Seasonal Research Technician - Alfalfa Breeding Program
Duration: Up to 9 months (seasonal, based on business needs)
About the Role Join our innovative alfalfa breeding team and gain hands-on experience in agricultural research! As a Seasonal Research Technician, you'll support critical field activities that drive advancements in crop science. This is an excellent opportunity for individuals interested in plant science, agriculture, or research, and who thrive in a dynamic, team-oriented environment.
Key Responsibilities
Assist Farm Manager in timing of field spraying, irrigation, fertilization, etc
Hands on farm field work
Planting, harvest, and mowing
Maintenance of equipment, field site, and shop areas
Assist with all aspects of alfalfa research, including transplanting, harvesting, and sample preparation.
Operate small lawn tractors, harvesters, and other vehicles to support station operations.
Perform sample grinding with a dust collection system (PPE provided).
Assist Farm Manager in extra day to day activities
Tasks will vary by season, offering a diverse and engaging work experience.
What We're Looking For
Detail-oriented individuals with strong eye-hand coordination and a commitment to quality record keeping.
Ability to work with plant materials and follow precise protocols.
Willingness to perform physical tasks in both indoor and outdoor environments.
Qualifications
High School Diploma or GED required.
Must be 18 years or older.
At least 6 months of continuous work experience.
Steel-toed shoes may be required for certain activities; PPE allowance provided for qualifying tasks.
Capable of lifting up to 50 lbs
Understanding of equipment operation and maintenance
Why Join Us?
Work alongside experienced researchers and gain valuable skills in plant breeding and agricultural science.
Contribute to projects that make a real impact on sustainable agriculture.
Enjoy a supportive team culture and opportunities for professional growth.
FGI is committed to providing a safe and inclusive workplace. All necessary personal protective equipment (PPE) will be supplied.
Compensation:
$20.00 per hour
About Land O'Lakes, Inc.
Join us and be part of a Fortune 250, farmer- and member-owned cooperative that is reimagining the business of food. We have been named a Top Workplace by Indeed and LinkedIn, and to the TIME 100 Most Influential Companies list.
We provide a broad portfolio of benefits to keep you and your family at your best. Land O'Lakes is Where Your Future Takes Root.
Land O'Lakes and our global entities support diversity in employment practices.
Neither Land O'Lakes, nor its affiliates or search firms, will ever contact you and ask for confidential information over the phone or in email. If you receive a call or email like this, please do not provide the information being requested.
If you need to submit a reasonable accommodation request to complete the employment application process, please call the HR Solution Center at 844-LOL-HR4U ************** M-F 8:00am-4:30pm CT.
$20 hourly 8d ago
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Online Research Participant - Earn Cash for Sharing Your Views
Opinion Bureau
Research associate job in Lawrence, KS
Take quick online surveys and earn rewards for sharing your thoughts. Join today - it's free and easy!
$32k-58k yearly est. 1d ago
Research Scientist - CTRL Labs
Meta 4.8
Research associate job in Topeka, KS
Reality Labs at Meta is seeking Research Scientists with experience in product-focused machine learning and signal processing research to advance our pioneering work in neuromotor interfaces, which has grown out of the acquisition of CTRL-labs. We're building a practical interface drawing on the rich neuromotor signals that can be measured non-invasively via surface electromyography (EMG) with single motor neuron resolution. This technology could become one of the main pillars for interaction with virtual and augmented worlds.We are a multi-disciplinary team of researchers investigating the nature of human neuromotor signals, developing novel signal processing and machine learning methods to infer a user's intent, and creating novel interaction techniques and user experiences. Help us unleash human potential by removing the bottlenecks between user intent and action.
