Research scientist jobs in Lenexa, KS

Research Scientist- Full-Time, 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. At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients' lives. Our 'Own It' culture is driven by four key values that bring us together as individuals and set us apart as an organization: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organization that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development. That's our vision. We're driven by it. And we need talented people who share it. If you're as driven as we are, join us. You'll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you'll be helping shape an industry. Desired Experience (flow cytometry experience required, LBA preferred) * Ligand binding assays * ELISA, ECLIA * PK, PD, and immunogenicity * Usage of relevant software (e.g. SoftMax Pro, Watson) * Flow cytometry * Panel design * Gating strategy design * Usage of cytometry software (e.g. FACSDiva, FCS express) * Cell culture * Use of aseptic technic to culture Primary Cells and Cell Lines in support of functional assays. Method Development * Designs and executes experiments for method development under supervision or independently depending on level * Develops new scientific approaches to method development and communicates these to the global science team * Depending on level the scientist may: * Mentor more junior scientists and advise operation on developed methods * Reviews and approves data of other scientists * Communicate with team members and management regarding project status, purpose, scheduling, problems, etc. * Communicate and/or participate in communication with clients regarding project status. Scientific * Maintain knowledge and skill in all techniques where you perform your work. * Provide scientific input to management and BD about new technology investments and lines of service. * Discusses scientific results with sponsors together with project manager * Promotes ICON/PRA utilizing their scientific skills through scientific communication such as external publication of posters and journal articles. * Perform R&D projects * Training of technicians on technical aspects * Mentor and train staff on scientific topics Quality and Timely Work Execution * Takes initiative in process development and SOP/WI writing * Legible, logical and reproducible documentation of all experimentation * Has a thorough understanding and complies with GLP and other appropriate regulations * Develops rugged and economical assays * Performs data review of other scientist's work Sample Analysis and Assay Validation * Provides key assay input to the validation and bioanalysis team(s) to ensure successful execution * Assay troubleshooting * May perform and document maintenance, trouble-shooting and repairs on advanced instrumentation with support of service engineers or other trained supervisory personnel. Qualifications * Read, write and speak fluent English * BS in Science + 3-5 years of experience in a relevant laboratory field * MS or PhD with applicable research in a relevant scientific field preferred * Presenter/Publisher in Regulated relevant field preferred * The level offered will be dependent on relevant experience and education Benefits of Working in ICON: Our success depends on the quality of our people. That's why we've made it a priority to build a culture that rewards high performance and nurtures talent. We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals - both ours and yours. We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead. But beyond the competitive salaries and comprehensive benefits, you'll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change. ICON is an equal opportunity and inclusive employer and 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 through the form below. 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

Job DescriptionDescription: 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.

Research Scientist- Full-Time, 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. At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients' lives. Our 'Own It' culture is driven by four key values that bring us together as individuals and set us apart as an organization: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organization that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development. That's our vision. We're driven by it. And we need talented people who share it. If you're as driven as we are, join us. You'll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you'll be helping shape an industry. **Desired Experience (flow cytometry experience required, LBA preferred)** + **Ligand binding assays** + **ELISA, ECLIA** + **PK, PD, and immunogenicity** + **Usage of relevant software (e.g. SoftMax Pro, Watson)** + **Flow cytometry** + **Panel design** + **Gating strategy design** + **Usage of cytometry software (e.g. FACSDiva, FCS express)** + **Cell culture** + **Use of aseptic technic to culture Primary Cells and Cell Lines in support of functional assays** **.** **Method Development** + Designs and executes experiments for method development under supervision or independently depending on level + Develops new scientific approaches to method development and communicates these to the global science team + Depending on level the scientist may: + Mentor more junior scientists and advise operation on developed methods + Reviews and approves data of other scientists + Communicate with team members and management regarding project status, purpose, scheduling, problems, etc. + Communicate and/or participate in communication with clients regarding project status. **Scientific** + Maintain knowledge and skill in all techniques where you perform your work. + Provide scientific input to management and BD about new technology investments and lines of service. + Discusses scientific results with sponsors together with project manager + Promotes ICON/PRA utilizing their scientific skills through scientific communication such as external publication of posters and journal articles. + Perform R&D projects + Training of technicians on technical aspects + Mentor and train staff on scientific topics **Quality and Timely Work Execution** + Takes initiative in process development and SOP/WI writing + Legible, logical and reproducible documentation of all experimentation + Has a thorough understanding and complies with GLP and other appropriate regulations + Develops rugged and economical assays + Performs data review of other scientist's work **Sample Analysis and Assay Validation** + Provides key assay input to the validation and bioanalysis team(s) to ensure successful execution + Assay troubleshooting + May perform and document maintenance, trouble-shooting and repairs on advanced instrumentation with support of service engineers or other trained supervisory personnel. **Qualifications** + Read, write and speak fluent English + BS in Science + 3-5 years of experience in a relevant laboratory field + MS or PhD with applicable research in a relevant scientific field preferred + Presenter/Publisher in Regulated relevant field preferred + The level offered will be dependent on relevant experience and education **Benefits of Working in ICON:** Our success depends on the quality of our people. That's why we've made it a priority to build a culture that rewards high performance and nurtures talent. We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals - both ours and yours. We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead. But beyond the competitive salaries and comprehensive benefits, you'll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change. ICON is an equal opportunity and inclusive employer and 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 through the form below. **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

