Scientist jobs in Saint Joseph, MO - 66 jobs

Grounded in safety, quality, and ethics, our experts lead their fields with dedication, a creative spirit, and a vision for growth. We draw from more than 20 technical specialties worldwide and are devoted to fostering a community of diverse talents, backgrounds, and expertise. Here, you can apply your passion and collaborate with top environmental professionals on work that's vital to our clients and the communities they serve. Your Opportunity Join a team that's naturally committed to the environment. We are seeking an exceptionally talented and enthusiastic individual with a keen interest in the natural sciences to join our team as a full-time, mid-to-senior level lead wetland scientist in the Overland Park (Kansas City), Kansas or St. Louis, Missouri office. The ideal candidate will have strong expertise in wetland delineation, plant identification, soil characterization, and ecological fieldwork in the Midwest. This role involves up to 60% travel, data collection, and reporting related to wetland assessments and other biological surveys. The candidate will work closely with project managers, senior scientists, and staff scientists with development, coordination, and delivery of environmental permitting, assessment, or compliance documents for projects involving wind and solar electric generation facilities, electric transmission lines, natural gas pipelines, and private development projects to fulfill federal, state, and local agency requirements. Your Key Responsibilities - Delineate wetlands and other water resources in accordance with the US Army Corps of Engineers Manual and the applicable Regional Supplements. - Perform independent field studies including botanical surveys, natural community mapping, wildlife habitat assessments, and ecological impact assessments. - Support project planning and task management for field assignments. - Assist with the preparation and review of technical documents, such as wetland and waterbody delineation reports, threatened and endangered species habitat assessments, environmental assessments, environmental impact statements, permit applications and other technical reports. - Assist Project Managers/Senior Scientists by contributing technical expertise during client/regulatory meetings and proposal development. - Prepare and manage data, reports, and tables for client and agency submission. - Utilize GPS and ArcGIS Field Maps/Survey123 for data collection and mapping. - Other technical duties may include ecological restoration planning and assessment. - May also assist with other duties as assigned, including biological surveys. Your Capabilities and Credentials The ideal candidate will demonstrate strong leadership abilities with experience both leading teams and contributing as a collaborative team member. They should possess exceptional oral and written communication skills, as well as strong analytical and creative problem-solving abilities. The role also requires excellent organizational and note-taking skills, along with the ability to work independently and make sound, timely decisions in the field without direct supervision. Travel will be expected - primarily throughout the Midwest, but also within the broader U.S., and should not be assumed to be local. Education and Experience Required: - Bachelor's degree in environmental science, ecology, botany, soil science, or a related field. - 5-10 years of relevant field experience in wetland delineation and environmental assessments. - Knowledge of local/regional vegetation and soils. - Valid driver's license required. Preferred: - Master's degree in environmental science, ecology, botany, soil science, or a related field. - Experience with and proficiency in data entry using ArcGIS tools (FieldMaps and Survey123). - Wetland Professional in Training or Professional Wetland Scientist Certification. - Familiarity with state and federal environmental permitting processes. - Ability to travel extensively and work outdoors in variable weather conditions. - Task or project management experience. Typical office environment working with computers and remaining sedentary for long periods of time. Field work may include exposure to the elements including inclement weather. This description is not a comprehensive listing of activities, duties or responsibilities that may be required of the employee and other duties, responsibilities and activities may be assigned or may be changed at any time with or without notice. Stantec is a place where the best and brightest come to build on each other's talents, do exciting work, and make an impact on the world around us. Join us and redefine your personal best. \#StayInquisitive **Primary Location:** United States | MO | Kansas City **Organization:** 2277 EnvSvcs-US Great Lakes West-St Louis MO **Employee Status:** Regular **Travel:** Yes **Schedule:** Full time **Job Posting:** 22/07/2025 09:07:24 **Req ID:** 1001639 Stantec provides equal employment opportunities to all qualified employees and applicants for future and current employment and prohibit discrimination on the grounds of race, colour, religion, sex, national origin, age, marital status, genetic information, disability, sexual orientation, gender identity or gender expression. We prohibit discrimination in decisions concerning recruitment, hiring, referral, promotion, compensation, fringe benefits, job training, terminations or any other condition of employment. Stantec is in compliance with laws and regulations and ensures equitable opportunities in all aspects of employment. At Stantec we are committed to ensuring our recruitment process is accessible to all. If you require reasonable adjustments to be made during the recruitment process then please inform a member of our Talent Acquisition team.

At Elanco (NYSE: ELAN) - it all starts with animals! As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets. At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose - all to Go Beyond for Animals, Customers, Society and Our People. At Elanco, we pride ourselves on fostering a diverse and inclusive work environment. We believe that diversity is the driving force behind innovation, creativity, and overall business success. Here, you'll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights. Making animals' lives better makes life better - join our team today! Your Role: Technical Services Manufacturing Scientist - Downstream The Technical Services & Manufacturing Science (TS/MS) Scientist is responsible for providing Primary and/or Secondary loop technical support for commercial downstream operations at the Elwood, Kansas monoclonal antibody (mAb) manufacturing facility. The position is a subject matter expert with respect to mAb products and processes and is engaged in tech transfer, scale-up, process optimization, validation, monitoring, troubleshooting and continuous improvement activities. The TSMS scientist plays a key role in day-to-day operations and delivery of technical projects. Your Responsibilities: Provide technical and on-floor support for the commercialization, manufacture, and life-cycle management of monoclonal antibody products. This includes troubleshooting, participate in product and process related technical investigations and root-cause analyses of process deviations, complaints, and OOS/OOE events. Act as the Process Teams product and process subject matter expert for purification processes which may include chromatography, tangential flow filtration, and centrifugation. Use scientific and statistical analysis tools to improve process understanding, ensure manufacturing processes are capable and operating in a state of control, and identify opportunities for process improvements. Develop / execute projects to address process performance issues and deliver improvement opportunities. Author and provide critical review of technical documents including, but not limited to; batch records, SOPs, PFDs, process recipes, risk assessments, investigations, technical studies, protocols, and reports. What You Need to Succeed (minimum qualifications): Education: Bachelor's degree (or equivalent experience) in Bio/Pharmaceutical Technology, Microbiology, Engineering, or a related discipline. Experience: Experience in the Biotech / Pharmaceutical industry. Detailed understanding of biopharmaceutical production processes and technologies. Working knowledge of cGMP standards and experience working in a regulated environment. Proven analytical thinking and problem-solving skills. What will give you a competitive edge (preferred qualifications): MSc or PhD in Bio/Pharmaceutical Technology, Microbiology, Engineering or a related discipline. Demonstrated experience in commercial monoclonal antibody / recombinant protein manufacturing processes. Experience in tech transfer, scale up, and validation of biopharmaceutical processes. Experience with SAP, JMP, Veeva Vault, RCI, FMEA and QRM tools. Working knowledge of USDA and/or EU GMP regulations for veterinary biologics. Additional Information: Location: Elwood, Kansas. Day shift position. Weekend work on a rotation to provide process support to ongoing operations. Don't meet every single requirement? Studies have shown underrepresented groups are less likely to apply to jobs unless they meet every single qualification. At Elanco, we are dedicated to building a diverse and inclusive work environment. If you think you might be a good fit for a role but don't necessarily meet every requirement, we encourage you to apply. You may be the right candidate for this role or other roles! Elanco Benefits and Perks: We offer a comprehensive benefits package focusing on financial, physical, and mental well-being while encouraging our employees to pursue our purpose! Some highlights include: Multiple relocation packages for eligible roles Two weeklong shutdowns (mid-summer and year-end) in the US (in addition to PTO) 8-week parental leave 9 Employee Resource Groups Annual bonus offering Up to 6% 401K matching #LI_MNLC Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status

