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<h3>Job Description</h3>
Job Description
10840 – Technical Operations Engineer &nbsp; Location: Costa Mesa, CA (5 days a week on-site)
 Company Overview &nbsp;
Hyundai AutoEver America (HAEA) is the dynamic IT powerhouse behind Hyundai Motor Corporation, a Fortune 500 global leader in the automotive industry. As a key affiliate, we provide cutting-edge IT services and support to top brands including Kia, Genesis, Hyundai Translead, Hyundai Mobis, Hyundai Capital, and Glovis.&nbsp;
HAEA offers a truly global and collaborative environment. Here, you’ll drive innovation, boost operational efficiency, and help shape the future of mobility for the Hyundai Motor Group.&nbsp;
At HAEA, we understand that IT is the cornerstone of today’s fast-evolving digital world. By uniting all IT resources under one roof, we deliver consistent, top-quality solutions while serving as the crucial information link between Hyundai’s Global Headquarters and North American operations.&nbsp;
If you’re passionate about technology and eager to make a real impact at a world-class company, Hyundai AutoEver America is the place to grow your career. Join us and be part of the transformation that’s driving the future of automotive innovation.&nbsp;
Website: <a href="http://www.haeaus.com&amp;nbsp" target="_blank">http://www.haeaus.com&amp;nbsp</a>;
Role Overview The selected candidate will perform validation of server-based route navigation for all navigation systems installed in Hyundai, Kia, and Genesis vehicles in order to enhancing the accuracy of traffic information, improving route quality, and providing recommended routes for user convenience. You will evaluate new features and quality enhancements relevant to our navigation systems by continuously analyzing and improving quality assessment and management efficiency in an effort to provide the best service to our customers and secure global competitiveness in navigation software quality.&nbsp;
<ul>
<li>You will be responsible for the North American Connected Routing (SBR - Server Based Routing) operation. You will collect, interpret, and visualize driving test data for the purpose of improving user experience by comparing, analyzing, and benchmarking tests against competitors to improve connected routing quality.&nbsp; &nbsp;</li>
<li>You will oversee the report on daily/monthly user usage trends by cross analyzing data from the connected car service (CCS) servers and geographic information systems (GIS) servers and analyze the accuracy of traffic data from the multiple providers using organizational scoring methods&nbsp;</li>
<li>Research and prepare required test environments and corresponding vehicles to confirm the functionality of software including planning and performing driving field tests for software updates, routes and traffic quality&nbsp;</li>
<li>You will collaborate with various teams including the HQ dev team and the various CCS teams regarding server issues, system maintenance, and client requests, as well as&nbsp;report maps related issues to the provider and test the corrections&nbsp;</li>
</ul>
Please note this job description is not designed to cover or contain a comprehensive list of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice. &nbsp;
Basic Qualifications&nbsp;
<ul>
<li>Bachelor's degree or equivalent experience in IT, Automotive, Mechatronics, Electrical, Electronic Computer Science, Industrial Engineering, Geographic Information Science and Information Technology majors or any related field preferred.</li>
<li>Minimum of 6 years of experience in quality assurance, engineering, or other related field</li>
<li>Minimum of 1 year at senior level or Subject Matter Expert (SME) using test automation tools</li>
<li>Understanding and ability to use collaboration tools (JIRA, Confluence, etc.)</li>
<li>Be able to drive for long periods of time and with previous experience using Connected Car Services such as OEM navigation systems from any car manufacturer</li>
</ul>
 Preferred Qualifications&nbsp;
<ul>
<li>Understanding quality processes related to software development and knowledgeable in test modeling</li>
<li>Understanding of server software and architecture</li>
<li>Skills with analyzing data using tools such as SQL and Excel&nbsp;</li>
</ul>
Team Culture&nbsp;
Our team thrives on collaboration, innovation, and continuous learning. We foster a supportive environment where every member is encouraged to share ideas and contribute to problem-solving. We value: &nbsp;
<ul>
<li>Passion for Technology: We are enthusiastic about emerging technologies and their potential to transform the automotive industry. &nbsp;</li>
<li>Agility: We work in an agile environment, adapting quickly to changes and continuously improving our processes. &nbsp;</li>
<li>Teamwork: We believe in the power of teamwork and collaboration, supporting each other to achieve common goals. &nbsp;</li>
<li>Growth: We prioritize personal and professional growth, offering opportunities for learning and development. &nbsp;</li>
<li>Inclusivity: We maintain an inclusive culture where diverse perspectives are valued and everyone feels welcome. &nbsp;</li>
</ul>
Base Salary Range:&nbsp;$36-44 /hour&nbsp;
Our Company adheres to the equal employment opportunity guidelines set forth by federal, state and local laws.&nbsp;The information requested on this form is sought in good faith and will not be used to discriminate against the applicant based on race, religion or creed, color, national origin, ancestry, physical disability, mental disability, medical condition, genetic characteristics, marital status, sex or gender (which includes pregnancy, childbirth, or related circumstances), gender identity, gender expression, age, citizenship, sexual orientation, family care or medical leave status, military and veteran status, political affiliation, or any other characteristic protected by federal, state and local laws. &nbsp;
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10840-Technical Operations Engineer (GIS)

<h3>Job Description</h3>
Job Description
Organization Overview
The National Institute for Children’s Health Quality (NICHQ) is a mission-driven nonprofit dedicated to driving dramatic and sustainable improvements in the complex issues facing children’s health. We provide deep expertise in building and managing effective change strategies that align partners and engage participants to achieve better outcomes for children’s health. 

