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<h3>Job Description</h3>
Job Description
T&amp;M Associates is seeking a GIS Solutions Engineer 2 to join our growing Geospatial Solutions Team. This mid-level role is ideal for a GIS professional with strong technical skills, experience with Esri technologies, and a passion for developing modern geospatial solutions. The successful candidate will support a wide range of GIS initiatives across municipal, utilities, transportation, environmental, and private-sector clients.
The position may be based out of our Philadelphia, King of Prussia, or Mt. Laurel offices, with opportunities for hybrid work.
Responsibilities:
GIS Application &amp; Workflow Development
<ul>
<li>Develop and deploy mobile data collection tools using Esri Field Maps, Survey123, ArcGIS Collector, and related platforms.</li>
<li>Build and configure ArcGIS Online (AGOL) web applications and dashboards using standard templates and capabilities (without customization).</li>
<li>Support the design and execution of data collection workflows to ensure accurate and efficient field operations.</li>
<li>Assist in data transformation and automation processes, including ETL operations.</li>
</ul>
GIS Database &amp; System Administration
<ul>
<li>Develop, maintain, and manage Enterprise GIS databases, including geodatabase design and administrative tasks.</li>
<li>Perform ArcGIS Enterprise configuration tasks under the guidance of senior staff.</li>
</ul>
Technical Support &amp; Project Assistance
<ul>
<li>Provide technical support to internal teams and external clients, escalating complex issues to senior GIS staff as needed.</li>
<li>Collaborate with engineers, planners, and other professionals to integrate GIS solutions into broader project workflows.</li>
<li>Prepare and deliver presentations to both technical and non-technical audiences, translating GIS concepts into understandable insights.</li>
<li></li>
</ul>
Qualifications:
<ul>
<li>Bachelor’s degree in Geography, GIS, Computer Science, Environmental Science, Engineering, or related field.</li>
<li>2–5 years of professional GIS experience.</li>
<li>Proficiency with Esri ArcGIS Pro, ArcGIS Online, ArcGIS Field Maps, Survey123, and related Esri solutions.</li>
<li>Working knowledge of Enterprise Geodatabases (e.g., SQL Server, PostgreSQL).</li>
<li>GISP Certification (preferred or ability to obtain).</li>
<li>Experience with Python for geoprocessing, ETL, or automation (preferred).</li>
<li>Esri Technical Certifications (GIS Desktop, Enterprise, or Specialty certifications preferred).</li>
<li>Experience with data pipelines, APIs, or web GIS technologies is a plus.</li>
<li>Strong understanding of GIS principles, mapping, analysis, and data management.</li>
<li>Ability to communicate clearly, manage priorities, and work independently or as part of a team.</li>
</ul>
T&amp;M Associates is committed to pay transparency and equitable compensation practices in compliance with applicable laws, including the New Jersey Equal Pay Act. T&amp;M estimates that the salary range for this position will fall between $80,000-$103,000. The actual salary offered may vary within this range, depending on a variety of factors including the candidate’s experience, educational qualifications, specific skills and knowledge, as well as internal pay equity and geographic location.
T&amp;M Associates offers a competitive and comprehensive benefits package designed to support the health, well-being, and professional growth of our employees. Benefits include comprehensive insurance (medical, dental and vision), a 401(k) with company match, paid time off, flexible work schedules, wellness programs, and professional development opportunities — all within a people-first, award-winning hybrid work environment. See more details about benefits here.
If this sounds like a company you want to be part of then apply now!
New Hires must have documents indicating they are eligible to work in the United States. EEO/AA Employer.
For California based applicants, our CCPA-CRPA Privacy Notice can be found on our Careers page at <a href="http://www.tandmassociates.com" target="_blank">www.tandmassociates.com</a>
#LI-HYBRID

