Scientist jobs in Shawnee, KS

Work Your Magic with us! Start your next chapter and join MilliporeSigma. Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US. Your Role: We are seeking a highly skilled and motivated Analytical Chemist with strong expertise in LC-MS to support the characterization of cell culture media used in biologics development and manufacturing. The Scientist III Upstream R&D, Cell Culture Media Analytics position in Lenexa, Kansas, will develop innovative analytical solutions to complex problems relating to cell culture media. The ideal candidate will develop, optimize, and execute analytical methods to characterize small molecules, metabolites, and other components in complex media matrices. This role will have a strong foundation in mass spectrometry, method development, and data interpretation, with the ability to work independently and collaboratively across teams. * Design, develop/optimize, and implement advanced LC-MS-based analytical methods for qualitative and quantitative characterization of cell culture media components with minimal guidance. * Perform routing LC-MS analysis to: * Support media production at a new site. * Demonstrate product comparability between different media production sites. * Ensure efficient technology transfer between different production sites. * Resolve media performance complaints. * Design and perform experiments with minimal supervision to support media development, process optimization, media performance investigations, and product characterization. * Collaborate with cross-functional teams, including Media Development, Customer Collaboration, and Quality Control. * Troubleshoot instrumentation and method-related issues and maintain LC-MS systems in good working condition. * Stay current with advances in analytical technologies and seek new opportunities to advance technologies and apply innovative approaches to improve workflows and services. * Be open to new ideas and always seek critical feedback from colleagues and demonstrate effective cooperation. * Work collaboratively with colleagues, including ability to navigate challenging interpersonal dynamics with professionalism. Who You Are Minimum Qualifications: * Bachelors in Microbiology, Chemistry, Biomedical Engineering, Chemical Engineering, or other Life Science or Engineering discipline * 5+ years hands-on LC-MS experience OR * Masters in Microbiology, Chemistry, Biomedical Engineering, Chemical Engineering, or other Life Science or Engineering discipline. * 3+ years hands-on LC-MS experience OR * PhD in Microbiology, Chemistry, Biomedical Engineering, Chemical Engineering, or other Life Science or Engineering discipline * 1+ years hands-on LC-MS experience Preferred Qualifications: * Strong understanding of mass spectrometric principles and procedures for LC-MS method development and characterization of small molecules or biologics. * Hands-on experience using LC-MS instrumentation (e.g., QTOF, Orbitrap, triple quadrupole) to analyze complex biological matrices such as cell culture media and fermentation broths is highly desirable. * Strong critical thinking skills, problem-solving skills, attention to detail, and ability to manage multiple priorities. * Good oral and written communication skills * Laboratory experience performing small or large molecule characterization using LC or LC-MS. * Experience using one or more of the following instruments is a plus: Waters, Sciex, and Thermo LC-MS systems. * Knowledge or experience using data analytics or programming skills for analysis of LC-MS data is a plus. * Experience with metabolomics workflows. Pay Range for this position: $76,600-$137,900. The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here. What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

At Corbion, we exist to champion preservation in all its forms, preserving food and food production, health, and our planet. Corbion has an exciting opportunity for an Analytical Scientist, located at our Lenexa, KS site within the Research, Development and Application Department (RD&A). Successful candidate will act as primary SME in organic, inorganic, and analytical chemistry, analytical instrumentation, methods development, analytical testing in support of business, network, internal projects, and customer requests, and ensure smooth operation and continuous improvement of the RD&A analytical laboratory. Responsibilities: Support routine and complex laboratory testing of flour, food, and raw materials following standard methods of analysis utilizing various analytical instruments and wet chemistry techniques. Act as subject matter expert in organic, inorganic, and analytical chemistry, as well as analytical instrumentation including but not limited to GCMS, GCFID, ICS, HPLC, UV/VIS, and AA. Conduct methods development and complex qualitative and quantitative analytical testing in support of internal projects, customer requests, and business/network needs. Implement and support established quantitative analytical methods and assays for in-house instrumentation, both directly and by mentoring others. Operate, maintain, and troubleshoot multiple analytical instrumentation directly and by instructing and mentoring others. Work with internal and external customers on projects and provide analytical expertise through data analysis, data processing, statistical analysis, technical reports, presentations, and recommendations. Support and conduct validation for new methods and re-validation of established methods, lab analytical data verification, statistical analysis, troubleshooting, and laboratory investigations. Support the creation, revision, review and maintenance of Standard Operating Procedures and training documents for new and existing methods and laboratory processes. Actively participate in maintaining the facilities, equipment, and ensuring the safety of all personnel and visitors in the labs. Support onboarding and training of colleagues and interns, including mentoring others. Maintain knowledge of current industry issues, technical advances, and sampling/analytical technologies through review of current literature, participation in appropriate professional society conferences, and communication with leading researchers and regulatory personnel. Participates in and helps foster open and collaborative teamwork between all Corbion analytical groups Collaborate with universities, research institutes, external labs, and consultants Other duties as determined by business needs Qualifications: Bachelor's Degree in Food Science, chemistry or related fields At least 5 years of experience in laboratory function within food, beverage, chemical or pharma industry or Master's Degree in food Science, chemistry or related fields with 2+ years of experience in laboratory function within food, beverage, chemical or pharma industry Expertise in organic, inorganic, and analytical chemistry Demonstrated experience with titrations, GC-MS and HPLC. Experience with additional analytical instruments and techniques, method development and validation, and data analytics preferred. Ability to work independently and in a team to complete tasks in a timely manner. Previous leadership experience or demonstrated ability to mentor colleagues preferred. Proven problem solving skills, initiative, and creativity Capable of self-management and multiple project/task management. About Corbion Corbion is the global market leader in lactic acid and its derivatives, and a leading supplier of emulsifiers, functional enzyme blends, minerals, vitamins, and algae ingredients. We use our unique expertise in fermentation and other processes to deliver sustainable solutions for the preservation of food and food production, health, and our planet. For over 100 years, we have been uncompromising in our commitment to safety, quality, innovation and performance. Drawing on our deep application and product knowledge, we work side-by-side with customers to make our cutting-edge technologies work for them. Our solutions help differentiate products in markets such as food, home & personal care, animal nutrition, pharmaceuticals, medical devices, and bioplastics. In 2024, Corbion generated annual sales of €1,288.1 million and had a workforce of 2,399 FTE. Corbion is listed on Euronext Amsterdam. For more information: *************** Corbion is an equal opportunity employer and committed to a diverse workplace. All applicants will be considered equally without regard to race, color, ethnicity, veteran status, religion, national origin, marital status, political affiliation, age, sex, sexual orientation, handicapping condition, membership in an organization or any other non-merit factors. Corbion provides reasonable accommodation to applicants. EOE/M/F/Vet/Disabled Corbion does not accept unsolicited resumes from individual recruiters or third party recruiting agencies in response to job postings. No fee will be paid to third parties who submit unsolicited candidates directly to our hiring managers. All candidates must be submitted by approved Corbion vendors who have been expressly requested to make a submission by our Talent Acquisition team for a specific job opening. No placement fees will be paid to any firm unless such a request has been made by the Corbion Talent Acquisition team and such candidate was submitted to the Corbion Talent Acquisition Team.