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.

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

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!

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

Senior Regulatory Specialist We are supporting a client on a program with complex, multi-region regulatory workstreams. The Senior Regulatory Specialist will independently execute the regulatory strategy defined by the project lead and drive high-quality CT submission deliverables across the US, EU, and China. Key Responsibilities Execute regional CT submission strategies aligned to the global plan for US, EU, and China. Prepare, review, and coordinate regulatory documents for clinical trial applications (e.g., IND amendments, CTA/CTC, protocol updates, IB revisions). Lead cross-functional collaboration with CMC, Clinical, Safety, and Project Management to ensure cohesive submission packages. Track regulatory timelines, risks, and dependencies; escalate issues and propose mitigation plans. Ensure compliance with applicable regional regulations and guidance (FDA, EMA, NMPA) for Phase II & III. Respond to authority queries and support deficiency resolution and follow-up commitments. Maintain submission quality standards and version control for source documents and dossiers. Contribute to regulatory meeting materials (briefing packages, Q&A grids) and participate in internal readiness reviews. Qualifications 7-10+ years of regulatory affairs experience in clinical stage development, with direct US, EU, and China CT submission responsibility. Solid experience with solid oral dosage programs preferred. Proven ability to work independently, execute against defined strategies, and deliver to aggressive timelines. Strong understanding of Phase II & III regulatory requirements, submission templates, and regional nuances. Excellent project coordination, document management, and stakeholder communication skills. Bachelor's or advanced degree in a life science or related field (MS/PhD preferred). Competencies Strategic execution, ownership, and decisiveness High attention to detail and submission quality Cross-functional collaboration and stakeholder influence Clear, concise scientific and regulatory writing Proactive risk management and problem solving

Hiring Department University of Missouri - Kansas City School of Science and Engineering Earth and Environmental Science - Natural and Building Environments Minerals and Interfaces in Terrestrial environment High-Resolution Laboratory (MITHRIL) The Minerals and Interfaces in Terrestrial environment High-Resolution Laboratory (MITHRIL) at UMKC studies the mineralogy and geochemistry of Earth surface conditions. The goals of the lab are to understand the fundamental geochemical processes controlling cycles of trace elements, including contaminants and critical elements, through adsorption on mineral surfaces, incorporation into crystal structure, and uptake by biomineralization processes. We use a combination of field observation, mineral synthesis, laboratory-and synchrotron-based X-ray techniques, (scanning) transmission electron microscopy, and geochemical methods to obtain an atomic resolution understanding to achieve these goals. UMKC is rated R1 by the Carnegie Research Classification of Institutions of Higher Education. Job Description The Minerals and Interfaces in Terrestrial environment High-Resolution Laboratory (MITHRIL) at University of Missouri-Kansas City invites applications for a postdoctoral research position, with an anticipated start date of February 1, 2026. This postdoc position will explore the fundamental interaction between critical elements and minerals at the Earth surface condition. Responsibilities include... * Conducting original research on the interactions of minerals and critical elements in aquatic systems using mineral synthesis, X-ray diffraction, electron microscopy, synchrotron X-ray and complementary approaches. * Preparing scientific findings for conferences and peer-reviewed publications. * Mentoring undergraduate and graduate students. * Assisting in laboratory management. * Involving in grant proposal writing. This is a 12-month, full-Time, benefit eligible, unranked academic position. Qualifications Applicants must have received their PhD. or equivalent degree (in mineralogy, low-temperature/environmental geochemistry, aquatic, soil, or marine chemistry, or related discipline) and all formal requirements for a PhD. must be completed before the start of the appointment. A proven record of research accomplishments and have prior experience with wet chemistry and analytical techniques such as (XRD, SEM, TEM, Raman, UV-Vis, and/or ICP-OES/MS). Demonstrated effective communication skills in a variety of settings. Applicants must write and converse fluently in English. 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 To be considered, you must complete the application at ******************************** including Legal Name, US employment eligibility, and current contact information. Upload all application materials (a letter of interest, curriculum vitae, a list of references). If you are experiencing technical problems, please email **************************. For questions about the position, please contact ************************** include the Job Identification number 57689 and name of the position. Official transcripts will be required if a contract is extended. Other Information For more information regarding 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 * Explore Jobs * Sign In * New User

