field_job_employment_type

field_job_occupational_field_parents_all

job_organization_name

city

state

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

Research and Development Medical Device Engineer

<h3>Job Description</h3>
Job Description
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 DescriptionDescription:
 The Process Engineer II is responsible for ensuring the organization is compliant with all applicable regulations and standards in the areas of process validations. In addition, this position leads process change and improvement throughout the different areas of the company, including manufacturing. Process Engineers also participate in technology transfer to ensure the processes necessary for new products are effectively translated to the manufacturing floor. The Process Engineer II makes use of statistical analysis methods, critical thinking, process development, and scaling principles to achieve the objectives mentioned above.
Requirements:
Duties and responsibilities
<ul>
<li>Provide backup support to the Director Research and Development Operations, as needed.</li>
<li>Perform critical review of Process Engineer I project plans and related documents to ensure implementation is accurate and timely.</li>
<li>Independently lead and coordinate cross-functional projects and related resources to ensure completion in a timely manner. Communicate to management of performance against plan.</li>
<li>Perform data and technical presentation reviews as needed.</li>
<li>Understand and apply the applicable regulations and standards for equipment qualification and process validation to ensure compliance.</li>
<li>Statistical and analytical methods to understand processes.</li>
<li>Use LEAN Manufacturing principles to analyze and make recommendations for process optimization and implementation.</li>
<li>Work with other department heads or designees on projects as delineated on project plans to ensure timely completion of projects.</li>
<li>Develop equipment and process validation protocols (IQ, OQ, PQ) and reports as needed.</li>
<li>Lead and perform equipment qualifications and process validations as needed. </li>
<li>Develop and monitor process and equipment metrics to use for optimization analysis.</li>
<li>Develop and implement solutions with minimal supervision.</li>
<li>Comply with FDA and AATB tissue banking standards. </li>
<li>Other duties as assigned.</li>
</ul>
Qualifications
<ul>
<li>BS in Biomedical, Mechanical, Industrial Engineering or other applicable engineering discipline. Advanced degree (Master’s) a plus.</li>
<li>A minimum of 3 years of experience in Tissue Banking, Device, Biologics, or pharmaceutical industry in a relevant engineering role. Leadership experience preferred.</li>
<li>Strong analytical, planning, project management, critical thinking, troubleshooting, and problem-solving skills.</li>
<li>Ability to effectively communicate with multidisciplinary teams. Excellent technical skills and writing.</li>
<li>Strong knowledge of LEAN manufacturing principles preferred. </li>
<li>Strong knowledge of 21CFR 1271 regulations and AATB guidelines.</li>
<li>Highly proficient in project planning software. Microsoft Project preferred.</li>
<li>CTBS certified (or certified within two years of employment). </li>
<li>Strong work ethics. </li>
</ul>
Working conditions
Job requires working in office. Must be willing to work weekends and evening hours, as necessary. Must be willing to accommodate travel, if necessary. The job may require work to be performed inside the controlled clean room processing area where the engineer would be exposed to tissue processing.
 
Physical requirements
Job is one where the incumbent is required to stand for extended periods of time, lift heavy objects, and do repetitive tasks with few breaks while executing engineering plans.
 
Direct reports
Intern
 
Nothing in this job description restricts management’s right to assign or reassign duties and 
responsibilities to this job any time. 
Vivex Biologics, Inc. is an equal opportunity employer (EEO) and expressly prohibits any form of workplace discrimination and/or harassment based on race, color, religion, gender, sexual orientation, gender identity or expression, national origin, age, genetic information, disability, or veteran status. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, transfers, leaves of absence, compensation, and training.
Vivex Biologics complies with the Americans with Disability Act (ADA) which prohibits discrimination against qualified individuals with disabilities who, with or without reasonable accommodation, can perform the essential functions of a job.

Process Engineer II

<h3>Job Description</h3>
Job Description
 
MoFe Engineer
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>
</ul>
<ul>
<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.
 