Hennesy Research Associates - a Kemin company is looking for an Associate Scientist with a strong focus on ELISA creation and development. Step into the heart of innovation as an ELISA Scientist, where your benchwork drives breakthroughs in veterinary medicine. You'll lead the charge in developing potency assays, crafting and executing ELISA protocols, and solving complex analytical puzzles that shape how the USDA evaluates product efficacy. This is more than R&D - it's your chance to define the science behind real-world impact. If you're passionate about precision, problem-solving, and pioneering research, this is where your expertise belongs. Join the Kemin Team and Transform Lives! We are a privately held, family-owned-and-operated global biotechnology company driven by curiosity and committed to transforming the quality of life for people, pets, and the planet. We create solutions that strengthen health and wellbeing, provide nutrition and immune support for pets and production animals, safeguard the planet's natural resources, and protect the global food supply chain for generations to come. We supply over 500 specialty ingredients for various industries, including human and animal health and nutrition, pet food, aquaculture, nutraceutical, food technologies, crop technologies, textiles, biofuels, and animal vaccines. We employ 3,500 global employees and operations in 90 countries, including manufacturing facilities in Belgium, Brazil, China, Egypt, India, Italy, San Marino, Singapore, South Africa, and the United States. As a valued member of our team, you'll enjoy a comprehensive benefits package designed to support your financial, physical, and professional well-being: * Competitive Financial Package: Enjoy a rewarding salary, uncapped bonus opportunities, a 401k match program, and generous paid vacation and holidays. * Career Development and Advancement: Unlock your potential with opportunities for growth and development throughout your entire career. * Continued Learning Opportunities: Grow your skills with our in-house learning platforms, offering thousands of training resources both live and online, and take advantage of tuition reimbursement for external post-secondary pursuits. * Service Opportunities: Make a positive impact with paid time off for volunteering in your community Responsibilities * Independently conduct innovative scientific experiments and translate research into practical applications. * Perform literature reviews and provide written summaries that are incorporated into strategy. * Designing and executing enzyme-linked immunoassay (ELISA) potency assays. * Independently develop and review SOP's, research protocols and research methods; design safety procedures. * Independently perform advanced data analysis and review other's data to provide input and insight. * Must keep detailed records of activities and prepare written documents including research reports and method protocols * Independently, collect, interpret and document research data. * Generate scientific publications for internal and external publication, with guidance and review. * Prepare and present data analytics and research in multiple formats both internally and externally. * Review internal publication across Kemin. * Identify and participate in external research collaborations. * Contribute to strategic planning process and customer meetings. * Provides instruction and training to interns and junior staff. * Ability to balance multiple projects, meet deadlines, meticulous record keeping skills, excellent oral and written communication skills, ability to work independently but also cooperate and work well with the entire R&D team. * Other duties/projects as assigned Qualifications * Education * Bachelor's Degree in a scientific field with 7+ years of relevant experience * Masters Degree or PhD in a scientific field with 3+ years of relevant experience is preferred * Skilled at experimental design, sterile technique, data evaluation, project management, and problem solving. * Experience in cell culture and sterile technique and knowledge of hybridoma based monoclonal antibody generation. * Expertise in standard laboratory procedures such as ELISA and SoftMax Pro Software. Experience with the JESS automated western blot system. * Must be able to work independently or on a team and have the ability to work in a fast-paced multidisciplinary environment. * Excellent Scientific skills in experiment design and data collection, able to maintain instruments. * Detail oriented, organized, prioritization skills and motivated by accomplishment. * Ability to understand and perform advanced statistical analysis. * Analytical lab skills with a strong scientific curiosity and innovative thinking. * Fluent in English. Excellent written and oral communication skills with ability to present ideas effectively. * Advanced computer knowledge (Word, Excel, Access, PowerPoint, etc.). * A post-offer background check and drug screen is required. Additional pre-employment requirements may be necessary based on position. Kemin is an equal opportunity employer, and all reasonable accommodations will be considered. Kemin is a drug-free and tobacco-free campus. #LI-MP1

Hennesy Research Associates - a Kemin company is looking for an Associate Scientist with a strong focus on ELISA creation and development. Step into the heart of innovation as an ELISA Scientist, where your benchwork drives breakthroughs in veterinary medicine. You'll lead the charge in developing potency assays, crafting and executing ELISA protocols, and solving complex analytical puzzles that shape how the USDA evaluates product efficacy. This is more than R&D - it's your chance to define the science behind real-world impact. If you're passionate about precision, problem-solving, and pioneering research, this is where your expertise belongs. Join the Kemin Team and Transform Lives! We are a privately held, family-owned-and-operated global biotechnology company driven by curiosity and committed to transforming the quality of life for people, pets, and the planet. We create solutions that strengthen health and wellbeing, provide nutrition and immune support for pets and production animals, safeguard the planet's natural resources, and protect the global food supply chain for generations to come. We supply over 500 specialty ingredients for various industries, including human and animal health and nutrition, pet food, aquaculture, nutraceutical, food technologies, crop technologies, textiles, biofuels, and animal vaccines. We employ 3,500 global employees and operations in 90 countries, including manufacturing facilities in Belgium, Brazil, China, Egypt, India, Italy, San Marino, Singapore, South Africa, and the United States. As a valued member of our team, you'll enjoy a comprehensive benefits package designed to support your financial, physical, and professional well-being: Competitive Financial Package: Enjoy a rewarding salary, uncapped bonus opportunities, a 401k match program, and generous paid vacation and holidays. Career Development and Advancement: Unlock your potential with opportunities for growth and development throughout your entire career. Continued Learning Opportunities: Grow your skills with our in-house learning platforms, offering thousands of training resources both live and online, and take advantage of tuition reimbursement for external post-secondary pursuits. Service Opportunities: Make a positive impact with paid time off for volunteering in your community Responsibilities Independently conduct innovative scientific experiments and translate research into practical applications. Perform literature reviews and provide written summaries that are incorporated into strategy. Designing and executing enzyme-linked immunoassay (ELISA) potency assays. Independently develop and review SOP's, research protocols and research methods; design safety procedures. Independently perform advanced data analysis and review other's data to provide input and insight. Must keep detailed records of activities and prepare written documents including research reports and method protocols Independently, collect, interpret and document research data. Generate scientific publications for internal and external publication, with guidance and review. Prepare and present data analytics and research in multiple formats both internally and externally. Review internal publication across Kemin. Identify and participate in external research collaborations. Contribute to strategic planning process and customer meetings. Provides instruction and training to interns and junior staff. Ability to balance multiple projects, meet deadlines, meticulous record keeping skills, excellent oral and written communication skills, ability to work independently but also cooperate and work well with the entire R&D team. Other duties/projects as assigned Qualifications Education Bachelor's Degree in a scientific field with 7+ years of relevant experience Masters Degree or PhD in a scientific field with 3+ years of relevant experience is preferred Skilled at experimental design, sterile technique, data evaluation, project management, and problem solving. Experience in cell culture and sterile technique and knowledge of hybridoma based monoclonal antibody generation. Expertise in standard laboratory procedures such as ELISA and SoftMax Pro Software. Experience with the JESS automated western blot system. Must be able to work independently or on a team and have the ability to work in a fast-paced multidisciplinary environment. Excellent Scientific skills in experiment design and data collection, able to maintain instruments. Detail oriented, organized, prioritization skills and motivated by accomplishment. Ability to understand and perform advanced statistical analysis. Analytical lab skills with a strong scientific curiosity and innovative thinking. Fluent in English. Excellent written and oral communication skills with ability to present ideas effectively. Advanced computer knowledge (Word, Excel, Access, PowerPoint, etc.). A post-offer background check and drug screen is required. Additional pre-employment requirements may be necessary based on position. Kemin is an equal opportunity employer, and all reasonable accommodations will be considered. Kemin is a drug-free and tobacco-free campus. #LI-MP1

