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<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 Description
We are looking for a Quality Engineer I to support the Quality Management System, design improvements and activities, analyze manufacturing processes to overall improve and maintain the quality standards of all Argen products. 
 
Schedule: M-F, 8:30 AM - 5:00 PM 
Location: 5855 Oberlin Dr. San Diego, CA 92121 
The day-to-day:
<ul>
<li>Coordinates with quality and engineering personnel to assure compliance to internal policies and procedures as well as to applicable external standards (GMP, QSR, ISO 13485, MDR, etc.).</li>
<li>Performs quality review and approval of regulated documentation including, but not limited to, part/component/system inspection reports, nonconforming material reports, deviations, engineering change orders, engineering change reports, and engineering work orders. </li>
<li>Reviews and approves supplier documentation (protocols, reports, specifications, etc.), as defined in the Quality Agreement. </li>
<li>Responsible for adherence to supplier and customer Quality Agreement provisions.</li>
<li>Interfaces with customer on quality activities.</li>
<li>Verifies, creates and/or revises SOPs, work instructions and associated forms, and participates in the implementation of these procedures.</li>
<li>Verifies engineering tests and measurement practices for new and existing products using appropriate tools (FMEA, DOE, SPC, Risk analysis, Process Capability).</li>
<li>Manages the CAPA, Complaints, Non-Conforming Material, Deviation systems; including generating Quality metrics.</li>
<li>Reviews and supports the generation of engineering specifications to assure that adequate quality assurance requirements are met.</li>
<li>Reviews drawings for adherence to design inputs, design control procedures, regulatory standards and quality system requirements.</li>
<li>Provides Quality oversight for Product Release and shipping activities.</li>
<li>Provides quality guidance and support to other departments.</li>
<li>Performs quality engineering activities for design changes to existing product designs by assisting engineering in the preparation of plans and DHF documentation.</li>
<li>Assists manufacturing in NPI activities.</li>
<li>Creates SOP’s and update exiting SOP’s.</li>
<li>Assists in the preparation of regulatory submissions to the U. S. FDA and other regulatory agencies.</li>
<li>Reviews and approves Device History Records for finished device release as required.</li>
<li>Serves as a technical resource for technicians, assemblers, and other Argen personnel</li>
</ul>
 
What does it take to be successful:
<ul>
<li>Successful Supplier Management (SCARs, Evaluations, scorecards)</li>
<li>Calibration ( prior experience in maintaining or supporting calibration activities).</li>
<li>Validation (IQ, OQ, PQ).</li>
<li>Bachelor’s degree in Quality Engineering, Quality Assurance, Biomedical Engineering or an equivalent degree from an accredited institution is required and 1-2 years’ experience in medical device quality engineer related work or equivalent experience in quality system such as ISO 9001; or Master’s degree with 1+ years’ experience</li>
</ul>
 
Other Important Qualifications: 
<ul>
<li>Demonstrated understanding of medical device design and process controls per FDA Quality System Requirements (QSRs)</li>
<li>Knowledge of cGMP regulations ISO 13485, 21CFR Part 820, CMDR SOR/98-282, 93/42/EEC, RDC 16 2013, MHLW MO 169 and TG(MD)R Sch3 preferred</li>
<li>Demonstrated understanding of required standards / regulations impacting medical devices </li>
<li>Knowledge of PFM, Crown and Bridge applications and their use in the dental lab is a plus </li>
<li>ASQ CQE certification is a plus</li>
</ul>
 
Our Awesome Benefits!
<ul>
<li>Medical, dental and vision Plans</li>
<li>401k with Employer Match</li>
<li>PTO</li>
<li>Employee Events</li>
<li>Wellness Programs</li>
<li>Discounts for home, travel, entertainment and relaxation!</li>
</ul>
 
About Us
At Argen, we’re in the business of creating healthy, confident smiles one case at a time. We are 500 team members strong. Founded more than 50 years ago as a precious metals company in South Africa, Argen has grown to become the largest dental zirconia manufacturer in North America, largest dental alloy provider worldwide, and leader in digital dentistry solutions with diverse product offerings. Our 140,000 square foot manufacturing center houses more than 150 3D printing and milling machines and operates six days a week. Argen embodies a culture of innovation, continuous improvement, and LEAN practices in support of our mission to help our dental laboratory customers succeed.