**Required Skills:**
Research Scientist - CTRL Labs Responsibilities:
1. Research and develop Deep Learning or other computational models
2. Design methods, tools and infrastructure to analyze and leverage rich multimodal data sets
3. Set technical direction for a project of 2-3 researchers and engineers
4. Help transition and deliver our work from research into product
5. Adapt standard machine learning methods to best leverage modern parallel environments (e.g. distributed clusters, multicore SMP, and GPU)
**Minimum Qualifications:**
Minimum Qualifications:
6. Bachelor's degree in Computer Science, Computer Engineering, relevant technical field, or equivalent practical experience
7. Ph.D. degree in Computer Science and Engineering, Electrical Engineering, Statistics/Mathematics
8. Experience with developing machine learning models at scale from inception to business impact
9. Programming experience in Python and hands-on experience with frameworks such as PyTorch
10. Exposure to architectural patterns of large scale software applications
11. Must obtain work authorization in the country of employment at the time of hire, and maintain ongoing work authorization during employment
**Preferred Qualifications:**
Preferred Qualifications:
12. Proven track record of achieving significant results as demonstrated by grants, fellowships, patents, as well as first-authored publications at peer-reviewed AI conferences (e.g. NeurIPS, CVPR, ICML, ICLR, ICCV, ACL, and ICASSP)
13. Demonstrated software engineer experience via an internship, work experience, coding competitions, or widely used contributions in open source repositories (e.g. GitHub)
14. Experience bringing machine learning-based products from research to production
**Public Compensation:**
$184,000/year to $257,000/year + benefits
**Industry:** Internet
**Equal Opportunity:**
Meta is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender, gender identity, gender expression, transgender status, sexual stereotypes, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics. We also consider qualified applicants with criminal histories, consistent with applicable federal, state and local law. Meta participates in the E-Verify program in certain locations, as required by law. Please note that Meta may leverage artificial intelligence and machine learning technologies in connection with applications for employment.
Meta is committed to providing reasonable accommodations for candidates with disabilities in our recruiting process. If you need any assistance or accommodations due to a disability, please let us know at accommodations-ext@fb.com.
$184k-257k yearly 60d+ ago
Medical Research Associate (PRN) - Lenexa, KS (Onsite) - ICON
Icon Clinical Research
Research associate job in Lenexa, KS
Medical ResearchAssociate (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 ResearchAssociate to join our diverse and dynamic team. As a Medical ResearchAssociate 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, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
+ Life assurance
+ Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site (************************************* to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here (******************************************************
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here (****************************************************** to apply
$37k-55k yearly est. 11d ago
Medical Research Associate (PRN) - Lenexa, KS (Onsite) - ICON
Icon Plc 4.8
Research associate job in Lenexa, KS
Medical ResearchAssociate (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 ResearchAssociate to join our diverse and dynamic team. As a Medical ResearchAssociate 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, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
* Life assurance
* Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here to apply
$41k-64k yearly est. 11d ago
Research Associate
Beck's Superior Hybrids 3.5
Research associate job in Salina, KS
Intermediate level position in the Research Department which we are seeking someone with some basic agriculture and field research knowledge. The main responsibility for this job will be conducting mini-strip and replicated testing as well as participating in other facets of Beck's Research Department.
As a member of the Beck's Family of employees, all full-time employees are eligible for a generous benefits package:
Health benefits including two medical plan options and company HSA contributions, dental, vision, employer paid life/AD&D for you and your dependents, disability insurance, and access to an onsite Nurse Practitioner
401k plan match & company sponsored pension plan and access to a Financial Advisor to help you manage your retirement savings
Paid time off, Paid Holidays, Wellness Programs, & Corporate Discounts
Company Christmas Party, Free Lunch, Two-Hundred Dollar Merchandise Allowance, & Much More
Responsibilities
Coordinate plot locations and logistics with plot cooperators
Measuring and setting flags
Working with cooperators to ensure proper seedbed preparation, fertility program and weed control
Seed Preparation
Prepare seed for mini-strip and replicated testing
Planting of mini-strip and replicated plots
Transporting planting equipment to outlying locations
Ensuring plots are planted as directed by the Testing Site Lead
Data Collection
Stand counts, early vigor, and plot ratings
Flowering data
Physical characteristics (Plant and ear heights, etc)
Disease evaluation and agronomic notes
Plot Maintenance
Work with cooperators to ensure plots are maintained to Beck's Hybrids' standards
Apply fertilizer, herbicide, and insecticide as needed
Plot Harvest
Transport harvest equipment to outlying locations
Collect fall agronomic notes (stability, plant integrity, etc)
Conduct harvest of mini-strip and replicated plots
Research Equipment Maintenance
Ensure machinery is maintained to Beck's Hybrids' standards to minimize downtime
Diagnose and make repairs as needed
Data Reporting
Some duties may include reporting notes, harvest data, and preparation of yield reports for Beck's Product Development Staff
Warehousing/distribution
Inventory incoming shipments
Organize and stage outgoing shipments
Load/unload trucks as needed
Perform seed deliveries as needed
Aid in isolated corn block, nursery, and winter nursery work
Supervise full time employees, part time employees, and interns that report to the ResearchAssociates as needed
Work in other areas of Beck's Hybrids' operations as directed by the Testing Site Lead to ensure efficient site operations.
