Research scientist jobs in Springfield, MO - 511 jobs

The Custom Protein Resources (CPR) group at the Stowers Institute for Medical Research is seeking an Associate Scientist II to support protein expression, purification, and characterization projects. The ideal candidate will combine strong technical and interpersonal skills with expertise in protein-protein interaction studies. Responsibilities: Express and purify proteins in bacterial, yeast, insect, and mammalian systems. Develop and troubleshoot purification workflows using diverse chromatography methods. Characterize proteins and protein-protein interactions using biophysical techniques such as BLI or ITC. Manage multiple projects, maintain clear records, and communicate progress with collaborators. Contribute to workflow development and mentor junior staff. Qualifications: Bachelor's or Master's degree in biochemistry, molecular biology, or a related field. 2-5 years of experience in protein expression, purification, and characterization. Familiarity with FPLC/HPLC systems and biophysical assays for protein interactions. Strong organizational, analytical, and communication skills. To Apply Submit the requested documents to ******************* or to Administration Department, Stowers Institute for Medical Research, 1000 E. 50th Street, Kansas City, MO 64110. Requested Documents Current Resume Cover Letter

$60-70K (Base) Auxvasse, MO - onsite About The Role You will assist in daily activities and operation of the Laboratory Sciences department including equipment maintenance, stocking supplies and general cleaning. You will also support and perform data collection activities including primarily focused on mass-spectrometry. What You'll Do Here Prepare materials, including animal blood and tissues, for analytical assays (e.g., ligand binding assays, flow cytometry, cell-based assays, mass-spectrometry, as assigned) and perform the assays according to Protocol or other guiding documents with accurate documentation. Maintain and document chain of custody for specimens, reagents, controls, and samples in the laboratory. Maintain and update facility records related to the laboratory and its analyses. Review laboratory records, procedures and study data for completeness and accuracy. Document deviations to laboratory procedures and study protocols and unforeseen circumstances in a timely manner and provide input for corrective actions. Assist in calibration, optimization, maintenance, and collection of data from analytical instruments. Follow the clients Standard Operating Procedures (SOPs), ensure compliance with GLP, ALCOA+, USDA, and AAALAC guidelines, and can identify areas for improvement. Perform routine laboratory maintenance (including cleaning, stocking supplies, equipment maintenance tasks, etc.). What You'll Need to Succeed Must have a Masters with 2-3 years in a GLP environment Must have GLP experience LCMS experience Problem solving and analysis Time management and organizational skills

Up To $1,000 Paid Depression Study! Those who Currently Experience At Least TWO Symptoms of Depression And the Current Depressive Episode Started More Than 4 Weeks Ago May Qualify For The Study!

We are seeking a dedicated Quality Control Scientist to join our team supporting both contract development and manufacturing organization operations and a new compounded pharmaceutical manufacturing line. This role emphasizes method development, validation, and technical problem-solving for small-molecule products and compounded formulations. The ideal candidate will possess strong analytical expertise and extensive experience in pharmaceutical quality systems. PAY - $48 - $72 Responsibilities + Design, develop, and validate analytical methods for compounded pharmaceutical products and small-molecule drug substances and products. + Support method transfer activities between internal teams and external partners. + Develop methods for impurity profiling, degradation studies, and stability testing. + Provide technical insights for complex analytical challenges, including root cause analysis for deviations and out-of-specification results. + Collaborate with Quality Assurance on investigations and corrective actions. + Ensure analytical methods and documentation meet regulatory requirements for FDA submissions and CMC packages. + Maintain compliance with cGMP and industry standards for laboratory operations. + Participate in CDMO development projects, contributing analytical expertise to formulation and process development. + Work at the bench as needed to execute laboratory studies and support project timelines. + Identify and implement process improvements within QC workflows to enhance efficiency and compliance. + Support audit readiness and contribute to maintaining a robust quality culture. Essential Skills + Minimum 10-15 years of experience in analytical method development and validation within a pharmaceutical environment. + Strong knowledge of HPLC, GC, MS, dissolution, and other analytical techniques. + Diverse experience with various drug product types, APIs, intermediates, small-molecule, and compounded pharmaceuticals. + Understanding of regulatory guidelines (FDA, ICH) and cGMP standards. + Excellent technical writing skills. Additional Skills & Qualifications + Bachelor's or advanced degree in Chemistry or a related field. + Familiarity with compounding operations and small-molecule development preferred. + Ability to mentor and coach others, with potential to lead teams. + Empathetic leadership skills and an understanding of diverse employee backgrounds. + Integrity, transparency, and a collaborative approach to decision-making. Work Environment The team currently includes three other chemists in the lab. The position offers a flexible day shift from Monday to Friday, along with two weeks of PTO and holiday pay. This is an excellent opportunity to join a rapidly growing business, with the chance to establish and shape processes in a dynamic environment equipped with new GC's and HPLC's, using the latest Open Lab Software with Agilent. Job Type & Location This is a Contract to Hire position based out of Springfield, MO. Pay and Benefits The pay range for this position is $48.08 - $72.11/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: - Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Springfield,MO. Application Deadline This position is anticipated to close on Jan 19, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.