Job DescriptionDescription: Food Scientist St. Joseph, MO and Leavenworth, KS Research & Development Come join our wonderful team culture, and be an integral part of our team! The Senior Food Scientist is responsible for our product development support, and technical services to our customers, sales, purchasing, regulatory, quality control, and operations. Promote company values and beliefs while performing job tasks . Primary responsibilities include, but not limited to: · Make “hands on” bench top samples as required by each project parameter in a timely manner. This may include ordering of ingredients. · Formulate with or without assistance, depending on formulation complexity. · Perform mathematical and formulation calculations. · Assist in trials to ensure compliance to approved formulas. · Develop specifications for new products. · Enter formulas in recipe management system accurately. · Reach out to current and potential suppliers and gather preliminary information to vet out ingredients. · Stay technically informed through suppliers, shows and literatures. · Follow CII's New Item/ Ingredient Approval (NIA) process. · Administration duties including labeling, organizing, shipping, and other related areas expected. · General Housekeeping Benefits: - Paid Time Off - Holiday Schedule - Medical - Dental - Vision - Life Insurance - 401k Retirement Plan Working Environment and Physical Demands: Indoors temperature-controlled environment-office, laboratory, manufacturing facility; the use of hearing protection may be required at times, along with other personal protective equipment as necessary. Position requires the ability to sit, stand, walk, climb, manual dexterity, ability to see details at close range and to differentiate colors, ability to listen and to understand spoken words and phrases, ability to communicate information verbally, ability to read and understand ideas presented in writing, ability to communicate information and ideas in writing so that others will understand. Must meet the physical abilities level of Two (2) as defined by the US Department of Labor. Requirements: BS in Food Science or closely related field required. · Minimum 5 years relevant work experience preferred. · Knowledge and experience in product development of granola, panning, and extrusion desirable. · Proficient in Word and Excel and other database management desirable. · Knowledge of ingredient functionality desirable · Some travel required. Customer visits and tradeshows.

UNIVERSITY of MISSOURI-KANSAS CITY SCHOOL of MEDICINE Department of Ophthalmology Vision Research Center The University of Missouri-Kansas City is rated R1 by the Carnegie Research Classification of Institutions of Higher Education. Our research supports advances in defense, health care, public safety, technology and more aimed at a brighter and more advanced future for all. We collaborate across campus, the UM System, the region and encourage our students to participate in our research. The UMKC School of Medicine is a partner of the UMKC Health Sciences District. The District strives to be a premier academic health district, engaging in cutting-edge biomedical research and entrepreneurship, delivering state-of-the-science health care, and educating the next generation of health care professionals. UMKC provides unique opportunities for research and health care collaboration across its Schools of: Medicine, Dentistry, Nursing & Health Studies, and Pharmacy as well as University Health Physicians, regional health care institutions, and the University of Missouri System's NextGen Data Science and Analytics Innovation Center. The Vision Research Center (VRC) at UMKC is the Department of Ophthalmology's research arm, providing residents and fellows with comprehensive research opportunities, including basic research, translational research and clinical trials. ************************************************************************************************** Job Description The Vision Research Group in the department of Ophthalmology at UMKC seeks a full-time Research Scientist or Senior Research Scientist. The successful candidate will engage in research exploring the molecular mechanisms underlying ocular degeneration and engage in collaborative proteomic analysis and research studies. This position offers an opportunity to join a dynamic and collaborative research environment supported by state-of-the-art facilities at UMKC and its partner institutes in the Kansas City area. Team members are integral contributors to research publications and will have the opportunity to participate in externally funded research collaboration and translational opportunities. This is a 12-month full-time, benefit eligible, unranked academic position. Qualifications To qualify for a Research Scientist position, applicants must hold a PhD or equivalent degree and must have a minimum of two years of postdoctoral experience. To qualify for a Senior Research Scientist position, applicants must hold a PhD or equivalent degree and must have a minimum of two years of postdoctoral experience and evidence of success in obtaining external funding. Preferred qualifications include expertise in one or more of the following areas: diseases that affect the retina, including age-related macular degeneration, diabetic retinopathy and glaucoma. 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, please apply online at ******************************** (Job Opening ID 57677). Application materials include: * Complete application on the UMKC recruitment portal including name, contact information, and questions therein. * Letter of research interest, experience, evidence of success in obtaining external funding that qualifies you as a Research Scientist or Senior Research Scientist * Curriculum Vita * List of at least 3 professional references with current contact information * Candidates will receive prior notification if references will be contacted. * Official copy of your transcripts with your highest degree earned * For credential verification Combine all materials into one PDF or Microsoft Word document 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 during application, please email ************************** . For questions about the position, please contact Megan Florance ******************, including the Job Identification number 57677 and name of the position. Reasonable accommodations may be requested during the application and recruitment process. If you need an accommodation, please contact the Office of Equity and Title IX at **************. Application Deadline Application review will begin upon receipt. Applications will be accepted until a qualified candidate is hired. Other Information UMKC is a public, urban, R1 research university with more than 15,000 undergraduate, graduate, and professional students. It is part of the larger University of Missouri System. Our university is committed to being a model urban university that is recognized for our partnerships with surrounding urban communities to effectively foster a healthy, safe, and more economically secure quality of life. ********************* Community Information Kansas City is a diverse and vibrant community with an affordable cost of living. Our UMKC campuses are centered in the hubs of business activity, cultural arts, (some great barbeque and ethnic cuisine!) and health science research engagement for both campuses. As one of the largest cities in Missouri, we are home to national championship sports teams, a rich history of cultural arts and music, NASCAR racing, an international airport, and a community that is very engaged with and supportive of our university initiatives. Our beautiful state has rolling hills, rivers, lakes, and long bike/hiking trails for those that enjoy time in the great outdoors. Kansas City offers something for everyone! 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 ************.