About Us American Century Investments is a leading global asset manager with over 65 years of experience helping a broad base of clients achieve their financial goals. Our expertise spans global equities and fixed income, multi-asset strategies, ETFs, and private investments. Privately controlled and independent, we focus solely on investment management. But there's an unexpected side to us, too. We direct over 40% of our profits every year-more than $2 billion since 2000-to the Stowers Institute for Medical Research. Our ongoing financial support drives the Institute's breakthrough work and mission of defeating life-threatening diseases like cancer and Alzheimer's. So, the better we do for our clients, the more we can do for everyone. All 1,400 of us across the globe are inspired every day by the unique difference our hard work can make in so many lives. It shows in the curiosity we bring to every initiative, the deep relationships we build with our clients, and the way we treat each other in the hallway. If you're excited to learn more about us, we can't wait to learn more about you. Role Summary This program is for currently enrolled undergraduate students. The deadline to apply is October 22, 2025. This position is not eligible for visa sponsorship. Applicants must be authorized to work in the U.S. without visa sponsorship, now or in the future. Are you seeking an opportunity to learn the basics of the financial services industry with a reputable firm in KC? How You Will Make an Impact Buildout of prompts and use of Copilot-AI capabilities in research and trading Documenting research framework and learning basic research capabilities Work on sector trend reporting Research for marketing pieces Natural Disaster reporting Help with basic Range Score modeling What You Bring to the Team (Required) Demonstrates the American Century Investments Winning Behaviors: Client Focused, Courageous and Accountable, Collaborative, Curious and Adaptable, Competitively Driven Financial, economic, and market analysis interest Financial statement analysis interest Analytical skills written and verbal communication skills Collaboration Technology skills (Copilot, Word, Excel) Additional Assets (Preferred) A current Junior or Senior Undergraduate student, currently enrolled full-time in any related field. Financial, Economic, and Market Analysis Ability to interpret macroeconomic trends, market movements, and financial data to support investment or policy decisions. Financial Statement Analysis Proficiency in reviewing and extracting insights from balance sheets, income statements, and cash flow statements. Analytical Thinking Skilled in breaking down complex problems, identifying patterns, and drawing data-driven conclusions. Communication Skills Clear and effective written and verbal communication, especially in presenting findings and collaborating across teams. Collaboration Comfortable working in team environments, contributing to group discussions, and supporting shared goals. Technology Proficiency Familiarity with tools such as Microsoft Excel, Word, and Copilot to streamline research, reporting, and analysis. What We Offer Our interns receive competitive pay, as well as 401k eligibility for contributions Mentor Program: a designated mentor will be assigned to you during your time with us to provide career coaching and mentorship Housing assistance for any interns that join us with a permanent residence outside of the Kansas City Metro Area Access to Business Resource Groups that you can ally and participate in (Diversity, Women in Finance, LGBTQ+, Emerging Professionals, Veterans) Casual dress code - be comfortable and express your unique self A robust social and philanthropic calendar of events hosted just for interns! Internship Structure 10 Week Program - June 1 - August 7 40 hours a week, between 8am-5pm CST Additional Requirements Employees are required to be in the office on a scheduled frequency. Adherence to this schedule is essential to fulfilling the expectations of the role. American Century Investments is committed to complying with the Americans with Disabilities Act and all other applicable Equal Employment Opportunity laws and regulations. As such, American Century strives to provide a reasonable accommodation to any qualified individual under the ADA to perform essential job functions. We encourage people of all backgrounds to join us on our mission. If you require reasonable accommodation for any aspect of the recruitment process, please send a request to HR-Talent_*******************************. All requests for accommodation will be addressed as confidentially as practicable. American Century Investments believes all individuals are entitled to equal employment opportunity and advancement opportunities without regard to race, religious creed, color, sex, national origin, ancestry, physical disability, mental disability, medical condition, genetic information, marital status, gender, gender identity, gender expression, age for individuals forty years of age and older, military and veteran status, sexual orientation, and any other basis protected by applicable federal, state and local laws. ACI does not discriminate or adopt any policy that discriminates against an individual or any group of individuals on any of these bases. #LI-Onsite American Century Proprietary Holdings, Inc. All rights reserved.

