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<h3>Job Description</h3>
Job Description Synthetic Aperture RADAR (SAR) Image Scientist
???? Location: Springfield, VA ???? Clearance: Active TS/SCI with polygraph 
About the Role TRIAEM LLC is seeking a SAR Image Scientist to support an Intelligence Community customer. This role focuses on product quality assessments, image science analysis, and sensor modeling. You’ll collaborate with government customers and subject matter experts while working on mission-critical GEOINT initiatives.
Responsibilities
<ul>
<li>
Perform sensor modeling and decompose image formation elements to evaluate system quality.
</li>
<li>
Conduct product evaluations, quality studies, and baseline system assessments.
</li>
<li>
Assess algorithms for mission application performance.
</li>
<li>
Monitor system performance, detect anomalies, and recommend corrective actions.
</li>
</ul>
Required Qualifications
<ul>
<li>
Active TS/SCI clearance with polygraph (or ability to obtain).
</li>
<li>
Bachelor’s degree in Image Science, Electrical Engineering, Physics, or related field (Master’s preferred).
</li>
<li>
5+ years with BS/BA or 3+ years with MS/MA.
</li>
<li>
Experience with SAR imagery, image processing, and digital signal processing.
</li>
<li>
Proficiency with coding languages (C, Python, MATLAB, IDL).
</li>
<li>
Strong background in image chain analysis and error estimation.
</li>
<li>
Excellent communication and teamwork skills.
</li>
</ul>
Preferred Skills
<ul>
<li>
Knowledge of NSG TCPED processes, especially SAR exploitation.
</li>
<li>
Familiarity with image quality standards (NIIRS, metrics, equations).
</li>
<li>
Experience in DoD or IC operational environments.
</li>
<li>
Expertise in sensor imaging systems and systems engineering lifecycle.
</li>
</ul>

Program Overview TRIAEM LLC is supporting a subcontract on an Intelligence Community program that provides expertise in Test Center operations, test tool automation and development, and image quality services.
About the Role TRIAEM is seeking a motivated Synthetic Aperture RADAR (SAR) Image Scientist to join a skilled team supporting a mission focused on product quality. This role offers the opportunity to collaborate with subject matter experts, work directly with government customers, and contribute to projects with a high degree of autonomy.
The SAR Image Scientist will support activities such as product evaluations, quality studies, new product initializations, algorithm assessments, and the development of image quality equations to model and quantify system performance under varying parameters. The position requires a strong background in modeling image formation paths—including sensor, detector, atmospheric, and material effects—as well as simulation and algorithm documentation for software development. Experience with GEOINT systems, exploitation tools, and test/verification methods is key. The selected candidate will work alongside an established team to address customer-driven priorities. Strong communication, collaboration, and a proven record of results are essential.
Key Responsibilities
<ul>
<li>
Perform sensor modeling and decompose image formation elements to evaluate system quality.
</li>
<li>
Assess algorithms to determine product performance for specific mission applications.
</li>
<li>
Conduct baseline assessments for system initialization and monitor performance over time.
</li>
<li>
Analyze detected errors/artifacts and provide recommendations for corrective actions.
</li>
</ul>
Required Qualifications
<ul>
<li>
Active Top Secret clearance (must be eligible for TS/SCI with polygraph).
</li>
<li>
Bachelor’s degree in Image Science, Electrical Engineering, Physics, or related field; advanced degree preferred.
</li>
<li>
5+ years of relevant experience with a BS/BA, or 3+ years with an MS/MA.
</li>
<li>
Demonstrated experience with SAR imagery and complex data products.
</li>
<li>
Proficiency in image processing and digital signal processing.
</li>
<li>
Strong understanding of image chain analysis (sensor modeling, calibration, signal/noise analysis, image formation).
</li>
<li>
Experience coding in C, Python, MATLAB, or IDL for algorithm development and repeatable processes.
</li>
<li>
Applied knowledge of error estimation methods.
</li>
<li>
Strong written and verbal communication skills, including briefing and technical documentation.
</li>
<li>
Ability to work independently and as part of a team in a dynamic environment.
</li>
</ul>
Preferred Skills
<ul>
<li>
Knowledge of NSG tasking, collection, processing, exploitation, and dissemination (TCPED), with emphasis on SAR imagery.
</li>
<li>
Experience in DoD or IC operational environments.
</li>
<li>
Familiarity with image quality standards (e.g., NIIRS), scales, metrics, and equations.
</li>
<li>
Expertise with sensor imaging systems, products, and exploitation workflows.
</li>
<li>
Understanding of systems engineering lifecycle, independent testing, and data verification.
</li>
</ul>