As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development, and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies' success. We realize that our strength and competitive advantage lie with our people. We support our employees in several ways to foster a healthy working environment, meaningful work, mobility, networking, and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim's high regard for our employees. The Senior Scientist, Clinical is responsible for the safety and efficacy in the target species for new animal pharmaceutical and biological research and development projects, line extensions and maintaining existing licensed products. This role provides clinical study design and implementation including resource and budget planning from protocol to execution and to final study report for submission to regulatory agencies for animal pharmaceutical and biological projects in both lab and field conditions. The incumbent fulfills a role as a subject matter expert in representing his/her function (e.g. on development teams, regulatory authority meetings and key Opinion Leaders). The Senior Scientist, Clinical acts as the Clinical Representative as assigned for all stages of product development. This role resents clinical content to regulatory authorities as required and ensures compliance with all applicable regulatory and animal welfare principles. The incumbent may lead a Clinical Team as Clinical Leader and is responsible for development and implementation of the clinical strategy. The Clinical Leader serves as the representative on the Core Team. **Duties & Responsibilities** + Independently initiates and coordinates strategic scientific experiments with a predefined goal including developing new methodologies, protocols and/or test procedures that contribute to innovation and core group/research goals and reflect expert knowledge. + Responsible for overall study design, execution, and reporting to achieve project milestones. + Designs clinical studies to earn label claims and new product licenses/marketing authorizations consistent with the TPP and in compliance with global regulatory guidance and corporate standards for data integrity and animal welfare. + May direct and oversee experimental study design and data analysis/results of junior-level scientists. + Demonstrates expertise in a specific project-relevant area or technology. + May provide guidance and expertise to advance specific projects or evaluate and propose new technologies and concepts in support of multiple projects. + Keeps abreast of relevant literature. + Develops visibility outside of functional area and effectively interacts scientifically with Key Opinion Leaders in relevant fields of research. + Publishes research in peer reviewed journals and presents data at national/international meetings as requested. + Skillfully collaborates across functions (internal and external stakeholders) to assure clinical plans and activities for project teams are delivered efficiently, while supporting continuous improvement in quality including, speed and value of processes supporting studies including protocol and forms, test article availability & suitability, monitoring effectiveness, statistical analysis, study event tracking, compliance, and excellent reporting. + Develops and leverages external providers, academia and Contract Research Organizations as necessary. + Mentors, coaches, and trains colleagues, especially clinical research associates/monitors, on best practices for study execution with flawless speed and compliance, professional & collaborative team member behaviors, accountability, and alignment within Pharma Clinical and with all stakeholders. + Provides technical content (safety and efficacy data) for local and international regulatory submissions and/or leads clinical discussions in authority meetings and/or develops clinical and regulatory strategy. + Develops the clinical strategy and works effectively toward achieving the project goals as defined in the TPP. + Assumes leadership (as the clinical leader or clinical representative) for clinical programs within multi-disciplinary Project Teams for the effective research and development of pharmaceutical projects. + Interacts with Project Leaders, members of the Project Teams and stakeholders. + Responsible for clinical project progress, including timelines, deliverable and budgetary responsibilities. **Requirements** + DVM preferred with five (5) years of experience in a related field with a proven track record of successfully implementing or investigating technologies and adding value to the organization required. OR + PhD (with significant experience in a veterinary-relevant field such as parasitology or animal nutrition) with five (5) years of experience in a related field with a proven track record of successfully implementing or investigating technologies and adding value to the organization required. OR + Master's Degree (with significant experience in a veterinary-relevant field such as parasitology or animal nutrition) with ten (10) years of experience in a related field with a proven track record of successfully implementing or investigating technologies and adding value to the organization required. + Board Certification and/or advanced degree (MS or PhD) in addition to DVM is a plus. + Clinical veterinary practice experience is preferred. + Interest in developing therapeutics a plus. + Minimum of five years (5) of broad experience in a related field with a proven track record of successfully implementing or investigating technologies and adding value to the organization or equivalent combination of education and experience. + Demonstrates industry-leading knowledge of field. + An analytical thinker. + Excellent skills in understanding data and scientific decision processes, and in interpreting and reporting these data in well supported conclusions targeted at achieving project objectives. + Strong leadership skills. + Able to lead (e.g. the Clinical team) without formal authority. + Research methodology experience. + Fosters innovation. + A problem solver. + Outstanding / Good communication and interpersonal skills. + A collaborative team player. + Possesses a customer service orientation, delivering results and executing in a fast and focused manner. + Exceptional planning and organizational skills with a quality orientation. + Strives for business process excellence. + Accepts accountability and ownership. + Exhibits integrity and trust. + Willingness to travel (>10% annual travel). + English: Fluent (read, write and speak). + Ability to communicate effectively both orally and in writing in an inter-disciplinary and international environment. + Leadership experience: One to three (1-3) years leading projects. + Demonstrated knowledge of the product life cycle process. + Experienced in project/program management. + Exhibits business and technical knowledge. **Eligibility Requirements** : + Must be legally authorized to work in the United States without restriction. + Must be willing to take a drug test and post-offer physical (if required). + Must be 18 years of age or older. **Desired Skills, Experience and Abilities** **Additional Duties & Responsibilites** : + Ensures that risks and changes to either the Research Target Profile (RTP) or Target Product Profile (TPP) are communicated into the project team. + Provides clinical input to the either RTP or TPP and influences the Project from the clinical veterinary and scientific perspective. + Takes on Clinical Lead, Study Director, Monitor and Investigator roles as necessary. + Responsible for the design, organization, conduct, timely completion and reporting of assigned clinical R&D studies to establish safety and efficacy of new pharmaceuticals, and to develop new claims and uses for existing products. + Ensures compliance around GSP, GLP, GCP, PV, animal welfare and local regulatory requirements. + Study Director responsibilities are described in the applicable GLP standards. + Contributes or leads internal initiatives such as SOP development, patent filings and due diligence. All qualified applicants will receive consideration for employment without regard to a person's actual or perceived race, including natural hairstyles, hair texture and protective hairstyles; color; creed; religion; national origin; age; ancestry; citizenship status, marital status; gender, gender identity or expression; sexual orientation, mental, physical or intellectual disability, veteran status; pregnancy, childbirth or related medical condition; genetic information (including the refusal to submit to genetic testing) or any other class or characteristic protected by applicable law.

**Senior Associate Scientist I (Dissolution)** + **Work Schedule:** Monday - Friday, 8AM - 4:30PM + 100% onsite (Kansas City) Catalent, Inc. is a leading global Contract Development and Manufacturing Organization (CDMO). Catalent's Kansas City (KCM) facility provides a range of integrated services for oral solid dosage forms, from formulation development and analytical testing to clinical and commercial-scale manufacturing. The facility is the commercial manufacturing Center-of-Excellence for accelerated development programs and roller compaction. The Senior Associate Scientist I will support the Analytics and Dissolution team for in-process, release, and stability sampling and use a variety of analytical instruments. With cutting-edge technologies and a collaborative work environment, this role offers opportunities for long-term advancement. **The Role:** + Execute laboratory work plans/schedules developed with input from a supervisor or senior team member. Sample types include in-process, release or stability. Techniques include HPLC, UV/Vis, Disintegration and Dissolution. Apparatus 1, 2, 3, 5, and 6. Under direction, may perform method development, validation, and transfer activities + Maintain accurate and high-quality laboratory documentation in accordance with regulatory guidance and Site SOPs + May draft technical documents such as methods or certificate of analysis + Performs parallel review of laboratory documentation and may become qualified to perform technical review of documents for accuracy, thoroughness and regulatory compliance + Assists in execution of efficiency improvement projects with guidance + Trains others on laboratory techniques + All other duties as assigned **The Candidate:** + Bachelor's degree in life science or physical science is required with at least two (2) years of related work experience OR a Master's degree is required without any formal industry experience + Knowledge and skills requirements include the ability to process, maintain, and interpret data, understand basic instrument troubleshooting techniques, and communicate clearly and professionally with clients and internal stakeholders + **Physical requirements:** On an average 8-hour day this position requires the ability to walk, sit and stand, use hands to handle or feel, reach with hands and arms at or above shoulder height and below waist height, climb or balance, stoop, kneel, crouch, or crawl; talk and hear, smell and lift up to 40 pounds. Specific vision requirements including reading of written documents, visual inspection of materials and use of computer monitor screen frequently **Why you should join Catalent:** + Defined career path and annual performance review and feedback process + Diverse, inclusive culture + Positive working environment focusing on continually improving processes to remain innovative + Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives + 152 Hours + 8 paid holidays + Several Employee Resource Groups focusing on D&I + Dynamic, fast-paced work environment + Community engagement and green initiatives + Generous 401K match + Company match on donations to organizations + Medical, dental and vision benefits effective day one of employment + Tuition Reimbursement - Let us help you finish your degree or start a new degree! + WellHub program to promote overall physical wellness + Perkspot - offers exclusive or private discounts from approximately 900+ merchants in a wide array of categories **Catalent offers rewarding opportunities to further your career!** Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference. personal initiative. dynamic pace. meaningful work. Visit Catalent Careers (*********************************** to explore career opportunities. Catalent is an Equal Opportunity Employer, including disability and veterans. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com . This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process. Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you. Important Security Notice to U.S. Job Seekers: Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to ***************** for us to investigate with local authorities. California Job Seekers can find our California Job Applicant Notice HERE (*************************************************************************************************************************** .