GIS Solutions Engineer 2

<h3>Job Description</h3>
Job DescriptionCompany Description 
Syngenta Seeds is one of the world’s largest developers and producers of seed for farmers, commercial growers,&nbsp;retailers&nbsp;and small seed companies. Syngenta seeds improve the quality and&nbsp;yields&nbsp;of crops. High-quality seeds ensure better and more productive crops, which is why farmers invest in them. Advanced seeds help mitigate risks such as disease and drought and allow farmers to grow food using less land, less&nbsp;water&nbsp;and fewer inputs.&nbsp;
Syngenta Seeds brings farmers more vigorous, stronger, resistant plants, including innovative hybrid varieties and biotech crops that can thrive even in challenging growing conditions.&nbsp;&nbsp;
Syngenta Seeds is headquartered in the United States.&nbsp;
Job Description 
At Syngenta, our goal is to build the most collaborative and trustworthy team in agriculture, providing top-quality seeds and innovative crop protection solutions that improve farmers' success. To support this mission, Syngenta's Germplasm Development Team is seeking a Soy Germplasm Process Scientist in Malta, IL, or Slater, IA.
The Soy Germplasm Process Scientist leads the development of elite soybean varieties through innovative pre-breeding discovery and genetic enhancement strategies. This role combines cutting-edge breeding methodologies with advanced analytics to accelerate genetic gain and drive product advancement for maturity groups 2-4, working in close collaboration with cross-functional teams across North &amp; South market segments.
Accountabilities:
<ul>
<li>Establish and lead the pre-breeding discovery pipeline for MG 2-4, developing elite soybean varieties through strategic identification, introgression, and testing of novel sources of value-added genetic diversity in collaboration with North &amp; South market segment teams.</li>
<li>Design and execute nurseries and yield trial experiments.</li>
<li>Collect field data and analyze varietal agronomic performance to drive product advancement decisions and accelerate genetic gain.</li>
<li>Develop and implement cutting-edge analytical methods (in partnership with data science teams) to quantitatively measure, characterize, and prescribe functional genetic diversity.</li>
<li>Leverage haplotype data and breeding pipeline insights to optimize selection strategies.</li>
<li>Design, develop, and execute innovative breeding methodologies and technical projects.</li>
<li>Test new approaches in the field to validate and scale breakthrough concepts that advance genetic gain.</li>
<li>Build strong partnerships with internal and external stakeholders to identify emerging opportunities.</li>
<li>Consistently document and communicate research findings, data mining results, and modeling approaches to ensure strategic alignment across cross-functional teams (plant breeders, data scientists, computational biologists, IT).</li>
</ul>
Qualifications 
Required:
<ul>
<li>Ph.D. in plant or animal breeding, with two years of experience in either a commercial or academic setting.</li>
<li>In-depth knowledge of plant breeding, quantitative genetics, and field experimental design.</li>
<li>Expertise with tools for data analysis, statistical computation, and visualization (such as Python or R); programming and pipeline development skills integrating large, complex datasets from structured and unstructured sources.</li>
<li>Demonstrated experience working with molecular marker-based studies applied to plant breeding, such as marker-assisted selection, genome-wide phenotype-to-genotype association, and genomic selection.</li>
<li>Project management experience in a team-oriented atmosphere; ability to develop and adhere to a budget.</li>
<li>Demonstrated skills to use simple interfaces to build visualization capabilities of analysis outputs and results.</li>
<li>Ability to work in a fast-paced, cross-functional, collaborative environment.</li>
<li>Creative, innovative, and strategic thinking; willingness to be bold and take risks on novel ideas.</li>
<li>Strong problem-solving and communication skills.</li>
<li>Curiosity and a desire to continuously learn and stay current on new emerging science and technology.</li>
</ul>
Desired:
<ul>
<li>Knowledge of molecular biology and gene editing technology.</li>
</ul>
 Additional Information 
Salary for the role is $101600 - $127,000 per year.
What We Offer:
<ul>
<li>A culture that celebrates diversity &amp; inclusion, promotes professional development, and strives for a work-life balance that supports the team members. Offers flexible work options to support your work and personal needs.</li>
<li>Full Benefit Package (Medical, Dental &amp; Vision) that starts your first day.</li>
<li>401k plan with company match, Profit Sharing &amp; Retirement Savings Contribution.</li>
<li>Paid Vacation, Paid Holidays, Maternity and Paternity Leave, Education Assistance, Wellness Programs, Corporate Discounts, among other benefits.</li>
</ul>
Syngenta has been ranked as a&nbsp;top employer&nbsp;by Science Journal. Learn more about our&nbsp;team&nbsp;and our mission here:&nbsp;<a href="https://www.youtube.com/watch?v=OVCN_51GbNI" target="_blank">https://www.youtube.com/watch?v=OVCN_51GbNI</a>
Syngenta is an Equal Opportunity Employer and does not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status.
WL: 4A
#LI-Hybrid

Soy Germplasm Process Scientist

<h3>Job Description</h3>
Job Description
About Dividend Assets Capital, LLC
Dividend Assets Capital, LLC is an employee-owned boutique wealth and investment management firm based in the heart of South Carolina's Lowcountry. With over a 40-year history of successful dividend growth investing at our foundation and a diverse, well-seasoned wealth and investment management team, we deliver personalized investment strategies and comprehensive wealth management services to our growing client base. We pride ourselves on bringing clarity, simplicity, and devotion to our clients, helping successful families, advisors, and institutions set and achieve their financial goals so they may preserve what is meaningful to them, their families, and their communities.
Position Summary
 
Dividend Assets Capital (DAC) is currently seeking a Senior Equity Analyst to join its growing investment team. This generalist equity research position will focus on identifying investments based on DAC's proprietary investment screens and performing fundamental research across several industries. Our disciplined investment process begins with bottom-up fundamentals and requires due diligence of industry and company-specific trends, company financial analysis, modeling, and valuation work. The Senior Analyst will then use this research to make specific investment recommendations for the client and institutional portfolios managed by DAC. The ideal candidate will be self-motivated with a high degree of personal and professional integrity. They also will value teamwork, be service-focused, and be able to work independently. This in-person opportunity (not remote or hybrid) is located in our Bluffton, SC office.
 
Responsibilities
 
• Learn and adopt DAC's dividend growth investment philosophy while embracing DAC's team-based culture, which supports an environment of mutual respect and shared rewards.
• Monitor DAC's existing equity investments, including posting quarterly earnings notes, maintaining price targets, and communicating current investment recommendations to Private Client and Institutional Asset Management teams.
• Screen DAC's investment universe to identify new opportunities within DAC's defined investment universe.
• Conduct a thorough fundamental analysis of a company's business and financial position, including cash flow assessment and dividend sustainability, balance sheet and income statement evaluation, and be able to draw insightful conclusions from their analysis.
• Responsible for all aspects of DAC's fundamental research process, including company research, setting up remote and in-person meetings with company management, writing company or industry research reports, developing detailed valuation analyses, and modeling financial projections.
• Monitor market conditions and evaluate current economic and investment trends.
• Communicate investment opportunities within DAC verbally and through written research reports.
• Contribute to DAC's client and institutional model portfolios as well as separate account non-model portfolios.
• Perform other duties as assigned by the Chief Investment Officer
• Be accountable and responsible for adhering to DAC's Core Values: Know Your Stuff, Devoted to Excellence, Serve With Integrity and Humility, Be Real and Transparent.
 