Quality Engineer I

<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.
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AEMS-2025-24 Environmental Engineer Trainee

<h3>Job Description</h3>
Job DescriptionDescriptionPrecision Neuroscience is pioneering a brain implant, known as a brain-computer interface (BCI), to restore communication and independence for people with neurological conditions. Our cutting-edge technology is designed to empower people with paralysis to control digital devices—such as computers and smartphones—with their thoughts alone, opening new possibilities for daily life.&nbsp;&nbsp;Precision’s multidisciplinary team brings together leading experts in diverse fields such as neurosurgery, artificial intelligence, machine learning, microfabrication, electrical engineering, and more. We are committed to turning breakthrough scientific advancements into real-world solutions for people affected by conditions such as spinal cord injury, stroke, and ALS. &nbsp; As a Precision employee, you will be joining one of the fastest moving and best-capitalized companies in the emerging field of BCI. Since our founding in 2021, Precision has secured over $155 million in funding, developed and validated our technology, and initiated human trials in collaboration with some of the nation’s top hospitals. We are seeking a Senior Mechanical Engineer to join our Implant Hardware team to design scalable solutions to chronically implanted electronics. This position will best suit someone who is experienced with mechanical design of Class III medical devices with implantable electronics such as IPG, DBS, spinal cord stimulator, cochlear implants, etc. This is an extraordinary opportunity to join our core team to help shape the future of our company. Your work will see commercialization quickly so that we improve the lives of patients who live with neurological disorders in a matter of months and years, not decades. This position is on-site at our Manhattan office. To be eligible for this role, you must currently be based in the United States, and have working rights. Key Responsibilities
<ul>
<li>Execute hands-on design, testing, and process development tasks for mechanical packaging of implantable electronic components.&nbsp;</li>
<li>Complete hands-on assembly, integration and testing tasks while ensuring rigorous quality control is being enforced.</li>
<li>Collaborate with the rest of our team to publish and present our work.</li>
<li>Create and update end-user technical documentation, product specifications and vendor procedures to ensure we are compliant with relevant regulations.</li>
</ul>
 Skills, Knowledge and Expertise
<ul>
<li>BS/MS in Mechanical Engineering (ME), Biomedical Engineering (BME) or similar.</li>
<li>5+ years of industry experience in mechanical engineering roles, preferably in the medical device industry.</li>
<li>Experience designing parts for CNC, injection molding, 3D printing, and die stamping manufacturing techniques.&nbsp;</li>
<li>Experience designing class III medical devices with implantable electronics</li>
<li>Experience with medical leads, connectors, and feedthroughs.&nbsp;</li>
<li>Experience designing, evaluating, and debugging hermetic seals, laser welded/brazed joints, and thick film metalization.</li>
<li>Experience with compression molding, liquid injection molding, or overmolding</li>
<li>Excellent organizational and communication skills; able to collaborate with neuroscientists, neurosurgeons, and electrical, software, materials, and bio engineers.</li>
<li>Expert in CAD (we use SolidWorks) and finite element analysis FEA</li>
<li>Track record of working towards accelerated timelines.</li>
<li>You should be comfortable with creative problem solving, collaborating, and taking charge of projects from concept to production.</li>
</ul>
 Diverse workforces create the best culture, company, and products. We at Precision are committed to an inclusive culture that celebrates the uniqueness and contributions of everyone.&nbsp; As an equal opportunity employer, Precision does not discriminate on the basis of sex, race, religion, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Senior Mechanical Engineer (Implant Hardware)