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

Performing critical work that impacts our industry and our world's health while problem solving and innovating in the field - that is what Associate Scientists at KCAS Bio get to do every day. If that gets you excited too, then maybe working as an Associate Scientist at KCAS Bio is the role for you. When you work as an Associate Scientist on the Molecular team, you get to further our mission by designing, developing, validating, and analyzing samples utilizing molecular and cell biology techniques such as qPCR, dd PCR and cell-based assays within a GLP (Good Laboratory Practice) environment laboratory environment. Our Molecular lab team uses a full range of services and viral vector capabilities to analyze gene replacement, gene addition, gene inhibition, gene editing, and cell therapy or transplantation. In this role, we will rely on you to: Demonstrate technical and scientific skills in molecular technologies, including PCR (qPCR and dd PCR) and handling DNA/RNA Experience with procedures for the extraction and quantification of nucleic acids Experience working with human blood, primary cells/tissue, and derived cell culture skills at the BSL-II level Experience with cell culture is preferred Plan and carry out assigned experiments. Including method development, method validation, sample analysis, data calculation, interpretation & review, and troubleshooting Design experiments & evaluate outcomes versus current SOPs, protocols, and other relevant standards. Recommend appropriate course of action as necessary Act as lead scientist and provide work instructions and technical training to more junior scientific staff in conducting assigned projects Perform all aspects of the job in a way that supports the company brand, mission, vision, and values To qualify specifically for this role, you will have: Bachelor's, Masters or PhD in microbiology, biochemistry, chemistry, immunology, or related field with 4 years' experience in a scientific laboratory environment Experience with design, method development, validation, and sample analysis Experience with GLP requirements and Good Documentation Practices (GDP) Manage material, equipment, and instrumentation Analyze and interpret data, prepare summary tables, and review raw data Assist with the preparation and review of SOPs, study plans, and reports Ability to multi-task and meet deadlines Excellent verbal and written communication and organizational skills Self-motivated and driven Flexible and adaptable - able to work independently and/or in a team environment Ability to troubleshoot and problem-solve - Critical Thinking (Please note this is a representative summary of responsibilities, not a comprehensive or exclusive list of the duties to be performed in any position. Employees must follow instructions and perform additional duties as requested.) WHO YOU AREYou will thrive at KCAS Bio if you enjoy a relational environment, are purpose- and values-driven, embrace constant development and supportive leadership, and enjoy being part of innovative work. WHAT YOU'LL GETOur benefits include, and extend beyond, the traditional package. At KCAS Bio, you will enjoy company sponsored events like food trucks, family days and spirit days. You will grow in your career with KCAS University. You will be able to connect with like-minded employees to further KCAS Bio's approach to key areas such as wellness, inclusion, and community outreach. You will engage as an owner in our stock ownership program. You will have access to the latest technology. And you will be able to invest in the community with paid time off to volunteer. Learn more about the Benefits at KCAS Bio WHO WE AREWe are a fast-growing contract research organization (CRO) headquartered in Kansas City, pioneering the latest drug development in both human and animal health fields. Demand for our expertise is growing and so is our need for great people to work in nimble, empowered teams committed to one another's growth. At KCAS Bio, we advance both great science AND great people. Learn more about what it is like to work at KCAS Bio KCAS Bio is proud to be an Equal Opportunity Employer. Among other things, we provide equal employment opportunities without regard to race, color, religion, national origin, ancestry, marital status, veteran status, age, disability, pregnancy, genetic information, sex, sexual orientation, gender identity, or any other legally protected category; we recruit qualified candidates without regard to citizenship status based on internal processes that enable us to hire the right candidates consistent with the appropriate U.S. Immigration framework; and (3) we work with and provide reasonable accommodations to individuals with disabilities and for sincerely held religious beliefs, observances, and practices. Anyone who needs reasonable accommodation may send an email to ************************** or call ************ (for TTY assistance call 711) and ask for Human Resources. IND123