Responsible for the development of Wet/Liquid/Paste dairy systems and dairy flavors for food and dairy industries from concept/opportunity through commercialization (at the customer). This person will be relied upon as an expert related to dairy flavors and emulsions including dairy science research, innovation, development, applications; relating to new product/solution development; but also, for formulation cost-out opportunities, process improvements, new technology scouting. Key driver of organic growth through monetization of the opportunity and innovation pipeline. Job Duties and Responsibilities: Research dairy science, food science and equipment for the purpose of innovating new technologies and the development of intellectual property (IP) for DFA Develop new wet and dry dairy systems, dairy flavors, dairy emulsions and solutions using DFA's plethora of ingredient options and manufacturing capabilities Reformulate products and stream-line processes appropriate to reduce cost Perform applications testing simulating the customer's end use to ensure the products developed exceed the customer's expectations for taste, functionality, and nutrition Utilize sensory science tools, available in the Innovation Center, to give data points to the customer demonstrating expectations are met/exceeded Perform pilot plant testing to ensure a successful scale-up for DFA manufacturing and ultimately the end customer Drive the commercialization of new products by partnering with the process technology team in the plants Support the customer in scale up and commercialization to ensure DFA people and products are part of the scale up and launch Effectively operate pilot plant equipment, for new products, cheeses, flavors and emulsion systems development. Develop effective concepts for benchtop sessions, in partnership with sales, to generate wins with customers Support sales in determining customer needs, problems, insights, and strategy that would ultimately require a DFA solution. Proactively initiate action plans to maintain, improve and develop the DFA solutions and capabilities Inspire and excite DFA customers through demonstration of unique new products and applications that are relevant to their consumers Partner with sales to understand customer's future needs, their brands, and strategies to anticipate new areas of capability development and innovative ideas for end use categories Provide technical and applications expertise to support the customer Drive opportunities to commercialization internally and close with the customer Co-create and effectively utilize the product lifecycle management (PLM) process and adhere to the Scientific Development Standards Process, including version control, development notes and documented learnings Effectively utilize CRM (Salesforce.com) as a tool to manage status of the opportunities, project milestones in the pipeline and track KPIs related to the opportunity pipeline continually improving our R&D service to customers, ultimately leading to faster speed-to-market driving increased customer connectivity. Collaborate with and influence technical sales, customer support and other stakeholders to “solve for yes” Contribute to technical content and make and review presentations for commercialization activities Provide effective, timely and relevant reporting to leadership Apply strong knowledge of the DFA's capabilities - including understanding the functional and technical aspects of the products and how DFA's capabilities differentiate us from others in the industry Demonstrate a “never stop learning” mindset and influence others to adopt this mindset Active participation in commercial project review by offering guidance and mentorship The requirements herein are intended to describe the general nature and level of work performed by employee, but is not a complete list of responsibilities, duties, and skills required. Other duties may be assigned as required

The Clinical Research Technician position offers flexible hours and a rewarding work environment in the drug research field. This position is primarily responsible for monitoring the study volunteers and ensuring the clinical study is being recorded, conducted, and reported in agreement with the study requirements. This position offers variety, and no two days are alike. The hours are scheduled on an as needed basis and can range from 0-29 hours per week. The essential duties are: Read and understand study documents, time and events, study restrictions and expectations of sponsor. Check in/out study volunteers and monitor their behavior for study compliance, safety, adverse events and concerns. Perform essential study duties such as recording mealtimes, performing vitals and recording results. Review raw data to ensure accuracy. Help to supervise events to ensure studies are done on time and in accordance with SOPs and Protocols. Maintain cleanliness of the clinics and all study-related areas. Experience Outstanding customer service skills High attention to detail Ability to work weekends is desirable Ability to work flexible hours Please visit Recruitment (adp.com) to apply for this position through the company website. QPS Bio-Kinetic (BKCA) provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability or genetics. In addition to federal law requirements, QPS Bio-Kinetic (BKCA) complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.