<h3>Job Description</h3>
Robotics Engineer and Interdisciplinary Scientist The Opportunity: To achieve an organization's mission, leaders need strong team members who can create processes, communicate requirements, and develop innovative solutions throughout the execution of the mission. Whether completing an immediate task, recognizing a process gap, recommending a solution, or flexing to support an immerging requirement, our clients need someone who can help manage operations while managing responses to external inquiries in a timely manner. That is why we need an experienced Robotics Engineer like you who can help conceptualize, create, and execute government funded research and development programs. As part of our team, you'll serve as a strategic technical advisor to the Advanced Research Projects Agency for Health ( ARPA-H ) , helping conceptualize, create, and execute advanced government-funded research and development programs to accelerate better health outcomes for everyone. You'll work with world-class scientists and engineers to support the development of high-impact solutions to society's most challenging health problems, and leverage technical expertise to provide strategic assessments of new technologies in support to senior ARPA-H decision makers. You'll maintain responsibility for producing and presenting findings and recommendations to a team of colleagues and clients on the feasibility and potential impact of future research programs, assisting with the management of current programs, and facilitating commer cia lization of successfully developed technologies. You'll support the research and development of robotic and unmanned systems across multiple operational domains and mission areas. You will be responsible for managing incoming requirements, facilitating e nga gements within offices and across the agency, and be readily available to shift your focus to fulfill emerging client requests. Your attention to detail, flexibility, communication skills, understanding of the client's mission, and problem-solving will enable the mission's success. Join us. The world can't wait. You Have: 
<ul>\n
<li>Experience interacting and communicating with senior-level executives, including SES or GS-15</li>
\n
<li>Experience using Micro sof t Office programs, including Excel, Word, and PowerPoint</li>
\n
<li>Ability to operate independently within a fast-paced, start-up environment</li>
\n
<li> Ability to obtain and maintain a Public Trust or Suitability/Fitness determination based on client requirements </li>
\n
<li>Master's degree in an EE, Mechanical Engineering, CS, Robotics, or Biomedical Engineering field and 5+ years of experience with engineering robotics or devices, or Doctorate degree in an EE, Mechanical Engineering, CS, Robotics, or Biomedical Engineering field and 2+ years of experience with engineering robotics or devices</li>
\n</ul>
\n Nice If You Have: 
<ul>\n
<li>Experience with programming languages such as Python, C++, Java, and MATLAB</li>
\n
<li>Experience with circuit design, microcontrollers, and embedded systems for robotic systems</li>
\n
<li>Experience with sensor or actuator integration and data fusion for simultaneous localization, mapping, and planning</li>
\n
<li>Experience with robotic operating systems for simulation, visualization, and communication between different components</li>
\n
<li>Experience with User- Center ed Design for customer needs-driven engineering development </li>
\n
<li>Experience supporting commer cia l innovation center s, university applied robotics center s, ARPA-like programs such as DARPA, IARPA, or APRA-E, or U.S. DoD advanced development programs</li>
\n
<li>Knowledge of AI and ML techniques for developing intelligent behaviors and robotic decision-making processes </li>
\n
<li>Possession of excellent verbal and written communication skills</li>
\n</ul>
\n Vetting: Applicants selected will be subject to a government investigation and may need to meet eligibility requirements of the U.S. government client . Compensation At Booz Allen, we celebrate your contributions, provide you with opportunities and choices, and support your total well-being. Our offerings include health, life, disability, financial, and retirement benefits, as well as paid leave, professional development, tuition assistance, work-life programs, and dependent care. Our recognition awards program acknowledges employees for exceptional performance and superior demonstration of our values. Full-time and part-time employees working at least 20 hours a week on a regular basis are eligible to participate in Booz Allen's benefit programs. Individuals that do not meet the threshold are only eligible for select offerings, not inclusive of health benefits. We encourage you to learn more about our total benefits by visiting the Resource page on our Careers site and reviewing Our Employee Benefits page. Salary at Booz Allen is determined by various factors, including but not limited to location, the individual's particular combination of education, knowledge, skills, competencies, and experience, as well as contract-specific affordability and organizational requirements. The projected compensation range for this position is $99,000.00 to $225,000.00 (annualized USD). The estimate displayed represents the typical salary range for this position and is just one component of Booz Allen's total compensation package for employees. This posting will close within 90 days from the Posting Date. Identity Statement As part of the application process, you are expected to be on camera during interviews and assessments. We reserve the right to take your picture to verify your identity and prevent fraud. Work Model Our people-first culture prioritizes the benefits of flexibility and collaboration, whether that happens in person or remotely. 
<ul>\n
<li>If this position is listed as remote or hybrid, you'll periodically work from a Booz Allen or client site facility.</li>
\n
<li>If this position is listed as onsite, you'll work with colleagues and clients in person, as needed for the specific role.</li>
\n</ul>
\n Commitment to Non-Discrimination All qualified applicants will receive consideration for employment without regard to disability, status as a protected veteran or any other status protected by applicable federal, state, local, or international law.