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

MoFe Engineer

<h3>Job Description</h3>
Job DescriptionR&amp;D Sustaining Engineer
100% ONSITE - Westlake Village CA
(This role is not eligible for work visa sponsorship)
Caldera Medical’s Mission - To Improve the Quality of Life for Women!
 
Message from the Hiring Manager: The R&amp;D Sustaining Engineer will lead projects and provide technical expertise to ensure the ongoing reliability, compliance, and cost-effectiveness of our existing medical device products. This role is crucial for supporting products throughout their lifecycle by resolving manufacturing issues, implementing design changes, and leading continuous improvement initiatives. The engineer will collaborate with cross-functional teams, including manufacturing, quality, supply chain, and regulatory affairs, to address challenges and maintain product quality. 
Duties and Responsibilities: 
Project Leadership: Lead small to intermediate-sized sustaining engineering projects, including product and process improvements, cost reduction initiatives, and component obsolescence management.
Manufacturing Support: Act a primary R&amp;D resource for manufacturing and production issues. Work closely with the manufacturing engineering team to troubleshoot and perform root cause analysis on product and process failures and implement effective corrective and preventive actions (CAPAs).
Design and Process Changes: Coordinate and complete the following as needed for all sustaining engineering objectives:
a. Project Schedule
b. Quality and Regulatory documents
c. Labeling and IFU changes
d. Design Requirements - Trace Matrix
e. Design Specifications - Trace Matrix
f. Real Time Aging retention, testing
g. V&amp;V testing, documentation
h. Testing protocols and reports
i. Support Engineering Evaluation of returned product when needed.
j. Competitive product evaluation including standard testing
k. Support change Orders, technical review, implementation when needed
 Required Knowledge, Skills and Abilities:
Education: Bachelor's degree in Biomedical Engineering, Mechanical Engineering, Electrical Engineering, or a related field.
Experience: 4+years of experience in a regulated industry, with a strong emphasis on medical device product development or sustaining engineering. Experience with Class II or Class III medical devices is preferred. Experience in medical device component and material processing, design, and manufacturing. A comprehensive understanding of ISO, GMP and FDA regulations for the development.
Other Requirements:
1. Strong analytical and problem-solving skills and comprehensive understanding of design control processes, risk management, and validation of processes/designs.
2. Proven project management skills.
3. Experience with lean manufacturing and continuous improvement methodologies
4. Effective verbal, presentation and written communication skills.
5. Proficient in Microsoft Office, and MS project.
6. Working experience in Solidworks.
7. Working knowledge of medical device development, sterilization requirements and techniques, and medical device regulations.
8. Additional responsibilities may be assigned as needed to support business objectives.
Travel Required
<ul>
<li>10%</li>
</ul>
Competitive Compensation, Comprehensive Benefits, and more!
<ul>
<li>100k-$120k Annual Salary</li>
<li>Medical and Dental Benefits – 75% paid for employee and family members</li>
<li>Vision Coverage</li>
<li>401(k) with 4% matching contributions after 90 days of employment</li>
<li>Basic Life and AD&amp;D</li>
<li>Unlimited Vacation Policy</li>
<li>6 Weeks Paid Maternity Leave</li>
<li>10 paid holidays- including your birthday!</li>
<li>Being surrounded by amazing people!</li>
</ul>
(This role is being filled directly by our in-house recruiting team. We are not working with outside agencies for this position.)
Our Culture- Where Career and Passion come together!
<ul>
<li>A Culture of family and team… not a corporate goliath where you’re just another number.</li>
<li>All employees get a seat at the table and have influence with management. We care about giving back to the community. Our team donates time to helping local charities throughout Southern California.</li>
<li>The Women’s Health Initiative is the heart of what we do, every day we put underprivileged women first.</li>
<li>Our goal is to treat 1 million women suffering from incontinence by 2027!</li>
</ul>
Who is Caldera Medical?
Caldera Medical is a growth stage medical device company dedicated to improving the quality of life for women. In 2018, Caldera was ranked one of Inc 5000’s fastest growing private companies in the United States and was ranked #38 fastest growing private company and #3 fastest growing Healthcare Company in Los Angeles by the LA Business Journal. We develop and market differentiated surgical implants specifically for the treatment of Stress Urinary Incontinence and Pelvic Organ Prolapse. Our products are used by Urogynecologists, Gynecologists, and Urologists worldwide.
Caldera Medical is an equal opportunity employer and considers all candidates for employment regardless of race, color, religion, sex, national origin, citizenship, age, disability, marital status, military or veteran's status (including protected veterans, as may be required by federal law), sexual orientation, gender identity or any other category protected by law.