8350 NW Roanridge Kansas City, MO 64151 < Back to search results This location is operated by an independent franchise owner. Benefits may vary by location. When applying, please note that current job availability is found by clicking the link to the franchise specific hiring website. Role Overview Our To-Go Specialists are responsible for providing fast service and great hospitality for our To-Go Guests. If you take pride in great team work and love making people feel special, then we want to hear from you! * Fast hiring process * Flexible part-time or full-time schedule * Growth opportunities * Great team atmosphere and culture Responsibilities * Have knowledge of the menu to explain offerings to Guests * Ensure an exceptional To-Go experience for every Guest * Answer phone within three rings and assist Guests with placing To-Go orders * Enter orders in proper sequence * Able to operate POS system for transactions About Us Chili's was born in Dallas, Texas in 1975. Since then, we've boldly claimed our place in the casual dining industry as the place to go for Big Mouth burgers, house smoked ribs, full on fajitas, and hand shaken margaritas! With a legacy deeply rooted in service, hospitality, and giving back, we are committed to delivering the best experience to every Guest, every day. About You * Dependable team player * Prefers to work in a fast-paced environment * Great multitasking skills * Welcoming demeanor

Full-time Description Job Title: Research Scientist I/II at Mosaic Diagnostics Department: Research and Development Reports To: Director of Research & Development Summary of position: The Research Scientist I/II is a motivated and detail-oriented professional responsible for supporting the development and validation of laboratory-developed tests (LDTs) using LC-MS, Analytical Chemistry, Molecular Biology, or Immunology-based methodologies. This hands-on laboratory position is essential to driving scientific innovation and operational excellence within the R&D department at Mosaic Diagnostics. Duties/Responsibilities: Assist in the design, development, and validation of LDTs targeting specific analytes in biological samples. Conduct routine lab tasks including sample preparation, daily experimental runs, and instrument calibration. Collaborate with scientific staff to optimize assay conditions and troubleshoot experimental procedures. Analyze and interpret experimental data to ensure accuracy, reliability, and reproducibility. Document experiments, findings, and conclusions in a clear, organized, and comprehensive manner. Draft SOPs, validation protocols, and technical reports. Support maintenance and troubleshooting of laboratory instruments, including both hardware and software. Uphold and promote a culture of safety, quality, and regulatory compliance. Perform additional duties as required to support departmental objectives. Requirements Required Skills/Abilities: Working knowledge of LC-MS, Molecular Biology, Immunology, or Analytical Chemistry methodologies. Proficiency with laboratory instruments, software platforms, and data processing tools. Strong analytical thinking and organizational skills with meticulous attention to detail. Demonstrated capability in experimental design and targeted troubleshooting. Excellent verbal and written communication abilities. Ability to work both independently and as part of a collaborative team. Dedication to maintaining quality, safety, and compliance standards. Education and Experience: Bachelor's or Master's degree in Analytical Chemistry, Molecular Biology, Immunology, Biochemistry, or a related scientific field. 1-5 years of laboratory experience, preferably in assay development and validation. Preferred: Experience troubleshooting analytical workflows and optimizing lab procedures. Familiarity with CLIA, CAP, and ISO standards and regulatory requirements for LDTs. Understanding of sample preparation and general laboratory best practices. Physical Requirements: Prolonged periods of computer use and sitting at a desk. Occasional standing and stair climbing. Visual acuity necessary for close work and making fine adjustments.

Job DescriptionDescription: Propio is on a mission to make communication accessible to everyone. As a leader in real-time interpretation and multilingual language services, we connect people with the information they need across language, culture, and modality. We're committed to building AI-powered tools to enhance interpreter workflows, automate multilingual insights, and scale communication quality across industries. We are seeking an AI Research Scientist that will conduct groundbreaking research in machine learning and natural language technologies to drive innovation at Propio. This role focuses on exploring novel algorithms, improving existing models for interpretation and speech tasks, and publishing high-impact research to strengthen Propio's position as an AI leader in language services. Key Responsibilities: Conduct research in NLP, speech, and machine learning, with focus on translation, interpretation, bidirectional communication, and low-resource language challenges Develop and prototype novel architectures and algorithms for real-world applications in Propio's core domains Publish in top AI and NLP conferences and journals (NeurIPS, ACL, ICML, EMNLP, Interspeech) Collaborate with engineering teams to transition research into production systems, ensuring research advances translate to product improvements Advise leadership on emerging technologies, research trends, and their applicability to Propio's roadmap Mentor junior researchers and foster a strong internal research culture within the expanded team Identify and explore emerging challenges in speech-to-speech systems, multilingual interpretation, and agentic AI Requirements: Qualifications: Master's Degree in Engineering, preferably in Computer Science, Statistics, or Data Science or equivalent work experience 2-3+ years of experience working with NLP or large-scale ML models in production Proven publication record in leading AI/NLP venues (NeurIPS, ACL, ICML, EMNLP, Interspeech) Expertise in ML, deep learning, NLP, or speech processing methods Proficiency in Python and research tooling (PyTorch, JAX, Transformers) Ph.D. in Computer Science, AI, or related field (or equivalent research experience) Strong problem-solving and scientific communication skills Interest in applied research with real-world impact; experience in production ML systems a plus #LI-JS1