Robotics Engineer and Interdisciplinary Scientist

<h3>Job Description</h3>
Job Description
Hi, I'm Yoav, the VP of Artificial Intelligence at EnsoData! I'm looking for an AI Engineer passionate about making healthcare better through use of the technology that powers EnsoData's systems. As an AI Engineer, you’ll design, develop, validate, and deploy AI systems used in real-world clinical settings. Your work will fuel products trusted by clinicians, by delivering safe, effective, and regulatory-compliant solutions. You’ll also have the opportunity to push the boundaries of healthcare AI through cutting-edge research, with pathways to publish in top peer-reviewed journals and present at leading conferences.
This is a role for ambitious engineers who thrive in a high-growth, fast-paced environment, want to see their work make a direct difference in patient care, and are eager to help shape the future of healthcare AI.
This hybrid/remote position offers a flexible work environment, competitive salary of $120,000 - $150,000 along with stock options and generous benefits, including paid time off.
About EnsoData
EnsoData strives to make healthcare more accurate, efficient, and affordable through waveform artificial intelligence (AI) technology. Using AI and machine learning, our software analyzes billions of data points collected from sensors placed throughout the human body. Our first solution, EnsoSleep, reduces the time clinicians spend analyzing, scoring and managing sleep studies. This results in a simplified and accelerated patient testing, diagnosis, and treatment workflow. Our AI-powered technology has the capability of informing health decisions beyond sleep medicine, from monitoring patient health in the ICU or through wearables, to detecting and capturing seizure data, to providing earlier detection of heart disease, diabetes, stroke, and Alzheimer’s.
Here is a little about what we are doing in the world of sleep medicine...
EnsoSleep - FDA-Cleared PSG and HSAT Scoring and Study Management
EnsoSleep PPG - FDA-Cleared, AI-Powered Sleep Diagnosis Using Pulse Oximeters
**Here is a link to learn a little about our Celeste app!
EnsoTherapy - AI-Powered PAP Therapy Adherence Support
Requirements
Qualifications
<ul>
<li>3+ years of hands-on ML experience, ideally in regulated or safety-critical domains.</li>
<li>Deep expertise in machine learning, deep learning, and modern data science methods.</li>
<li>Proficiency with physiological signals, time series, or sensor data.</li>
<li>Strong coding skills in Python, as well as proficiency with ML/DL libraries such as TensorFlow, PyTorch, and Scikit-learn.</li>
<li>Experience with medical data (imaging, physiological, EHR) a plus.</li>
<li>Experience with addressing model interpretability, bias, and real-world deployment challenges.</li>
<li>Familiarity with SaMD regulatory frameworks (FDA 510(k), MDSAP, ISO 13485) a plus.</li>
<li>Startup mindset: adaptable, resourceful, comfortable with autonomy, and impact-driven.</li>
</ul>
Education and Experience
<ul>
<li>B.Sc. or M.Sc. in Computer Science, Biomedical Engineering, Electrical Engineering, or related field (Ph.D. a plus).</li>
<li>Experience with cloud platforms (AWS, GCP) and containerization (Docker, Kubernetes).</li>
<li>Experience with data engineering tools such as BigQuery, Mongo, Airflow, Dagster.</li>
<li>Published research or patents in healthcare AI, and/or contributions to open source software</li>
</ul>
Company Culture - Embrace the Pineapple! 
How do we do this? <a href="https://www.ensodata.com/blog/why-the-pineapple/" target="_blank">https://www.ensodata.com/blog/why-the-pineapple/</a>
<ul>
<li>Make Healthcare Better - is passionate about moving healthcare to a better place for everyone everywhere</li>
<li>Put Customers First - delights customers by working closely with them to support their initiatives</li>
<li>Be a Great Teammate - spreads the good vibes and is a joy to work with; also understands the value of helping one's teammates</li>
<li>Gets $#!t Done - bias toward action and intrinsically motivated to go above and beyond; demonstrates the ability to work autonomously as well as across teams</li>