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

Who We Are: Spring Venture Group is a leading digital direct-to-consumer sales and marketing company with product offerings focused on the senior market. We specialize in distributing Medicare Supplement, Medicare Advantage, and related products via our family of brands and dedicated team of licensed insurance agents. Powered by our unique technologies that combine sophisticated marketing, comparison shopping, sales execution, and customer engagement - we help thousands of seniors across the country navigate the complex world of Medicare every day. Job Description Overview At SVG, we are a leader in driving business solutions using analytics and data. The Data Science team operates at the very heart of this culture, constantly investigating how machine learning can optimize business, automate processes, improve KPIs, and forecast trends. The Data Science team is ideal for those who like to be where business and science intersect. They collaborate with stakeholders across SVG to identify business problems, and then apply data science skills to optimize objectives and directly impact key performance indicators. About the role As a Junior Data Scientist on the DS team you will receive exposure to all facets of data science at SVG and be given self-development and skills training opportunities. You will work as part of a team to solve business-related problems using data-driven techniques. You will help transform our data into tangible business value by performing statistical analysis, contributing to production services, and communicating the outcomes across business verticals. * This is a hybrid role 2-3 days a week in our dowtown office, so you must currently be in Kansas City. We are unable to sponsor for this role, so can not consider candidates with their EAD/OPT. Also, no third parties. Responsibilities Learn about and improve existing AI and machine learning systems, or build new ones altogether. Train and Deploy great models, then create tangible value with them. Develop lead engagement strategies that utilize model outputs. Train a close rate model and apply it to customer outreach. Derive actionable insights from transcripts using LLMs. Test a hypothesis and utilize the data to drive the way forward. Run thorough A/B tests that show and validate measurable improvements. Conduct analyses of business topics and present actionable insights to team leadership. Build Tableau dashboards to investigate business questions and analyze ML systems. Begin writing production-level machine learning and engineering code. Create automated solutions that solve operational pain-points and reduce manual work. Develop understanding of and utilize our tech stack - including MySQL, Python, AWS (esp. SageMaker), Git, FastAPI, and LangChain. Share ownership of production workflows, in collaboration with senior team members. Demonstrate consistent initiative and follow-through. Work through every step of the Machine Learning Lifecycle; take a problem definition all the way through to a deployed and tracked production model. Build trust throughout the organization. Perform other duties and responsibilities as assigned. Qualifications Bachelor's degree in analytical or technical field, or 2+ years of relevant work experience. Experience analyzing data and using it to drive decisions. Demonstrated problem-solving skills. Passionate about mathematical and statistical applications in business. Strong sense of accountability and integrity with exceptional written and verbal communication skills. Adaptable, acting with appropriate urgency when needed. General understanding of SQL and relational databases. Fluency in at least one programming language, preferably Python. Familiarity with basic machine learning concepts. Interest in AI and LLMs for engineering and analysis tasks. A strong work ethic combined with self-awareness and a commitment to continuous improvement. Demonstrated ability to receive and incorporate feedback effectively. Preferred Graduate coursework in Data Science, Statistics, or similar. Experience using version control systems and performing code reviews. Familiarity with owning 24/7 operational systems. Experience in a highly-productive work environment where ambiguity is the norm. Additional Information Benefits: The Company offers the following benefits for this position, subject to applicable eligibility requirements: Competitive Compensation Medical, Dental and vision benefits after a short waiting period 401(k) matching program Life Insurance, and Short-term and Long-term Disability Insurance Optional enrollment includes HSA/FSA, AD&D, Spousal/Dependent Life Insurance, Travel Assist and Legal Plan Generous paid time off (PTO) program starting off at 15 days your first year 15 paid Holidays (includes holiday break between Christmas and New Years) 10 days of Paid Parental Leave and 5 days of Paid Birth Recovery Leave Annual Volunteer Time Off (VTO) and a donation matching program Employee Assistance Program (EAP) - health and well-being on and off the job Rewards and Recognition Diverse, inclusive and welcoming culture Training program and ongoing support throughout your Venture Spring Venture Group career Security Responsibilities: Operating in alignment with policies and standards Reporting Security Incidents Completing assigned training Protecting assigned organizational assets Spring Venture Group is an Equal Opportunity Employer

KEY RESPONSIBILITIES: Data Governance, Strategy and Architecture * Define and drive the organization's overall vision, data strategy, roadmap, and architecture vision. This includes the data AI architecture vision, strategy, and roadmap. This includes the design of scalable data lakes, data warehouses, and data fabric architectures. * Establish and enforce data governance policies and standards to ensure data quality, consistency, and compliance with all relevant regulations (e.g., GDPR, CCPA). Lead the implementation of a comprehensive data governance framework, including data quality management, data lineage tracking, and master data management (MDM). Collaborate with data owners and stewards across business units to establish clear roles, responsibilities, and accountability for data assets. * Establish clear rules and policies governing the responsible usage of data within AI and ML models, including documentation of data lineage for model training. Design data infrastructure specifically optimized for AI workloads, including data pipelines for machine learning models, and architect solutions for large language models (LLMs). Develop bias mitigations strategies to ensure diverse and representative datasets to prevent AI biases, and architect monitoring systems for model drift. * Evaluate, recommend, and select appropriate data management technologies, including cloud platforms (e.g., AWS, Azure, GCP), storage solutions, and governance tools. * Architect complex data integration patterns to connect disparate data sources across the organization, ensuring seamless data flow and a unified data view. Data Security and Privacy * Design and implement a robust data security architecture to protect sensitive data from unauthorized access, breaches, and corruption. * Develop security protocols, such as encryption, access controls (IAM), and masking techniques to safeguard data in transit and at rest. * Conduct regular security audits and vulnerability testing to identify gaps in security architecture and develop remediation plans. * Ensure the data architecture and its supporting systems are compliant with internal policies and external data protection regulations. Data Modeling and Management * Design and maintain conceptual, logical, and physical data models for transactional and analytical systems. * Oversee the development of database schemas, metadata management, and data cataloging efforts to improve data discoverability and understanding. * Define and standardize data architecture components, including storage solutions (data lakes, warehouses, etc.), data pipelines, and integration patterns. * Evaluate and recommend new data technologies, tools, and platforms that align with the organization's strategic needs. Data Classification * Design and implement a robust data security architecture, including controls for access management, encryption, and data masking to protect sensitive information. * Create and manage an organization-wide data classification scheme based on data sensitivity and importance (e.g., public, internal, confidential, restricted). * Implement technical controls and processes to automatically classify and tag data assets, ensuring proper handling and security. * Collaborate with business and legal teams to define and apply data classification rules consistently. Team Collaboration and Leadership * Provide technical guidance and mentorship to data engineers, analysts, developers, and other IT teams on best practices for data management and security. * Work closely with business stakeholders to understand their data requirements and translate them into effective architectural solutions. * Foster a data-centric culture across the organization, promoting awareness and understanding of data governance principles. ABOUT THE COMPANY: Bluebird Fiber is a premier fiber telecommunications provider of internet, data transport, and other services to carriers, businesses, schools, hospitals, and other enterprises in the Midwest. To learn more, please visit bluebirdfiber.com. Join an amazing team of telecommunication professionals! Bluebird is a dynamic growing company in need of a Data Architect to be a part of a collaborative team. This is a full-time, benefit eligible position in our Kansas City Office. All of us at Bluebird work hard to meet objectives for the organization and live the mission and values of this growing company to meet a common goal. Check out this video that highlights our amazing company culture. JOB SUMMARY: We are seeking a highly skilled and strategic Data Architect to lead our data governance, security, and management initiatives. This senior role will be responsible for designing and implementing the organization's enterprise data architecture, ensuring that our data is secure, reliable, and accessible for business-critical functions. The ideal candidate is a proactive leader who can define data strategy, enforce best practices, and collaborate with cross-functional teams to align our data ecosystem with business goals. REQUIRED QUALIFICATIONS: * Bachelor's or master's degree in Computer Science, Information Technology, or a related technical field. * 10+ years of hands-on experience in data architecture, data modeling, and data governance, with a proven track record of designing and implementing complex data ecosystems. Experience working in regulated industries is a plus. * Proven experience (8+ years) designing and implementing enterprise-level data architectures. * Extensive experience with data modeling, data warehousing, and modern data platforms (e.g., cloud environments like AWS, Azure, or GCP). * Deep expertise in data modeling, data warehousing, database technologies (SQL, NoSQL), big data technologies (e.g., Spark), and modern cloud platforms (e.g., AWS, Azure, GCP). * Deep expertise in data governance and security principles, including regulatory compliance frameworks. * Strong knowledge of how to structure data for machine learning and AI workloads, including experience with MLOps platforms. * Hands-on experience with data classification and data cataloging tools (e.g., Collibra, Alation). * Excellent communication, interpersonal, and leadership skills, with the ability to influence and build consensus across the organization. PREFERRED QUALIFICATIONS: * Professional certifications in data architecture, data governance, or cloud platforms. * Experience with big data technologies (e.g., Hadoop, Spark). * Familiarity with data integration and ETL/ELT frameworks.