Image Scientist

<h3>Job Description</h3>
Job Description
Description:
<ul>
<li>
The Quantitative, Translational ADME Sciences (QTAS) department at is seeking a highly motivated and energetic bioanalytical scientist to join the biologics bioanalysis, characterization and proteomics (BBCP) group. 
</li>
<li>
The primary responsibility of this position is to support LC-MS (liquid chromatography-mass spectrometry)-based bioanalysis and method development for biologic entities, such as monoclonal antibodies, multi-specific antibodies, antibody-drug conjugates (ADCs), and other novel modalities. 
</li>
<li>
The successful candidate will have experience in optimizing and implementing hybrid LC-MS-based bioanalytical methods to support non-regulated preclinical PK and TK studies. 
</li>
<li>
Responsibilities include routine sample preparation, method development, instrument maintenance, data analysis, report writing, and presenting data at internal and external meetings.
</li>
<li>
Perform affinity purification and digestion of biological therapeutics (including but not limited to monoclonal and bispecific antibodies, antibody drug conjugates, antibody-siRNA conjugates, and fusion proteins) from biological matrices manually or using automation systems.
</li>
<li>
Operate and maintain LC/MS instruments to generate high-quality experimental data.
</li>
<li>
Optimize and develop LC/MS methods to meet assay specificity and sensitivity requirements.
</li>
<li>
Analyze data and maintain detailed, accurate and comprehensive study documentation in electronic laboratory notebooks.
</li>
<li>
Communicate data interpretation internally and externally.
</li>
</ul>
Qualifications:
<ul>
<li>
BS with 5+ years or MS with 2+ years in a pharmaceutical industry setting with a focus on mass spectrometry. 
</li>
<li>
Degree in chemistry, pharmacology or other related fields. 
</li>
<li>
Prior industry experience in drug discovery/development is highly desired.
</li>
<li>
Highly motivated, self-driven and results-oriented with excellent communication and presentation skills; capable of working both as a team player and individual contributor.
</li>
<li>
Hands-on experience with QQQ (SCIEX) is required, additional experience with qTOF (Agilent, Bruker, SCIEX) and/or Orbitrap (Thermo) mass spectrometers is a plus.
</li>
<li>
Hands-on experience with biologics bioanalysis is highly desired, additional experience with oligonucleotide analysis is a plus.
</li>
<li>
Hands-on experience with immuno-affinity purification and automation systems (e.g., TECAN, AssayMap Bravo or Hamilton) is highly desired.
</li>
<li>
In-depth understanding of PK, TK and PK/PD studies is preferred.
</li>
</ul>
Benefits:
Healthcare Insurance: Synectics offers eligible employees and their dependents healthcare coverage through BlueCross BlueShield of Illinois. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. Premiums are subsidized by Synectics. 
Dental Insurance: Synectics offers eligible employees and their dependents a dental plan through MetLife. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. 
Vision Insurance: Synectics offers eligible employees vision insurance through VSP. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics.401(k) Plan: The Synectics Inc. Investment Savings Retirement Plan. Synectics offers all employees who are 21 years of age or older the opportunity to invest in the 401(k) Plan on the first enrollment date that is at least 30 days after employment begins. Enrollment dates are each January 1st, April 1st, July 1st, and October 1st.
Technical Certification Bonus: Synectics is pleased to award its employees a bonus of up to $500 for an approved professional certification. In determining the bonus amount, Synectics will consider the cost of the test(s) for any certification relating to your current position, achieved during your employment with us. Only one Certification Bonus per calendar year may be awarded per employee. Only current, active employees will be eligible to receive this bonus. It will be awarded 90 days after the Synectics office has received documentation confirming the successful completion of the certification.
Synectics is an equal opportunity employer.