<li>We also practice a Focus on Quality and look for teammates who don't cut corners and demonstrate integrity and attention to detail</li>
</ul>
Benefits
The benefits package includes, but is not limited to, the following:
Remote and flexible schedule - we are a remote company with hybrid options and support for flexible schedules! That being said, we have an amazing office headquarters in downtown Madison, WI with views of the capitol that you are welcome to work at anytime. In case you didn't know, Madison has consistently been ranked as one of the top places to live in the US (businessinsider.com, money.com, livability.com)!
Health, dental, and vision insurance with options to choose a plan that fits you and your dependents needs. 
Paid time off options - we want our employees to rest, recharge, and feel better.
Stock options - we want team members to feel ownership in the organization. When EnsoData does well, you do well.
401k to help people invest in the future.
Team Summits! We look forward to opportunities to gather in person and enjoy a few days together. We participate in team events and gain some great in-person time. (Hint: check out our blog for info from former team gatherings!)
Interview Process
<ol>
<li>Submit a resume online and our hiring team will choose those that seem like the best candidates.</li>
<li>We look forward to meeting you face-to-face! A few candidates will be chosen for a video call to get to know each other, discuss your experience, and explain the position in more detail.</li>
<li>Expect an opportunity to show your skills.</li>
<li>The final candidates will have a chance to meet a few people from the team.</li>
<li>Offer!</li>
</ol>
Let’s talk 
EnsoData seeks to recruit, hire, and retain the most talented people from a diverse candidate pool. Research shows that while men apply to jobs when they meet an average of 60% of the criteria, women and other marginalized folks tend to only apply when they check every box. If you think you’re a great fit, but don't necessarily check every box on the job description, please still get in touch.
To learn more about our ongoing commitment to diversity, check here.
Note: this role is based in the continental United States and currently EnsoData is unable to support sponsorships so candidates must be legally eligible to work and reside in the United States now and in the future.
Equal Employment Opportunity 
EnsoData is proud to be an Equal Employment Opportunity employer. We do not discriminate against, nor do we tolerate unlawful harassment against, team members or any other covered persons on any basis of race, color, protective hairstyles, national, social, or ethnic origin, gender, pregnancy, childbirth, gender orientation, identity or expression, sexual, relationship, or romantic orientation, marital, civil union or domestic partnership status, family or parental status, age, protected veteran status, arrest record, expunged or sealed convictions, criminal history, source of income, credit history, housing status, physical, mental, or sensory disability, medical condition, genetic information, religion, or any other status protected by the laws or regulations in the locations where we operate.
We value, celebrate, and support diversity, inclusion, and our differences. We are committed to providing a safe work environment and a company culture of mutual respect where equal employment opportunities are available to all applicants and teammates. We seek to recruit, hire, and retain the most talented people from a diverse candidate pool. We strongly encourage women, people of color, LGBTQIA+ individuals, people with disabilities, members of ethnic minorities, intersectional individuals, foreign-born residents, and veterans to apply. We have a deep conviction that diversity and inclusion among our teams, our communities, and our physical and virtual workplaces is vital to the success of EnsoData’s mission to improve healthcare access, outcomes, and affordability for patients and communities everywhere globally.
If you are a job seeker applying to EnsoData and you feel that you need to request an accommodation or alternative application, please contact Angela at <a href="mailto:angela@ensodata.com" target="_blank">angela@ensodata.com</a>.