R&D Sustaining Engineer

<h3>Job Description</h3>
Job Description 
Location: Bethesda, MD 
Work Type: Hybrid Work (Minimum 2 Days Onsite) 
Required Clearance: Ability to obtain Public Trust 
LCG, Inc. provides insight into the impact of public programs that advance our society. For more than 20 years, LCG, Inc. has been a leading provider of technology-based consulting services, biomedical research support, grants management, decision analytics, software engineering and IT operations that enhance the transparency, efficiency, and empowerment of programs with health and science missions 
Job Title: Scientific Systems Integration Engineer 
Job Overview: The Scientific Systems Integration Engineer provides strategic and technical leadership in the design, configuration, and management of complex biomedical informatics systems, with a focus on terminology processing, semantic data integration, and ontology-based software environments. This role supports key infrastructure such as the NCI Thesaurus and Metathesaurus by ensuring the quality, scalability, and semantic integrity of information systems used across cancer research and public health informatics domains. 
Key Responsibilities 
Strategic Systems Consulting 
<ul>
<li>Serve as a senior consultant on complex IT and scientific informatics projects, advising stakeholders on system architecture, technical methodologies, and automation strategies for biomedical information processing. </li>
<li>Participate in high-level studies and analyses to support the planning, acquisition, and implementation of major system components and modifications. </li>
<li>Lead feasibility assessments, develop functional specifications, and evaluate system security and integration concerns. </li>
</ul>
MEME5 and Terminology Management 
<ul>
<li>Configure, operate, and update MEME5 software for terminology development, including managing source insertions, inversions, and UMLS updates. </li>
<li>Execute and manage the full MEME5 production cycle for the NCI Metathesaurus. </li>
<li>Run QA scripts and export to Rich Release Format (RRF), converting for NCI-specific Metathesaurus loads. </li>
</ul>
NCI Thesaurus and Semantic Infrastructure 
<ul>
<li>Support development and maintenance of the NCI Thesaurus by producing configuration scripts, evaluating software, and managing linked data and RDF-based components. </li>
<li>Work closely with software developers, DBAs, and QA specialists to support the EVS terminology server and search applications. </li>
<li>Maintain and enhance EVS semantic systems, including Triplestore databases, OWL ontologies, and SPARQL query operations. </li>
</ul>
Application Configuration and Cloud Integration 
<ul>
<li>Assist in the development and configuration of client-server Java systems and web applications used in semantic processing. </li>
<li>Collaborate with DevOps teams to ensure Elasticsearch-based EVS search engine indexing is optimized and stable in a cloud-based environment. </li>
</ul>
Communication and Documentation 
<ul>
<li>Prepare technical reports, feasibility studies, executive presentations, and system documentation. </li>
<li>Serve as a point of contact for scientific and technical inquiries, bridging domain expertise and IT implementation. </li>
</ul>
Qualifications 
<ul>