Qualifications
<ul>
<li>Bachelor's degree and completion or progress toward CFA® Level III are required; an advanced degree in Finance or Accounting is a plus</li>
<li>Minimum of 5 years of relevant experience (public or private equity investing)</li>
<li>Strong understanding of finance and accounting</li>
<li>Proficient with financial modeling and discounted cash flow analysis</li>
<li>Proficient in Word, Excel, and PowerPoint</li>
<li>Working knowledge of FactSet and/or Bloomberg</li>
<li>Strong communication skills, both written and verbal</li>
<li>Flexible and team-oriented, with the ability to pivot from one task to another with minimal supervision</li>
<li>Self-motivated and entrepreneurial, with a demonstrated passion for investing</li>
<li>Intellectual curiosity with an ability to engage in thoughtful debates over the merits of an investment.</li>
</ul>
 
If you're the right candidate and an offer is made, please note that we conduct a job-relevant, comprehensive background check and drug screen prior to your start date.

Sr. Equity Research Analyst

<h3>Job Description</h3>
Job Description
 
 Associate Scientist/Scientist - Biologics - BDDS Full Time Exton, PA Frontage Laboratories Frontage Laboratories Inc. is an award winning, full-service, CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada and China. Our core competencies include drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials. Biologics Frontage’s biologics teams have an average of 10-15 years in complex drug development and have worked with large molecule applications throughout its evolution in product development. We can handle projects for a range of large molecule development projects including peptides, proteins, monoclonal antibodies, bispecific antibodies, biosimilars, oligonucleotides, biomarkers , and antibody drug conjugates. Gain access to comprehensive biologics services in support of advanced development programs with Frontage’s bioanalytical laboratory. We have the capabilities to analyze virtually any peptide, protein, or antibody, and have built a reputation for solving technical challenges related to assay development and validation. Position Summary This is a technical bench scientific position within the Biologics Service Team. The Biologics Service Team is responsible for conducting bioanalytical methods Pharmacokinetics (PK), and Anti-drug Antibody (ADA) related to large molecule biotherapeutic drug development across all therapeutic areas, spanning nonclinical studies to post-market clinical development. The scientist will assist with the interpretation of data resulting from analyses of bioanalytical samples, and work with senior staff to assess, troubleshoot, develop, and validate new assays. They may also perform other duties, as assigned, to meet business needs. Responsibilities 
<ul>
<li> Responsible for qualification and preparation of controls and reagents to support PK, and ADA assay methods to quantify concentrations of therapeutic proteins.</li>
<li> Required to assist with assay validations, routine lab operations.</li>
<li> Responsible for maintaining an electronic lab notebook, participation in GLP compliance activities and other duties as needed.</li>
<li>Performs job duties with some supervision. Collaborates effectively with fellow team members following priorities, checkpoints, and timelines in support of objectives set by direct supervisors.</li>
<li>Communicates with internal and external team members regarding assigned tasks through written and oral communication. </li>
</ul>
Requirements 
<ul>
<li> BS or MS in biochemistry, biomarker, molecular biology, or a related field.</li>
<li> Experience in immunoassay development and validation in a GLP lab (21CFR part 11 compliant) is preferred.</li>
<li> Experience with Meso Scale Discovery (MSD) immunoassays or ELISA.</li>
<li> Experience in a biopharma company, Clinical Research Organization (CRO) or diagnostic lab environment is preferred. </li>
</ul>
Salary And Benefits Frontage Laboratories offers a competitive compensation and benefits package including health and dental insurance, a 401(k) plan, disability insurance, and life insurance Frontage Laboratories Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, among other things, or status as a qualified individual with disability.

