent interpersonal and negotiating skills; ability to adapt to changing work priorities</li>
<li>Polished communicator and presenter with excellent listening, teaching, and program evaluation skills.</li>
<li>Effective interpersonal interactions, both within the commercial group and in accounts</li>
<li>Proficiency with PC-based office computers, including familiarity with Microsoft Word, Excel, PowerPoint, and Outlook required</li>
<li>Ability to work independently</li>
<li>Valid driver's license</li>
<li>Compliance with relevant county, state, and Federal rules regarding vaccinations.</li>
</ul>
What We Offer:
At Calyxo, you will be part of a knowledgeable, high-achieving, experienced and fun team. You will work in a diverse work environment with experienced, proven leaders and have an opportunity to shape our company culture. You will experience constant learning and dynamic challenges to help you grow and be the best version of yourself. 
We also offer an attractive compensation package, which includes:
<ul>
<li>A competitive base salary of $115,000 to $145,000 and variable incentive plan</li>
<li>Stock options – ownership and a stake in growing a mission-driven company</li>
<li>Employee benefits package that includes 401(k), healthcare insurance and paid vacation</li>
</ul>
Calyxo is deeply committed to fostering an environment where diversity and inclusion are not only valued but also prioritized. We believe a diverse and inclusive community empowers us to act courageously, care deeply, and dream boldly to impact people in big ways. Diverse viewpoints bring diverse capabilities, which strengthen our focus and fuel our growth. Calyxo is proud to be an equal opportunity employer, seeking to create a welcoming and diverse environment. All applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran status or any other applicable legally protected characteristics
Legal authorization to work in the United States is required. In compliance with federal law, all persons hired will be required to verify their identity and eligibility to work in the United States and to complete the required employment eligibility verification form upon hire. 
Disclaimer:
At Calyxo, we prioritize a transparent and structured interview process to ensure the best fit for both our candidates and our team. Please be aware of the following:
<ul>
<li>Structured Interview Process: Our hiring process includes multiple stages of interviews where you will have the opportunity to communicate directly with Calyxo employees. This ensures that you gain a comprehensive understanding of the role and our company culture.</li>
<li>Verification of Identity: We do not extend job offers without first meeting candidates, either virtually or in person. This step is crucial to maintain the integrity of our hiring process and to ensure mutual alignment.</li>
<li>Beware of Scams: Calyxo will never request sensitive personal information, such as your full name, address, phone number, or identification documents, via email or online forms before an official interview. Calyxo representatives will always contact you using an email format of <a href="mailto:firstname.lastname@calyxoinc.com" target="_blank">firstname.lastname@calyxoinc.com</a>. If you receive a request for information from any other domain, please contact us directly at <a href="mailto:info@calyxoinc.comto" target="_blank">info@calyxoinc.comto</a> verify the legitimacy of the communication.</li>
</ul>
We appreciate your interest in joining Calyxo and look forward to getting to know you through our official channels.

Clinical Development Engineer - Pleasanton, CA

<h3>Job Description</h3>
Job Description
DeepSight Technology Inc. is a stealth mode startup company that has developed breakthrough technology in ultrasound imaging. This new technology will both extend the range and clarity over current systems by 10x - 100x! We are setting new standards that will dramatically improve the capabilities of ultrasound for many years. 
In order to develop and improve this technology, we need dedicated team members. Not only do we offer a great team-oriented environment, but we also offer competitive compensation of $150,000-$250,000 per year and generous benefits in both our St. Louis, MO and Santa Clara, CA offices.
Job Description
We are looking for an Engineer with a strong background in Ultrasound Image Analysis to work on our new ultrasound imaging platform. This is a crucial role in our design and development process. 
As the Image Analysis Engineer, your responsibilities are: 
<ul>
<li>Lead image analysis from probe bring-up to final optimization </li>
<li>Lead ultrasound imaging feature definition, development, implementation, and verification to ensure successful product release. </li>
<li>Reconcile image artifacts with the development team to resolve system performance leading to the highest quality imaging for the company </li>
<li>Support the clinical evaluation of the ultrasound system </li>
</ul>
This position is suited for you if you are familiar with:
<ul>
<li>Development of image performance parameters that result in maximizing the ultrasound system and probe performance </li>
<li>Image optimization based on tissue characterization and blood flow visualization and quantification. </li>
<li>Taking ownership of image quality, system performance verification, engineering and clinical image optimization, and customer support. </li>
<li>Developing and using imaging tools to verify image feature development for transfer to software implementation </li>
<li>Driving innovation and continual improvement of imaging performance all the way from concept generation to prototyping and product implementation. </li>
<li>Contributing to teamwork in an Agile development environment. </li>
</ul>
Required Qualifications:
<ul>
<li>M.S. in Electrical/Biomedical Engineering </li>
<li>7+ years industry experience in medical imaging product development </li>
<li>Expertise in ultrasound physics and system design, signal and image processing, algorithm specification and development </li>
<li>Demonstrated experience using MATLAB/Python for fast prototyping; C/C++ programming </li>
<li>Demonstrated technical abilities in coordinating development efforts of a highly technical group </li>
<li>Excellent oral and written communication skills </li>
<li>Able to adapt quickly to change and work in a rapidly evolving environment </li>
<li>Willing to relocate to either the St. Louis, MO or Santa Clara, CA areas </li>
<li>Willing to travel up to 10% </li>
</ul>
Preferred Qualifications:
<ul>
<li>PhD in Electrical/Biomedical engineering with a dissertation topic related to ultrasound imaging or therapy </li>
<li>Direct experience in R&amp;D ultrasound image optimization and system development for general imaging applications (e.g. Abdominal, Small Parts, Musculoskeletal, Vascular, Pediatric, CEUS, and Color Doppler. </li>
</ul>
Other Qualities We Are Looking For
<ul>
<li>Positive - a can-do attitude that helps you rise to challenges </li>
<li>Collaborative - a team player who can effectively communicate with others </li>
<li>Attentive to detail - nothing gets by you </li>
<li>Efficient - a knack for effectively prioritizing tasks and managing your time</li>
<li>Pride in your work - real desire to do quality work </li>
<li>Career-minded - looking for more than a job </li>
<li>Empathy - a mindset of producing quality products that help people </li>
</ul>
Benefits and Perks
We offer great benefits and perks: 
<ul>
<li>Competitive salary </li>
<li>Stock options </li>
<li>Medical, dental, and vision insurance </li>
<li>401(k) retirement plan</li>
</ul>
 Job Posted by ApplicantPro