Job Requirements
Education and training:
Minimum of high school diploma or GED equivalent, advanced degree preferred
Class A CDL required
Pesticide applicator license or the ability to obtain
Must possess and maintain valid driver's license and insurable driving record as determined by Beck's automobile insurance policy
Technical knowledge:
Excellent verbal and written communication skills
Possess strong agronomic and mechanical skills
Possess positive attitude
Ability to establish priorities, work independently, work as a team member, and proceed with objectives without supervision.
Skill to use personal computer and various software packages
3. Physical demands:
Ability to pass DOT physical examination and obtain Medical Examiner's Certificate is required
Overnight travel is required
Must be able to lift up to 70 pounds unassisted
Experience:
Field Research and/or Agriculture experience preferred
Previous experience with replicated test plots preferred
Previous experience with operating combine harvesters preferred
** In an effort to provide a safer, drug-free workplace for employees, all full-time applicants to whom offers of employment are made must submit to a drug test and background check, subject to applicable local, state, or federal laws or regulations. Employment at Beck's is contingent upon passing these pre-employment screenings.
$35k-55k yearly est. Auto-Apply 60d+ ago
Research Scientist I
Mosaic Diagnostics LLC
Research associate job in Overland Park, KS
Job DescriptionDescription:
Job Title: Research Scientist I/II at Mosaic Diagnostics
Department: Research and Development
Reports To: Director of Research & Development
Summary of position:
The Research Scientist I/II is a motivated and detail-oriented professional responsible for supporting the development and validation of laboratory-developed tests (LDTs) using LC-MS, Analytical Chemistry, Molecular Biology, or Immunology-based methodologies. This hands-on laboratory position is essential to driving scientific innovation and operational excellence within the R&D department at Mosaic Diagnostics.
Duties/Responsibilities:
Assist in the design, development, and validation of LDTs targeting specific analytes in biological samples.
Conduct routine lab tasks including sample preparation, daily experimental runs, and instrument calibration.
Collaborate with scientific staff to optimize assay conditions and troubleshoot experimental procedures.
Analyze and interpret experimental data to ensure accuracy, reliability, and reproducibility.
Document experiments, findings, and conclusions in a clear, organized, and comprehensive manner.
Draft SOPs, validation protocols, and technical reports.
Support maintenance and troubleshooting of laboratory instruments, including both hardware and software.
Uphold and promote a culture of safety, quality, and regulatory compliance.
Perform additional duties as required to support departmental objectives.
Requirements:
Required Skills/Abilities:
Working knowledge of LC-MS, Molecular Biology, Immunology, or Analytical Chemistry methodologies.
Proficiency with laboratory instruments, software platforms, and data processing tools.
Strong analytical thinking and organizational skills with meticulous attention to detail.
Demonstrated capability in experimental design and targeted troubleshooting.
Excellent verbal and written communication abilities.
Ability to work both independently and as part of a collaborative team.
Dedication to maintaining quality, safety, and compliance standards.
Education and Experience:
Bachelor's or Master's degree in Analytical Chemistry, Molecular Biology, Immunology, Biochemistry, or a related scientific field.