Thanks for your interest in Children's Mercy! Do you envision finding a meaningful role with an inclusive and compassionate team? At Children's Mercy, we believe in making a difference in the lives of all children and shining a light of hope to the patients and families we serve. Our employees make the difference, which is why we have been recognized by U.S. News & World Report as a top pediatric hospital, for eleven consecutive years. Children's Mercy is in the heart of Kansas City - a metro abounding in cultural experiences, vibrant communities and thriving businesses. This is where our patients and families live, work and play. This is a community that has embraced our hospital and we strive to say thanks by giving back. As a leader in children's health, we engage in meaningful programs and partnerships throughout the region so that we can improve the lives of children beyond the walls of our hospital. Overview The Center for Children's Healthy Lifestyles & Nutrition is seeking multiple postdoctoral fellows broadly focused on obesity, physical activity, and/or nutrition research in children and/or adults. Applicants will be accepted from the fields of Nutrition, Exercise Physiology, Public Health, Psychology, or a related field. We are specifically seeking candidates who plan to pursue NIH funding, likely by submitting an F or K application during their fellowship, and who are interested in future research faculty positions. To help align the training with the fellow's individualized career goals, fellows will receive guidance from a primary mentor and a 4-member scholarship oversight committee comprised of faculty selected by the fellow. The fellowships are fully research positions, with hours toward licensure only available after specific negotiation when relevant. Applicants must have completed all requirements for their doctoral degree prior to beginning the fellowship. The positions are for two years and have a flexible start date in the latter part of 2026. Salary will follow current NIH guidance for postdoctoral fellows. The Center for Children's Healthy Lifestyles & Nutrition (*************** is a joint partnership between the University of Kansas Medical Center and Children's Mercy Hospital. Applicants must select a primary mentor in their application materials from the following list of primary mentors accepting applicants: Ann Davis, PhD, MPH, ABPP; Jordan Carlson, PhD; Helena Laroche, MD, FAAP, ABOM; Robin Shook, PhD; Brooke Sweeney, MD, FAAP, FACP, DABOM HOW TO APPLY: To apply, please submit the following documents to Julie Aust at *************** 1) A cover letter indicating your interest in the position, qualifications, specific research interests, selected primary mentor, and goals for the postdoctoral training years 2) Curriculum vitae 3) Names and titles for three professional references. 4) apply to the position At Children's Mercy, we are committed to ensuring that everyone feels welcomed within our walls. A successful candidate for this position will join us as we strive to create a workplace that reflects the community we serve, as well as our core values of kindness, curiosity, inclusion, team and integrity. Additionally, it's important to us that we remain transparent with all potential job candidates. Because we value the safety of the patients and families we serve, as well as the Children's Mercy staff, we want to let you know that the seasonal influenza vaccine is a condition of employment for all employees in our organization. New employees must be willing to be vaccinated if found non-immune to measles, mumps, rubella (MMR) and chicken pox (varicella) and/or without evidence of tetanus, diphtheria, acellular pertussis (Tdap) vaccination since 2005. If you are selected for this position, you will be asked to supply your immunization records as proof of vaccination. If you and have any concerns about receiving these vaccines, medical and/or religious exemptions can be further discussed with Human Resources. Qualifications Ph.D. or MD or related doctoral level degree in a relevant discipline and 1-2 years experience Benefits at Children's Mercy The benefits plans at Children's Mercy are one of many reasons we are recognized as one of the best places to work in Kansas City. Our plans are designed to meet the changing needs of our employees and their families. Learn more about Children's Mercy benefits. Starting Pay Our pay ranges are market competitive and we follow the NIH guidelines for Post Docs. The pay range for this job begins at $28.39/hr, but your offer will be determined based on your education and experience. EEO Employer/Disabled/Vet Children's Mercy hires individuals based on their job skills, expertise and ability to maintain professional relationships with fellow employees, patients, parents and visitors. A personal interview, formal education and training, previous work experience, references and a criminal background investigation are all factors used to select the best candidates. The hospital does not discriminate against prospective or current employees based on the race, color, religion, sex, national origin, age, disability, creed, genetic information, sexual orientation, gender identity or expression, ancestry or veteran status. A drug screen will be performed upon hire. Children's Mercy is smoke and tobacco free. CM is committed to creating a workforce that supports the diverse backgrounds of our patients and families. We know that our greatest strengths come from the people who make up our team, so we hire great people from a wide variety of backgrounds, not just because it's the right thing to do, but because it makes our hospital stronger and our patient care more compassionate. If you share our values and our enthusiasm for service, you will find a home at CM. In recruiting for our team, we welcome the unique contributions that you can bring, including education, ideas, culture, and beliefs.

Job DescriptionIndustrial Cybersecurity Consultant - SOC Operations (Extended Night-Shift) Location: Remote (must reside in Kansas City, MO) Training: Onsite in Kansas City, MOShift Options: Full-TimeNight Shift: Four 10-hour shifts, typically 6:00 PM - 4:00 AMPart-Time Night Shift: AvailableWeekend Coverage: Open to candidates willing to work weekends Position Overview The Industrial Cybersecurity Consultant will be an integral member of a Security Operations Center (SOC) team, responsible for both operational and consulting tasks. This role combines real-time security monitoring and incident response with project-based cybersecurity consulting. Key duties include triaging security events, providing recommendations through a case management system, and participating in client calls for incident response or escalation. In addition, the consultant will support ICS/OT security projects, vulnerability assessments, penetration testing, and compliance initiatives aligned with frameworks such as NIST CSF and RMF. Key Responsibilities Security Event Management Monitor and triage security events, analyze alerts, and prioritize incidents for remediation. Provide actionable recommendations through the case management system to ensure timely resolution. Participate in client calls for incident response or escalation as needed. Cybersecurity Consulting Execute planning, design, development, and implementation of technical controls, procedures, and policies associated with cybersecurity compliance and regulatory standards. Conduct network penetration tests and vulnerability assessments of IT and Operational Technology (OT) networks for compliance and security purposes. Perform detailed post-event analysis of unusual events and recommend procedural changes. Develop policies and procedures for secure process control network design, including technical recommendations for firewalls and other security controls. Compile technical documentation of network traffic and firewall services/solutions, including diagrams and explanations. Collaboration & Compliance Work with internal teams and client stakeholders to resolve technical issues and communicate implications effectively. Maintain confidentiality and security of all client and project information. Comply with all applicable policies and standards. Job Requirements Education: Bachelor's degree in Cybersecurity, Computer Science, Computer Engineering, Electrical Engineering, or related technical field. Experience: Minimum 3 years of related experience in cybersecurity operations and consulting. Certifications: Security+ preferred (other advanced certifications a plus). Technical Skills: Advanced knowledge of security principles and cybersecurity technologies. Experience with vulnerability assessments, penetration testing, and associated tools/techniques. Familiarity with cybersecurity controls (firewalls, access control, authentication, anti-virus/anti-malware, patching, logging). Knowledge of control systems used in utilities, manufacturing, oil & gas, transportation, smart buildings, and cities. Strong written and oral communication skills for client interaction and reporting. Ability to operate under pressure and meet tight deadlines in industrial, corporate, and government environments. Understanding of business principles and operational security practices specific to engineering/security consulting. Strong technical writing skills and knowledge of modern and legacy networking and telecommunications. Experience 2ith physical cabling for network communications and control system I/O. Other: Ability to obtain and maintain access to client sites, including applicable U.S. security clearances.