Artificial Intelligence Engineer

<h3>Job Description</h3>
Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Cepheid, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.&nbsp;
You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.
At Cepheid, we are passionate about improving health care through fast, accurate, molecular diagnostic systems and tests. As a member of our team, you’ll get to make an immediate, measurable impact on a global scale, within an environment that fosters career growth and development. Our mission drives us to develop groundbreaking solutions for the world’s most complex health challenges. Together, we bring MORE change to the world.
Learn about the Danaher Business System which makes everything possible.
The Senior Quality Engineer is responsible for driving manufacturing and product lifecycle quality by implementing a risk-based approach to ensure compliance with corporate policies, 21 CFR 820, ISO 13485, and other regulatory standards, while championing continuous improvement. You will play a pivotal role in New Product Introduction (NPI) and Change Control processes, ensuring accurate and complete quality deliverables during design transfer to manufacturing. This includes reviewing change orders and deviations to confirm clear, well-documented rationales and comprehensive impact assessments for significant changes. By developing robust qualification strategies, you will proactively mitigate risks associated with design and process modifications, enhancing product reliability and supporting innovative product development.
This position reports to the Sr Manager of Quality Engineering and is part of the Quality Engineering team located in Sunnyvale, CA, and will be an on-site role. &nbsp;
In this role, you will have the opportunity to:
<ul>
<li>
Lead quality engineering efforts for PCR-based assay development, including analytical method validation, reagent qualification, and system-level performance verification.
</li>
<li>
Serve as the primary Quality Engineering representative on cross-functional teams for new product introduction and manufacturing sustainment, providing strategic input on design control, risk management, and quality compliance.
</li>
<li>
Drive risk assessment activities including safety, design and process FMEA, with a focus on assay sensitivity, reagent compatibility, specificity, and robustness.
</li>
<li>
Create project-specific documents, such as validation master plans, risk management plans, and qualification protocols, to meet compliance requirements.
</li>
<li>
Address nonconformities and deviations through risk assessment, root cause identification, failure mode analysis, and proposing disposition.
</li>
</ul>
The essential requirements of the job include:
<ul>
<li>
BS degree in chemistry, molecular biology, biomedical engineering, or related field with 5+ years of quality engineering experience, master’s degree with 3+ years experience, OR Doctoral degree with 1+ year(s) experience.
</li>
<li>
Proven experience in working with the assay development, including method validation, troubleshooting, performance characterization and continuous process improvement for biological assays and processes.
</li>
<li>
Experienced in NPI Quality for complex systems, including design verification and validation, part qualification and test method validation.
</li>
<li>
Experience in the application of process control plans, statistical process control, and quality system regulations (e.g., 21 CFR 820, ISO 13485).
</li>
<li>
Demonstrated ability to lead cross-functional teams and guide product development from concept to commercialization.
</li>
</ul>
It would be a plus if you also possess previous experience in:
<ul>
<li>
Experience in biomedical or medical device manufacturing
</li>
<li>
Certified Quality Engineer and/or Lead Auditor certification
</li>
</ul>
Cepheid, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it’s a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info.
The annual salary range for this role is $111,100 – 135,500. This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting.
This job is also eligible for bonus/incentive pay.
We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees.
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company’s sole discretion, consistent with the law.
#LI-LCS
Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. 
For more information, visit <a href="http://www.danaher.com" target="_blank">www.danaher.com</a>. 
Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. 
The U.S. EEO posters are available here.
We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact:1-202-419-7762 or <a href="mailto:applyassistance@danaher.com" target="_blank">applyassistance@danaher.com</a>.

Senior Quality Engineer

<h3>Job Description</h3>
Job Description
Description
Verista's 500 experts team up with the world's most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve some of the world's most pressing healthcare challenges. Verista provides innovative solutions and services that empower informed decision-making and are the result of our significant investment in our people and our capabilities.
Our ability to grow is driven by world-class people who thrive in a team environment and share our mission to enable life sciences clients to improve lives. Our talented and dedicated professionals are committed to making an impact every day.
Company Culture Guidelines &amp; Values:
<ul>
<li>We empower and support our colleagues</li>
<li>We commit to client success at every turn</li>
<li>We have the courage to do the right thing</li>
<li>We encourage an inclusive environment where our colleagues feel respected, engaged, and challenged.</li>
<li>We constantly acquire new skills and learn from our experiences to enhance our collective expertise</li>
</ul>
CQV Engineer Responsibilities (Typical):
<ul>
<li>Managing and working collaboratively with clients' quality representative to complete deviation investigation and resolution for problems and issues encountered during execution activities. Includes ability to complete root cause analysis</li>
<li>Supporting clients change management program – including authoring proposed changes, executing impact assessments/ regression analysis, and supporting client documentation of change results and release</li>
<li>Authoring, editing, and executing technical commissioning, qualification and validation documentation for standard equipment/systems/ software, and processes as part of team as directed by the project leader</li>
<li>Running test scripts and documenting results</li>
<li>Adherence with project schedule for all assigned activities</li>
<li>Maintaining clear, detailed records qualification and validation</li>
<li>Documenting impact and risk assessments as part of a team</li>
<li>Completing user interface testing, software verification, and complete alarm testing on automated systems</li>
<li>Developing, reviewing, and executing testing documentation</li>
<li>Making recommendations for design or process modification based on test results when executing test scripts</li>
<li>Reading technical schematics to identify, locate, and test photo sensors, verify part numbers, and complete I/O testing on automated manufacturing equipment</li>
<li>General understanding of capital equipment implementation and process knowledge</li>
<li>Understanding validation documents, URS, IQ, OQ, PQ</li>
<li>Verifying system drawings including ability to review and as-built P&amp;IDs (piping and instrumentation drawings) and I&amp;C (instrumentation and controls) drawings as well as verifying electrical schematics with support of an electrical engineer</li>
</ul>