Associate Scientist/Scientist-Biologics

<h3>Job Description</h3>
Job DescriptionCompany Description 
LGC is a leading, global life science tools company, providing mission-critical components and solutions into high-growth application areas across the human healthcare and applied market segments. Our high-quality product portfolio is comprised of mission-critical tools for genomic analysis and for quality assurance applications, which are typically embedded and recurring within our customers’ products and workflows and are valued for their performance, quality and range.
Our tools play a key role in customer workflows from discovery applications through to commercial manufacture and enable its customers to: bring new diagnostics and therapies to market; progress research and development; optimize food production; and continuously monitor and enhance the quality of food, the environment and consumer products.
Job Description 
The Associate Scientist II, Production is responsible for the manufacture of site product within one or more portfolios in a cost-effective manner and in compliance with appropriate quality and safety standards. This role supports departmental success by following approved operational protocols, using good documentation practices, escalating process variances, and helping to maintain a clean and safe work environment. This position is also expected to support or participate in process improvement activities, quality investigations, and operational excellence (OE) initiatives.
To perform this job successfully, an individual must be able to capably perform each of the following essential duties:&nbsp;
<ul>
<li>Contribute to operations teams performing manufacturing, quality control, and production maintenance activities in a manner consistent with&nbsp;the company quality and safety standards&nbsp;</li>
<li>Assist&nbsp;in&nbsp;the&nbsp;fermentation and purification of recombinant proteins from different expression systems&nbsp;</li>
<li>In accordance with&nbsp;designated procedures and work instructions, prepare and&nbsp;operate&nbsp;chromatography systems, dialysis/TFF operations, and reagent preparation&nbsp;&nbsp;</li>
<li>Support and follow production protocols geared towards robust and cost-effective supply of molecular biology&nbsp;product and&nbsp;NGS proteins&nbsp;</li>
<li>Process, record, and&nbsp;analyze&nbsp;data following approved protocols and using good documentation practices&nbsp;&nbsp;</li>
<li>Identify&nbsp;and escalate events that deviate from normal operations&nbsp;&nbsp;</li>
<li>Support process improvements, nonconformance reporting, investigations, and corrective/preventative actions as assigned&nbsp;</li>
<li>Effectively communicate results to&nbsp;immediate team, and other stakeholders as directed&nbsp;</li>
<li>Maintain cleanliness and orderliness of operational area&nbsp;and work environment&nbsp;&nbsp;</li>
<li>Conscientiously learn and diligently follow the requirements of the site’s quality management system&nbsp;</li>
<li>Adhere to company Personal Protection Equipment (PPE) policy&nbsp;</li>
<li>Perform other duties as&nbsp;required, or assigned by management, to meet business needs&nbsp;</li>
</ul>
Qualifications 
<ul>
<li>Bachelor’s degree in relevant life sciences field (molecular biology, microbiology, biochemistry, etc.)—or applicable industry experience&nbsp;&nbsp;</li>
<li>Prior experience operating standard laboratory equipment (e.g.&nbsp;pH meters, conductivity meters, pipettes)&nbsp;</li>
<li>Ability to follow standard operating procedures (SOP’s) and/or manufacturing protocols&nbsp;</li>
<li>Familiarity&nbsp;with standard biological and analytical techniques, including PCR, SDS-PAGE, and western blotting&nbsp;</li>
<li>Prior experience with&nbsp;manual&nbsp;or&nbsp;automated&nbsp;chromatography&nbsp;systems&nbsp;or processes&nbsp;(e.g.,&nbsp;AKTA platform)&nbsp;</li>
<li>Proven ability to effectively communicate work results, including technical data, to colleagues&nbsp;</li>
<li>Working knowledge of Microsoft Office, including Word, Excel, and PowerPoint&nbsp;</li>
</ul>
Desired&nbsp;Knowledge &amp;&nbsp;Qualifications:&nbsp;
<ul>
<li>Prior experience performing fermentation, protein&nbsp;production&nbsp;and purification in an industrial setting&nbsp;</li>
<li>Prior experience performing operations on the&nbsp;AKTA platform&nbsp;and executing&nbsp;depth-filtration and Tangential Flow Filtration operations&nbsp;</li>
<li>Experience with functional testing (PCR, LAMP, etc.)&nbsp;&nbsp;</li>
<li>Experience with bacteria fermentation&nbsp;</li>
</ul>
 Additional Information 
About LGC:
LGC is a leading, global life science tools company, providing critically important components and solutions into high-growth application areas across the human healthcare and applied market segments. Its high-quality product portfolio is comprised of critical tools for genomic analysis and for quality assurance applications, which are typically embedded and recurring within our customers’ products and workflows and are valued for their performance, quality, and range.
Our values
<ul>
<li>PASSION</li>
<li>CURIOSITY</li>
<li>INTEGRITY</li>
<li>BRILLIANCE</li>
<li>RESPECT</li>
</ul>
Equal opportunities
LGC strongly believes that every job applicant and employee should be valued for their individual talents regardless of age, disability, race, color, ethnic or national origin, sex, sexual orientation, gender reassignment, marital or civil partnership, pregnancy or parental status, religion, or belief. Short listing, interviewing and selection will always be carried out without regard these factors.
For more information about LGC, please visit our website <a href="http://www.lgcgroup.com" target="_blank">www.lgcgroup.com</a>
#scienceforasaferworld