Hiring Department University of Missouri - Kansas City School of Science and Engineering - Energy, Matter and Systems (EMS) Research Laboratory of Dr. Zhu Li UMKC is rated R1 by the Carnegie Research Classification of Institutions of Higher Education. Job Description The Research Laboratory of Dr. Zhu Li is seeking a full-time postdoctoral researcher. The position will focus on the following: Conducting cutting edge research and algorithm development in area of learning based compression, immersive media compression, especially the point cloud and gaussian splatting based 3D content coding, assists in teaching, and developing research grants, publishing research results. A good publication record and system development experience is a plus for this position. This is a 9-month, full-time, unranked, benefit eligible academic position. Qualifications PhD in CS, ECE, or related area, with a good publication record and system dev experience Preferred Qualifications: Familiar with MPEG standardization research process, solid Python, Matlab and/or C/C++ programming and deep learning tools. Anticipated Hiring Range Salary is determined by a variety of factors, including but not limited to, the individual's particular combination of education, skills, and experience, as well as organizational requirements. Your total compensation goes beyond the number on your paycheck. The University of Missouri provides generous leave, health plans, and retirement contributions that add to your bottom line. Application Materials For consideration, you must apply online at ****************** click in Academic Positions (Job Opening ID 57741). Please combine all application materials (application form, personal letter of interest and applicable experience with accompanying curriculum vitae and a current list of references) into one PDF or Microsoft Word document not to exceed 11MB and upload as your resume attachments. Limit document name to 50 characters and do not include any special characters (e.g., /, &, %, etc.). If you are experiencing technical problems, please email **************************. Finalists will be asked to provide their transcripts which reflect the required degree for determination of the position title. Appointment is contingent upon verification of PhD degree. For questions about the position, please contact Dr. Zhu Li at **************. Other Information The School of Science and Engineering (SSE) was established through UMKC Forward, a university initiative that called for the joining of all the computing, science, mathematics and engineering programs into a single academic unit. This was a bold move by the university to create multidisciplinary learning, academics, research and civic outreach for the benefit of all students, faculty, alumni and friends. This new structure will create opportunities for shared experiences, interdisciplinary course options, broader learning engagement and inspired new research endeavors. For more information about the School of Science and Engineering, visit: ********************** Community Information Kansas City offers the best of both worlds-a vibrant, urban community with Midwestern appeal. The city's rich history and its modern-day, innovative thinking come together to create an eclectic group of neighborhoods that offer a little something for everyone. From thriving arts districts, an energetic downtown nightlife, casual to upscale shopping and champion sports teams, you will have no problem making yourself at home. Of course, one of Kansas City's biggest claims to fame is its food, especially its world-famous barbecue. Foodies will delight in the culinary scene found throughout the city. Ranging from award-winning chefs to cozy pizza joints, Kansas City definitely is not lacking any flavor. UMKC's campuses are conveniently nestled in the middle of all the action. Volker Campus is just minutes from the legendary Country Club Plaza, perfect for shopping or restaurants for lunch or after-work happy hours. Surrounded by hip neighborhoods and eateries, the Health Sciences Campus is located downtown near University Health Truman Medical Center and Children's Mercy Hospital. UMKC is proud to be "Kansas City's university," and the campus and its people celebrate all the characteristics of the surrounding community. To learn more about life in Kansas City and find more resources, visit VisitKC.com. Benefit Eligibility This position is eligible for University benefits. As part of your total compensation, the University offers a comprehensive benefits package, including medical, dental and vision plans, retirement, and educational fee discounts for all four UM System campuses. For additional information on University benefits, please visit the Faculty & Staff Benefits website at *********************************************** Equal Employment Opportunity The University of Missouri is an Equal Opportunity Employer. To request ADA accommodations, please call the Office of Equity & Title IX at ************. Apply for Job * Careers * Sign In * New User

Research Associate (RA) Glass Lewis is a trusted ally to more than 1,300 investors globally who use our corporate governance research, custom policy recommendations, engagement services and tools, and industry-leading proxy vote management solution to help drive value across their governance activities. We also work with over 3,000 corporate issuer clients, providing research reports, thought leadership, customized voting policies, equity plan models, and opportunities for direct engagement on material governance and disclosure practices. Glass Lewis' industry-leading research and analysis covers more than 30,000 meetings each year across approximately 100 global markets. Our clients include many of the world's leading pension funds, mutual funds, and asset managers, collectively managing over $40 trillion in assets. We have teams located across the United States, Europe, and Asia-Pacific regions, giving us global reach with a local perspective on the most important governance issues. Founded in 2003, Glass Lewis is headquartered in San Francisco, California with additional offices in Kansas City, Missouri; London, U.K.; Paris, France; Limerick, Ireland; Karlsruhe, Germany; Stockholm, Sweden; Manila, Philippines; Toronto, Canada; Sydney, Australia; Timișoara, Romania; and Tokyo, Japan. Our team includes more than 400 full-time employees globally, over half of which are dedicated to research. For more information, please visit ******************* Position Details Contract Type: Full-time, temporary (~5 months from January/February 2026 - May/June 2026) Location: Kansas City, Missouri Work Model: Hybrid, 3 days per week in office Level: Entry-level Compensation: USD $1,906.25 semi-monthly (15th and last day of each month) Position Description Research Associates (“RAs”) work with Glass Lewis' research teams to produce unbiased, independent research (Proxy Papers). RA positions are separated into two areas of focus: Governance covers meeting proposals for board of director elections, committee memberships, environmental and social issues, skills matrices, auditor appointments, etc. Compensation covers meeting proposals for executive pay practices, incentive plans, pay-for-performance, etc. Glass Lewis is an equal opportunity employer in compliance with applicable state and federal laws. Accordingly, we take affirmative action to ensure that all employment and recruiting activities are conducted on a non-discriminatory basis without regard to race, color, religious creed, age, marital status, national origin, ancestry, sex, gender identity or expression, intellectual, mental, or physical disability, veteran status, or other characteristics protected by law. Requirements Bachelor's degree Strong English writing and editing skills Strong analytical research skills (emphasis on qualitative analysis) Able to quickly synthesize new information and apply to unique scenarios Thorough, accurate, organized and productive Able to work effectively under tight and overlapping deadlines Flexibility to navigate shifting priorities Desire to learn, with ability to receive and apply feedback Able to effectively communicate in a collaborative environment Genuine interest in areas of corporate law, economics, finance, public policy and governance is helpful Desire to work in a professional, fast-paced atmosphere with other bright people

Medical Research Associate - PRN - (Onsite) Lenexa, KS ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We are currently seeking a Medical Research Associate to join our diverse and dynamic team. As a Medical Research Associate at ICON, you will be responsible for meeting/greeting clinical research volunteers as they come into the clinic, checking their vitals (height, weight, blood pressure, BMI), and essentially making sure the study participants are healthy eNugh to participate in the clinical trial according the protocol of a study. What you will be doing * Your compassion and dedication will be at the forefront as you take vital signs and perform phlebotomy on study subjects, ensuring their comfort and well-being throughout the research process. * You will be entrusted with following our clients' protocols when conducting vital sign assessments and phlebotomy procedures. * Joining us means being part of a collaborative environment where your active participation in meetings and other assignments will be valued and recognized. * Your role will extend beyond the clinical aspects as you chaperone study subjects during their breaks outside, offering personalized care and ensuring their comfort. Your profile * A strong command of both English and the host country's language is essential, enabling effective communication and collaboration. * A High School Diploma or G.E.D. qualification * If you possess an undergraduate degree in a clinical or health-related area, or have equivalent work experience in a similar role, we want to hear from you. * 1+ years of work experience in a medical or clinical field is preferred * If you hold certifications such as Basic Life Support (BLS) or Phlebotomist Certification, it will be a great advantage * Preferred Background: Medical Assistant, Certified Nursing Assistant, Certified Medication Aide, Telemetry Technician, or Laboratory Technician backgrounds are highly desired What ICON can offer you: Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: * Various annual leave entitlements * A range of health insurance offerings to suit you and your family's needs. * Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. * Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being. * Life assurance * Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles. Are you a current ICON Employee? Please click here to apply