Biologist

<h3>Job Description</h3>
Job Description
Job Title: QC Chemist
Job Description
The QC Chemist will perform various wet chemistry testing on raw materials, including IR Spectroscopy, Melting Point Temperature, and Viscosity, following USP methodology. The role involves conducting a range of identification, limit, and physical tests to ensure the quality and compliance of materials.
Responsibilities
<ul>
<li>Conduct wet chemistry testing on raw materials.</li>
<li>Perform IR Spectroscopy, Melting Point Temperature, and Viscosity tests.</li>
<li>Follow USP methodologies for testing procedures.</li>
<li>Perform Identification Tests including Thin Layer Chromatography.</li>
<li>Conduct Limit Tests such as Chloride and Sulfates, Heavy Metals, and Elemental Impurities.</li>
<li>Conduct Other Tests and Assays including Karl Fischer, Acid Value, and Peroxide Value.</li>
<li>Perform Physical Tests including Viscosity, Melting Range, and Congealing Temperature.</li>
<li>Utilize laboratory equipment such as Refractometer, Densitometer, pH meter, Auto-titrator, UV-VIS Spectrophotometer, and FTIR.</li>
</ul>
Essential Skills
<ul>
<li>Bachelor's Degree in Chemistry or related scientific field.</li>
<li>1-3 years of experience in a GMP regulated laboratory.</li>
<li>Proficiency in wet chemistry techniques.</li>
<li>Experience performing raw material qualification testing.</li>
<li>Experience with IR Spectroscopy and Melting Point Temperature testing.</li>
<li>Familiarity with USP Methodology preferred (open to other methodologies such as AOCS, ASTM, etc.)</li>
</ul>
Work Environment
<ul>
<li>The position is based in a Quality Control laboratory, operating from 8:00 AM to 4:30 PM, Monday through Friday. The company provides a supportive environment with growth opportunities, being part of a family-owned business that values health-focused products.</li>
</ul>
Job Type &amp; Location
This is a Contract to Hire position based out of Lombard, IL.
Pay and Benefits
The pay range for this position is $25.00 - $25.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Lombard,IL.
Application Deadline
This position is anticipated to close on Dec 30, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

QC Chemist

<h3>Job Description</h3>
Job DescriptionPay range: $24.00+ per hour, based on experience, plus shift differential pay
 
First several weeks of training on first shift 
Available positions: 3rd shift (M-Th 4x10 hour schedule)

GFS Chemicals is a family owned and operated business in Columbus, Ohio serving customers worldwide since 1928. You will be joining an established, close knit family organization that has been proudly dedicated to quality, service, and innovation in the specialty chemicals market. GFS offers a comprehensive compensation package that includes a generous 401k, profit sharing plan, paid time off, 2:1 HSA match, company paid life insurance, medical, vision, dental, and much more. 
 
Apply now to learn more about GFS Chemicals. Let’s see if we have “Chemistry”!

Qualifications:
<ul>
<li>High school diploma or equivalent; technical or vocational training in chemistry or related field is a plus.</li>
<li>Proven experience as a chemical operator or in a similar manufacturing environment.</li>
<li>Solid understanding of chemical processes, equipment, and safety procedures.</li>
<li>Ability to read and interpret technical documents, including SOPs and manuals.</li>
<li>Strong attention to detail and a proactive approach to problem-solving.</li>
<li>Ability to work effectively in a team and communicate clearly.</li>
<li>Physical ability to lift heavy objects, stand for extended periods, and work in various weather conditions.</li>
<li>Familiarity with operating and troubleshooting process control systems a plus.</li>
</ul>