GENERAL STATEMENT OF RESPONSIBILITY: Coordinate the day-to-day activities of the Certifying Scientists and the specific duties associated with the hair testing department. Ensure the daily processing is conducted in an accurate and efficient manner, following guidelines and regulations. ESSENTIAL FUNCTIONS: * Manage team performance by evaluating, hiring, training, coaching, disciplining and motivating; initiating disciplinary action when appropriate. * Maintain teamwork schedules to ensure assignments to expedite work flow, operational coverage and staff coverage. * Establish and maintain department SOP's and ensure compliance. * Consult with MRO's and clients about drug test results. * Perform the duties of a Certifying Scientist when necessary. * Keep current with Federal Register, NLCP Guidance Documents, NRC requirements, CAP requirements, state requirements, etc. * Work with the QC department to resolve audit issues and ensure regulatory requirements are being met. * Ensure department meets production goals and expected turnaround time for samples. * Provide and maintain good communication with staff, other departments, and administration. * Carry out supervisory responsibilities in accordance with CRL's policies and applicable laws. * Maintain and protect the confidentiality of all CRL, CRL subsidiaries, legal entities and client information. * Be able to comply with all applicable federal, state, and local safety and health regulations that would apply to this job. * Be proactive in bringing ideas to Management's attention to improve productivity, service, quality, policies and procedures, cost savings, and utilization of company resources. * Continuously improve management skills through in-house training, self-study methods, and other available training resources. * Ensure concerns are raised to the appropriate level of management. * Keep work area neat and clean. Other duties as assigned. JOB QUALIFICATIONS: EDUCATION: A doctoral, master's, or bachelor's degree in medical technology, clinical laboratory, chemical, or biological science. EXPERIENCE: 4 years of pertinent laboratory experience. Must meet NYS Technical Supervisor requirements. SKILLS & ABILITIES: * Excellent interpersonal skills - positive, professional demeanor, attentive listener * Excellent verbal and written communication and documentation skills - spelling, grammar and proofreading * Strong working knowledge of MS office (MS Outlook, Word, Excel, PowerPoint) * Strong judgment/decision making skills * Ability to perform highly detailed work on multiple, concurrent task with constant interruptions and changing deadlines * Must be able to read, understand, and develop strong working knowledge of appropriate SOP's and other relevant information services. * Detail oriented * Strong analytical and organizational skills * Ability to work under pressure * Ability to be at work and on time * Ability and judgment to interact and communicate appropriately with other employees, clients and management PHYSICAL REQUIREMENTS: The physical demands described here are representative of those that must be met to successfully perform the essential functions of this job. Reasonable accommodations may be available to enable qualified individuals with disabilities to perform the essential functions. The following physical attributes are required for this position: * Sitting for extended lengths of time * Close vision requirements due to computer work * Repetitive use of hands, fingers, wrists, and elbows for operating a computer and telephone * Light lifting, up to 10 pounds * The ability to discriminate between different colors visually is considered an essential function for the position. EQUIPMENT: PC and communications equipment OTHER: Overtime and weekend work as necessary according to workload and/or projects; occasional travel required. The employer shall, in its discretion, modify or adjust this position to meet the company's changing needs. This job description is not a contract and may be adjusted as deemed appropriate in the employer's sole discretion. * denotes essential job function An Equal Opportunity Employer Pay Range: $26.00 - $48.00 Benefits for Full Time Employees: * Medical, Dental, Vision * Life/AD&D * Supplemental Life/AD&D * Section 125 FSA Plan * 401(k) * Short and Long-Term Disability * Paid Time Off * Holidays * Tuition Reimbursement