Associate Scientist II, Production

<h3>Job Description</h3>
Job Description
Senior Scientist III (iPSC-Derived Gut Models) Cambridge, MA (Lab Based Position) Pay Rate: $70 -77/hr W2
This 24+ Month Contract Position Has A Tentative Start Date of 2/2/26 Role Overview: We are seeking a hands-on Scientist with strong experimental biology expertise to advance iPSC-derived gut models for evaluating combination therapies for inflammatory diseases (e.g., IBD). Working closely with DAGS, Immunology, and Pharmacology colleagues, the contractor will culture and differentiate human iPSCs into intestinal lineages (e.g., epithelial monolayers and 3D organoids/enteroids), establish microphysiological systems, and design and execute combination therapy studies. The successful candidate will optimize functional assays, perform dose–response and matrixed combination experiments, analyze synergy/antagonism, and deliver clear, actionable data packages to cross-functional teams. Required Qualifications: • MS with 5+ years or PhD with 1–2+ years of relevant experience in molecular/cellular biology, immunology, pharmacology, or related field • Hands-on experience with human cell culture and at least one of: o iPSC maintenance and differentiation into epithelial/endodermal lineages o Intestinal organoids (enteroids) or epithelial monolayers • Proven ability to execute and troubleshoot functional assays; experience running dose–response studies and quantitative assay analysis • Strong documentation, data analysis, and presentation skills; success working in collaborative, cross-functional settings • Following aseptic processes Preferred Qualifications • Direct experience with iPSC-derived intestinal models, including 3D organoids, 2D monolayers, Transwells, and/or gut-on-chip systems • Expertise in barrier function assays (TEER, permeability), imaging-based analyses, and cytokine profiling • Experience with automation, liquid handling, and high-throughput assay development • Background in inflammatory disease biology and prior industry experience in preclinical combination testing or pharmacology Job Description: The Merck Genome Sciences (GS) iPSC disease modeling group within the Department of Data, AI, and Genome Sciences (DAGS) partners with Immunology and cross-functional teams to evaluate therapeutic strategies based on human-relevant models. Our mission is to build and apply robust iPSC-derived systems to understand mechanisms in human disease and to test mono- and combination therapies under controlled, scalable in vitro conditions. We leverage genetic and pharmacological perturbations in iPSC-derived gut models to inform therapeutic combination design and prioritization. The contractor is expected to work both independently and collaboratively in a dynamic early discovery environment. • Develop, optimize, and execute iPSC-derived gut model systems: o Differentiation of iPSCs into 3D intestinal organoids. o Co-cultures with immune cells (e.g., macrophages, dendritic cells, T cells), and 3D organoid model system. o Microphysiological platforms to model barrier and tissue microenvironment • Design and run combination therapy studies: o Plan mono- and pairwise/multi-drug matrices; include biologics, small molecules, and pathway-targeted agents o Execute dose–response and time-course experiments; incorporate inflammatory stimuli (e.g., cytokine cocktails, bacterial products) to model disease-relevant contexts o Analyze combination effects for synergy/additivity/antagonism and generate decision-enabling summaries • Apply quantitative, mechanism-informed readouts: o Barrier integrity and function assays (TEER, permeability, wound healing, mucus layer assays) o Inflammatory and cell-state profiling (cytokine/chemokine panels via ELISA/MSD, qPCR/RT-qPCR, flow cytometry, high-content imaging, immunofluorescence) o Transcriptomic profiling (bulk or single cell preferred) for pathway engagement; collaborate with data scientists for analysis. • Implement perturbations and model qualification: o Genetic and pharmacological perturbations to dissect mechanisms and predict combination responsiveness. o Assess reproducibility, dynamic range, and throughput; adapt assays to plate-based formats (96-/384-well) and support automation readiness. • Collaborate cross-functionally: o Partner with immunology, pharmacology, and data science teams to prioritize combinations, refine hypotheses, and align in vitro models with translational endpoints. o Present experimental plans and results to internal stakeholders, including senior leadership; maintain rigorous documentation and SOPs. • Ensure compliance with safety practices and proper maintenance of cell lines, reagents, and equipment. Johnson Service Group, Inc. (JSG) is a North American leader in the staffing and consulting services industry, with over 35 years of experience investing in people and companies. Johnson Service Group (JSG) is an Equal Opportunity Employer. JSG provides equal employment opportunities to all applicants and employees without regard to race, color, religion, sex, age, sexual orientation, gender identity, national origin, disability, marital status, protected veteran status, or any other characteristic protected by law.
Company DescriptionOur people and culture make JSG a great place to work. JSG’s mission is to empower people, help our clients reach their goals, and hire motivated individuals. Johnson Service Group, Inc. (JSG) is a North American leader in the staffing and consulting services industry, with 40 years of experience investing in people and companies. We are always looking for great people to join our team—we want to see your success here at JSG! We can be found locally in more than 30 offices throughout the United States and Canada. JSG continues to work diligently to offer our clients and candidates world-class service and diversified offerings to fit their evolving needs. We offer medical, dental, vision, life insurance options, 401(k), weekly pay, and more. Johnson Service Group (JSG) is an Equal Opportunity Employer. JSG provides equal employment opportunities to all applicants and employees without regard to race, color, religion, sex, age, sexual orientation, gender identity, national origin, disability, marital status, protected veteran status, or any other characteristic protected by law. 
<h3>Company Description</h3>
Our people and culture make JSG a great place to work. JSG’s mission is to empower people, help our clients reach their goals, and hire motivated individuals.\r\n\r\nJohnson Service Group, Inc. (JSG) is a North American leader in the staffing and consulting services industry, with 40 years of experience investing in people and companies. We are always looking for great people to join our team—we want to see your success here at JSG! We can be found locally in more than 30 offices throughout the United States and Canada. JSG continues to work diligently to offer our clients and candidates world-class service and diversified offerings to fit their evolving needs.\r\n\r\nWe offer medical, dental, vision, life insurance options, 401(k), weekly pay, and more.\r\n\r\nJohnson Service Group (JSG) is an Equal Opportunity Employer. JSG provides equal employment opportunities to all applicants and employees without regard to race, color, religion, sex, age, sexual orientation, gender identity, national origin, disability, marital status, protected veteran status, or any other characteristic protected by law.