Position Overview 
The Senior Analyst brings knowledge of and experience in applied research and evaluation and applies that knowledge to lead the successful design, execution and management of projects in the context of NICHQ’s maternal child health work. The Senior Analyst works closely and collaboratively with the Senior leadership in Programs and in the Department of Applied Research and Evaluation (DARE), project leads, Quality Improvement Advisors, expert faculty members, funders, and project teams to design and execute applied research and evaluation work that provides high-quality, relevant data analysis and recommendations across the lifecycle of projects. The Senior Analyst plays an integral and leadership role on NICHQ’s Applied Research and Evaluation team, guiding the department’s work (under the supervision of the Associate Director and senior leadership in DARE), as well as in the team’s work to capture, develop, and spread innovative approaches. The Senior Analyst may provide additional research consulting services and assist in elevating NICHQ’s standing in the scientific community by driving strategic planning for publications and conference presentations. 

Summary 
Career Level: Experienced 
Status: Full-Time, Exempt Employee, US Based Remote
Education: Master’s degree required; doctoral degree in relevant discipline preferred 
Reports to: Principal Analyst Department of Applied Research and Evaluation (DARE) 
Salary: $84,000 

Responsibilities 
<ul>
<ul>
<li>Applied research and evaluation tasks including
<ul>
<li>Planning
<ul>
<li>Create and implement plans for data management and analytic file creation</li>
<li>Collaborate with program staff to meet project deliverables on schedule</li>
</ul>
</li>
<li>Data collection and management
<ul>
<li>Design, build and maintain REDCap databases to support research data collection efforts</li>
<li>Create and optimize data collection instruments ensuring alignment with research objectives and reporting requirements</li>
<li>Develop and implement data collection protocols, including date entry guidelines, access controls and validation rules</li>
<li>Establish and maintain quality assurance and quality control systems</li>
<li>Perform data validation checks and produce reports for internal teams and external stakeholders</li>
<li>Investigate, track, and resolve data queries, support extant data transfer efforts</li>
<li>Lead data harmonization efforts across data sources</li>
<li>Provide technical guidance and support on REDCap functionalities and best practices to project teams</li>
</ul>
</li>
<li>Data analysis
<ul>
<li>Clean, transform, and validate data to ensure accuracy and readiness for analysis</li>
<li>Conduct descriptive and inferential analysis using statistical software such are SAS to inform research findings</li>
<li>Utilize knowledge of statistical methodology to inform study design and operations.</li>
<li>Provide consultation to other project teams on statistical analysis techniques (e.g., sampling, random assignment, application scoring and weighting), as needed</li>
<li>Keep abreast of current trends in statistical methods and program evaluation</li>
</ul>
</li>
<li>Reporting and dissemination
<ul>
<li>Prepare comprehensive summaries and graphic representations of statistical findings across different formats</li>
<li>Review abstracts for professional conferences and manuscripts for peer-reviewed publications</li>
<li>Provide consultation to project teams in their development of reports and other materials that include research data</li>
</ul>
</li>
</ul>
</li>
<li>Identifies and appropriately brings complex project insights, concerns, and potential solutions in a timely manner to project and DARE lead(s) and collaborates to implement solutions</li>
<li>May be responsible for the supervision and development of individuals working in applied research and evaluation</li>
<li>Represents the Applied Research and Evaluation team on projects in a collaborative and supportive manner and participates in other activities of the applied research and evaluation team as needed</li>
</ul>
</ul>

Skills and Knowledge
<ul>
<li>Demonstrates subject matter expertise in data management, biostatistics and/or epidemiology</li>
<li>Synthesizes complex information into usable formats</li>
<li>Works independently, capable of making decisions with limited oversight</li>
<li>Ability to manage multiple projects and meet deadlines with minimal support from supervisor while working remotely</li>
<li>Strong communications skills (both verbal and written)</li>
</ul>
 Qualifications and Characteristics
<ul>
<li>Master’s degree or MPH in biostatistics or epidemiology; at least 3 years’ work experience in a health services, social science, or clinical research setting doing quantitative research</li>
<li>Experience designing, building and maintaining REDCap databases</li>
<li>Extensive experience and strong programming skills in statistical software programs (e.g. SAS and R)</li>
<li>Proficient in Microsoft Office, visualization software and database management; adept at quickly learning new technologies</li>
<li>Detail-oriented “achiever” who takes initiative</li>
</ul>

Benefits 
We offer a generous benefits package for employees including competitive compensation; US based remote work; paid time off including vacation, sick and holidays; insurance including medical, dental, vision, disability and life; flexible spending accounts; employee assistance programs; paid parental leave and professional development benefits.
NICHQ is committed to increasing the representation of people from culturally and linguistically diverse backgrounds in our workforce and to value and embrace their skills, perspectives and experiences for the benefit of our mission. NICHQ is an equal opportunity employer; all qualified applicants will receive consideration for employment without regard to race, color, religion, national origin, gender or gender expression, sexual orientation, age marital status or disability. NICHQ strongly encourages applications from candidates who identify as BIPOC, LGBTQIA+, or from any other minoritized group.
To Apply 
To apply for this employment opportunity, please complete and submit an online application at NICHQ.org.