This is a grant-funded position with a current limit of 2 years 9 months with progress reviewed after one year. Investigate parameters of stellar structure and evolution to improve the match between models and observations, particularly related to asteroseismology, using evolutionary models, expected to be MESA and GYRE. The successful candidate is also expected to disseminate results in appropriate journals and conferences and supervise undergraduate students in project-related research. It is expected that the Faculty Research Associate is a specialist with experience in the physics of stellar structure pertaining to hot compact (subdwarf B) stars and will receive additional on-the-job training as needed for other required activities (e.g., supervising students and possibly outreach and teaching activities) This position will include travel to multiple national and international meetings/conferences. The candidate will also include and advise undergraduate research projects related to the grant and should be available to participate in outreach activities. Physics, Astronomy & Material Science

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Research Technician II - Hall Lab Are you fascinated by the bizarre world of small, wiggly, often regenerative invertebrates? The Stowers Institute for Medical Research is seeking a Research Technician II to join the Hall Lab. Our lab is motivated by the simple premise that we shouldn't be limited to studying biology only in established “model” organisms. We are developing a suite of molecular and imaging tools to enable genetic engineering in diverse emerging model organisms, with the goal of understanding how stem cells support regeneration across the tree of life. Roles & Responsibilities The selected candidate will work closely with the PI to support the lab's research efforts by: Developing and refining techniques to maintain and expand an array of emerging model invertebrates (with a strong emphasis on flatworms). Contributing to molecular cloning that support transgenesis and gene editing strategy development. Performing experiments to characterize regeneration, life history traits, and phenotype variation across species. Maintaining thorough documentation (protocols, experimental records, colony/line tracking) and contributing to lab organization and best practices. The ideal candidate is curious, creative, and resilient in the face of experimental setbacks. They work independently when needed, communicate clearly, and consistently incorporate feedback to improve. What You'll Be Doing Animal husbandry to maintain several species of emerging model flatworms and related invertebrates. Working with the Invertebrate Culture Facility to develop and implement more automated, standardized husbandry workflows. Characterizing life-cycle traits and regenerative capabilities across diverse flatworm species (including phenotyping with immunohistochemistry and in situ hybridization, and performing genetic perturbations with CRISPR and RNAi). Performing molecular cloning using techniques such as bacterial transformation, minipreps, PCR, gel electrophoresis, restriction digestion, Golden Gate assembly, and Gibson assembly. What We Offer Close mentorship and support to help you meet your scientific and professional goals. The opportunity to work with unusual and exciting emerging model organisms in the field of regenerative biology. The opportunity to work closely with our fantastic technology centers while gaining important leadership skills. Professional development opportunities (lab meetings, institute seminars, and conference attendance as appropriate). Competitive compensation and benefits (medical, dental, vision, 403(b)), and relocation assistance as applicable. Campus perks including café access, and fitness facilities. Minimum Qualifications BS or MS in a relevant field (e.g., Molecular Biology, Bioengineering, Synthetic Biology, Biophysics, Chemical Biology, Ecology, Microbiology, or related discipline). 3+ years of laboratory experience. Preferred Qualifications Hands-on experience with molecular biology and/or genetics (cloning, PCR, gel electrophoresis, etc.). Comfort with careful organization and recordkeeping (tracking cloning projects, animal lines, and experimental details). Familiarity with sequence/plasmid design tools (e.g., Geneious, Benchling, SnapGene). Imaging experience (widefield fluorescence, confocal, or similar). Strong attention to detail and observational skill (e.g., recognizing “happy worms,” regeneration phenotypes, and subtle health changes). A love and excitement for the organisms we work with. How to Apply Please compile the following materials into a single PDF and name the file using the format: LastName_2026_HallLab_RTechII.pdf Submit applications to: ******************* Application materials: Cover letter Statement of career goals and research interests (1 page max) Summary of prior research experience CV Unofficial college transcripts Contact information for up to three professional references We look forward to reviewing your application!

Up To $1,000 Paid Depression Study! Those who Currently Experience At Least TWO Symptoms of Depression And the Current Depressive Episode Started More Than 4 Weeks Ago May Qualify For The Study!