<li>Advanced degree in Computer Science, Information Systems, Engineering, Library Sciences, or a related scientific or technical discipline. </li>
<li>Minimum of ten (10) years of progressive professional experience in systems analysis, configuration, and scientific informatics. </li>
<li>Familiarity with terminology systems such as the NCI Metathesaurus and NCI Thesaurus. </li>
<li>Proficiency in description logic tools, OWL2, and RDF/linked data. </li>
<li>Experience with Triplestore technology and SPARQL. </li>
<li>Understanding of Elasticsearch configuration in a cloud-based environment. </li>
<li>Ability to coordinate across multidisciplinary teams, including software engineers, informaticians, and system administrators. </li>
<li>Demonstrated ability to lead and manage large-scale system implementation efforts. </li>
<li>Experience configuring and running MEME5 production cycles. </li>
<li>Strong scripting skills for data analysis, configuration, and automation tasks. </li>
<li>Analytical thinker with deep technical knowledge and systems-level insight. </li>
<li>Effective communicator who can translate complex technical topics into strategic decisions. </li>
<li>Detail-oriented problem-solver comfortable in high-stakes, high-visibility environments. </li>
</ul>
Compensation and Benefits 
The projected compensation range for this position is $90,000 to $130,000 per year benchmarked in the Washington, D.C. metropolitan area. Salary at LCG is determined by various factors, including but not limited to role, location, the combination of education/training, knowledge, skills, competencies, certifications, and work experience. 
LCG offers a competitive, comprehensive benefits package which includes health insurance options (medical, dental, vision), life and disability insurance, retirement plan contributions, as well as paid leave, federal holidays, professional development, and lifestyle benefits. 
Devoted to Fair and Inclusive Practices 
All qualified applicants will receive consideration for employment without regard to sex, race, ethnicity, age, national origin, citizenship, religion, physical or mental disability, medical condition, genetic information, pregnancy, family structure, marital status, ancestry, domestic partner status, sexual orientation, gender identity or expression, veteran or military status, or any other basis prohibited by law. 
If you are interested in applying for employment with LCG and need special assistance or an accommodation to apply for a posted position, contact our Human Resources department by email at <a href="mailto:hr@lcginc.com" target="_blank">hr@lcginc.com</a>. 
Securing Your Data 
Beware of fraudulent job offers using LCG's name. LCG will never request payment-related details or advancement of money during the application process. Legitimate communication will only come from lcginc.com or <a href="mailto:system@hirebridgemail.com" target="_blank">system@hirebridgemail.com</a> emails, not free commercial services like Gmail or WhatsApp. If you receive suspicious emails asking for payment or personal information, contact us immediately at <a href="mailto:hr@lcginc.com" target="_blank">hr@lcginc.com</a>. 
If you believe you are the victim of a scam, contact your local law enforcement and report the incident to the U.S. Federal Trade Commission.