1-5 years of laboratory experience, preferably in assay development and validation.
Preferred:
Experience troubleshooting analytical workflows and optimizing lab procedures.
Familiarity with CLIA, CAP, and ISO standards and regulatory requirements for LDTs.
Understanding of sample preparation and general laboratory best practices.
Physical Requirements:
Prolonged periods of computer use and sitting at a desk.
Occasional standing and stair climbing.
Visual acuity necessary for close work and making fine adjustments.
$51k-77k yearly est. 16d ago
Research Assistant - School of Law
Washburn University 4.0
Research associate job in Topeka, KS
Research Assistant - School of Law
Department: School of Law
Advertised Pay: 12.00
The Research Assistant will contribute to faculty research projects; perform legal research, analysis, and writing for a professor related to the professor's scholarly or pedagogical work.
About Washburn University:
Washburn University is a teaching-focused, student-centered, public institution located in the metropolitan setting of Topeka that has earned national recognition for its high-impact programs for first-generation students. Washburn has a student body of over 5,500 undergraduate, graduate, and law students, a significant and growing number of whom are first-generation and Pell-Grant eligible. The University has created educational pathways for all students to be successful and achieve their educational goals.
Washburn is dedicated to recruiting and retaining a dynamic faculty, staff, and student body and cultivating a robust learning and working environment and curriculum. We employ more than one thousand faculty and staff on our campuses throughout Topeka and strive to offer competitive wages, an excellent benefits program, and a supportive culture and a healthy work/life balance. Washburn seeks to create an environment that reflects our core values for creating positive IMPACT: inclusion, modernization, partnership, achievement, community and transformation. In 2024, Washburn was recognized as one of the best colleges in the nation to work for, according to Great Colleges to Work For program.
Essential Functions:
-Research legal issues and topics identified by professor.
-Review and summarize articles and book chapters.
-Provide analysis of how the material applies to the issues under examination.
Non-Essential Functions:
Answering phones, filing, and typing.
Required Qualifications:
Must have completed or plan to take, in the second year, the courses pertaining to the professor's research.
-Professionalism.
-Ability to maintain confidentiality.
-Computer/keyboarding skills.
-Excellent grammar; written and verbal communication.
-Interpersonal skills.
-Ability to multi-task.
-Understand legal terminology.
Applicant must be enrolled as a 2L, 3L, or LLM at Washburn University Law School.
Preferred Qualifications:
Hourly
Background Check Not Required
$37k-49k yearly est. 4d ago
R&D Food Scientist
Flora Food Group
Research associate job in Hugoton, KS
We offer consumers a compelling choice in four growing categories: butters and spreads, creams, liquids and cheeses. We hold leadership positions in many of the 100 countries we operate in, with iconic brands including Flora, Becel+ProActiv, Blue Band, Country Crock, I Can't Believe It's Not Butter, Rama, and Violife, together with our local brands and Professional business.
Global branded food champion Flora Food Group, offers the next generation of delicious, natural, nutritious food. Our products are more affordable and more sustainable than their dairy equivalents.
Location: On-Site at Hugoton, KS Factory Reports To: Pilot Plant Supervisor / Senior R&D Manager
About the Role
We're looking for a Food Scientist to support pilot plant operations and industrial implementation of new products. In this role, you'll assist with trial execution, data collection, and commissioning of new production lines, while ensuring hygiene, safety, and efficiency in our experimental platform. You'll also coordinate the collection of sales samples and contribute to continuous improvement initiatives.
This is a hands-on role for someone passionate about food science and process engineering who thrives in a collaborative, fast-paced manufacturing environment.
What You'll Do
Pilot Plant Operations
Assist in planning and executing pilot plant trials with R&D project leads.
Prepare equipment configurations and manage raw material and packaging inventory.
Support trial execution, troubleshooting, and post-trial cleaning (CIP).
Collect, format, and analyze trial data from acquisition systems.
Maintain hygiene, safety, and first-level maintenance of pilot plant equipment.