Ultrasound Image Analysis Engineer

<h3>Job Description</h3>
Job Title - Test Engineer II - Exempt
Number of Positions - 1
Job Location - 195 McDermott Rd, North Haven, Connecticut, United States of America, 06473
Job Start Date - 8/25/25
Job End Date - 8/28/26
Job Description - 
Top 3 technical skills that you are required for this role:
<ol>
<li>Execute and document System tests</li>
<li>Author Test Reports and route documents for approval (strong writing skills) </li>
<li>Communicate test related activities and results with multi-disciplinary team members</li>
</ol>
Will the contractor be working 40 hours a week? If not, weekly estimate? Yes, the contractor will be working 40 hours a week.
Does this position require the candidate to be onsite or remote, if hybrid what does the onsite vs remote schedule look like? The position requires the candidate to be onsite.
What product line will this person support? This position will be a part of a R&amp;D Systems Engineering team and will interface with cross-functional team members
Responsibilities may include …
JOB DESCRIPTION
1st shift hours are 8:00am-5:00pm M-F
The Test Engineer shall support test activities to best meet the project’s requirements. This position will be a part of a R&amp;D Systems Engineering team and will interface with cross-functional team members. You will be responsible for executing tests, analyzing data, documenting results, and ensuring that all documentation passes quality review.
 
You will:
<ul>
<li>Execute and document System tests</li>
<li>Author Test Reports and route documents for approval (strong writing skills)</li>
<li>Create quality and safety related documentation to support validity of test.</li>
<li>Communicate test related activities and results with multi-disciplinary team members</li>
<li>Perform gauge repeatability and reproducibility</li>
<li>Provide input to engineers to assist in the development of test protocols and prototype builds.</li>
<li>Perform mechanical and electrical testing to evaluate new and existing products.</li>
<li>Generate and analyze test data, and report results per departmental procedures.</li>
<li>Prepare and operate various lab equipment such as Instron mechanical testers, visual inspection, autoclaves, etc.</li>
<li>Participate in continuous improvement activities of a Testing Services team.</li>
<li>May serve as an extended team member for engineering team meetings.</li>
<li>Train operators to appropriate SOP’s</li>
<li>Adhere to safety policies and procedures.</li>
</ul>
 
Must Have:
<ul>
<li>Bachelor’s Degree and 0-1 years of relevant experience</li>
</ul>
 
Nice to have:
<ul>
<li>Bachelor’s Degree in a technical discipline, preferably engineering (Biomedical, Mechanical, or Electrical Engineering) with 1 year working in a STEM field. </li>
<li>Understanding of creating test methods for verifying product requirements</li>
<li>Familiarity with basic statistics and use of Minitab</li>
<li>Ability to work with QA to ensure testing meets Quality and Regulatory needs.</li>
<li>Ability to work with Systems, Mechanical, Electrical and Software engineers when discovering, documenting, and resolving issues.</li>
<li>Experience using oscilloscope, force gauges, and LabVIEW</li>
</ul>