Senior Analyst, Applied Research and Evaluation

<h3>Job Description</h3>
Job Description
 Associate Scientist (Pharmacokinetics) – Biologics
 
Job Title: Associate Scientist (Pharmacokinetics) – Biologics
Location: 760 Pennsylvania Dr, Exton, PA 19341
Full-time
 
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.
 
Job Summary: We are seeking a highly motivated and detail-oriented Associate Scientist to join our Pharmacokinetics (PK) group. The successful candidate will support bioanalytical method development, validation, and sample analysis using ligand binding assays (LBA) to assess pharmacokinetics for preclinical and clinical studies. This role requires expertise in bioanalytical techniques, data analysis, and regulatory compliance.
 
Key Responsibilities:
<ul>
<li>Develop, optimize, and validate ligand binding assays (e.g., ELISA, MSD, Gyrolab) for quantifying therapeutic molecules in PK studies.</li>
<li>Perform routine bioanalysis of preclinical and clinical samples under GLP and non-GLP conditions.</li>
<li>Analyze and interpret experimental data, ensuring accuracy, reproducibility, and regulatory compliance.</li>
<li>Troubleshoot and resolve technical issues related to assay performance and instrumentation.</li>
<li>Maintain detailed and organized records of experimental procedures and results in laboratory notebooks and electronic systems.</li>
<li>Contribute to the preparation of bioanalytical reports, method validation reports, and regulatory submissions.</li>
<li>Collaborate with pharmacokinetics, toxicology, clinical, and regulatory teams to support drug development programs.</li>
<li>Ensure compliance with regulatory guidelines (GLP, FDA, EMA) and company policies for bioanalytical studies.</li>
</ul>
Qualifications:
<ul>
<li>Bachelor’s or master’s degree in Biochemistry, Molecular Biology, Immunology, Pharmaceutical Sciences, or a related field.</li>
<li>Entry-level candidates, including recent graduates, are encouraged to apply. Hands-on experience in ligand binding assay development, validation, and sample analysis through coursework, internships, or research projects is a plus.</li>
<li>Familiarity with bioanalytical techniques such as ELISA, MSD, and Gyrolab.</li>
<li>Knowledge of pharmacokinetics, immunogenicity assessment, and bioanalytical regulatory requirements.</li>
<li>Experience in a GLP-compliant environment is a plus.</li>
<li>Strong analytical and problem-solving skills with the ability to troubleshoot assay performance issues.</li>
<li>Excellent organizational skills and attention to detail.</li>
<li>Effective communication and teamwork skills to collaborate with multidisciplinary teams.</li>
</ul>
Preferred Qualifications:
<ul>
<li>Experience with automated liquid handling systems for bioanalysis is a plus; training opportunities will be provided for candidates eager to learn automation.</li>
<li>Proficient in coding language for data analysis and automation (e.g., Python, Kotlin).</li>
<li>Familiarity with software for data analysis (e.g., SoftMax Pro, Watson LIMS, GraphPad Prism).</li>
<li>Understanding of regulatory expectations for bioanalytical method validation (FDA, EMA, ICH guidelines).</li>
<li>Bilingual (Mandarin/English) preferred.</li>
</ul>
Why Join Us?
<ul>
<li>Be part of a collaborative and innovative bioanalytical team supporting groundbreaking drug development.</li>
<li>Gain exposure to cutting-edge bioanalytical techniques and regulatory-driven workflows.</li>
<li>Opportunity for career growth within a dynamic and fast-paced research environment.</li>
</ul>
If you are passionate about bioanalysis and eager to contribute to the development of novel therapeutics, we encourage you to apply for this exciting opportunity.
 
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

<h3>Job Description</h3>
Job DescriptionSalary: 
Join Our Trailblazing Team In Creating The Future Of Public Affairs Risk Analysis
 
Who We Are: Delve is not just a competitive intelligence and risk advisory firm; we're a beacon for those who dare to think differently in the realm of political and public affairs analysis. Our firm is a hub for the curious, detail-oriented, and ambitious professionals who thrive on cutting through the noise and conventional narratives to provide insights that truly matter.
 
Since our inception in 2015, we've carved a niche in delivering mission critical analysis to major corporations, trade associations, advocacy groups, and political organization who are navigating the complexities of highly scrutinized policy debates and heavily regulated industry sectors. Featured by The Washington Post, Politico, and more, our insights arm clients with the information advantage they need to mitigate political and reputational risks effectively.
 
As we serve our clients in a range of industries and policy areas, we are also developing the next generation of technology, combining the strength of artificial intelligence with our sharp analysts to make our services more efficient, effective, and accessible.
 
The Opportunity: Join us as a Research Analyst or Senior Research Analyst and embark on a journey that's not just about conducting research but about making a significant impact. Your role involves crafting forward-looking reports, analyzing trends, and keeping our clients ahead of the curve in public affairs.
 