Role Purpose: The Intern will play a vital role in advancing the company's capabilities in computer vision and fraud detection projects, as well as contributing to research and development initiatives. The incumbent will assist in various tasks related to biometric data collection, algorithm testing, and model validation. Proficiency in Python, along with knowledge of machine learning and MATLAB, is essential for success in this role. Familiarity with AWS, and SageMaker is advantageous. Example Responsibilities: Assist in computer vision and fraud detection projects by contributing to algorithm testing, model validation, and biometric data collection. Utilize Python, MATLAB, and deep learning libraries such as PyTorch and TensorFlow for image processing and analysis tasks. Collaborate with the research team to implement benchmarking metrics and perform ROC analysis. Ensure accuracy in data collection, labeling, and algorithmic testing by paying meticulous attention to detail. Travel to Jumio's Lenexa, KS office 2-4 times a week to collaborate with team members and participate in project discussions. Communicate effectively with team members through written and verbal channels to provide updates on project progress and findings. Experience and Qualifications: Availability to start immediately is required. Enrollment in a graduate program in computer science, computer/electrical engineering, or related fields. Proficiency in Python with working knowledge of image processing libraries. Understanding of benchmarking metrics. Attention to detail and ability to adapt and learn quickly in a fast-paced environment. Great to have Experience and Qualifications: Knowledge of different biometric modalities, eKYC, and presentation attacks. Understanding of databases, cloud computing, and storage, particularly AWS data and ML pipelines such as SageMaker and S3 buckets. Key Characteristics and Attitudes In a recent global survey these attributes were valued by Jumios in all locations and functions - we firmly believe in hiring for mind-set as well as skill. Friendly and supportive Adaptable and flexible Articulate and persuasive High IQ and EQ Curious and coachable Commercially Aware Resilient and tenacious Big picture and the detail Jumio Values IDEAL: Integrity, Diversity, Empowerment, Accountability, Leading Innovation Jumio Values: IDEAL: Integrity, Diversity, Empowerment, Accountability, Leading Innovation Equal Opportunities: Jumio is a collaboration of people with different ideas, strengths, interests and cultures. We welcome applications and colleagues from all backgrounds and of all statuses. About Jumio: Jumio is a B2B technology company dedicated to eradicating online identity fraud, money laundering and other financial crimes to help make the internet safer. We leverage AI, biometrics, machine learning, liveness detection and automation to create solutions that are trusted by leading brands worldwide and respected by industry thought leaders. Jumio is the leading provider of online identity verification, eKYC and AML solutions. With a global footprint, we're expanding the team to meet strong client demand across a range of industries including Financial Services, Travel, Sharing Economy, Fintech, Gaming, and others. Applicant Data Privacy We will only use your personal information in connection with Jumio's application, recruitment, and hiring processes, as described in Jumio's Applicant Privacy Notice. If you have any questions or comments, please send an email to privacy@jumio.com.