Medical Research Associate (PRN) - Lenexa, KS - ICON 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 #LI-LB1 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, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised 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, subsidised 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 DescriptionStep into a pivotal role as a Clinical Laboratory Scientist with KU Medical Center in Kansas, where your precision, curiosity, and care translate directly into better patient outcomes. In this dynamic setting, you'll lead complex testing across multiple disciplines, interpret results with confidence, and collaborate with a multidisciplinary team dedicated to excellence. Your expertise will power timely, accurate diagnoses, support cutting-edge patient care, and fuel continuous learning as you navigate an ever-evolving clinical landscape. This opportunity isn't just a job-it's a chance to shape the standard of care in a premier academic health system while expanding your own professional horizon on a national stage. Separately, Kansas is a state of sweeping beauty and unexpected charm. From the rolling prairies and expansive skies to the distinctive allure of the Flint Hills, the Sunflower State offers breathtaking sunrises, wide-open roads, and welcoming communities. Explore the Tallgrass Prairie National Preserve, marvel at Monument Rocks, and enjoy the warmth of neighborhoods where culture, history, and forward momentum mingle. Whether you're drawn to outdoor adventures, vibrant city life, or quiet small-town charm, Kansas provides a picturesque backdrop for your next career chapter and a balanced rhythm for life beyond the lab. Location Benefits: Working at KU Medical Center in Kansas blends academic rigor with practical impact. You'll be part of a leading teaching hospital environment that champions evidence-based practice, advanced instrumentation, and interdisciplinary collaboration. The role offers proximity to a thriving medical campus where research, education, and patient care intersect, providing opportunities to learn from top-tier professionals and to contribute to translational outcomes. For those who relish variety, the assignment additionally opens the doors to potential placements across diverse locations within the U.S., expanding your professional exposure and network. Enjoy the region's affordable living, a welcoming community, and a quality of life that supports focused lab work and meaningful downtime. The position offers weekly pay in the $2,155-$2,247 range, with a multi-week assignment designed to fit your goals. Start date is 02/08/2026, with the flexibility of weeks as the engagement duration, and a pathway to extension depending on performance and project needs. Role Specifics and Benefits: As a Clinical Laboratory Scientist, you'll perform and supervise routine and specialized laboratory testing across chemistry, hematology, microbiology, immunology, and coagulation. You'll operate, troubleshoot, and maintain a broad array of analyzers; ensure strict quality control and QA compliance; verify and validate results, correlate with clinical information, and communicate critical findings promptly to the care team. You'll document procedures with precision, mentor junior staff, and participate in process improvement initiatives to streamline workflows and enhance accuracy. This role emphasizes professional growth through hands-on experience with state-of-the-art platforms, cross-training across departments, and opportunities to pursue board certification or advanced certifications aligned with your interests. Competitive benefits include a welcome bonus, housing assistance, and extension opportunities to maximize continuity of care and career advancement. The program provides comprehensive support, including 24/7 assistance for traveling clinicians, ensuring you're never alone when navigating challenges or new environments. KU Medical Center's collaborative culture champions your development, recognizing the value of your expertise and investing in your continued education and career progression. Company Values: Our organization is dedicated to empowering staff, fostering a supportive, inclusive environment where every clinician can thrive. We champion continuous learning, professional autonomy, and teamwork, with leadership committed to clear pathways for advancement and recognition of your contributions. You'll find classmates and colleagues who value integrity, patient-centered care, and resilient problem-solving-together building a workplace where your skills are respected, your voice matters, and your professional trajectory is amplified through mentorship, training, and opportunities to lead. Call to Action: If you're ready to apply your clinical laboratory expertise in a vibrant academic setting, to explore Kansas and the broader U.S. through your work, and to grow within a supportive, forward-thinking organization, seize this chance. Submit your application to join KU Medical Center for a meaningful, multi-week assignment beginning 02/08/2026, with favorable extension prospects and a pathway to advancing your career in clinical laboratory science. Embrace the opportunity to contribute, learn, and thrive-your next chapter starts here. Please note: The hours and pay rates listed are estimates and may vary. Final compensation packages and guaranteed hours will be confirmed during the hiring process. Privacy & Consent By applying, you agree to TLC Healthforce's Privacy Policy and consent to receive job-related text messages; message/data rates may apply. Reply STOP to opt out. About TLC Nursing TLC Healthforce is a nationwide travel healthcare staffing agency pairing Nursing and Allied Health professionals with high-quality travel and local contracts across the U.S. ShiftShield™ - Traveler Protection ShiftShield™ protects travelers from preventable facility-driven cancellations and ensures fair compensation for schedule disruptions. Why Travelers Choose TLC Competitive weekly pay Fast credentialing 24/7 recruiter & clinical support Nationwide assignments Referral Bonus Earn up to $1,000 per referral - no employment required. EEO Statement TLC Healthforce is an Equal Opportunity Employer. Powered by JazzHR g40cwQOECw

The Assistant Environmental Scientist will assist in conducting environmental and siting studies, preparing permitting applications and analyzing environmental data for various types of projects, including high-voltage transmission line routing, power generation construction activities and water treatment facilities. + Assist in conducting field surveys, assessments and collecting project-related data for analysis in environmental impact projects. + Assist in preparation of technical reports, environmental impact statements and environmental field studies. + Provide assistance in utilizing GIS data for map production in accordance with standards and industry best practices. + Assist with performing environmental site investigations, support erosion control efforts and subsurface soil sampling. + Assist in conducting environmental compliance audits. + Assist in preparing a wide variety of permitting applications such as air, land use and cultural resources permitting. + Support site selection studies and preparation of related National Environmental Policy Act (NEPA) documentation. + Ensure compliance with company and site safety policies. + Performs other duties as assigned. + Complies with all policies and standards. Qualifications + Bachelor Degree in Environmental Studies, Science, or a related natural science degree from an accredited program required. + Prior internship or natural science field experience preferred. + Strong analytical and problem solving skills. + Ability to clearly communicate both verbal and written technical information. + Basic knowledge of environmental site assessment methods. + Basic knowledge of environmental compliance and compliance audits. + Basic knowledge of the environmental permitting process. + Basic knowledge of GPS and working in the ArcGIS desktop environment. + Must be proficient in the use of computer software (i.e., Microsoft Word, Excel, PowerPoint). + Must meet standards to qualify for and maintain the Company's vehicle driving privileges as outlined in the Company's Motor Vehicle Safety Policy. + Valid driver's license required. + Minimum of a 3.0 GPA strongly preferred. + Involvement on campus or in the community preferred. + Candidates must be legally authorized to work permanently (i.e., without time limitations, without restrictions or without need for work sponsorship) in the country where this position is located. This job posting will remain open a minimum of 72 hours and on an ongoing basis until filled. EEO/Disabled/Veterans Job Environmental Primary Location US-MO-Kansas City Schedule: Full-time Travel: Yes, 25 % of the Time Req ID: 253377 Job Hire Type New Grad #LI-JF #ENS