Here, your insights are not just valued they're essential to the success of our high-profile clients. Our work delves into the heart of public affairs challenges, going beyond surface-level reporting and conventional thinking to empower our high-profile clients with the insights they need to navigate a broad range of stakeholders impacting their policy and business landscapes. At the same time, your work will enable you to build practical knowledge and functional expertise in key industries and policy areas.
 
Who You Are: You're not just looking for a job; you're seeking a career where your meticulous attention to detail, relentless pursuit of knowledge, and passion for public affairs will be celebrated and nurtured.
 
Your profile:
<ul>
<li>A voracious learner, fueled by intellectual curiosity in politics and public policy and an eye for capturing details others miss.</li>
<li>An experienced professional (minimum 2 years post-undergrad or equivalent) with a background in a fast-paced, non-academic public affairs setting, such as a political campaign, association, lobbying or public affairs firm, or Congressional or state legislative office.</li>
<li>Driven to make an impact, with a firm belief in the power of a robust free market to shape society.</li>
<li>An exceptional writer, able to turn complex research into compelling narratives.</li>
<li>Thrives on independent work but values collaboration and knowledge sharing.</li>
</ul>
 
Your Role and Growth Path:
 
<ul>
<li>Craft comprehensive reports on key public figures and organizations, influencing our clients' strategic decisions.</li>
<li>Stay ahead of trends by monitoring news, social media, and a broad range of primary and secondary sources, synthesizing them into indispensable analysis for our clients.</li>
<li>Collaborate with a team of like-minded professionals, sharing knowledge and growing together.</li>
<li>Develop and share your expertise in the political and reputational challenges and opportunities within key industry sectors and policy areas, such as energy, life sciences, financial services, Artificial Intelligence and other technology issues, and beyond.</li>
<li>Analysts have access to weekly formal trainings and ongoing informal coaching, along with the opportunity to grow into larger roles such as Senior Analyst, Lead Analyst, and Manager.</li>
<li>For Senior Analysts: Lead, mentor, and uplift your team members, shaping the future of our research capabilities.</li>
</ul>
 
Life At Delve: Delve is a place where work-life balance is not just a buzzword. Our hybrid work environment prioritizes results over location. Employees enjoy our office, featuring a fitness center and a rooftop view of the White House, and a culture that values your personal time as much as your professional development. Teamwork and continuous learning are at the core of our DNA. We invest in your growth, offering educational opportunities and a suite of benefits including health insurance, 401(k) matching, and unlimited telecommuting. Your well-being is our priority, ensuring that your vacation days are truly yours to enjoy.
 
Ready to Shape the Future of Public Affairs? Apply now and embark on a career that satisfies your intellectual hunger, shapes public discourse, and fosters continuous personal and professional growth.

Research Analyst or Senior Research Analyst

<h3>Job Description</h3>
Job Description
Arcaea is building a new ingredient toolset for the beauty and personal care industry - one rooted in biotechnology with the aim of delivering radical performance and unparalleled sustainability that will also present new opportunities for storytelling.
We're hiring an Associate Scientist to contribute to the development and evaluation of innovative hair care products. This role focuses on executing scientific protocols, performing efficacy testing, and providing data-driven insights to support product claims. The ideal candidate is a detail-oriented researcher with a strong foundation in laboratory techniques and a passion for hair science.
WHAT YOU'LL DO
<ul>
<li>Conduct standardized Testing Procedures (SOPs) for product efficacy using consumer-relevant predictive assays.</li>
<li>Design robust experiments, perform comprehensive data analysis, and present findings to help guide product direction.</li>
<li>Evaluate the performance of formula prototypes and raw materials through rigorous bench testing.</li>
<li>Develop simplex formulas to screen new ingredients and assess their functional benefits within hair care applications.</li>
<li>Utilize microscopy, spectroscopy, and mechanical/thermal analysis to characterize hair properties and the effects of various products.</li>
<li>Manage the preparation and standardized treatment of hair substrates for consistent and reproducible testing.</li>
<li>Conduct literature reviews to stay current on hair science, competitor products, and ingredient innovations.</li>
<li>Maintain laboratory equipment and ensure a clean, safe, and efficient working environment.</li>
</ul>
WHAT WE SEEK
<ul>
<li>BS in Chemistry, Chemical Engineering, Materials Science, Biochemistry, or a related scientific discipline.</li>
<li>1–3 years of experience in a personal care laboratory setting, with a strong preference for hair care.</li>
<li>Proven experience in cosmetic product efficacy testing or claims substantiation.</li>
<li>Proficiency in mechanical testing, surface analysis, or thermal analysis. Experience with delicate, hands-on laboratory tasks and precise measurements is essential.</li>
<li>Proficiency in searching and interpreting scientific literature. Experience with image analysis and statistical software is a plus.</li>
<li>Strong knowledge of hair care product categories and consumer needs.</li>
<li>Exceptional attention to detail and a conscientious approach to data integrity.</li>
<li>Strong problem-solving skills with the ability to work independently in a fast-paced environment.</li>
</ul>
The full compensation package is based on candidate experience. 
Pay Range$85,000—$95,000 USD
We are committed to diversity, equality, and inclusion in all its practices. It is the policy of Arcaea to provide equal employment opportunities to all employees and employment applicants.
Agency and Third Party Recruiter Notice: Agencies that submit a resume to Arcaea must have a current executed Arcaea Agency Agreement executed by the Director, People Operations. In addition Agencies may only submit candidates to positions for which they have been invited to do so by an Arcaea Recruiter. All resumes must be sent to the Arcaea Recruiter under these terms or they will not be considered.
If you have a disability under the Americans with Disabilities Act or similar law, or you require religious accommodation, and you wish to discuss potential accommodations related to applying for employment at our company, please contact <a href="mailto:recruiting@arcaea.com" target="_blank">recruiting@arcaea.com</a>.
Arcaea participates in E-verify to determine employment eligibility.
Disclaimer: This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee.