Job Title: Senior Data Science/Analytics Consultant JOB PURPOSE: The Senior Data Science/Analytics Consultant is responsible for the full stack of data analytics, from querying or procuring data, cleaning data, feature generation, problem formulation, error/success metric choice, machine learning/predictive model building, and translation of results into business action. This role will help advanced Transportation Insight's data strategy and data-related business decision making. The Sr. Consultant will be expected to wear multiple hats, seek out new opportunities from the business and apply technology to solve a variety of data problems across our organization. ESSENTIAL DUTIES AND RESPONSIBILITIES: Act as a cross functional consultant on data science, data analytics related efforts that span the enterprise. Identifies appropriate analytical tools and methods; uses advanced knowledge of business analysis to perform quantitative analyses and predictive modeling Be able to communicate and explain the results of more technical analyses to business partners in a digestible, visual fashion Lead strategy development for data and analytics products to ensure the program becomes pervasive throughout the organization. Develop a high performing team focused on building strong analytical, data strategy, research and business skill sets while sustaining leading employee engagement and retention. Be a stakeholder in developing and maturing the Data Science strategy PERFORMANCE METRICS: Deliver solutions according to the delivery schedule Design and architect complete end-to-end DS solutions Continuous improvement on predictive and machine learning models Conform to industry standards for quality and effective data visualization and reporting JOB REQUIREMENTS: Qualified applicants should have a Bachelor's degree in Computer Science, Information Science or related field; equivalent work experience and aptitude is acceptable in place of degree Experienced with Data Science practices and tools, such as Alteryx, R, Python, Gurobi Familiar with 3PL business and supply chain concepts Experience with ETL design and data warehousing concepts 5+ years with reporting / analytic tools such as Tableau or Cognos Experience with Oracle, MySQL and/or MS SQL Server and SQL query language required Experience with CRM tools like Salesforce Possess excellent communication and presentation skills required Strong Work Ethic **MAY PERFORM OTHER DUTIES AS ASSIGNED** WORK ENVIRONMENT: Standard office environment, usually indoors away from the elements with moderate noise. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. PHYSICAL EFFORT: Maintain a stationary position for extended periods; move about the office, operate computers and files, as needed; and frequently communicate with others. The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. While performing the duties of this job, the employee is regularly required to sit and talk or hear. The employee is required to stand, walk, and reach with hands and arms. Occasionally, the employee is required to lift boxes up to 20 pounds. SCHEDULING: This is a full-time benefits-eligible position, working Monday through Friday; 8:00 a.m. - 5:00 p.m. An employee in this position must be available to work occasionally on weekends and evenings, during peak periods. TRAVEL: Local travel is required. Out of state travel is limited, but may be required for special projects , training, and conferences. DISCLAIMER: The above statements are intended to describe the general nature and level of work being performed. They are not intended to be an exhaustive list of all responsibilities, duties, and skills required.

Your New Company! At Altasciences we all move in unison to assist and work in the discovery, development, and manufacturing of new drug therapies to get them faster to people who need them. No matter your role, we all play an important part and you will have a significant impact on the health and well-being of people across the globe. By living our values of Employee Development, Customer Focus, Quality and Excellence, Respect and Integrity, we look to foster a passionate and collaborative work environment and we are looking for talented and enthusiastic people, like you, to join our growing team! Whether you're a recent college graduate or seeking your next career opportunity, it's time to discover your future at Altasciences. We are better together and together We Are Altasciences. About The Role The Clinical Research Technician II will work with Clinic teams to execute clinical trial activities in compliance with study protocol, Good Clinical Practices (GCP) and Standard Operating Procedures (SOP)s. What You'll Do Here Ensure the confidentiality of clinical trial participants and sponsors is respected. Understand protocol driven timed study events and acceptable collection windows (protocol and/or SOP driven) for the timed events. Report procedural deviations to appropriate supervisory team members. Preparation and proper clean-up of applicable workstations (i.e. urine collection station, blood processing station, etc.) Maintain and advocate a high level of customer service, quality and safety within the department. Perform clinical trial activities may include but not limited to, sample handling, safety measurements, in-house testing and questionnaire administration. Conduct all clinical trial activities and participant interaction with a high standard of customer service. Report significant participant misbehavior to Study/Clinical Operations management teams. Provide feedback, where necessary, to appropriate team members of study progress. Proactively communicate issues and/or problem resolutions to departmental supervisors and managers. Act as a mentor and coach for newly hired staff. Complete and/or maintain training as required per jobs needs. What You'll Need to Succeed High School Diploma or GED and related job experience required; college degree preferred. Good communication (French and English for Montreal location), Excellent customer service skills, Ability to work in a fast-paced environment. #LI-TN1 MOVING IN UNISON TO DELIVER A BIG IMPACT WITH A PERSONAL TOUCH Altasciences is an equal opportunity employer committed to diversity and inclusion. Our goal is to attract, develop and retain highly talented employees from diverse backgrounds, allowing us to benefit from a wide variety of experiences and perspectives. All qualified applicants will receive consideration for employment without regard to age, race, color, religion, creed, sex, sexual orientation, gender identity, national origin, disability or any other protected grounds under applicable legislation. Reasonable accommodations for persons with disabilities during the recruitment process are available upon request. Join us at Altasciences!

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

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

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