UP TO $15 PER HOUR BASED ON YOUR AVAILABILITY 4pm-11pm: BARRY Rd, by PowerPlay As a local, independent McDonald's franchise, we are looking for talented & enthusiastic people. We will give you the tools to be what you want to be. Once hired, you may want to take advantage of $2500 a year in FREE college tuition, while working as few as 15 hours a week.... or you may develop skills & earn promotions into restaurant management!! Either way, we want to meet YOU! ALL positions are needed. CREW MEMBERS ARE RESPONSIBLE FOR: * Greeting customers with a smile *Taking accurate food orders * Working with the Team to meet Target Goals for the Shift * Preparing McDonald's World Famous food *Cleanliness of Store * Being on Time *Ensuring Store is Well-Stocked This job posting is not a complete , as McDonald's employees perform a number of different tasks every day. BENEFITS MAY INCLUDE: * Competitive Pay *Free Uniforms *Free Meals * Paid Vacation after 1 year *Discounted Family Meals * $2500 FREE college/trade school tuition after 90 days * Team Building *Advancement Opportunities * Health Insurance Plans Available *Flexible Schedule * Monthly Bonuses *401k with Employer Match Student Jobs, No Experience Jobs, Teen Jobs, Part-Time Jobs Additional Info: This job posting contains some information about what it is like to work in a McDonald's restaurant, but it is not a complete job description. People who work in a McDonald's restaurant perform a number of different tasks every day, and this posting does not list all of the essential functions of this job. This job posting is for a position in a restaurant owned and operated by an independent franchisee and not McDonald's USA. This franchisee owns a license to use McDonald's logos and food products, for example, when running the restaurant. However, this franchisee is a separate company and a separate employer from McDonald's USA. If you are hired for the job described in this posting, the franchisee will be your employer, not McDonald's USA. Only the franchisee is responsible for employment matters at the restaurant, including hiring, firing, discipline, supervisions, staffing, and scheduling employees. McDonald's USA has no control over employment matters at the restaurant. McDonald's USA will not receive a copy of your employment application and it will have no involvement in any employment decisions, including whether you receive an interview for the job or whether you are hired. By applying to this position, I understand that I am applying to work at a restaurant that is owned and operated by an independent franchisee, not McDonald's USA. I understand that this franchisee is a separate company and a separate employer from McDonald's USA. Any information I provide in this application will be submitted only to the independent franchisee, who is the only company responsible for employment matters at this restaurant. I recognize that the independent franchisee alone will make all decisions concerning employment matters, including hiring, firing, discipline, supervision, staffing and scheduling. By applying for a job at a franchisee operated restaurant, I understand that the information I provide will be forwarded to the franchisee organization in order for that organization to reach out to me and process and evaluate my application. I acknowledge that McDonald's USA will not receive a copy of my employment application and will have no involvement in any employment decisions regarding me, including whether I receive an interview or whether I am hired to work for the franchisee. I understand that I need to contact the franchise organization for information about its privacy practices.

At Elanco (NYSE: ELAN) - it all starts with animals! As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets. We're driven by our vision of ‘Food and Companionship Enriching Life' and our approach to sustainability - the Elanco Healthy Purpose™ - to advance the health of animals, people, the planet and our enterprise. At Elanco, we pride ourselves on fostering a diverse and inclusive work environment. We believe that diversity is the driving force behind innovation, creativity, and overall business success. Here, you'll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights. Making animals' lives better makes life better - join our team today! Your Role: Technical Services & Manufacturing Science (TSMS) Associate -Pilot Scale The Technical Services & Manufacturing Science (TSMS) Associate is responsible for providing operational and technical support for commercial and pilot laboratory operations at the Elwood, Kansas, monoclonal antibody (mAb) manufacturing facility. The position is a subject matter expert with respect to mAb products and processes and is engaged in tech transfer, scale-up, process optimization, validation, monitoring, troubleshooting, and continuous improvement activities. Your Responsibilities: Support the execution and troubleshooting of upstream and/or downstream manufacturing processes for biologics (e.g., mammalian cell culture, purification). Collaborate with Manufacturing, Development, and Quality teams in the execution of technical / development studies, investigations, validation activities, and technical transfer programs, and collaborate with team members to identify potential risks, sources of variability, improvement, and value engineering opportunities to maximize project return and likelihood of technical success. Provide on-floor support during manufacturing campaigns, including troubleshooting and deviation investigations. Use scientific and statistical analysis tools to improve process understanding, ensure manufacturing processes are capable and operating in a state of control, and identify opportunities for process improvements. Author and provide critical review of technical documents, including, but not limited to: batch records, SOPs, PFDs, risk assessments, investigations, technical studies, commissioning and qualification protocols, and reports. Assist in implementing changes through the change control system (e.g., BOM updates, process changes). What You Need to Succeed (minimum qualifications): Education: Bachelor's degree or equivalent in Bio/Pharmaceutical Technology, Microbiology, Engineering, or a related discipline. Experience: 0 - 2 years' experience in the Biotech / Pharmaceutical industry. Familiarity with tools such as JMP or Excel for data analysis is a plus. Ability to work in a team environment and support manufacturing activities on the production floor, including occasional off-shift or weekend support if required. Detailed understanding of biopharmaceutical production processes and technologies with working knowledge of cGMP standards and experience working in a regulated environment. What will give you a competitive edge (preferred qualifications): MSc in Bio/Pharmaceutical Technology, Microbiology, Engineering, or a related discipline. 3+ years' experience in the Biotech / Pharmaceutical industry. Demonstrated experience in commercial monoclonal antibody / recombinant protein manufacturing processes. Experience in tech transfer, scale-up, and validation of biopharmaceutical processes. Experience in capital project design, development, validation, and execution. Experience with electronic quality systems (e.g., Veeva QMS, TrackWise) and MES platforms. Additional Information: Location: Elwood, Kansas Day shift position. Weekend and evening work is not usual, although it may be required to provide process support to ongoing operations. Minimal travel requirements < 10%. Don't meet every single requirement? Studies have shown underrecognized groups are less likely to apply to jobs unless they meet every single qualification. At Elanco we are dedicated to building a diverse and inclusive work environment. If you think you might be a good fit for a role but don't necessarily meet every requirement, we encourage you to apply. You may be the right candidate for this role or other roles! Elanco Benefits and Perks: We offer a comprehensive benefits package focusing on financial, physical, and mental well-being while encouraging our employees to pursue our purpose! Some highlights include: Multiple relocation packages Two weeklong shutdowns (mid-summer and year-end) in the US (in addition to PTO) 8-week parental leave 9 Employee Resource Groups Annual bonus offering Flexible work arrangements Up to 6% 401K matching Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status

Full-time Description Food Scientist St. Joseph, MO and Leavenworth, KS Research & Development Come join our wonderful team culture, and be an integral part of our team! The Senior Food Scientist is responsible for our product development support, and technical services to our customers, sales, purchasing, regulatory, quality control, and operations. Promote company values and beliefs while performing job tasks . Primary responsibilities include, but not limited to: · Make “hands on” bench top samples as required by each project parameter in a timely manner. This may include ordering of ingredients. · Formulate with or without assistance, depending on formulation complexity. · Perform mathematical and formulation calculations. · Assist in trials to ensure compliance to approved formulas. · Develop specifications for new products. · Enter formulas in recipe management system accurately. · Reach out to current and potential suppliers and gather preliminary information to vet out ingredients. · Stay technically informed through suppliers, shows and literatures. · Follow CII's New Item/ Ingredient Approval (NIA) process. · Administration duties including labeling, organizing, shipping, and other related areas expected. · General Housekeeping Benefits: - Paid Time Off - Holiday Schedule - Medical - Dental - Vision - Life Insurance - 401k Retirement Plan Working Environment and Physical Demands: Indoors temperature-controlled environment-office, laboratory, manufacturing facility; the use of hearing protection may be required at times, along with other personal protective equipment as necessary. Position requires the ability to sit, stand, walk, climb, manual dexterity, ability to see details at close range and to differentiate colors, ability to listen and to understand spoken words and phrases, ability to communicate information verbally, ability to read and understand ideas presented in writing, ability to communicate information and ideas in writing so that others will understand. Must meet the physical abilities level of Two (2) as defined by the US Department of Labor. Requirements BS in Food Science or closely related field required. · Minimum 5 years relevant work experience preferred. · Knowledge and experience in product development of granola, panning, and extrusion desirable. · Proficient in Word and Excel and other database management desirable. · Knowledge of ingredient functionality desirable · Some travel required. Customer visits and tradeshows.