Associate Scientist - Hair

<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 
The SST Associate Scientist I shall assist other SST Laboratory personnel in general lab duties.&nbsp;&nbsp; The SST Associate Scientist I shall be responsible for ensuring quality and accurate data in a timely fashion.
Responsibilities and Duties
General:
<ul>
<li>Communicate effectively internally and externally.</li>
<li>Work cooperatively.</li>
<li>Propose and communicate process improvements for technical area.</li>
<li>Participate in general laboratory maintenance.</li>
<li>Ensure quality and accurate data in a timely fashion in all processes in a given area.</li>
<li>Follow work instructions and direct sample flow for efficiency.</li>
<li>Perform sample analysis and document results.</li>
<li>Participate in lab and equipment maintenance.</li>
<li>Communicate inventory needs to appropriate staff.</li>
<li>Communicate sample/test issues to appropriate responsible manager.</li>
<li>Identify and report any opportunities to improve efficiency, customer satisfaction, and quality.</li>
<li>Perform their assigned tasks according to company procedures and work instructions in the most cost-effective way.&nbsp;&nbsp;</li>
<li>May be required to sit for 8 hours; May be required to stand for 8 hours.</li>
</ul>
Specific:
<ul>
<li>Ensure ALL goals are met for the day and encourage others to meet their goals as well.</li>
<li>Will perform evaluation tests according to work instructions and follow AOSA, Canada, or ISTA rules depending on testing requested.</li>
<li>Performs tasks as defined by lab manager.</li>
<li>Be able to drive the process and motivate individuals to get the work done.</li>
<li>Ensure the consistent and repeatability of results in a timely fashion.</li>
<li>Propose and communicate process improvements for planting and/or evaluation.</li>
<li>Be able to evaluate TZ Tests (both Post Germ and straight TZ Tests).</li>
<li>Maintain appropriate inventory and organizing supplies.</li>
<li>Based on years of experience, be able to guide or assist newer staff with questions.
<ul>
<li>Direct newer staff in the right direction if the answer of the question is unknown.</li>
</ul>
</li>
<li>Ensure accurate and efficient execution of work instructions.
<ul>
<li>Minimize the number of mistakes made throughout the workday/week.</li>
</ul>
</li>
<li>Reliable work schedule.</li>
<li>During the months of October through March, may be requested to work (but not required) at least 45 hours per week to assist the lab manager in maintaining the SST lab.</li>
</ul>
Qualifications 
Education/Experience:
<ul>
<li>HS degree recommended with an aptitude for science.&nbsp;</li>
</ul>
Certificates/Licenses:
<ul>
<li>Certification by the Society of Commercial Seed Technologists is recommended.</li>
</ul>
Supervisory Responsibilities:
<ul>
<li>None required.</li>
</ul>
Skills:
<ul>
<li>Attention to detail, ability to maintain focus, mental addition and subtraction, computer operation including email and LIMS.&nbsp; Be able to work under pressure to meet deadlines for test completion, be self- motivated, understand priorities, willingness to learn new things, gets along with team members, takes the initiative, and be flexible.</li>
</ul>
Other Factors:
<ul>
<li>None required.</li>
</ul>
 Additional Information 
Schedule:
<ul>
<li>Monday-Friday&nbsp;8:00am-4:30pm</li>
</ul>
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 Genomic Services is a Disabled and Veteran Equal Employment Opportunity employer.