Essential Responsibilities:
You will be trained in performing fascinating processes to manufacture chemicals used in automotive, pharmaceuticals, electronics, agrochemical, and energy commercial applications. You will learn multiple work centers over time allowing a changing work environment each day.
Daily activities:
<ul>
<li>Utilize pumps to load raw materials into vessels.</li>
<li>Monitor reaction conditions using our electronic PLC systems.</li>
<li>Work closely with Quality Control to test and adjust batches in process.</li>
<li>Package finished goods into containers ranging from 1 liter to 55 gallon drums. </li>
<li>Use a fork-lift to stage pallets of raw materials for upcoming batches.</li>
<li>We empower operators to participate in problem solving and continuous improvement.</li>
<li>Focus on industrial housekeeping and personal protective equipment usage.</li>
<li>Follow written operating procedures including the record keeping of information.</li>
<li>Most importantly.. help to create a positive, productive, and safe work environment.</li>
</ul>
 
 Additional Qualifications
The company will only employ those who are legally authorized to work in the United States for this position. This is not a position for which sponsorship will be provided. Individuals with temporary visas or who need sponsorship for work authorization now or in the future are not eligible for hire.
EEO/AA/M/F/Vets/Disabled
No agency calls or emails please!

Chemical Operator - 3rd Shift

<h3>Job Description</h3>
Job DescriptionCompany Description 
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;<a href="http://www.abbvie.com" target="_blank">www.abbvie.com</a>. Follow @abbvie on&nbsp;X,&nbsp;Facebook,&nbsp;Instagram,&nbsp;YouTube,&nbsp;LinkedIn&nbsp;and&nbsp;Tik Tok.
Job Description 
Purpose
Generate and analyze precise, reliable, and reproducible data in a timely manner, under the direction of a more senior scientific leader. Demonstrate experimental precision and should possess general understanding of core discipline.
Responsibilities
<ul>
<li>Completely follow established experimental protocols and assess results with supervision.</li>
<li>Recognize and report experimental variances.</li>
<li>Apply basic scientific principles to research.</li>
<li>Learn and effectively implement new experimental protocols and/or techniques. Maintain laboratory equipment and optimize laboratory operations for efficient use of time and laboratory supplies and reagents, when appropriate.</li>
<li>Consult literature to understand scientific purpose of assignments. Impact projects predominantly through lab and/or pilot plant based activities.</li>
<li>Understand and adhere to corporate standards regarding code of conduct, safety, appropriate handling of materials, controlled drug and radioactive compounds, GxP compliance, and animal care where applicable.</li>
</ul>
Qualifications 
Qualifications
<ul>
<li>Bachelor’s Degree, or equivalent education.</li>
<li>Theoretical and practical knowledge to carry out job functions.</li>
</ul>
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or&nbsp;local law:&nbsp;​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company&nbsp;believes in&nbsp;good faith it will pay for this role at the time&nbsp;of this posting based on the job grade for this position.&nbsp;Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and&nbsp;we&nbsp;may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the&nbsp;future. ​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),&nbsp;medical/dental/vision&nbsp;insurance and 401(k) to eligible&nbsp;employees.​
</li>
<li>
This job is eligible to participate in our short-term incentive&nbsp;programs.&nbsp;​
</li>
</ul>
​
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and&nbsp;determinable.&nbsp;The amount and availability of any bonus,&nbsp;commission, incentive, benefits, or any other form of&nbsp;compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and&nbsp;absolute&nbsp;discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with&nbsp;applicable law.&nbsp;
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>

Associate Scientist, I

<h3>Job Description</h3>
Job DescriptionCompany Description
We are Olsson. We engineer and design solutions that improve the world around us. As a company, we promise to always be responsive, transparent, and focused on results – for our people, our clients, and our company.
We're a people-centric firm, so it's no surprise our greatest asset is our people. The impact this creates is an environment that encourages our people to grow and be creative with their talents. This approach builds a culture that is uniquely Olsson. It allows us to grow our people as we grow our business. This, in turn, creates a lasting impact on the world around us.
Job Description
As a Geotechnical Engineer, you will perform geotechnical engineering design, project proposal and management duties with integrity and a drive to succeed. You will also process design calculations, develop project scopes and schedules, and travel to job sites for observation. You will be required to ensure high client service by providing constructible designs, meeting deadlines and creating clear communications with our clients. 
We have one current opening and will consider candidates being located out of our Lincoln, NE, Oklahoma City, OK, Fayetteville, AR or Springfield, MO office locations. 
Qualifications
You are passionate about:
<ul>
<li>Working collaboratively with others.</li>
<li>Having ownership in the work you do.</li>
<li>Using your talents to positively affect communities.</li>
</ul>
You bring to the team:

<ul>
<li>Strong communication skills</li>
<li>Ability to contribute and work well on a team</li>
<li>Bachelor's Degree in civil/geotechnical engineering required</li>
<li>Must be a registered professional engineer</li>
<li>4+ years of related Geotechnical analysis and design experience</li>
<li>The ability to work in a constant state of alertness and safe manner</li>
</ul>
#LI-DD1
Additional Information
Olsson specializes in engineering and design, client advisory services, planning, field services, and environmental. Improving the world has been our mindset from the very beginning, back when Olsson first opened for business in 1956. And it will be our mindset for years to come.
As an Olsson employee, you will:
<ul>
<li>Receive a competitive 401(k) match</li>
<li>Be empowered to build your career with tailored development paths</li>
<li>Have the possibility for flexible work arrangements</li>
<li>Engage in work that has a positive impact on communities</li>
<li>Participate in a wellness program promoting balanced lifestyles</li>
</ul>
In addition, full-time employees will receive our traditional benefits package (health care, vision, dental, paid time off, etc.) and the opportunity to participate in a bonus system that rewards performance.
Olsson is an Equal Opportunity Employer. We encourage qualified minority, female, veteran, and disabled candidates to apply and be considered for open positions. We do not discriminate against any applicant for employment or any employee because of race, color, religion, national origin, sex, sexual orientation, gender identity, gender, disability, age, military status, or other protected status.
Olsson understands the importance of privacy and is committed to protecting job applicants' personal information. Pursuant to the California Consumer Privacy Act, as amended by the California Privacy Rights Act (collectively, the "CCPA"), this notice explains Olsson's practices regarding the collection, use, and disclosure of personal information for job applicants residing in California. Please read this Notice carefully to understand our privacy practices.
For more information about the types of information we collect and how we use it in connection with your general access and use of our website, please review our general California Privacy Notice here.