Scientific Systems Integration Engineer

<h3>Job Description</h3>
Job Description 
Location: Bethesda, MD 
Work Type: Hybrid Work (Minimum 2 Days Onsite) 
Required Clearance: Ability to obtain Public Trust 
LCG, Inc. provides insight into the impact of public programs that advance our society. For more than 20 years, LCG, Inc. has been a leading provider of technology-based consulting services, biomedical research support, grants management, decision analytics, software engineering and IT operations that enhance the transparency, efficiency, and empowerment of programs with health and science missions 
Job Title: Senior Scientific Software Engineer 
Job Summary: The Senior Scientific Software Engineer is a technical and strategic leader responsible for the design, implementation, and management of advanced software applications and systems in support of biomedical and scientific informatics initiatives. This role demands extensive experience in full-stack Java development, terminology systems, cloud-based architecture, and biomedical data standards. The candidate will serve as a task lead and subject matter expert, contributing to the successful delivery of highly complex systems and applications used across scientific research and public health domains. 
Key Responsibilities 
Project and Systems Leadership
<ul>
<li>Lead software development life cycle (SDLC) activities including planning, analysis, design, implementation, testing, documentation, and delivery. </li>
<li>Serve as the day-to-day point of contact for assigned development tasks and lead cross-functional teams to ensure timely and high-quality deliverables. </li>
<li>Interpret complex technical and scientific requirements and translate them into effective software solutions. </li>
<li>Act as a senior advisor to customers and stakeholders on technical architecture, software strategies, and research applications. </li>
<li>Oversee project reporting and resource allocation, ensuring alignment with scope, objectives, and milestones. </li>
</ul>
Development and Technical Expertise 
<ul>
<li>Design, develop, test, and implement robust and scalable Java-based web applications, including both front-end and back-end components. </li>
<li>Develop applications using modern frameworks such as the Spring Framework, integrating open-source tools and libraries. </li>
<li>Maintain secure development practices, analyzing and addressing security vulnerabilities in applications. </li>
<li>Implement and manage terminology editing tools and processes, particularly those based in OWL and description logic. </li>
<li>Configure, manage, and operate MEME software, including experience running full MEME production cycles for systems such as the NCI Metathesaurus. </li>
<li>Utilize Triplestore databases and write advanced SPARQL queries for semantic data retrieval and processing. </li>
<li>Manage source code using Git/GitHub and automate builds and deployments using Jenkins CI/CD pipelines. </li>
<li>Work comfortably within Linux environments and utilize command-line tools for configuration, monitoring, and debugging. </li>
<li>Support development in cloud-based environments (e.g., AWS), focusing on scalability, performance, and integration. </li>
</ul>
Terminology and Semantic Integration 
<ul>
<li>Apply knowledge of biomedical vocabularies and ontologies such as LOINC, ICD-9/10, ICD-O, Gene Ontology, and SNOMED. </li>
<li>Participate in ontology modeling and terminology development efforts using OWL and other semantic standards. </li>