Requirements:
<ul>
<li>Must be able to meet onsite work requirements in Holly Springs, NC</li>
<li>Bachelor's Degree or equivalent required (STEM degree, Biomedical Engineering, Chemical Engineering preferred)</li>
<li>2-4 years of relevant industry experience</li>
<li>Proficiency using PC and Microsoft Office tools</li>
<li>Outgoing personality with strong ability to communicate effectively with peers in clear, concise terms</li>
<li>Ability to work as part of a team</li>
<li>Strong problem-solving and critical thinking skills</li>
<li>Excellent organizational and time management skills</li>
<li>Strong attention to detail</li>
<li>GMP and Good Documentation Practice training (may be completed at onboarding)</li>
<li>Intermediate skills with WORD (authoring/editing large technical documents with styles, tables, TOCs, track changes)</li>
<li>Basic skills with EXCEL and PowerPoint</li>
<li>Strong interpersonal skills and clear communication capabilities</li>
</ul>
For US geography, the salary range for this position is shown below. The actual salary is dependent upon a variety of job-related factors such as professional background, training, work experience, location, business needs, market demand, and competitive market practice. Therefore, in some circumstances, the actual salary could fall outside of this expected range. This salary range is subject to change and may be modified in the future.
*Verista is an equal opportunity employer.
National (US) Range$65,000—$104,439 USD
Benefits
Why Choose Verista?
<ul>
<li>High growth potential and fast-paced organization with a people-focused culture</li>
<li>Competitive pay plus performance-based incentive programs</li>
<li>Company-paid Life, Short-Term, and Long-Term Disability Insurance.</li>
<li>Medical, Dental &amp; Vision insurances</li>
<li>FSA, DCARE, Commuter Benefits</li>
<li>Supplemental Life, Hospital, Critical Illness and Legal Insurance</li>
<li>Health Savings Account</li>
<li>401(k) Retirement Plan (Employer Matching benefit)</li>
<li>Paid Time Off (Rollover Option) and Holidays</li>
<li>As Needed Sick Time</li>
<li>Tuition Reimbursement</li>
<li>Team Social Activities (We have fun!)</li>
<li>Employee Recognition</li>
<li>Employee Referral Program</li>
<li>Paid Parental Leave and Bereavement</li>
</ul>
Verista collects and processes personal data in accordance with applicable data protection laws. If you are a California Job Applicant, see the privacy notice for further details. 
For more information about our company, please visit us at Verista.com

5832- CQV Engineer / Validation Engineer 2

<h3>Job Description</h3>
Job Description
Corporate Overview
SD Solutions, LLC is a fast-growing professional services company, providing Cybersecurity, Strategy &amp; Governance, IT Modernization, Management Consulting, and Professional Services solutions to large and small clients in the federal government sector. Our broad spectrum of services also includes digital &amp; legacy transition, decommissioning, communications, event planning &amp; logistics, and operations. It is our mission to deliver enduring results to our clients using strong business acumen, technical solutions, and management services. Our core values include quality, timeliness, integrity, trusted relationships, and corporate citizenship.
Position Overview
This role offers a unique opportunity for a skilled scientist with expertise in Robotics Engineering and interdisciplinary research to contribute directly to the mission of the U.S. Advanced Research Projects Agency for Health (ARPA-H). The selected candidate will serve as a technical advisor to an ARPA-H Program Manager, supporting the development and execution of a new, high-impact research initiative.
In this role, you will collaborate with the ARPA-H Program Manager and team to effectuate bold ARPA-H research initiatives, support the development, funding, and management of new and existing R&amp;D programs to meet ARPA-H's mission to accelerate better health outcomes for everyone.  More detailed requirements below.
Position Requirements:
<ul>
<li>Collaborate with a multidisciplinary team to advance safe, affordable autonomous robotic assistive technologies that enhance mobility and independence for elderly and disabled individuals in real-world environments.</li>
<li>Offer expert guidance on integrated robotics systems, addressing design, safety, and deployment challenges in applications involving direct physical interaction with humans, especially in healthcare and assistive contexts.</li>
<li>Review and assess technical proposals for scientific quality and innovation; synthesize reviewer feedback, draft recommendations, and prepare clear summaries and presentation materials for decision-making.</li>
<li>Conduct market research, technical evaluations, and literature reviews; produce concise briefing documents on autonomous mobile robots and exoskeletons for elderly and disability-focused healthcare applications.</li>
<li>Prepare technical and administrative documentation under tight deadlines, detailing program objectives, progress, cost, schedule, and risk for advanced robotics initiatives supporting health and mobility outcomes.</li>
</ul>
 