Associate Scientist I

<h3>Job Description</h3>
Job Description
Support the DuPage Forest Preserve as a Seasonal Entomology Preprofessional by completing monitoring and research efforts related to mosquito surveillance and management. This position provides hands-on field and laboratory experience, assisting with ecological studies that protect public health information to the community. This position is ideal for anyone with emerging professionals interested in entomology, ecology, or environmental science.
What You'll Do
<ul>
<li>Conduct field sampling and identification of invertebrates such as mosquitoes, spongy moths, rusty patched bumble bees, and ticks.</li>
<li>Maintain and operate field equipment including insect traps and monitoring tools.</li>
<li>Test mosquito samples for viruses and support management efforts using established scientific protocols.</li>
<li>Collect and record GPS data to support project mapping and reporting.</li>
<li>Operate a 4-wheel drive truck and other vehicles to access field sites.</li>
<li>Assist with wildlife surveys, native seed collection, restoration activities, and lab work as needed.</li>
<li>Manage invasive plant species using herbicides and gas-powered equipment.</li>
<li>Follow safety procedures and support a clean, organized, and hazard-free work environment.</li>
<li>Contribute to a collaborative team culture and provide excellent service to internal and external partners.</li>
<li>Perform other related duties to support ecological projects.</li>
</ul>
What You'll Need
<ul>
<li>18 years of age or older at time of hire.</li>
<li>Valid Driver's License in good standing.</li>
<li>Pursuing or recently completed a degree in entomology, ecology, wildlife management, or a related field.</li>
<li>Must be able to obtain an IL Department of Agriculture Pesticide Operator's license within 1 month of employment.</li>
<li>Experience working with insects or other wildlife preferred.</li>
<li>Basic knowledge of insect taxonomy and identification, field research methods, and data collection techniques.</li>
<li>Comfortable working independantly on and off trail in wilderness and remote areas.</li>
</ul>
Schedule &amp; Pay
<ul>
<li>Monday-Friday | 7:00 AM - 3:30 PM.</li>
<li>This position starts around May 11th and lasts until around October of 2026.</li>
<li>$15 - 16 /hour.</li>
</ul>
Work Setting
<ul>
<li>This position reports to District Headquarters in Wheaton, IL and includes daily travel in a District vehicle to forest preserves throughout DuPage County.</li>
<li>Uniform shirts, hats, and PPE will be provided. Safety boot allowance available. Hiring for this position begins after January 1, 2026.</li>
</ul>
Apply Today
Follow the link to apply directly and be considered for the position.
Additional information about the position and job duties can be found in the attached job description or on our website.
The Forest Preserve District of DuPage County is an equal opportunity employer.

Seasonal Entomology PreProfessional May 2026

<h3>Job Description</h3>
Job Description
Job ID: 264 Job Title: Scientist III, Biologics Downstream Process Development Location: Alameda, CA Contract: 6 Months (Renewable) Pay Rate: Up to $77/hr. W2 Group: Bio CMC - Downstream Process Development Biologics CMC Development &amp; Manufacturing
 
TECHNICAL SKILLS
· &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; AEX
· &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; AKTA (Chromatography Technology)
· &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Anion Exchange Chromatography
· &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Cation Exchange Chromatography
· &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Downstream Process Development
· &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; High-Performance Liquid Chromatography (HPLC)
· &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Hydrophobic Interaction Chromatography
· &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Protein A
· &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Tangential Flow Filtration (TFF)
 
The Scientist III, Biologics Downstream Process Development will independently conduct laboratory experiments with limited supervision to develop purification processes and support technology transfer and manufacturing of biological drug candidates. The incumbent will utilize their technical expertise in downstream/purification process development of biologics (therapeutic proteins, antibodies, bispecifics, ADCs, etc) to advance CMC development and manufacturing for pre-IND and in-clinic therapeutic proteins. A strong technical focus is critical to ensure the speed, cost effectiveness, and technical quality of our CMC activities. The incumbent should have excellent hands-on technical abilities and a strong theoretical grasp of purification unit operations such as affinity chromatography, ion exchange chromatography (IEX), ultrafiltration/diafiltration (UF/DF), viral filtration, etc. The incumbent is expected to work in the laboratory full time, including operating state-of-art downstream equipment (FPLC, TFF, depth filtration systems, etc), performing routine instrument maintenance, and providing training to peers. The incumbent is also expected to effectively document lab results and draft test methods/SOPs in accordance with company, departmental, and regulatory guidelines.&nbsp; The individual should have familiarity with upstream process development, analytics, and formulation development, as they will be working closely with these groups, in addition to a general working knowledge of Biologics CMC.
 
ESSENTIAL DUTIES AND RESPONSIBILITIES:
· &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Under minimal supervision, develop and execute laboratory studies in downstream process development (chromatography purification, viral filtration, TFF, etc) to support unit operation scale up and technology transfers to enable clinical production.
· &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Undertake production campaigns from Lab - Pilot Scale
· &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Collaborate with internal and external partners in upstream process development, analytical development, and formulation development groups to advance CMC biologics programs
· &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Maintain complete and accurate records of laboratory work in conformance with company standard operating procedures (SOPs) and training.
· &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Provide detailed reviews of peer generated data as well as that generated from contracted service providers.
· &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Maintain the inventory of laboratory consumables and clean glassware.
· &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Coordinate vendors service calls for repair and maintenance of laboratory instruments, perform routine maintenance of laboratory instrumentation, and maintain complete and accurate records of instrument service and repairs in conformance with company SOPs and policies.
· &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Work to establish, maintain, and lead internal downstream process development and scale up lab capabilities in CMC Biologics
 
Education/Experience:
· &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Bachelor’s degree in chemistry, biochemistry, biochemical engineering, chemical engineering or related field and a minimum of three (3) years of relevant drug discovery/development experience; or,
· &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Master’s degree in chemistry, biochemistry, biochemical engineering, chemical engineering or related field and a minimum of one (1) year of relevant drug discovery/development experience; or,
· &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Equivalent combination of education and experience.
 