Senior Associate Scientist I (Dissolution) Work Schedule: Monday - Friday, 8AM - 4:30PM 100% onsite (Kansas City) Catalent, Inc. is a leading global Contract Development and Manufacturing Organization (CDMO). Catalent's Kansas City (KCM) facility provides a range of integrated services for oral solid dosage forms, from formulation development and analytical testing to clinical and commercial-scale manufacturing. The facility is the commercial manufacturing Center-of-Excellence for accelerated development programs and roller compaction. The Senior Associate Scientist I will support the Analytics and Dissolution team for in-process, release, and stability sampling and use a variety of analytical instruments. With cutting-edge technologies and a collaborative work environment, this role offers opportunities for long-term advancement. The Role: Execute laboratory work plans/schedules developed with input from a supervisor or senior team member. Sample types include in-process, release or stability. Techniques include HPLC, UV/Vis, Disintegration and Dissolution. Apparatus 1, 2, 3, 5, and 6. Under direction, may perform method development, validation, and transfer activities Maintain accurate and high-quality laboratory documentation in accordance with regulatory guidance and Site SOPs May draft technical documents such as methods or certificate of analysis Performs parallel review of laboratory documentation and may become qualified to perform technical review of documents for accuracy, thoroughness and regulatory compliance Assists in execution of efficiency improvement projects with guidance Trains others on laboratory techniques All other duties as assigned The Candidate: Bachelor's degree in life science or physical science is required with at least two (2) years of related work experience OR a Master's degree is required without any formal industry experience Knowledge and skills requirements include the ability to process, maintain, and interpret data, understand basic instrument troubleshooting techniques, and communicate clearly and professionally with clients and internal stakeholders Physical requirements: On an average 8-hour day this position requires the ability to walk, sit and stand, use hands to handle or feel, reach with hands and arms at or above shoulder height and below waist height, climb or balance, stoop, kneel, crouch, or crawl; talk and hear, smell and lift up to 40 pounds. Specific vision requirements including reading of written documents, visual inspection of materials and use of computer monitor screen frequently Why you should join Catalent: Defined career path and annual performance review and feedback process Diverse, inclusive culture Positive working environment focusing on continually improving processes to remain innovative Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives 152 Hours + 8 paid holidays Several Employee Resource Groups focusing on D&I Dynamic, fast-paced work environment Community engagement and green initiatives Generous 401K match Company match on donations to organizations Medical, dental and vision benefits effective day one of employment Tuition Reimbursement - Let us help you finish your degree or start a new degree! WellHub program to promote overall physical wellness Perkspot - offers exclusive or private discounts from approximately 900+ merchants in a wide array of categories Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference. personal initiative. dynamic pace. meaningful work. Visit Catalent Careers to explore career opportunities. Catalent is an Equal Opportunity Employer, including disability and veterans. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process. Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you. Important Security Notice to U.S. Job Seekers: Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to ***************** for us to investigate with local authorities. California Job Seekers can find our California Job Applicant Notice HERE.

Who We Are: Spring Venture Group is a leading digital direct-to-consumer sales and marketing company with product offerings focused on the senior market. We specialize in distributing Medicare Supplement, Medicare Advantage, and related products via our family of brands and dedicated team of licensed insurance agents. Powered by our unique technologies that combine sophisticated marketing, comparison shopping, sales execution, and customer engagement - we help thousands of seniors across the country navigate the complex world of Medicare every day. Job Description Overview At SVG, we are a leader in driving business solutions using analytics and data. The Data Science team operates at the very heart of this culture, constantly investigating how machine learning can optimize business, automate processes, improve KPIs, and forecast trends. The Data Science team is ideal for those who like to be where business and science intersect. They collaborate with stakeholders across SVG to identify business problems, and then apply data science skills to optimize objectives and directly impact key performance indicators. About the role As a Junior Data Scientist on the DS team you will receive exposure to all facets of data science at SVG and be given self-development and skills training opportunities. You will work as part of a team to solve business-related problems using data-driven techniques. You will help transform our data into tangible business value by performing statistical analysis, contributing to production services, and communicating the outcomes across business verticals. * This is a hybrid role 2-3 days a week in our dowtown office, so you must currently be in Kansas City. We are unable to sponsor for this role, so can not consider candidates with their EAD/OPT. Also, no third parties. Responsibilities * Learn about and improve existing AI and machine learning systems, or build new ones altogether. * Train and Deploy great models, then create tangible value with them. * Develop lead engagement strategies that utilize model outputs. * Train a close rate model and apply it to customer outreach. * Derive actionable insights from transcripts using LLMs. * Test a hypothesis and utilize the data to drive the way forward. * Run thorough A/B tests that show and validate measurable improvements. * Conduct analyses of business topics and present actionable insights to team leadership. * Build Tableau dashboards to investigate business questions and analyze ML systems. * Begin writing production-level machine learning and engineering code. * Create automated solutions that solve operational pain-points and reduce manual work. * Develop understanding of and utilize our tech stack - including MySQL, Python, AWS (esp. SageMaker), Git, FastAPI, and LangChain. * Share ownership of production workflows, in collaboration with senior team members. * Demonstrate consistent initiative and follow-through. * Work through every step of the Machine Learning Lifecycle; take a problem definition all the way through to a deployed and tracked production model. * Build trust throughout the organization. * Perform other duties and responsibilities as assigned. Qualifications * Bachelor's degree in analytical or technical field, or 2+ years of relevant work experience. * Experience analyzing data and using it to drive decisions. * Demonstrated problem-solving skills. * Passionate about mathematical and statistical applications in business. * Strong sense of accountability and integrity with exceptional written and verbal communication skills. * Adaptable, acting with appropriate urgency when needed. * General understanding of SQL and relational databases. * Fluency in at least one programming language, preferably Python. * Familiarity with basic machine learning concepts. * Interest in AI and LLMs for engineering and analysis tasks. * A strong work ethic combined with self-awareness and a commitment to continuous improvement. Demonstrated ability to receive and incorporate feedback effectively. Preferred * Graduate coursework in Data Science, Statistics, or similar. * Experience using version control systems and performing code reviews. * Familiarity with owning 24/7 operational systems. * Experience in a highly-productive work environment where ambiguity is the norm. Additional Information Benefits: The Company offers the following benefits for this position, subject to applicable eligibility requirements: * Competitive Compensation * Medical, Dental and vision benefits after a short waiting period * 401(k) matching program * Life Insurance, and Short-term and Long-term Disability Insurance * Optional enrollment includes HSA/FSA, AD&D, Spousal/Dependent Life Insurance, Travel Assist and Legal Plan * Generous paid time off (PTO) program starting off at 15 days your first year * 15 paid Holidays (includes holiday break between Christmas and New Years) * 10 days of Paid Parental Leave and 5 days of Paid Birth Recovery Leave * Annual Volunteer Time Off (VTO) and a donation matching program * Employee Assistance Program (EAP) - health and well-being on and off the job * Rewards and Recognition * Diverse, inclusive and welcoming culture * Training program and ongoing support throughout your Venture Spring Venture Group career Security Responsibilities: * Operating in alignment with policies and standards * Reporting Security Incidents Completing assigned training * Protecting assigned organizational assets Spring Venture Group is an Equal Opportunity Employer