Geotechnical Engineer

<h3>Job Description</h3>
Job Description
Hybrid in Deerfield, IL Description:
Hybrid in Deerfield Job Summary: We are seeking a hands-on Technical Manager to lead the development and deployment of AI and automation solutions. This role is ideal for a technically skilled leader with deep experience in healthcare and manufacturing, who thrives on building intelligent systems, streamlining operations, and delivering measurable impact. You’ll be directly involved in designing, and implementing solutions using leading automation platforms while managing a high-performing technical team in various time zones Key Responsibilities: AI &amp; Automation Development • Design, build, and deploy AI/ML models and automation workflows to enhance device intelligence and operational efficiency. • Develop and maintain solutions using Power Automate, Power apps • Rapidly prototype and test automation tools for use in manufacturing, quality control, and regulatory compliance. • Build intelligent AI Agents using low-code platforms to accelerate automation adoption and scalability. Process Optimization • Analyze and re-engineer business processes to identify automation opportunities across R&amp;D, supply chain, and clinical operations. • Integrate automation solutions with enterprise systems (ERP, MES, QMS) to reduce manual effort and improve compliance. AI Governance &amp; Strategy • Establish and lead an AI governance framework to ensure ethical, compliant, and secure deployment of AI solutions. • Define policies, standards, and monitoring mechanisms for AI and automation initiatives across the organization. Technical Leadership • Lead by example by hand-on development, conduct code reviews, and guide the team through technical challenges. Define design standards, and best practices for AI and automation projects. • Mentor junior engineers and ensure continuous upskilling within the team. Architecture &amp; Infrastructure • Collaborate with enterprise architecture teams to propose and implement next-generation infrastructure for AI and automation solutions aligned with the organization’s futuristic vision. • Evaluate emerging technologies and recommend scalable, secure, and cost-effective architectures. Cross-Functional Collaboration • Work closely with clinical, regulatory, and manufacturing teams to align solutions with industry-specific needs and compliance standards. • Translate business requirements into technical specifications and deliver working solutions. • Present technical insights and project outcomes to stakeholders in a clear, actionable format. Skills and Qualifications: • Technical Proficiency: • Expertise in Power Automate • Strong programming skills in Python and experience with AI/ML frameworks • Tools and Software: • Project Management: Proficiency in Jira and MS Project for managing and tracking project progress • Data Analysis: Expertise in Power BI for analyzing and visualizing data to support decision-making and performance monitoring Certifications: • Microsoft Certified: Power Automate RPA Developer Associate • Azure AI Engineer Associate or AWS Certified Machine Learning – Specialty • AI Governance Professional (AIGP) for governance expertise. • Industry Experience: • Extensive experience in healthcare and manufacturing, with a deep understanding of industry-specific challenges and regulatory requirements • Professional Experience: • 10+ years of relevant experience in automation and AI • Proven track record of successful project delivery and leading small to mid-size geographically located teams. • Education: • Master’s degree in Automation and AI, Computer Science, or equivalent Key Performance Indicators (KPIs): • Automation Conversion: Migrate 40+ automations to Power Automate within the Vantive environment. • Team Development: Build and sustain a fully operational automation team. • Cost Efficiency: Deliver 4+ cost-saving automation solutions with measurable financial impact. • Project Delivery: Ensure all automation projects are completed on time, within budget, and meet quality standards. Professional Development: We offer continuous learning opportunities and support for professional development to help you stay at the forefront of automation and AI technologies
Company DescriptionSelect Source International (SSI) is a distinguished staffing company with nearly 25 years of experience, renowned for delivering top-tier workforce solutions encompassing staffing, recruiting, and managed services. As a proud supplier, we bring a wealth of expertise and best-in-business differentiators to comprehensively support your diverse workforce needs. Based in Minneapolis, Minnesota, USA, SSI has established itself as a global leader, serving a broad clientele across industries with unwavering dedication and excellence. SSI is ISO 9001, 14001, and Soc2 Type2 certified, underscoring our commitment to quality and security. We have garnered numerous sustainability and supplier diversity awards, further validating our industry-leading capabilities 
<h3>Company Description</h3>
Select Source International (SSI) is a distinguished staffing company with nearly 25 years of experience, renowned for delivering top-tier workforce solutions encompassing staffing, recruiting, and managed services. As a proud supplier, we bring a wealth of expertise and best-in-business differentiators to comprehensively support your diverse workforce needs.\r\n\r\nBased in Minneapolis, Minnesota, USA, SSI has established itself as a global leader, serving a broad clientele across industries with unwavering dedication and excellence. SSI is ISO 9001, 14001, and Soc2 Type2 certified, underscoring our commitment to quality and security. We have garnered numerous sustainability and supplier diversity awards, further validating our industry-leading capabilities