Biological Scientist

<h3>Job Description</h3>
Job Description
Purpose and Scope
The Technical Manager is responsible for managing and supporting customer-focused technical projects. This role ensures that customer requirements for material performance, processing, and application are met through effective formulation development, testing, and technical service.
The position works closely with customers, sales, production, and quality teams to develop and modify compounds, support product trials, and resolve technical issues. The Technical Manager also collaborates with the Group R&amp;D organization to transfer new technologies, share application knowledge, and align local development activities with global initiatives.
This role oversees day-to-day laboratory operations, ensuring accurate formulation work, proper documentation, and compliance with company and regulatory standards. The Technical Manager plays a key role in supporting continuous improvement of products and processes to meet evolving customer and market needs.
Essential Duties and Responsibilities
This list of duties and responsibilities is not all-inclusive and may be expanded to include other duties and responsibilities, as management may deem necessary from time to time. Duties may be accomplished by the incumbent or through the utilization of appropriate staff and resources.
&nbsp;Leadership and Team Management
<ul>
<li>Lead and develop the local technical team at the Broadview facility, including laboratory and technical support staff.</li>
<li>&nbsp;Manage R&amp;D resources, including budgets, equipment, staffing, and workload planning.</li>
<li>&nbsp;Oversee recruitment, training, performance evaluations, and employee development to build technical capability and career growth.</li>
<li>&nbsp;Establish clear priorities and ensure timely completion of customer projects, testing, and product development activities.</li>
<li>Promote a positive, collaborative culture across departments and within the technical team.</li>
</ul>
Customer and Commercial Support
<ul>
<li>&nbsp;Maintain strong relationships with key customers and suppliers, providing technical support and collaboration on new product initiatives.</li>
<li>Serve as the primary technical contact for customers, offering formulation guidance, processing recommendations, and troubleshooting assistance.</li>
<li>&nbsp;Support the sales team with product development, technical data, and customer presentations or training.</li>
</ul>
&nbsp;Product and Process Development
<ul>
<li>&nbsp;Manage and execute technical projects involving new product development, compound modification, and process optimization.</li>
<li>&nbsp;Develop and test formulations to meet customer performance, regulatory, and cost targets.</li>
<li>Oversee product approval processes, testing protocols, and specification management.</li>
<li>Evaluate and approve raw materials and ensure accurate item master, finished compound recipe, and test specifications maintenance within the ERP system.</li>
<li>Support production scale-up, ensuring smooth transitions from laboratory to full-scale manufacturing.</li>
</ul>
Regulatory and Quality Compliance
<ul>
<li>Ensure all products and raw materials comply with applicable regulatory and product safety standards (e.g., REACH, RoHS, FDA, Proposition 65).</li>
<li>Maintain technical documentation and regulatory data to support customer and internal compliance requirements.</li>
<li>Develop and maintain R&amp;D procedures and standard work practices in alignment with ISO and company management systems.</li>
<li>Ensure full technical compliance with federal, state, and local safety and environmental regulations.</li>
</ul>
Continuous Improvement and Collaboration
<ul>
<li>&nbsp;Work with Group R&amp;D and VP of Operations to share knowledge, transfer technology, and support global development initiatives.</li>
<li>Drive continuous improvement in product quality, process efficiency, and operational consistency.</li>
<li>Participate in cross-functional initiatives to improve production output, reduce costs, and support sustainability objectives.</li>
<li>Provide technical training internally and externally as needed.</li>
</ul>
Ideal Competencies Required for Role
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodation may be made to enable individuals with disabilities to perform essential functions.
<ul>
<li>Technical Expertise: Deep knowledge of thermoplastic compounding and related R&amp;D processes. Experience with thermoplastic elastomers is highly desirable.</li>
<li>&nbsp;Able to provide guidance, make informed decisions, and support the success of the technical team.</li>
<li>Leadership and Staff Management: Proven ability to lead, develop, and empower employees, fostering a collaborative, high-performing team environment. Skilled in providing feedback, mentoring, and creating development plans.</li>
<li>&nbsp;Planning and Process Management: Strong skills in organizing, prioritizing, and overseeing technical projects, ensuring timely completion and alignment with organizational goals.</li>
<li>&nbsp;Forward-Thinking and Innovation: Ability to identify opportunities for product, process, and organizational improvements. Open to new ideas, technologies, and approaches.</li>
<li>&nbsp;Effective Communication: Excellent communication skills, capable of conveying complex technical information clearly to both technical and non-technical stakeholders. Skilled at listening and providing constructive feedback.</li>
<li>Collaboration: Works effectively across departments, including marketing, production, quality, and sales, to ensure technical efforts support broader organizational objectives.</li>
<li>Resource Management: Skilled in managing budgets, equipment, and personnel efficiently to optimize research efforts.</li>
<li>Problem Solving and Analytical Skills: Strong mathematical, reasoning, and troubleshooting abilities to resolve technical and material challenges.</li>
<li>Attention to Detail: High level of diligence, accuracy, and focus on quality in all technical and operational activities.</li>
<li>Time Management and Adaptability: Able to manage multiple priorities, meet tight deadlines, remain calm under pressure, and adjust plans as needed to respond to changing circumstances.</li>
</ul>
Education and/or Experience
<ul>
<li>Requires a master’s degree in Polymer Chemistry or related discipline.</li>
<li>Requires a minimum of 10 years of experience in thermoplastic chemistries and experience in a plastic compounding manufacturing environment.</li>
<li>&nbsp;Knowledge of analytical instrumentation and testing methods is highly desirable</li>
<li>Requires proficiency in Microsoft Office including Word, Excel, Access, and Outlook.</li>
<li>&nbsp;Requires experience with Project management, CRM, ERP, and MRP systems.</li>
</ul>
Physical Requirements
While performing the duties of this Job, the employee is regularly required to talk or hear. The employee is frequently required to sit; use hands to finger, handle, or feel and reach with hands and arms. The employee is occasionally required to stand; walk; climb or balance and stoop, kneel, crouch, or crawl. The employee must occasionally lift and/or move up to 60 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus.
Work Environment
While performing the duties of this position, the employee is frequently exposed to moving mechanical parts. The employee is occasionally exposed to high, precarious places; fumes or airborne particles; extreme heat; risk of electrical shock and vibration. The noise level in the work environment varies from loud when in the plant area to quiet in the office areas.
Company DescriptionHexpol TPE is a leading provider of custom-engineered thermoplastic elastomer (TPE) compounds, serving a wide range of industries including automotive, consumer goods, healthcare, and industrial applications. As part of the global Hexpol Group, Hexpol TPE combines deep technical expertise with a strong commitment to innovation, sustainability, and customer-focused solutions. With advanced manufacturing capabilities and a dedicated team our US location in Broadview IL offers high-performance materials tailored to meet the evolving needs of customers across the Americas region. 
<h3>Company Description</h3>
Hexpol TPE is a leading provider of custom-engineered thermoplastic elastomer (TPE) compounds, serving a wide range of industries including automotive, consumer goods, healthcare, and industrial applications. As part of the global Hexpol Group, Hexpol TPE combines deep technical expertise with a strong commitment to innovation, sustainability, and customer-focused solutions. With advanced manufacturing capabilities and a dedicated team our US location in Broadview IL offers high-performance materials tailored to meet the evolving needs of customers across the Americas region.