We are seeking a dedicated Quality Control Scientist to join our team supporting both contract development and manufacturing organization operations and a new compounded pharmaceutical manufacturing line. This role emphasizes method development, validation, and technical problem-solving for small-molecule products and compounded formulations. The ideal candidate will possess strong analytical expertise and extensive experience in pharmaceutical quality systems. PAY - $48 - $72 Responsibilities * Design, develop, and validate analytical methods for compounded pharmaceutical products and small-molecule drug substances and products. * Support method transfer activities between internal teams and external partners. * Develop methods for impurity profiling, degradation studies, and stability testing. * Provide technical insights for complex analytical challenges, including root cause analysis for deviations and out-of-specification results. * Collaborate with Quality Assurance on investigations and corrective actions. * Ensure analytical methods and documentation meet regulatory requirements for FDA submissions and CMC packages. * Maintain compliance with cGMP and industry standards for laboratory operations. * Participate in CDMO development projects, contributing analytical expertise to formulation and process development. * Work at the bench as needed to execute laboratory studies and support project timelines. * Identify and implement process improvements within QC workflows to enhance efficiency and compliance. * Support audit readiness and contribute to maintaining a robust quality culture. Essential Skills * Minimum 10-15 years of experience in analytical method development and validation within a pharmaceutical environment. * Strong knowledge of HPLC, GC, MS, dissolution, and other analytical techniques. * Diverse experience with various drug product types, APIs, intermediates, small-molecule, and compounded pharmaceuticals. * Understanding of regulatory guidelines (FDA, ICH) and cGMP standards. * Excellent technical writing skills. Additional Skills & Qualifications * Bachelor's or advanced degree in Chemistry or a related field. * Familiarity with compounding operations and small-molecule development preferred. * Ability to mentor and coach others, with potential to lead teams. * Empathetic leadership skills and an understanding of diverse employee backgrounds. * Integrity, transparency, and a collaborative approach to decision-making. Work Environment The team currently includes three other chemists in the lab. The position offers a flexible day shift from Monday to Friday, along with two weeks of PTO and holiday pay. This is an excellent opportunity to join a rapidly growing business, with the chance to establish and shape processes in a dynamic environment equipped with new GC's and HPLC's, using the latest Open Lab Software with Agilent. Job Type & Location This is a Contract to Hire position based out of Springfield, MO. Pay and Benefits The pay range for this position is $48.08 - $72.11/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Springfield,MO. Application Deadline This position is anticipated to close on Jan 19, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

This is a grant-funded position with a current limit of 1 year and 3 months and is contingent upon available funds. The primary accountabilities below are intended to describe the general content of and requirements of this position and are not intended to be an exhaustive statement of duties. Incumbents may perform all or some of the primary accountabilities listed below. Specific tasks or responsibilities will be documented in the incumbents' performance objectives as outlined by the incumbents' immediate supervisor or manager. The scholar will work on projects that aim to advance knowledge, practice, and policy at the intersection of K-12 computer science education and research practice partnerships that serve minoritized communities. The overarching goal of the appointment is to strengthen capacity (i.e., knowledge, skills, practices, literacies) among recent education doctoral graduates whose scholarship engages with Computer Science (CS) and other STEM disciplines among learner groups traditionally marginalized in STEM + C fields (e.g., predominantly Hispanic-serving K-12 environments). The scholar will participate in a co-generative mentorship model that will involve participation in existing K-12 social science research projects-with the goal of additionally developing and implementing independent research programs in related fields within their time as post-doctoral researchers. The scholar will be co-mentored by project investigators (i.e., PI/Co-PIs/Senior Personnel) who will provide apprenticeship in: designing and enacting research projects, competitively pursuing extramural funding to support research, and mentoring students. Responsibilities: * Collaborate with faculty investigators to carry out such responsibilities to include, but not limited to, the following: * Developing and implementing lines of inquiry aligned with the scholar's interests, expertise, and social science research goals in one or more areas: K-12 computer science student learning, teaching practice, or policy * Writing/Amending IRB applications and obtaining IRB approvals * Collecting/Analyzing/Managing one or multiple education-related data sources * Collaborating with and Mentoring undergraduate and graduate students * Publishing and presenting research findings in competitive peer-reviewed venues * Writing grant funding proposals to seek extramural support * Engaging in participatory approaches to research, practice and policy development and implementation * Coordinating and working with diverse community stakeholders (i.e., district-, school- and community-based within existing partnerships of the College of Education * Assisting with project management, and * Collaborating with other team members at the University of Texas at El Paso [via distance]. Graduate College Administration

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Up To $1,000 Paid Depression Study! Those who Currently Experience At Least TWO Symptoms of Depression And the Current Depressive Episode Started More Than 4 Weeks Ago May Qualify For The Study!

This position is grant funded and any term limits set out in that grant and/or that funding for the position is contingent upon continued grant funding. * Clean and analyze ecological datasets pulled from databases in accordance with the Inventory and Monitoring Division's data publication standards * Generate Ecological Metadata Language (EML) metadata using the NPSdataverse R package to promote the discoverability of the data it describes * Contribute to R packages developed by other data managers to automate data cleaning tasks, where appropriate * Write reports using RMarkdown to document data management processes Computer Science

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Up To $1,000 Paid Depression Study! Those who Currently Experience At Least TWO Symptoms of Depression And the Current Depressive Episode Started More Than 4 Weeks Ago May Qualify For The Study!

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Up To $1,000 Paid Depression Study! Those who Currently Experience At Least TWO Symptoms of Depression And the Current Depressive Episode Started More Than 4 Weeks Ago May Qualify For The Study!