<li>Collaborate with biomedical content specialists and informatics teams to align application functionality with domain-specific semantic needs. </li>
</ul>
Qualifications 
<ul>
<li> Bachelor’s degree (BA or BS) in Computer Science, Information Systems, Engineering, or related technical or scientific discipline.</li>
<li>Minimum of ten (10) years of progressive experience in scientific software development and systems analysis.</li>
<li>Familiarity with biomedical informatics or scientific research environments.</li>
<li>Experience with description logic-based systems and editing tools (e.g., Protégé). </li>
<li>Proficiency in Triplestore technologies and semantic query languages (e.g., SPARQL). </li>
<li>Experience in DevOps, cloud infrastructure (e.g., AWS), and containerization tools. </li>
<li>Knowledge of biomedical terminologies including but not limited to LOINC, ICD9/10, SNOMED CT, and Gene Ontology. </li>
<li>Proven expertise in full-stack Java application development, including Spring Framework. </li>
<li>Experience working with terminology/ontology tools and systems, including MEME and OWL-based editors. </li>
<li>Strong analytical and problem-solving skills with ability to translate scientific needs into technical solutions.</li>
<li>Excellent communication and leadership skills for interfacing with clients, team members, and stakeholders. </li>
</ul>
Compensation and Benefits 
The projected compensation range for this position is $90,000 to $130,000 per year benchmarked in the Washington, D.C. metropolitan area. Salary at LCG is determined by various factors, including but not limited to role, location, the combination of education/training, knowledge, skills, competencies, certifications, and work experience. 
LCG offers a competitive, comprehensive benefits package which includes health insurance options (medical, dental, vision), life and disability insurance, retirement plan contributions, as well as paid leave, federal holidays, professional development, and lifestyle benefits. 
Devoted to Fair and Inclusive Practices 
All qualified applicants will receive consideration for employment without regard to sex, race, ethnicity, age, national origin, citizenship, religion, physical or mental disability, medical condition, genetic information, pregnancy, family structure, marital status, ancestry, domestic partner status, sexual orientation, gender identity or expression, veteran or military status, or any other basis prohibited by law. 
If you are interested in applying for employment with LCG and need special assistance or an accommodation to apply for a posted position, contact our Human Resources department by email at <a href="mailto:hr@lcginc.com" target="_blank">hr@lcginc.com</a>. 
Securing Your Data 
Beware of fraudulent job offers using LCG's name. LCG will never request payment-related details or advancement of money during the application process. Legitimate communication will only come from lcginc.com or <a href="mailto:system@hirebridgemail.com" target="_blank">system@hirebridgemail.com</a> emails, not free commercial services like Gmail or WhatsApp. If you receive suspicious emails asking for payment or personal information, contact us immediately at <a href="mailto:hr@lcginc.com" target="_blank">hr@lcginc.com</a>. 
If you believe you are the victim of a scam, contact your local law enforcement and report the incident to the U.S. Federal Trade Commission.