Research and Development Manager

<h3>Job Description</h3>
Job DescriptionCelerion is committed to swift, exceptional clinical research through translational medicine.&nbsp;&nbsp;Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.&nbsp;&nbsp; We're seeking an Instrument Scientist/Associate Scientist&nbsp;to join our Dose Formulation team at our facility in Lincoln, NE, located just south of downtown.&nbsp;In this lab-based role, you'll execute critical tests to ensure compounds from our in-house pharmacy meet all required specifications for use in clinical research trials.&nbsp;If you're driven by tight timelines and passionate about advancing human health, this could be the role for you. You'll leverage your expertise in analytical chemistry to ensure every dose is ready for delivery on schedule.Essential Functions:
<ul>
<li>Partner with senior scientists to develop chromatographic in support of dose formulation testing</li>
<li>Complete tasks necessary for daily operation in the laboratory: execute analytical tests to ensure the accuracy, homogeneity and precision to support on-site compounding by the Celerion Pharmacy team.</li>
<li>Preparation of standard calibrators, quality controls, mobile phases, and solutions for the purpose of testing dose formulations.</li>
<li>Inventory and re-order parts when used for instrument maintenance and repair</li>
<li>Assist in troubleshooting instrumentation aspects of studies</li>
<li>Take part in instrumentation upkeep by observing the maintenance schedule and performing calibrations and preventative maintenance</li>
<li>Communicate results effectively and in a timely manner to other associates</li>
<li>Initiate, introduce, and implement new guidelines and procedures through the development of working instructions</li>
<li>Optimize instruments to support ruggedness testing, production flexibility, and production</li>
<li>Prepare documentation to share method development results with the sponsor</li>
<li>Write detailed methodologies and provide feedback on Dose Formulation Protocols.</li>
</ul>
Requirements:
<ul>
<li>Bachelor's degree in Chemistry, Biochemistry, or related scientific field</li>
<li>3-5 years of hands-on experience with analytical instrumentation and/or method development (highly preferred)</li>
<li>Self-directed, self-motivated, and detail-oriented</li>
<li>Strong desire to learn new techniques with openness to cross-training opportunities</li>
<li>Flexibility to work outside normal business hours as needed to meet testing timelines, including occasional long days, evenings and weekends</li>
</ul>
Celerion Values:&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Integrity&nbsp; &nbsp;Trust&nbsp; &nbsp;Teamwork&nbsp; &nbsp;Respect Celerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

Instrument Scientist /Associate Scientist - Dose Formulation

<h3>Job Description</h3>
Job DescriptionCompany Description 
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.
Eurofins is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. The Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 50 countries. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.
Job Description 
Eurofins Medical Device Services is seeking a highly experienced Senior Scientific Advisor with deep expertise in medical device biocompatibility and chemistry to provide scientific leadership and strategic guidance for our testing services. This role is critical in supporting clients with complex regulatory and technical challenges, ensuring compliance with ISO 10993 and related standards, advancing Eurofins’ position as a trusted partner in the medical device industry.
As a senior technical advisor, you will collaborate with clients, internal teams, and regulatory bodies to design scientifically robust testing programs, interpret results, and deliver actionable insights. This position is ideal for professionals who combine advanced scientific knowledge with strong communication and advisory skills.
Key Responsibilities:
<ul>
<li>Serve as the subject matter expert in biocompatibility and chemistry services for medical devices, including an understanding of toxicological risk assessments, biological plans and reports.</li>
<li>Actively prospect, engage, and close new client relationships to drive top-line revenue growth and expand market share in the microbiological and sterilization testing space.</li>
<li>Collaborate with Sales and Key Account Managers to position Eurofins’ microbiology and sterilization services as a best-in-class solution, improving quote-to-win ratios.</li>
<li>Lead the development of technical scopes of work and respond to RFQs/RFPs with compelling, scientifically robust proposals.</li>
<li>Provide strategic insights to business development and operations leadership to ensure alignment of service offerings with market demands.</li>
<li>Represent Eurofins at conferences, trade shows, and industry events to enhance visibility and establish thought leadership.</li>
<li>Facilitate seamless handoffs to project management and operations teams, ensuring successful project execution and client satisfaction.</li>
<li>Monitor the competitive landscape and market trends to support pricing strategy and service differentiation.</li>
<li>Travel 30–50% to meet with clients, attend events, and support on-site collaboration with Eurofins teams.</li>
</ul>
Qualifications 
<ul>
<li>Bachelor’s degree in Biology, Chemistry, Biochemistry, or a related field is required; advanced degree is strongly preferred.</li>
<li>Minimum 7+ years of experience in biocompatibility and chemical characterization within a CRO or medical device environment.</li>
<li>In-depth knowledge of ISO 10993 standards, FDA and international regulatory requirements.</li>
<li>Strong analytical and problem-solving skills with the ability to interpret complex data sets.</li>
<li>Excellent verbal and written communication skills; ability to present technical concepts clearly to diverse audiences.</li>
<li>Collaborative mindset with proven ability to influence and guide cross-functional teams.</li>
<li>Authorized to work in the U.S. without restriction or sponsorship.</li>
</ul>
 Additional Information 
Full-time, Monday–Friday, 8 a.m.–5 p.m. (flexibility required). Remote position with preference for candidates near a major airport for travel to client sites and industry events.
What we offer:
<ul>
<li>Excellent full time benefits including comprehensive medical coverage, dental, and vision options</li>
<li>Life and disability insurance</li>
<li>401(k) with company match</li>
<li>Paid vacation and holidays</li>
</ul>
Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.