Experience/The Ideal for Successful Entry into Job:
· &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Experience applying their technical knowledge to drive critical objectives for CMC biologics across the product life cycle
· &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Hands-on experience in recombinant protein purification and downstream process development
· &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Familiarity with harvest and clarification unit operations
· &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Hands-on experience with Fast Protein Liquid Chromatography (FPLC) systems (e.g. Akta Avant, Akta Pilot, Akta Ready, etc) for chromatography-based purification development.
· &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Experience developing scalable chromatography purification unit operations (Affinity, IEX, HIC, SEC, mixed mode, etc).
· &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Experience developing scalable viral filtration and TFF unit operations.
· &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Working knowledge of CMC upstream process development, analytical development, formulation development, bioconjugation process development, technology transfer, and GMP quality requirements
· &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Ability to run basic analytical purity assays (SEC-HPLC) and in-process impurity clearance assays (HCP, res DNA, res ProA) independently
· &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Demonstrated capability to work independently on complex technical problems, effectively in cross-functional teams, and with external CDMOs and partners
· &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Experience planning, generating, analyzing, and linking experimental capabilities and results to critical CMC objectives
 
Knowledge/Skills:
· &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Expertise in downstream (purification) process development
· &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Broad and deep knowledge of CMC biologics downstream processes
· &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Working knowledge of upstream process development, analytics, formulation development, and bioconjugation process development.
· &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Ability to apply technical knowledge to CMC development and manufacturing for biologics across the product life cycle
· &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Ability to multi-task in a fast-paced dynamic environment while delivering high quality work
· &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Strong understanding of cGMP quality and regulatory requirements for CMC biologics
· &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Sets goals with understanding of priority and impact to the program, department, and organization
· &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Excellent interpersonal, presentation, and written communication skills
· &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Excellent organizational and documentation skills and habits
· &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Creative thinker and complex problem solver
 
TechData is proud to be an equal opportunity workplace and is an affirmative action employer. We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status.
Company Description<a href="http://www.techdataservice.com" target="_blank">www.techdataservice.com</a> 
<h3>Company Description</h3>
<a href="http://www.techdataservice.com" target="_blank">www.techdataservice.com</a>

Scientist III, Biologics Downstream Process Development (264)

<h3>Job Description</h3>
Job Description
Palermo Villa Inc. is looking for a high-energy, poised, and confident individual to assist in the development of concepts, products, and optimization projects through Palermo's vigorous consumer-driven R&amp;D process.
Associate Food ScientistWho you’ll work for…
While most companies that sell Pizza have no real connection to Italy, Palermo’s passion for food and family reaches all the way back to the country where Pizza was born. “Papa Palermo” carried the cherished recipes to America from Sicily!
Innovation is at the heart of who we are. We use an entrepreneurial, forward-thinking approach resulting in high quality products that are consistently recognized by both the industry and consumers.
Our commitment to quality has made Palermo’s a leader in private label frozen Pizza and contract manufacturing!
Perks…
<ul>
<li>20 free Pizzas per month</li>
<li>Opportunity for training and career advancement</li>
<li>Paid Time Off and Floating Holiday of your choice</li>
<li>401k &amp; Roth with company match and fully vested on the 1st of the Month after Hire</li>
<li>Fantastic benefit offering starting on the 1st of the Month after Hire</li>
</ul>
Where you’ll work…
Located in Milwaukee’s Menomonee River Valley, Villa Palermo is a state-of-the industry manufacturing facility that adjoins our company headquarters.
Our high-tech pizza manufacturing operations include an on-site bakery to produce best-in-class crusts, robotic packaging equipment, and a 24-hour shipping and receiving facility.
When you’ll work…
The Associate Food Scientist role works predominantly day shift hours with occasional nights/weekends to complete projects.
What you’ll do…
<ul>
<li>Execute Product Development and/or improvement projects including formulating finished product and sub-assembly for pizzas.</li>
<li>Prepare small-scale samples for testing, document study results according to company procedures, and maintain a clean and organized environment with accurate recordkeeping.</li>
<li>Demonstrate strong knowledge of food science best practices to test materials, develop formulas improvements and/or new formulas, and prepare lab sheets.</li>
<li>Assist with PR events, food shows, food presentations and production presentations.</li>
</ul>
Why you’ll be successful…
<ul>
<li>Proven ability to provide support to the organization in the areas of food technology, product design, food manufacturing, and food safety.</li>
<li>Utilizing knowledge from your Bachelor’s Degree in Food Science, Biology, Chemistry, Culinary and any experience with food manufacturing, major food companies or restaurant industry.</li>
<li>Organized and methodical approach to problem solving – often in a time-sensitive, tight-deadline situation where accuracy is critical.</li>
<li>Passionate lifelong learner with a strong interest in mastering new techniques in the culinary arts and food science.</li>
<li>Team player with excellent communication skills ready to work hard to ensure the whole Palermo’s team succeeds.</li>
</ul>

Associate Food Scientist

<h3>Job Description</h3>
Job DescriptionSalary: $19 - $23.57/hour 
Interested in Fishery Sustainability, Management and Hands on Marine Biology Work? Become a Marine Biologist!
 