Senior Scientific Software Engineer

<h3>Job Description</h3>
Job Description 
Location: Bethesda, MD 
Work Type: Hybrid Work (Minimum 2 Days Onsite) 
Required Clearance: Ability to obtain Public Trust 
LCG, Inc. provides insight into the impact of public programs that advance our society. For more than 20 years, LCG, Inc. has been a leading provider of technology-based consulting services, biomedical research support, grants management, decision analytics, software engineering and IT operations that enhance the transparency, efficiency, and empowerment of programs with health and science missions 
Job Title: Scientific Software Engineer, Associate 
Job Summary: The Associate Scientific Engineer supports the design, development, and maintenance of software applications and systems for biomedical and scientific informatics initiatives. This role requires a solid foundation in full-stack Java development, a working knowledge of terminology systems and semantic technologies, and a strong interest in contributing to public health and research infrastructure. The candidate will work under the guidance of senior engineers and scientists, supporting the successful delivery of systems and services that enhance biomedical data integration, analysis, and standards adoption. 
Key Responsibilities 
Technical Support and Development
<ul>
<li>Assist in the development and maintenance of Java-based web applications, supporting both front-end and back-end components. </li>
<li>Participate in the software development life cycle (SDLC), including requirements gathering, coding, testing, debugging, and documentation. </li>
<li>Use frameworks such as Spring and open-source libraries to build scalable and maintainable applications. </li>
<li>Help identify and resolve software bugs and participate in vulnerability mitigation tasks. </li>
</ul>
Semantic Technologies and Terminology Support
<ul>
<li>Support the configuration and operation of terminology development tools such as MEME and Protégé. </li>
<li>Assist in implementing and managing OWL-based ontologies and participate in quality control processes. </li>
<li>Work with Triplestore technologies and write SPARQL queries under senior staff guidance. </li>
</ul>
Collaboration and Communication
<ul>
<li>Collaborate with technical teams and biomedical domain experts to ensure alignment of system functionality with scientific and data standards requirements. </li>
<li>Contribute to internal documentation, reports, and technical deliverables. </li>
<li>Participate in team meetings and status reviews to report progress and identify blockers. </li>
</ul>
Infrastructure and Deployment
<ul>
<li>Use Git/GitHub for source control and Jenkins for automated build and deployment processes. </li>
<li>Operate within Linux environments for basic configuration and troubleshooting tasks. </li>
<li>Learn and support deployment activities in cloud-based environments (e.g., AWS). </li>
</ul>
Qualifications
<ul>
<li>Bachelor’s degree (BA or BS) in Computer Science, Information Systems, Engineering, or a related technical or scientific discipline. </li>
<li>3–5 years of experience in software development, ideally in biomedical or scientific environments. </li>
<li>Experience in Java development and working knowledge of frameworks such as Spring. </li>
<li>Familiarity with Git, Jenkins, and Linux command-line tools. </li>
<li>Understanding of software security best practices. </li>
<li>Exposure to or experience with biomedical informatics, ontologies, or terminology standards (e.g., SNOMED, LOINC, ICD, Gene Ontology). </li>
<li>Experience or coursework in semantic technologies (OWL, RDF, SPARQL). </li>
<li>Familiarity with cloud computing services and environments such as AWS. </li>
<li>Experience supporting ontology editing tools such as Protégé and terminology management tools such as MEME. </li>
<li>Strong written and verbal communication skills, with an interest in collaborative development. </li>
<li>Eager to learn and grow within a fast-paced, research-oriented environment. </li>
<li>Comfortable working in a team setting and accepting direction from senior team members. </li>
<li>Detail-oriented with strong organizational skills and a proactive attitude toward problem-solving. </li>
</ul>
Compensation and Benefits 
The projected compensation range for this position is $90,000 to $130,000 per year benchmarked in the Washington, D.C. metropolitan area. Salary at LCG is determined by various factors, including but not limited to role, location, the combination of education/training, knowledge, skills, competencies, certifications, and work experience. 
LCG offers a competitive, comprehensive benefits package which includes health insurance options (medical, dental, vision), life and disability insurance, retirement plan contributions, as well as paid leave, federal holidays, professional development, and lifestyle benefits. 
Devoted to Fair and Inclusive Practices
All qualified applicants will receive consideration for employment without regard to sex, race, ethnicity, age, national origin, citizenship, religion, physical or mental disability, medical condition, genetic information, pregnancy, family structure, marital status, ancestry, domestic partner status, sexual orientation, gender identity or expression, veteran or military status, or any other basis prohibited by law. 
If you are interested in applying for employment with LCG and need special assistance or an accommodation to apply for a posted position, contact our Human Resources department by email at <a href="mailto:hr@lcginc.com" target="_blank">hr@lcginc.com</a>. 
Securing Your Data 
Beware of fraudulent job offers using LCG's name. LCG will never request payment-related details or advancement of money during the application process. Legitimate communication will only come from lcginc.com or <a href="mailto:system@hirebridgemail.com" target="_blank">system@hirebridgemail.com</a> emails, not free commercial services like Gmail or WhatsApp. If you receive suspicious emails asking for payment or personal information, contact us immediately at <a href="mailto:hr@lcginc.com" target="_blank">hr@lcginc.com</a>. 
If you believe you are the victim of a scam, contact your local law enforcement and report the incident to the U.S. Federal Trade Commission