Medical Research Associate - PRN - (Onsite) Lenexa, KS ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We are currently seeking a Medical Research Associate to join our diverse and dynamic team. As a Medical Research Associate at ICON, you will be responsible for meeting/greeting clinical research volunteers as they come into the clinic, checking their vitals (height, weight, blood pressure, BMI), and essentially making sure the study participants are healthy eNugh to participate in the clinical trial according the protocol of a study. **What you will be doing** + Your compassion and dedication will be at the forefront as you take vital signs and perform phlebotomy on study subjects, ensuring their comfort and well-being throughout the research process. + You will be entrusted with following our clients' protocols when conducting vital sign assessments and phlebotomy procedures. + Joining us means being part of a collaborative environment where your active participation in meetings and other assignments will be valued and recognized. + Your role will extend beyond the clinical aspects as you chaperone study subjects during their breaks outside, offering personalized care and ensuring their comfort. **Your profile** + A strong command of both English and the host country's language is essential, enabling effective communication and collaboration. + A High School Diploma or G.E.D. qualification + If you possess an undergraduate degree in a clinical or health-related area, or have equivalent work experience in a similar role, we want to hear from you. + 1+ years of work experience in a medical or clinical field is preferred + If you hold certifications such as Basic Life Support (BLS) or Phlebotomist Certification, it will be a great advantage + Preferred Background: Medical Assistant, Certified Nursing Assistant, Certified Medication Aide, Telemetry Technician, or Laboratory Technician backgrounds are highly desired **What ICON can offer you:** Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: + Various annual leave entitlements + A range of health insurance offerings to suit you and your family's needs. + Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. + Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being. + Life assurance + Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others. Visit our careers site (************************************* to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here (****************************************************** Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles. Are you a current ICON Employee? Please click here (****************************************************** to apply

Mindlance is a national recruiting company which partners with many of the leading employers across the country. Feel free to check us out at ************************* Its a simple route driver job and company will be providing the car. Job Description: Perform accurate and timely testing of routine and some non-routine lab samples in accordance with appropriate GMP and safety guidelines. Completes second person verification of test results. Participates in laboratory root cause investigations and quality system improvement initiates by executing well defined protocols and procedures. Shares technical information and best practice within the group. Design and evaluation of experiments, methods development and characterization, support of process development/optimization and the analysis and interpretation of data. Conduct studies to validate methods, develop methods, evaluate new technologies. Sample Analysis. Sample preparation, instrument set-up and operation, data entry, primary data review. Coordination of method transfers and co-validations. Qualifying, calibrating, and maintaining analytical instrumentation. All laboratory work will be conducted and documented in accordance with the appropriate Quality System. Act as a resource for insuring adherence to quality systems. Request preferences / nice to haves: Fundamental knowledge of cGMP compliance requirements, instrument qualification procedures and computer system validation principles. Good documentation skills and ability to author and/or review standards, guidelines, SOPs, templates, protocols, and other GMP documentation. Excellent general computer skills (MS Excel, Word, etc.) and the ability to compile summarize and present information to a diverse group. Excellent communication skills and willingness to interact with laboratory personnel, contractors and management. Ability to troubleshoot problems and identify solutions. Ability to influence and partner with individuals both within and outside of a formal reporting relationship towards realization of team goals. Assist in addressing laboratory investigations within specified timeframe. Primary Position Responsibilities (major or daily tasks): Perform analytical and physical testing on in-process, finished product and stability samples. Assist laboratory leader in ensuring compliance with all procedures, safety and regulatory commitments in Quality Control. Perform review and approval of analytical data. Maintain analytical methods in the laboratory in a state of validation. Assist in addressing laboratory investigations within specified timeframe. Promote elimination of problems by identifying and addressing root cause. Qualifications Request preferences / nice to haves: Fundamental knowledge of cGMP compliance requirements, instrument qualification procedures and computer system validation principles. Good documentation skills and ability to author and/or review standards, guidelines, SOPs, templates, protocols, and other GMP documentation. Excellent general computer skills (MS Excel, Word, etc.) and the ability to compile summarize and present information to a diverse group. Excellent communication skills and willingness to interact with laboratory personnel, contractors and management. Ability to troubleshoot problems and identify solutions. Ability to influence and partner with individuals both within and outside of a formal reporting relationship towards realization of team goals. Assist in addressing laboratory investigations within specified timeframe. Additional Information All your information will be kept confidential according to EEO guidelines.

This position is responsible for support of CMC activities as well as working with Scientists and management for specific compound development at CritiTech in support of CritiTech product development and associated affiliates/partners for the global development and regulatory approval of New Chemical Entities (NCE's), Active Pharmaceutical Ingredients (APIs) and support of research and development of any/all product activities. RESPONSIBILITIES Participates in lab development in support of Chemistry, Manufacturing and Controls (CMC) section of NDA or SNDA by direction and interaction with Quality Operations/Regulatory Affairs and CritiTech. Provides analytical support for proof of concept studies, feasibility studies, routine manufacturing, and troubleshooting using CritiTech's Supercritical Precipitation equipment. Provides analytical support for proof of concept studies, feasibility studies, routine manufacturing, and troubleshooting using CritiTech's spray drying equipment. Perform production activities in support of clinical trials, including filling, environmental monitoring, visual inspection, and packaging of vials for further processing. Suggest changes and improvements to CritiTech's analytical services and product characterization, facilities, utilities, and other systems. Performs preventative maintenance and calibration checks on analytical equipment. Participates in the qualification of new equipment and facilities. Generates support data for CritiTech to be used in 3rd party development activities. Generates data in support of CMC documents, including out-of-specification (OOS) or deviation investigations, and helps execute action plans to meet sound scientific practices. Provides technical support for QO on complaint samples and manufacturing/packaging problems. Performs and assists in CritiTech compatibility and feasibility assessments for compounds being considered for development. Participate in the onsite review of data, facilities and laboratory operations of contract manufacturing and analytical laboratory. Suggests changes or edits to appropriate SOP's for CritiTech. Performs release and stability analytical testing with QO in the coordination and management of retest/expiration dating. Executes testing and lab work in support of technology transfer and stability protocols, stability packaging and manufacturing jobs for CritiTech activities. Other duties as assigned. EDUCATION, EXPERIENCE AND SKILLS Required BS in chemistry, biology, engineering or related pharmaceutical field with 3+ years industry background in pharmaceutical product development - or - MS in chemistry, biology, engineering or related pharmaceutical field with 2+ years industry background in pharmaceutical product development. 2+ years preparing and supporting CMC documentation for IND's and NDA's. Experience in working with people in a multi-disciplinary team environment. Preferred Advanced degree in chemistry or pharmacy or equivalent experience. Experience in pharmaceutics, analytical and organic chemistry. Experience in technology transfers to contract facilities. Experience with interactions with regulatory agencies. Experience in preparing and supporting Chemistry, Manufacturing and Control (CMC) documentation regulatory filings. KNOWLEDGE AND SKILLS Knowledgeable (including hands-on experience) in the use of analytical methods for active pharmaceutical ingredients and drug product (i.e. HPLC, GC, IR, etc.) and formulation development/manufacturing and the relation of these to overall pharmaceutical development. Knowledge and understanding of current Good Manufacturing Practices (cGMP) as well as other pertinent national regulations. Current knowledge of CMC regulatory and ICH guidelines. Knowledgeable in the overall drug development process. Knowledgeable in the application of compendia requirements and procedures to testing and developing pharmaceutical products. Leadership Skills - knowledge and interpersonal skills to help others towards the accomplishment of CritiTech's goals and objectives. Analytical and Problem-Solving Skills - ability to identify problems or opportunities using appropriate information; determines the causes and possible solutions to the problem. Teamwork - the ability to work well and manage personnel in a highly cross-functional team environment. Communication Skills - ability to express one's self clearly and concisely to CritiTech personnel over the phone or with others within the team; documents issues and/or concerns concisely and comprehensively; adjusts language and/or terminology appropriate for the audience. Interpersonal Flexibility - ability to adapt to other personalities in a respectful manner that is conducive to goal achievement. Knowledge Sharing - ability to capture knowledge within the organization; improves solutions, processes, an deliverables through the use of information; improves information capital by contributing experience, theories, deliverables, and models for others to use. Resource Management - ability to work with internal and external resources and to coordinate individual goals and objectives to align with business imperatives.