A.I.S., Inc. (AIS) is a national scientific services firm supporting maritime activities requiring certification of compliance with environmental regulations as well as collecting data for use by Federal, State, Municipal, and other government agencies along the US coastline. AIS is looking forMarine Biologists(At-Sea Monitors)to work at sea collecting and recording data and biological samples for the National Marine Fisheries Service (NMFS) Northeast Fisheries Science Center (NEFCS) aboard commercial fishing vessels.
 
The primary goals of Northeast federal fishery observation programs are to provide quantitative biological, vessel, and gear-selectivity information for various New England and Mid-Atlantic fisheries. The At-Sea Monitor program focuses specifically on the groundfish industry, a grouping of fish that includes many commonly consumed fish such as cod, haddock and various flounder species. Each fishery observer or monitor operates on commercial fishing vessels operating in ports throughout New England and the Mid-Atlantic.If you ever wanted to make a difference, this is how.
 
Commercial fishing dates back hundreds of years. Today commercial fishing continues to be possible due to cooperation between fishermen and fisheries management scientists like yourself. In order to facilitate that cooperation, marine biologists collect data pertaining to fishing programs, economics, catch data, and fishing efficiency. Collected data is used to document stock information which is then used to protect the environment and preserve future generations of fish/fishermen. Commit to the journey!
 
Click to Learn More about Becoming a Fisheries Observer
 
At-Sea Monitors record detailed information on the gear and fishing activity of the vessels. Monitors work on deck on vessels ranging from 20 to 100 on trips roughly ranging from 1 to 14 days collecting data on fish catch and discard and incidental takes such as marine mammals, seabirds, and marine turtles. After attending a 3-week paid training in-person training inFalmouth, MAmonitors are deployed from ports throughout New England and Mid-Atlantic states. Gear types assessed include, trawl, gillnet, longline and handline.
 
Accommodations and meal reimbursement during in person session of training are provided.Training includes instructions on sampling protocols, gear, fisheries, fish identification, marine mammal/sea turtle identification, and safety.
 
This is a challenging job, and candidates must be mentally prepared to be away from home for multiple days, and must be physically able to handle heavy lifting, working odd hours, and long days in rough seas. Observing provides an excellent career in marine biology, as observers and monitors are widely recognized as being excellent field biologists. A broad range of advancement opportunities are available to those who demonstrate appropriate capabilities. Those opportunities include, but are not limited to, project management, field supervisors, and fieldwork in other programs.
 
Compensation:Monitorsstarting pay is $19.00/hour.Dependent on enrollment in our H&amp;W benefit, biologists may also be eligible for anadditional $4.57/hourfor the first 40 hours worked on each calendar week for a total of$23.57 hour. This is a fulltime position with benefits.Annually, monitors earn between $35K - $55K a yeardependent on their availability to deploy offshore and their personal sea day accomplishments. Monitors will be paid a minimum of 12 hours for each calendar day offshore and are also eligible for additional compensable activities while on land.
 
AIS benefits package includes health and dental insurance, vacation, sick and holiday benefits.Potential additional compensation consists of Data quality bonuses, Service awards, Fitness center reimbursement, Candidate Referral bonus.
 
Travel is reimbursedat an hourly rate along with compensation for miles accrued on a personal vehicle as well as per diem at the specified Government rate.
 
Minimum Qualifications:
<ul>
<li>High school diploma is required.</li>
<li>Experience with data entry on computers.</li>
<li>Monitor candidates must be U.S. citizens, or be legally authorized to work in the U.S.</li>
<li>Candidates must be physically able, as determined by a licensed physicians certification to perform observer duties.</li>
<li>Your own transportation is required.</li>
<li>Candidates are expected to commit to the program for at least one year.</li>
</ul>
 
Preferred Qualifications:
<ul>
<li>Bachelor's degree in biology or a related field from an accredited college or university with 30 credits of biology coursework, 6 credits of marine science is preferred.</li>
<li>At least one undergraduate course in math or statistics preferred.</li>
<li>At-sea experience</li>
<li>Coursework in Dichotomous Keys</li>
<li>Experience collecting Field Data and entering databases.</li>
</ul>
 
Locations:
<ul>
<li>Applicants must be currently living or be willing to live within 50 miles of Gloucester, Ma.</li>
</ul>
 
Contact:
If you would like to apply for one of these exciting new openings, please click the following link Careers Pageto submit the following information.
 
<ul>
<li>Resume</li>
<li>Cover Letter detailing sea and fish experience.</li>
<li>3 to 5 academic/professional references (name, email address and phone number)</li>
<li>Unofficial copies of your college (or high school if applicable) transcripts. </li>
</ul>
All documents must be submitted for your application to be considered. If you have any questions pertaining to this opening, please feel free to reach out to the Talent Team or 774-770-5833
 
An Equal Opportunity Employer
It is the policy of A.I.S. to recruit, hire, train, promote, transfer and compensate our employees and provide all other conditions of employment including Company sponsored events without regard to race, color, creed, religion, national origin, age, sex, gender identity, genetic information, marital status, lawful alien status, sexual orientation, physical or mental disability, citizenship status, veteran status or any other status protected by applicable law.
 
Must be able to work in the U.S. VEVRAA Federal Contractor Request Priority Protected Veteran Referrals Equal Opportunity Employer

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