Test Engineer II

<h3>Job Description</h3>
Job Description
Location: Alachua, FL 
RTI Surgical is now Evergen!
This rebranding reflects our strategic evolution as a leading CDMO in regenerative medicine and comes at the end of a significant year for the business, including the successful acquisitions of Cook Biotech in IN. and Collagen Solutions, MN. Our new brand identity emphasizes our unique positioning as the only CDMO offering a comprehensive portfolio of allograft and xenograft biomaterials at scale.
Evergen is a global industry-leading contract development and manufacturing organization (CDMO) in regenerative medicine. As the only regenerative medicine company that offers a differentiated portfolio of allograft and xenograft biomaterials at scale, Evergen is headquartered in Alachua, FL, and has manufacturing facilities in West Lafayette, IN., Eden Prairie and Glencoe, MN., Neunkirchen, DE., Glasgow, UK., and Marton, NZ. 
Read more about this change and Evergen’s commitment to advancing regenerative medicine here: <a href="https://lnkd.in/eMSfVJkM" target="_blank">https://lnkd.in/eMSfVJkM</a>
RESPONSIBILITIES
<ul>
<li>Leads project workstreams in the design and development of new implants and improvements to existing designs leveraging previous experience with minimal support to derive unique solutions and approaches to contribute to project success</li>
<li>Applies sound engineering problem-solving techniques to resolve challenges during the product development process and analyzes data to draw conclusions using statistically sound and scientifically based methodology</li>
<li>Leverages experience and technical knowledge to proactively develop strategies and plans of execution to derive unique solutions and approaches to contribute to project success</li>
<li>Writes protocols, reports, Standard Operating Procedures (SOPs), and other technical documents in accordance with Good Documentation Practices with a high attention to detail</li>
<li>Designs, develops, and validates test methods to meet design requirements</li>
<li>Effectively leads discussions and builds consensus with quality, regulatory, engineering, and production teams throughout the product development process to meet project objectives</li>
<li>Leads discussions with internal or external customers to obtain design requirements and feedback on prototype designs with a high level of customer service</li>
<li>Maintains project timelines by providing appropriate inputs, target times, and resource needs</li>
<li>Applies clinical knowledge in relevant surgical procedures and disease states within a clinical segment to develop innovative solutions to satisfy customer needs</li>
<li>Evaluates product design for manufacturability and suggest design process adjustments and quality improvements</li>
<li>Participates in the selection, development, and testing of tools, fixtures, machinery, and equipment used in manufacturing</li>
<li>Other duties as assigned</li>
</ul>
REQUIREMENTS
Education
<ul>
<li>Bachelor of Science Degree in biomedical engineering or another relevant engineering disciple </li>
</ul>
Experience
<ul>
<li>4-6 years engineering experience designing or modifying medical devices or implants </li>
</ul>
Certification
<ul>
<li>N/A</li>
</ul>
Skills 
<ul>
<li>Excellent verbal and written communication </li>
<li>Microsoft Office Suite</li>
<li>Project Management </li>
<li>Computer Aided Drafting (CAD) software</li>
<li>Statistical analysis software</li>
<li>Design Control and Design History File </li>
</ul>
Travel 
<ul>
<li>10% or less</li>
</ul>
SAFETY
Physical Requirement
<ul>
<li>Move or lift objects up to 25 pounds</li>
<li>Frequent (&gt;75%) stationary position (standing or sitting) while utilizing digital displays</li>
<li>Frequent (&gt;75%) fine manipulation using hands and fingers (typing, opening, writing, clicking, paper sorting, etc.)</li>
</ul>
Working Environment
<ul>
<li>Onsite: Office environment with assigned workstation</li>
<li>Remote positions only: Home office environment with minimum distractions</li>
</ul>
More about Evergen:
Evergen provides customers across a diverse set of market segments with leading-edge expertise, scale, and flexibility across end-to-end services including design, development, regulatory support, verification and validation, manufacturing, and supply chain management. 
 Evergen is rooted in a steadfast commitment to quality, integrity, and patient safety with a focus on five key values: 
<ul>
<li>Accountable: We own our actions and decisions.</li>
<li>Agile: We embrace change to stay ahead of the curve and evolve to drive innovation and growth. </li>
<li>Growth Mindset: We embrace challenges as opportunities for continuous learning.</li>
<li>Customer-Centric: We prioritize customers at every touch point. </li>
<li>Inclusive: We thrive on the richness of our diversity and ensure every voice is heard, respected, and celebrated. </li>
</ul>
At Evergen, we are committed to fostering an inclusive workplace where we embrace the richness of our diversity and ensure that every voice is heard, respected, and celebrated. We believe that by embracing diversity and promoting inclusivity, we not only uphold our values but also strengthen our position as the CDMO of Choice in regenerative medicine solutions. We recognize that cultivating a growth mindset is essential to our success, and we are dedicated to continuous learning and improvement in our diversity, equity, and inclusion efforts. Through accountability and action, we strive to create an environment where individuals can thrive, innovate, and contribute their unique perspectives to drive our collective success.
Montagu Private Equity (“Montagu”), a leading European private equity firm, acquired RTI in 2020 and has supported the transformation of the company to its next level of potential.
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R&D Engineer 2