AI/ML Engineer

<h3>Job Description</h3>
Job Description
Chemical Process Engineer Pasadena, TX Full-time | Exempt | Engineering Department About the Company We are a global chemical manufacturing and services company supporting refineries, gas processing facilities, and industrial plants worldwide. Our focus is on delivering safe, reliable, and efficient process solutions that help clients improve performance and sustainability. Position Summary The Process Engineer plays a key role in overseeing and optimizing production operations at our Pasadena, Texas facility. This position focuses on ensuring efficient, safe, and high-quality processes while driving continuous improvement and supporting capital and maintenance projects. Key Responsibilities
<ul>
<li>Monitor and improve day-to-day production processes and utility systems.</li>
<li>Troubleshoot technical and equipment issues in coordination with operators and supervisors.</li>
<li>Analyze process data and lab results to identify trends and implement performance improvements.</li>
<li>Collaborate with Production, Maintenance, and HSE teams to resolve technical challenges.</li>
<li>Support capital and maintenance projects, including planning, scope development, and contractor oversight.</li>
<li>Develop and maintain standard operating procedures and process documentation.</li>
<li>Provide training and technical guidance to operations personnel.</li>
<li>Participate in safety meetings and promote a strong culture of safety and compliance.</li>
<li>Prepare material balance reports and utility usage calculations to support production efficiency.</li>
<li>Communicate regularly with customer service and management regarding process performance and scheduling.</li>
</ul>
Qualifications
<ul>
<li>Bachelor’s degree in Engineering (Chemical Engineering preferred).</li>
<li>7+ years of experience in a chemical, petrochemical, or refining manufacturing environment.</li>
<li>Strong analytical and problem-solving skills.</li>
<li>Proficient with Microsoft Office and production or inventory management systems.</li>
<li>Excellent communication and technical writing abilities.</li>
<li>Familiarity with ISO-9001 quality systems preferred.</li>
<li>Professional Engineer (P.E.) license a plus.</li>
</ul>
Core Competencies
<ul>
<li>Analytical Thinking and Process Optimization</li>
<li>Technical Troubleshooting and Design</li>
<li>Effective Communication and Collaboration</li>
<li>Safety and Environmental Awareness</li>
<li>Cost and Resource Efficiency</li>
</ul>
Work Environment This role is based in a chemical manufacturing facility and involves regular time spent in production areas. The position may require standing, walking, climbing, and occasional lifting (up to 50 lbs). Strict adherence to all safety and operational procedures is required. Why Join Us
<ul>
<li>Contribute to innovative projects in a growing industry.</li>
<li>Collaborate with a knowledgeable, safety-first engineering team.</li>
<li>Access opportunities for professional growth and development.</li>
</ul>

Chemical Process Engineer

<h3>Job Description</h3>
Job Description
THIS POSITION IS 100% ON-SITE IN GERMANTOWN, MARYLAND. 
Relocation Support to the Germantown area may be provided.
Global Engineering &amp; Technology (GET) is seeking a Nuclear Weapons Subject Matter Expert (SME) with expertise in nuclear weapon science to support the Department of Energy's Office of Classification in Germantown, Maryland.
This is a highly compensated full-time position with benefits, with work performed primarily at the DOE facility in Germantown, Maryland. This long-term position provides relocation support to the Germantown area for those who live outside of the DMV (region encompassing the District of Columbia, Maryland, and Virginia). 
Salary Range: Compensation for this position will range from $175,000 to $190,000 per year, depending on qualifications.
Duties:
<ul>
<li>This position requires expert-level knowledge to advise senior DOE management on current technical issues related to the SME's area of expertise in nuclear weapons research (e.g., nuclear weapon design, materials science research, stockpile management, special nuclear materials production, developments relating to improvised nuclear devices, or other areas of expertise)</li>
<li>This leadership and policy guidance position requires the ability to lead working groups and develop white papers and presentations</li>
<li>This senior professional prepares classification guidance and classification/declassification policy documents and guides in accordance with applicable laws, regulations, DOE Orders, and DOE Office of Classification procedures for Restricted Data (RD), Formerly Restricted Data (FRD), National Security Information (NSI), and Unclassified Controlled Nuclear Information (UCNI), including but not limited to the technical areas described below</li>
</ul>
Requirements
Security Clearance: 
Candidate MUST be a United States citizen and have a current DoD Top Secret security clearance or DOE Q security clearance
Education and Experience:
<ul>
<li>Applicant MUST have earned an advanced degree in nuclear engineering or a physical science</li>
<li>Applicant MUST have hands-on nuclear weapon science experience</li>
<li>This position requires excellent writing and verbal communication skills. The individual must demonstrate the ability to read and understand written English at or above academic grade 15 (Nelson Denny reading assessment).</li>
</ul>
Minimum of ten (10) years' total field experience in the subject area of nuclear weapons is required. Hands-on experience with nuclear weapons-related matters such as any of the following is highly valued:
<ul>
<li>Computer Codes and Simulation Tools</li>
<li>Nuclear Weapon Design</li>
<li>Weapon Science</li>
<li>Use Control and other surety aspects of nuclear weapons</li>
<li>Knowledge of Improvised Nuclear Devices (INDs)</li>
<li>Advanced understanding of Radiation Exposure Devices and Radiological Dispersal Devices, including their basic science and technological principles</li>
<li>Expert knowledge of programs such as Second Line of Defense to interdict nuclear materials </li>
<li>Hands-on knowledge of computer code development to support the nuclear weapon complex is desirable, as is experience with XML computer language</li>
<li>Experience working with DOE / NNSA / DoD / DHS / NRC and the national nuclear weapon laboratories</li>
</ul>
The following are also highly valued:
<ul>
<li>Expertise in Inertial Confinement Fusion (ICF)</li>
<li>Experience teaching and developing testing and educational materials for subjects such as IND or ICF is highly desirable</li>
</ul>
Benefits
We provide exceptional benefits to our full-time employees (spouse/family coverage option is available at a company-subsidized rate). 
Benefits include: 
<ul>
<li>Medical Plan Options With UnitedHealthcare</li>
<li>Dental Insurance</li>
<li>Long-term and Short-term Disability Insurance</li>
<li>Life Insurance</li>
<li>AD&amp;D Insurance</li>
<li>Generous 401(k) Match</li>
</ul>
All benefits are effective on day one of employment.
Global Engineering &amp; Technology, Inc. (GET) does not discriminate on the basis of race, sex, color, religion, age, national origin, marital status, disability, veteran status, genetic information, sexual orientation, gender identity or any other reason prohibited by law in provision of employment opportunities and benefits.