APTIM is seeking an early career Environmental Scientist on a full-time basis to participate in a variety of environmental compliance support tasks, such as permitting/management of hazardous waste, hazardous materials, above ground and/or underground storage tanks, spill prevention, and DOT and RCRA compliance. The successful candidate will be experienced in supporting an environmental team. This position will primarily be in an office environment but may also require travel to client facilities to conduct environmental compliance reviews and/or gather related data. Key Responsibilities/Accountabilities: Executing various work scopes, while meeting project schedules and budgets Working independently and as part of a project team and be able to adjust to changing conditions Research and understanding regulatory regulations Working as a team member and/or team lead to assist in preparation of regulatory reports and permit applications Data entry and management, likely on multiple software platforms Work in client asset management systems to document research and findings Interfacing with client personnel at a corporate and facility level Managing time to ensure a quality product is prepared to meet project deadlines Applying knowledge and skills to a wide range of standard and nonstandard situations Following defined processes explicitly while also being able to identify and accommodate new or changing scenarios as well as developing processes for new activities. Basic Qualifications: Bachelor's degree in a core science (such as geology, chemistry, physics, or biology) Some business courses recommended. External Job Description: engineering, environmental science, or related area required. Related work experience of 1 - 2 years recommended. Prior experience or training regarding environmental compliance and related federal and state environmental regulations desirable. Strong written and oral communication skills. Strong computer skills required. Must have a demonstrated strength and proficiency in Microsoft applications such as MS Excel, MS Word, MS Teams, SharePoint Online, etc. and the ability to learn other software applications. Willing and able to work in the field and travel to complete work. ABOUT APTIM APTIM is committed to accelerating the transition toward a clean and efficient energy economy, building a sustainable future for our communities and natural world, and creating a more inclusive and equitable environment that celebrates the diversity of our communities. We specialize in environmental, resilience, and sustainability and energy solutions, as well as technical and data solutions, program management, and critical infrastructure. For every challenge our clients face, there is an opportunity for APTIM to innovate a fit-for-purpose solution that will raise your organization or community to a new standard of excellence. What you can expect from APTIM: Work that is worthy of your time and talent Respect and flexibility to live a full life at work and at home Dogged determination to deliver for our clients and communities A voice in making our company better Investment into your personal and professional development As of the date of this posting, a good faith estimate of the current pay range for this position is $24.04- $31.25 per hour. Compensation depends on several factors including: experience, education, key skills, geographic location of the position, client requirements, external market competitiveness, and internal equity among other employees within APTIM. Employee Benefits APTIM Environmental and Infra, LLC is committed to providing an extensive range of benefits that protect and promote the health and financial well-being of our employees and their families through the APTIM Benefits Marketplace ************************************ Medical, vision, and dental insurance: Through the marketplace, our employees can choose benefits from five metallic levels and 10+ carriers to find the right benefits that work for them in their location. Life insurance Short-term and long-term disability insurance Paid holidays, vacation, and sick leave (eligibility based on company policy and applicable law) 401(k) APTIM offers three 401k plans through the Aon Pooled Employer Plan (PEP). The specific plan you are eligible for depends on the business unit you are in. The details of the largest plan are found here: APTIM 2025 401(k) Plan Features (makeityoursource.com) APTIM - Helpful Documents Watch our video: About APTIM - In Pursuit of Better #LI-BN1 #LI-ONSITE

Job Posting The Kansas Department of Agriculture is devoted to the total support of agriculture in Kansas. The department works for the entire Kansas agriculture sector including farmers, ranchers, food establishments and agribusinesses. The agency has a balanced approach to providing an environment that enhances and encourages economic growth of the agriculture industry and Kansas economy while promoting and advocating for the agriculture industry, the state's largest industry, employer, and economic contributor. KDA helps to ensure a safe food supply, protects natural resources, promotes public health and safety, protects animal health, and provides consumer protection to the best of our ability. Kansas Department of Agriculture: 1320 Research Park Drive, Manhattan, KS 66502 About the Position: * Who can apply: Anyone * Classified/Unclassified Service: Unclassified * Full/Part-time: Full-Time * Work Schedule: Days (8am to 5pm) * Eligible to Receive Benefits: Yes * Veteran Preference Eligible: Yes * Disability Preference Eligible: Yes Compensation: * Annual Salary: $55,000 per year * Hourly Pay: $26.44 per hour Employment Benefits: * Comprehensive medical, mental, dental, vision, and additional coverage * Sick & Vacation leave * Work-Life Balance programs: parental leave, military leave, jury leave, funeral leave * Paid State Holidays (designated by the Governor annually) * Fitness Centers in select locations * Employee discounts with the STAR Program * Retirement and deferred compensation programs Visit the Employee Benefits page for more information… Position Summary & Responsibilities: This position will remain posted until filled. Location: Topeka Field Office - Topeka, KS Job Summary: * Work with a diverse team of technical staff in our field offices and headquarters. * Conduct water right inspections in the field to ensure compliance with regulatory requirements and collect data used to certify water rights. * Prepare reports, maps, and drawings used to assist in decision making by DWR Water Commissioners and the Chief Engineer. * Use technical equipment such as global positioning system devices, ultrasonic water flowmeters, and stream gaging equipment. * Assist in the administration and distribution of surface water and groundwater in eastern Kansas, including enforcement of minimum desirable streamflow requirements. * Assist water users and the public with filing water use data, completing application forms, maps, plats, and other associated documents. * Communicate directly with water users, government officials, heads of industries or corporations, public water supply systems and the public regarding water rights and regulatory requirements. * Utilize GIS computer software to prepare maps and analyze data. * Conduct water level measurements in wells to monitor and evaluate the status of the groundwater resource. * Research historical documents to determine water right development. * Prepare notices and orders to ensure water right compliance. Minimum Qualifications: * Professionally minded individuals with four years experience in environmental science, physical sciences, biological sciences, mathematics and/or engineering. Candidates may also qualify through a combination of relevant education, work experience, training or certification. * Capable of performing outdoor assignments for long hours in extreme temperatures during summer/winter. * Good oral and written communication skills are essential. * Employee must have a valid Class C (or higher) Kansas driver's license or equivalent license from another state. Employee is responsible to maintain an acceptable driving record to safely drive state vehicle and be willing and able to fulfill all job-related travel normally associated with this position. Preferred Qualifications (Not Required): * Knowledge of the Kansas Water Appropriation Act and water rights preferred. * Courses or work experience in hydraulics, hydrology, geology, natural resource management, agricultural, or earth science preferred. Post-Offer/Pre-employment Requirements: Kansas Tax Clearance Certificate required in accordance with Executive Order 2004-03. Each applicant (even non-residents) who is selected for a State of Kansas job vacancy must apply for a Tax Clearance Certificate within 10 days from the date of the offer letter by accessing the Kansas Department of Revenue's (KDOR) website at ********************************************** . If you need assistance with the tax clearance, please contact KDOR at ************** or by email at kdor_********************** Recruiter Contact Information: * Name: Alyssa Satterthwaite * Email: *************************** * Phone: ************** * Fax: ************** * Mailing Address: 1320 Research Park Drive, Manhattan, KS 66502 Required Documents for this Application to be Complete: * On the My Job Applications page, verify these documents are present and valid. Upload or delete and replace if needed. * DD214 (if you are claiming Veteran's Preference) * Inside your Job Application, upload these documents: * Resume (or choose existing resume if you have one) * Cover Letter Job Application Process * Sign in to your existing account or Register for a new account. * Review and complete your contact information on the My Contact Information page. * Upload documents listed in the Required Documents section of this job posting to the appropriate location. * Complete and Submit your application. * Check your email and My Job Notifications for written communications from the Recruiter. * Email - the email listed on the Careers>My Contact Information page. * Notifications - view the Careers>My Job Notifications page. See the helpful links below to assist in completing your application: * Instructions: * Job Search * Registration & User Account * Application * Frequently Asked Questions How to Claim Veterans Preference Veterans' Preference Eligible (VPE): Former military personnel or their spouse that have been verified as a "veteran"; under K.S.A. 73-201 will receive an interview if they meet the minimum competency factors of the position. The veterans' preference laws do not guarantee the veteran a job. Positions are filled with the best qualified candidate as determine by the hiring manager. Learn more about claiming Veteran's Preference How to Claim Disability Hiring Preference Applicants that have physical, cognitive and/or mental disabilities may claim an employment preference when applying for positions. If they are qualified to meet the performance standards of the position, with or without a reasonable accommodation, they will receive an interview for the position. The preference does not guarantee an applicant the job, as positions are filled with the best qualified candidate as determined by the hiring manager. Learn more about claiming Disability Hiring Preference PLEASE NOTE: The documentation verifying a person's eligibility for use of this preference should not be sent along with other application materials to the hiring agency but should be sent directly to OPS. These documents should be sent either by fax to *************, scanned and emailed to *************************, or can be mailed/delivered in person to: ATTN: Disability Hiring Preference Coordinator Office of Personnel Services Landon State Office Building 900 SW Jackson, Rm 401 Topeka, KS 66612 Equal Employment Opportunity The State of Kansas is an Equal Opportunity Employer. All qualified persons will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, political affiliation, disability or any other factor unrelated to the essential functions of the job. If you wish to identify yourself as a qualified person with a disability under the Americans with Disabilities Act and would like to request an accommodation, please address the request to the agency recruiter.