Scientific Software Engineer, Associate

<h3>Job Description</h3>
Job DescriptionOpen to: General Public Work Week:&nbsp;NE (35-hour) Work Week Salary:$66,894.99 (Non-negotiable) Opening Date: 9/24/2025 Closing Date:&nbsp;When all vacancies are filled Existing Vacancies: TBD Program/Location Department of Environmental Protection Air, Energy, &amp; Materials Sustainability&nbsp; Air Quality and Radiation Protection&nbsp; 401 East State Street Trenton, NJ 08625 NJ Department of Environmental Protection Air, Energy, &amp; Materials Sustainability&nbsp; Sustainable Waste Management&nbsp;&nbsp; 401 East State Street Trenton, NJ 08625 NJ Department of Environmental Protection Air, Energy, &amp; Materials Sustainability&nbsp; Climate Change Mitigation &amp; Monitoring &nbsp;&nbsp;&nbsp; 401 East State Street Trenton, NJ 08625 Scope of Eligibility Open to applicants who meet the requirements below. Description Under the close supervision of a supervisory official, in an Environmental Engineering Program in a State department, institution, agency, or local government agency, learns to conduct routine surveys, studies, inspections, and/or investigations relating to the improvement and/or monitoring of environmental conditions; learns to review engineering plans; learns to gather data, and research and analyze information as it relates to the enforcement of environmental laws/regulations; does other related duties as required. Requirements Education:&nbsp; Graduation from an accredited college or university with a Bachelor’s degree in Civil, Chemical, Mechanical, Environmental, Ocean, Coastal, Bio-Resource, Biomedical, Sanitary, Industrial, Agricultural, or Mining Engineering, or other field of engineering related to the environment. NOTE:&nbsp; An Engineer-In-Training (EIT) certification issued by the Division of Consumer Affairs, New Jersey Office of the Attorney General, may be substituted for the above education requirement.&nbsp; Applicants must submit proof of the EIT certification and the Fundamentals of Engineering (FE) exam results.&nbsp; The area of discipline indicated on the FE exam results must be in Chemical, Civil, Environmental, Industrial &amp; Systems, Mechanical, or other disciplines. NOTE:&nbsp; All U.S. degrees and transcripts must be from an accredited college or university.&nbsp; All foreign degrees and transcripts must be evaluated for accreditation by a recognized evaluation service by the closing date of this posting.&nbsp; Failure to provide documentation may result in ineligibility. License Appointees will be required to possess a driver's license valid in New Jersey only if the operation of a vehicle, rather than employee mobility, is necessary to perform the essential duties of the position. SAME Applicants If you are applying under the NJ SAME program, your supporting documents (Schedule A or B letter) must be submitted along with your resume by the closing date indicated above. For more information on the SAME program, please visit SAME Program, email <a href="mailto:SAME@csc.nj.gov" target="_blank">SAME@csc.nj.gov</a>, or call CSC at (609) 292-4144 and select Option #3. Veteran's Preference To qualify for New Jersey Veteran's Preference/status, you must establish Veteran's Preference through the Department of Military and Veteran's Affairs. Please submit proof of your Veteran's Preference along with your resume as indicated. For more information, please visit <a href="https://www.nj.gov/military/veterans/services/civil-service-preference/" target="_blank">https://www.nj.gov/military/veterans/services/civil-service-preference/</a> Residency All persons newly hired on or after September 1, 2011, have one year from the date of employment to establish, and then maintain principal residence in the State of New Jersey subject to the provisions of N.J.S.A. 52:14-7 (L.2011, Chapter 70), also known as the “New Jersey First Act”. Benefits As a New Jersey State Department, NJDEP offers a comprehensive benefits package that includes:&nbsp;
<ul>
<li>Paid Benefit Leave</li>
<li>Holiday Pay</li>
<li>Alternative Workweek Program*</li>
<li>Telework*</li>
<li>Pension</li>
<li>Deferred Compensation</li>
<li>Health Benefits (medical, prescription drug, dental &amp; vision care) and Life Insurance</li>
<li>Flexible and Health Spending Accounts (FSA/HSA)</li>
<li>Commuter Tax Savings Program</li>
<li>Public Service Loan Forgiveness (PSLF)</li>
<li>Tuition Reimbursement*</li>
</ul>
*Pursuant to the State/Department's policy, procedures, and/or guidelines. Authorization to Work Selected candidates must be authorized to work in the United States per the Department of Homeland Security, United States Citizenship, and Immigration Services regulations. NOTE: The State of New Jersey does not provide sponsorship for citizenship to the United States. Equal Opportunity Employment The State of New Jersey seeks to increase the richness and diversity of its workforce, and in doing so, become the employer of choice for all people seeking to work in State Government.&nbsp; To evaluate the effectiveness of our efforts to attract and employ a diverse workforce, applicants are asked to voluntarily answer a few brief questions on the NJ Affirmative Action Information Form.&nbsp; All information is considered confidential and will be filed separately with the agency's affirmative action officer.&nbsp; This information will not be part of your application for employment and will not be considered in any hiring decision.&nbsp; &nbsp;
DEP Notices of Vacancy have a 4:00 p.m. deadline on the closing date. When filing for these opportunities, please be sure to have your letter of interest and credentials sent electronically before 4 p.m. on the closing date.
The New Jersey Department of Environmental Protection is an Equal Opportunity Employer and is committed to inclusive hiring and a diverse workforce. We strongly encourage people from all backgrounds to apply. Accommodations under ADA will be provided upon request.
Powered by JazzHR
Q5kc5D4pWX

731 biomedical engineer Jobs