Scientist / Nuclear Weapons SME

<h3>Job Description</h3>
Job Description
BEYOND International Inc. is seeking a Lab Assistant/Chemical Technician for our Chemical &amp; Quality Department. The assistant/technician will support production, products quality control test, regular lab &amp; production instruments maintenance etc.
Responsibilities:
<ul>
<li>Assist the Lead Chemist and Chemical Engineer in new product research and development (R&amp;D)</li>
<li>Prepare sample for Quality Control test, complete the testing records, maintain protocols, SOPs, test reports and related documents, have good documentation practice</li>
<li>Inspect and track the stability of raw materials, R&amp;D products and finished products</li>
<li>Work safely and maintain a clean work area in accordance with production requirement and standard lab practices (May lift up to 25 lbs and/or move up to 50 lbs)</li>
<li>Maintenance of the raw material inventory and monthly usage</li>
<li>Maintain lab equipment and perform test apparatus verifications/calibrations</li>
<li>Effectively communicate with colleagues, customers and outside vendors</li>
</ul>
Qualifications:
<ul>
<li>Have a legal job status in the United States (H1B sponsored if approved by supervisor)</li>
<li>Chemistry and other related degree preferred (0-2 years experience required)</li>
<li>Attention to quality including familiarity with ISO 13485 concepts</li>
<li>Familiar with production environment and laboratory procedures</li>
<li>Proficiency in Microsoft Office (Word, Excel, Outlook)</li>
<li>Be able to do literature search independently or as instructed</li>
<li>Team oriented, self-motivated and flexible to working overtime when needed</li>
</ul>
Job Type: Full-time
Pay: $13.00 - $18.00 per hour
Benefits:
<ul>
<li>Health insurance</li>
<li>Paid time off</li>
</ul>
Schedule:
<ul>
<li>8 hour shift</li>
</ul>
Ability to commute/relocate:
<ul>
<li>Sugar Land, TX 77478: Reliably commute or planning to relocate before starting work (Required)</li>
</ul>
Application Question(s):
<ul>
<li>Familiarity with ISO 13485 concepts and procedures</li>
</ul>
Experience:
<ul>
<li>Chemical engineering: 1 year (Required)</li>
</ul>
Work Location: In person

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