# Job Description: AI Task Evaluation & Statistical Analysis Specialist ## Role Overview We're seeking a data-driven analyst to conduct comprehensive failure analysis on AI agent performance across finance-sector tasks. You'll identify patterns, root causes, and systemic issues in our evaluation framework by analyzing task performance across multiple dimensions (task types, file types, criteria, etc.). ## Key Responsibilities - **Statistical Failure Analysis**: Identify patterns in AI agent failures across task components (prompts, rubrics, templates, file types, tags) - **Root Cause Analysis**: Determine whether failures stem from task design, rubric clarity, file complexity, or agent limitations - **Dimension Analysis**: Analyze performance variations across finance sub-domains, file types, and task categories - **Reporting & Visualization**: Create dashboards and reports highlighting failure clusters, edge cases, and improvement opportunities - **Quality Framework**: Recommend improvements to task design, rubric structure, and evaluation criteria based on statistical findings - **Stakeholder Communication**: Present insights to data labeling experts and technical teams ## Required Qualifications - **Statistical Expertise**: Strong foundation in statistical analysis, hypothesis testing, and pattern recognition - **Programming**: Proficiency in Python (pandas, scipy, matplotlib/seaborn) or R for data analysis - **Data Analysis**: Experience with exploratory data analysis and creating actionable insights from complex datasets - **AI/ML Familiarity**: Understanding of LLM evaluation methods and quality metrics - **Tools**: Comfortable working with Excel, data visualization tools (Tableau/Looker), and SQL ## Preferred Qualifications - Experience with AI/ML model evaluation or quality assurance - Background in finance or willingness to learn finance domain concepts - Experience with multi-dimensional failure analysis - Familiarity with benchmark datasets and evaluation frameworks - 2-4 years of relevant experience

Ready to dive into a fast-paced, ever-evolving research environment where innovation thrives and curiosity leads the way? Hennessy Research Associates - a Kemin Company is hiring a Research Associate. Are you passionate about animal health and eager to make a real impact across species? As a Research Associate, you'll be part of a vibrant team working on projects that span both companion animals and livestock-well beyond the vaccine space. This role offers hands-on experience in a dynamic lab environment, where you'll spend half your time preparing solutions for downstream processing and helping refine biological materials after growth. With a wide variety of projects and no set routine, every day brings new challenges and discoveries. If you thrive on multitasking, scientific exploration, and contributing to meaningful research, this is the opportunity you've been waiting for. This position is based on-site at our Lenexa, Kansas location. Join the Kemin Team and Transform Lives! We are a privately held, family-owned-and-operated global biotechnology company driven by curiosity and committed to transforming the quality of life for people, pets, and the planet. We create solutions that strengthen health and wellbeing, provide nutrition and immune support for pets and production animals, safeguard the planet's natural resources, and protect the global food supply chain for generations to come. We supply over 500 specialty ingredients for various industries, including human and animal health and nutrition, pet food, aquaculture, nutraceutical, food technologies, crop technologies, textiles, biofuels, and animal vaccines. We employ 3,500 global employees and operations in 90 countries, including manufacturing facilities in Belgium, Brazil, China, Egypt, India, Italy, San Marino, Singapore, South Africa, and the United States. As a valued member of our team, you'll enjoy a comprehensive benefits package designed to support your financial, physical, and professional well-being: Competitive Financial Package: Enjoy a rewarding salary, uncapped bonus opportunities, a 401k match program, and generous paid vacation and holidays. Career Development and Advancement: Unlock your potential with opportunities for growth and development throughout your entire career. Continued Learning Opportunities: Grow your skills with our in-house learning platforms, offering thousands of training resources both live and online, and take advantage of tuition reimbursement for external post-secondary pursuits. Service Opportunities: Make a positive impact with paid time off for volunteering in your community Responsibilities Perform lab experiments within well-defined guidelines and under direct supervision; operate laboratory equipment. Perform literature reviews and provide written summary. Draft SOP's, research protocols and research methods, with supervision. Perform basic data analysis, with supervision. Collect, interpret and document research data, with supervision. Prepare and present research data and analytics in multiple formats. Contribute to scientific publications used for internal purposes. Qualifications Education Associates Degree in a chemistry or biology related field with 2+ years of relevant experience Bachelors Degree with 1+ year of relevant experience Demonstrated sterile technique. Lab instrumentation upkeep/maintenance. Lab notebook/recording. Solution preparation. Cell culture/virus and/or microbial experience up to 1L volume or T-100 flasks (or larger). Ability to work under pressure and able to handle multiple projects efficiently. Analytical lab skills with a strong scientific curiosity and innovative thinking. Reliable and self-motivated. Good understanding of Microsoft office products (Word, Excel, Powerpoint, etc.) Good written and oral communication skills. Basic understanding of English, both written and oral. Ability to interact well with others in a team environment. A post-offer background check and drug screen is required. Additional pre-employment requirements may be necessary based on position. Kemin is an equal opportunity employer, and all reasonable accommodations will be considered. Kemin is a drug-free and tobacco-free campus. #LI-MP1