<h3>Job Description</h3>
Job Description
Principal R&amp;D Engineer, Microcatheter Development
Potential Role Expansion to VP R&amp;D for the right hands-on candidate
Location: Milpitas, CA
Department: Engineering
Reports to: Chief Operating Officer
Salary Range: $100,000 – $200,000
Experience: 10+ years in medical device development
About Galaxy Therapeutics Inc.
Galaxy Therapeutics is a private, US-based, clinical stage medical device company pioneering implant technology to treat brain aneurysms. Our Saccular Endovascular Aneurysm Lattice treatment system, Seal™, addresses a $1B+ market opportunity. We have demonstrated proof of concept and clinical safety in our Pre-SEAL IT trial and are currently enrolling in our Pre-Market Approval SEAL-IT trial in the US and internationally. Our core team is based in Milpitas, CA.
About the Role
As Principal R&amp;D Engineer, you will lead product development for our microcatheter product line, from concept through market release. This hands-on role is ideal for a technical leader who thrives in a collaborative, fast-paced environment and is passionate about innovation in medical devices.
Key Responsibilities
<ul>
<li>Lead projects from concept to market release, acting as Project Leader.</li>
<li>Design, develop, test, and validate microcatheter systems and supporting devices.</li>
<li>Mentor and guide engineers and technicians; foster cross-functional collaboration.</li>
<li>Develop and execute engineering specifications, feasibility plans, cost analysis, risk assessments, FMEAs, and product verification/validation testing.</li>
<li>Ensure compliance with quality system procedures and regulatory requirements.</li>
<li>Document detailed drawings and specifications throughout R&amp;D stages.</li>
<li>Build prototypes and participate in animal studies as required.</li>
<li>Drive process improvements to enhance performance, efficiency, and production yields.</li>
<li>Write and submit intellectual property disclosures; participate in patent reviews.</li>
<li>Perform additional duties as needed to support company objectives.</li>
</ul>
Qualifications
<ul>
<li>Bachelor’s degree in Biomedical, Mechanical, or Biomedical Science, or related field (advanced degree preferred).</li>
<li>10+ years of experience in medical device design and development, including 7+ years with intravascular products (catheters, guidewires, balloons, stents).</li>
<li>Proven experience as a technical lead, taking products from concept to launch (microcatheter experience preferred).</li>
<li>Proficiency in SolidWorks/CAD, word processing, spreadsheets, and project management software.</li>
<li>Strong skills in product design/testing, statistical data analysis, technical writing, and communication.</li>
<li>Ability to work under pressure, meet deadlines, and collaborate effectively.</li>
<li>Knowledge of vascular interventional medical products and regulatory requirements (GMPs, GLPs).</li>
<li>Ability to attend clinical cases and interact professionally with hospital staff.</li>
</ul>
Supervisory Responsibilities
<ul>
<li>R&amp;D Technician (all levels)</li>
</ul>
Why Join Us?
<ul>
<li>Opportunity to make a significant impact in a growing, innovative company.</li>
<li>Work alongside leading physicians and engineers in the field.</li>
<li>Potential for role expansion to VP R&amp;D for the right candidate.</li>
</ul>
Equal Opportunity Employer
Galaxy Therapeutics Inc. is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.
Ready to make a difference? Apply now and join us in revolutionizing brain aneurysm treatment!
Company DescriptionGalaxy Therapeutics is a private, US-based, clinical stage medical device company pioneering implant technology to treat brain aneurysms. Our Saccular Endovascular Aneurysm Lattice treatment system, SealTM, addresses a $1B+ market opportunity. We have demonstrated proof of concept and clinical safety in our Pre-SEAL IT trial and are currently enrolling in our Pre-Market Approval SEAL-IT trial in the US and internationally. Our core team is based in Milpitas, CA. 
<h3>Company Description</h3>
Galaxy Therapeutics is a private, US-based, clinical stage medical device company pioneering implant technology to treat brain aneurysms. Our Saccular Endovascular Aneurysm Lattice treatment system, SealTM, addresses a $1B+ market opportunity. We have demonstrated proof of concept and clinical safety in our Pre-SEAL IT trial and are currently enrolling in our Pre-Market Approval SEAL-IT trial in the US and internationally. Our core team is based in Milpitas, CA.

Principal R&D Engineer, Microcatheter Development

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

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