Qualifications:
<ul>
<li>Ph.D. in electrical, mechanical, or computer science; robotics; biomedical engineering; or a related field with at least years' experience preferred; a master's degree in a related field with at least five years' experience acceptable.</li>
<li>Proficiency in programming languages, including Python, C++, Java, and MATLAB for robotics and system-level development.</li>
<li>Proficiency in circuit design, microcontroller programming, and embedded systems integration for robotic platforms.</li>
<li>Proficiency in sensor and actuator integration, data fusion, and algorithms for localization, mapping, and motion planning.</li>
<li>Knowledge of robotic operating systems for simulation, visualization, and component-level communication and control.</li>
<li>Knowledge of AI and machine learning methods for autonomous decision-making and intelligent robotic behavior.</li>
<li>Demonstrated experience applying user-centered design principles to engineer solutions driven by real-world customer needs.</li>
<li>Strong team collaboration skills with excellent communication, technical writing, and organizational capabilities.</li>
<li>Prior involvement with federal advanced research programs (ARPA-H, DARPA, IARPA, ARPA-E) preferred; prior involvement with commercial, academic, or U.S. Department of Defense research and development programs desired.</li>
<li>Metro DC area preferred; remote locations acceptable. </li>
<li>Ability to successfully pass a background investigation and maintain a federal clearance.</li>
</ul>
Employment Type
<ul>
<li>Full-time, W2 employment</li>
</ul>
<ul>
<li>Exempt, salaried</li>
</ul>
<ul>
<li>Eligible for paid benefits</li>
</ul>
<ul>
<li>Remote is acceptable.</li>
</ul>
Clearance, Citizenship, and Work Location
<ul>
<li>      Clearance requirement: Active or able to obtain Public Trust.</li>
</ul>
<ul>
<li>      U.S. citizenship </li>
</ul>
SD Solutions Culture
We are a fast-growing company who puts people first. Our focus is on building the right team to provide exceptional services to our customers and to grow with our organization. We offer very competitive compensation and a very attractive benefits package. We believe in corporate citizenship and provide several levels of support to students, schools, teachers, and other organizations in our local community. If you are looking for a new opportunity to make a difference and build your career in a positive way, please join us. We're waiting for you.
 
Equal Opportunity Employer
SD Solutions, LLC is an equal opportunity employer and does not unlawfully discriminate against employees or applicants for employment based on an individual's race, color, religion, creed, sex, national origin, age, disability, marital status, veteran status or any other status protected by applicable law. This policy applies to all terms, conditions, and privileges of employment, including recruitment, hiring, placement, compensation, promotion, discipline, and termination.
Whenever possible, SD Solutions makes reasonable accommodation for qualified individuals with disabilities to the extent required by law.
 
Candidate Referral Fee Program
SD Solutions wants to reward you for helping us identify qualified, talented professionals to join our team. Send us your friends and professional connections and we'll reward you with a cash bonus!
To submit a qualified referral, please visit our website. You'll need to send the candidate's contact information and/or resume to SD Solutions and include "Candidate Referral" in the subject line. Your referral must be an active candidate interested in new opportunities. You must include the candidate's full name and contact information (i.e., email address and phone number).
Please visit Careers - SD Solutions, LLC (sdsolutionsllc.com) for more details of the Candidate Referral Fee Program.

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