Mindlance is a national recruiting company which partners with many of the leading employers across the country. Feel free to check us out at ************************* Its a simple route driver job and company will be providing the car. Job Description Job Title: Chemist Job ID : LLYJP00006309 Duration: 6+ Months (Possible Of Extension) Location: Overland Park, KS Job Details: QC Chemist position, they will be doing HPLC Analyses with possible dissolution testing. They will be working in a lab environment using GMP skills with a GC headspace, potentially could be running it. They will be an influx of testing required for the lab move which is requiring them to do comparative testing between the two spaces. There is a potential for hormone exposure so there is a respirator testing required. Perform accurate and timely testing of routine and some non-routine lab samples in accordance withappropriate GMP and safety guidelines. Completes second person verification of test results. Participates in laboratory root cause investigations and quality system improvement initiates by executingwell defined protocols and procedures. Shares technical information and best practice within the group. Design and evaluation of experiments, methods development and characterization, support of processdevelopment/optimization and the analysis and interpretation of data. Conduct studies to validate methods, develop methods, evaluate new technologies. Sample Analysis. Sample preparation, instrument set-up and operation, data entry, primary data review. Coordination of method transfers and co-validations. Qualifying, calibrating, and maintaining analytical instrumentation. All laboratory work will be conductedand documented in accordance with the appropriate Quality System. Act as a resource for insuring adherence to quality systems Requirements / have to haves not listed elsewhere Bachelor of Science in Chemistry or related field Request preferences / nice to haves • Fundamental knowledge of cGMP compliance requirements, instrument qualification procedures and computer system validation principles. • Good documentation skills and ability to author and/or review standards, guidelines, SOPs, templates, protocols, and other GMP documentation. • Excellent general computer skills (MS Excel, Word, etc.) and the ability to compile summarize and present information to a diverse group. • Excellent communication skills and willingness to interact with laboratory personnel, contractors and management. • Ability to troubleshoot problems and identify solutions. • Ability to influence and partner with individuals both within and outside of a formal reporting relationship towards realization of team goals. • Assist in addressing laboratory investigations within specified timeframe. Promote elimination Primary Position Responsibilities (major or daily tasks) • Perform analytical and physical testing on in-process, finished product and stability samples. • Assist laboratory leader in ensuring compliance with all procedures, safety and regulatory commitments in Quality Control. • Perform review and approval of analytical data. • Maintain analytical methods in the laboratory in a state of validation. • Assist in addressing laboratory investigations within specified timeframe. Promote elimination of problems by identifying and addressing root cause. Qualifications Requirements / have to haves not listed elsewhere Bachelor of Science in Chemistry or related field Request preferences / nice to haves • Fundamental knowledge of cGMP compliance requirements, instrument qualification procedures and computer system validation principles. • Good documentation skills and ability to author and/or review standards, guidelines, SOPs, templates, protocols, and other GMP documentation. • Excellent general computer skills (MS Excel, Word, etc.) and the ability to compile summarize and present information to a diverse group. • Excellent communication skills and willingness to interact with laboratory personnel, contractors and management. • Ability to troubleshoot problems and identify solutions. • Ability to influence and partner with individuals both within and outside of a formal reporting relationship towards realization of team goals. • Assist in addressing laboratory investigations within specified timeframe. Promote elimination Primary Position Responsibilities (major or daily tasks) • Perform analytical and physical testing on in-process, finished product and stability samples. • Assist laboratory leader in ensuring compliance with all procedures, safety and regulatory commitments in Quality Control. • Perform review and approval of analytical data. • Maintain analytical methods in the laboratory in a state of validation. • Assist in addressing laboratory investigations within specified timeframe. Promote elimination of problems by identifying and addressing root cause. Additional Information All your information will be kept confidential according to EEO guidelines.

APTIM is seeking an early career Environmental Scientist on a full-time basis to participate in a variety of environmental compliance support tasks, such as permitting/management of hazardous waste, hazardous materials, above ground and/or underground storage tanks, spill prevention, and DOT and RCRA compliance. The successful candidate will be experienced in supporting an environmental team. This position will primarily be in an office environment but may also require travel to client facilities to conduct environmental compliance reviews and/or gather related data. Key Responsibilities/Accountabilities: * Executing various work scopes, while meeting project schedules and budgets * Working independently and as part of a project team and be able to adjust to changing conditions * Research and understanding regulatory regulations * Working as a team member and/or team lead to assist in preparation of regulatory reports and permit applications * Data entry and management, likely on multiple software platforms * Work in client asset management systems to document research and findings * Interfacing with client personnel at a corporate and facility level * Managing time to ensure a quality product is prepared to meet project deadlines * Applying knowledge and skills to a wide range of standard and nonstandard situations * Following defined processes explicitly while also being able to identify and accommodate new or changing scenarios as well as developing processes for new activities. Basic Qualifications: * Bachelor's degree in a core science (such as geology, chemistry, physics, or biology) * Some business courses recommended. * External Job Description: engineering, environmental science, or related area required. * Related work experience of 1 - 2 years recommended. * Prior experience or training regarding environmental compliance and related federal and state environmental regulations desirable. * Strong written and oral communication skills. * Strong computer skills required. * Must have a demonstrated strength and proficiency in Microsoft applications such as MS Excel, MS Word, MS Teams, SharePoint Online, etc. and the ability to learn other software applications. * Willing and able to work in the field and travel to complete work. ABOUT APTIM APTIM is committed to accelerating the transition toward a clean and efficient energy economy, building a sustainable future for our communities and natural world, and creating a more inclusive and equitable environment that celebrates the diversity of our communities. We specialize in environmental, resilience, and sustainability and energy solutions, as well as technical and data solutions, program management, and critical infrastructure. For every challenge our clients face, there is an opportunity for APTIM to innovate a fit-for-purpose solution that will raise your organization or community to a new standard of excellence. What you can expect from APTIM: * Work that is worthy of your time and talent * Respect and flexibility to live a full life at work and at home * Dogged determination to deliver for our clients and communities * A voice in making our company better * Investment into your personal and professional development As of the date of this posting, a good faith estimate of the current pay range for this position is $24.04- $31.25 per hour. Compensation depends on several factors including: experience, education, key skills, geographic location of the position, client requirements, external market competitiveness, and internal equity among other employees within APTIM. Employee Benefits APTIM Environmental and Infra, LLC is committed to providing an extensive range of benefits that protect and promote the health and financial well-being of our employees and their families through the APTIM Benefits Marketplace ************************************ * Medical, vision, and dental insurance: Through the marketplace, our employees can choose benefits from five metallic levels and 10+ carriers to find the right benefits that work for them in their location. * Life insurance * Short-term and long-term disability insurance * Paid holidays, vacation, and sick leave (eligibility based on company policy and applicable law) * 401(k) APTIM offers three 401k plans through the Aon Pooled Employer Plan (PEP). The specific plan you are eligible for depends on the business unit you are in. The details of the largest plan are found here: * APTIM 2025 401(k) Plan Features (makeityoursource.com) * APTIM - Helpful Documents Watch our video: About APTIM - In Pursuit of Better #LI-BN1 #LI-ONSITE