Senior Scientific Advisor - Biocompatibility & Chemistry

<h3>Job Description</h3>
Job Description
Kahala, a globally recognized leader in quick-service restaurant franchising, has an opportunity for a Research and Development Chef to join its Ops Services Team in Scottsdale, Arizona. Kahala franchisees and partners operate a portfolio of many QSR brands including Cold Stone Creamery, Blimpie, Baja Fresh, Pinkberry, among others, in over 20 countries around the world.
Equal Opportunity Employer M/F/D/V
POSITION SUMMARY
Serve as an R&amp;D Chef for Kahala Brands. Develop new products, procedures and processes for various savory brands. Work with internal teams and suppliers to make improvements to existing products. Work closely with Operations and Purchasing to procure products as needed. Mentor R&amp;D Manager to promote knowledge, skills, and growth. Monitor current industry trends, consumer insights and competitive restaurant/menu strategies. Assist with the setup, execution and breakdown of headquarters meetings, events and employee activities.
 
KEY RESPONSIBILITIES
<ul>
<li>Create and develop new products, menu items and product lines for a variety of savory brands</li>
</ul>
<ul>
<li>Lead product development ideation process and create LTO/promotional menu items</li>
<li>Develop and refine specifications for new and/or existing products</li>
<li>Conduct product evaluations while maintaining food safety and regulatory requirements specific to the menu development</li>
<li>Provide technical expertise and resolve any technical, operational and performance issues that arise during product development </li>
<li>Analyze feedback and results from product cuttings</li>
<li>Complete accurate food costing and ingredients for developed products </li>
<li>Work with multiple departments on all aspects of test programs and product rollouts, including Purchasing, Distribution, Marketing, Operations and Training</li>
<li>Conduct equipment testing</li>
<li>Meet with suppliers for prospective new products, ideations for new items and improvements for existing items</li>
<li>Develop new menus for emerging brands</li>
<li>Assist with product photoshoots and pre-shoot preparation of products</li>
<li>Mentor R&amp;D Manager to promote knowledge, skills, and growth</li>
<li>Share responsibilities for nutritional analysis using ESHA Genesis nutrition software</li>
<li>Monitor current industry trends, consumer insights and competitive restaurant/menu strategies</li>
<li>Support various Ops Services team responsibilities and assist with headquarters events such as dry run fundraisers, employee lunches and employee activities (e.g., planning/setting up/hosting/breaking down headquarters events)</li>
</ul>

KNOWLEDGE / SKILLS
<ul>
<li>Culinary Arts degree; preferred Bachelor’s in culinary, foodservice, food science or hospitality</li>
<li>Minimum 1-3 years of experience in restaurant back of house </li>
<li>Basic knowledge of food production and processing</li>
<li>Basic culinary knowledge, technical skills and understanding of restaurant equipment and services</li>
<li>Thorough knowledge of food products, recipes and procedural writing, and food costing</li>
<li>Thorough knowledge of food safety standards, HAACP and Serve Safe Certification</li>
<li>Excellent verbal and written communication skills</li>
<li>Strong skills in Microsoft (e.g., Word, Publisher, PowerPoint and Excel)</li>
<li>Ability to handle a variety of different tasks at once, prioritizing and sequencing actions/decisions to move tasks toward execution</li>
<li>Organized, detail-oriented and able to work independently, as well as part of a team</li>
<li>Enthusiastic, optimistic and service-minded team player</li>
<li>Demonstrated desire for continuous learning and improvement</li>
</ul>
Benefits (Subject to Change):
<ul>
<li>401(k) matching, including Roth options</li>
<li>3 Medical insurance plans</li>
<li>Dental insurance</li>
<li>Vision insurance</li>
<li>Employee assistance program</li>
<li>Flexible spending account</li>
<li>Health savings account</li>
<li>Life insurance</li>
<li>Short-term disability insurance</li>
<li>Long-term disability insurance</li>
<li>Paid time off (10 holidays, 3 weeks PTO)</li>
<li>Tuition reimbursement</li>
<li>Referral program</li>
<li>Wellness programs</li>
<li>Hybrid work schedule</li>
</ul>

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