Production Support & Industrial Implementation
Support commissioning of new production lines by verifying process parameters and product specifications.
Collaborate with R&D, Quality, Engineering, and Operations for smooth product scale-up.
Participate in factory audits and identify optimization opportunities.
Monitor product quality during production runs and assist in root cause analysis.
Continuous Improvement & Documentation
Contribute to shop floor improvement initiatives focused on performance KPIs.
Update SOPs and maintain documentation related to pilot plant operations and safety.
Stay current with food processing technologies and propose equipment upgrades.
Training & Collaboration
Assist in training interns and temporary staff on pilot plant procedures and safety protocols.
Participate in technical workshops and cross-functional collaboration for product launches.
About You
Bachelor's degree in Food Science, Chemical Engineering, Bioprocessing, or related field
5+ years of experience in food manufacturing operations.
Internship or academic experience in a pilot plant or food manufacturing preferred.
Strong foundation in food science and process engineering; hands-on experience on the plant floor.
Basic understanding of food processing equipment and hygienic design.
Experience in improving processes, recipes, equipment upgrades, and testing methodologies.
Strong communication, organization, and problem-solving skills.
Team-oriented with the ability to thrive in a fast-paced environment.
Proficiency in Microsoft Excel and data analysis tools.
What's next
If this position sounds interesting, please hit the apply button now!
#LI-AM1
#LI-Onsite
We understand your resume might not be up to date and recommend that you apply with what you have or your LinkedIn Profile. Flora Food Group is dedicated to building an inclusive and diverse workplace, we understand that you might not meet all the requirements stated in the description, but we encourage you to apply anyway. You might be the right candidate for this role or other roles.
Flora Food Group is an employer committed to diversity and inclusion in the workplace and equal opportunities for all. We recruit based only on values, qualifications, performance, skills, behaviours, experience, and knowledge. We ensure job advertisements are free from unintentional bias.
No personal characteristics should be a barrier to joining Flora Food Group. We prohibit discrimination and harassment based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or other personal characteristics.
$55k-82k yearly est. Auto-Apply 1d ago
Scientist 3
Merck KGaA
Research associate job in Lenexa, KS
Work Your Magic with us! Start your next chapter and join MilliporeSigma. Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.
This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.
Your Role:
We are seeking a highly skilled and motivated Analytical Chemist with strong expertise in LC-MS to support the characterization of cell culture media used in biologics development and manufacturing. The Scientist III Upstream R&D, Cell Culture Media Analytics position in Lenexa, Kansas, will develop innovative analytical solutions to complex problems relating to cell culture media. The ideal candidate will develop, optimize, and execute analytical methods to characterize small molecules, metabolites, and other components in complex media matrices. This role will have a strong foundation in mass spectrometry, method development, and data interpretation, with the ability to work independently and collaboratively across teams.
* Design, develop/optimize, and implement advanced LC-MS-based analytical methods for qualitative and quantitative characterization of cell culture media components with minimal guidance.
* Perform routing LC-MS analysis to:
* Support media production at a new site.
* Demonstrate product comparability between different media production sites.
* Ensure efficient technology transfer between different production sites.
* Resolve media performance complaints.
* Design and perform experiments with minimal supervision to support media development, process optimization, media performance investigations, and product characterization.
* Collaborate with cross-functional teams, including Media Development, Customer Collaboration, and Quality Control.
* Troubleshoot instrumentation and method-related issues and maintain LC-MS systems in good working condition.
* Stay current with advances in analytical technologies and seek new opportunities to advance technologies and apply innovative approaches to improve workflows and services.
* Be open to new ideas and always seek critical feedback from colleagues and demonstrate effective cooperation.
* Work collaboratively with colleagues, including ability to navigate challenging interpersonal dynamics with professionalism.
Who You Are
Minimum Qualifications:
* Bachelors in Microbiology, Chemistry, Biomedical Engineering, Chemical Engineering, or other Life Science or Engineering discipline
* 5+ years hands-on LC-MS experience
OR
* Masters in Microbiology, Chemistry, Biomedical Engineering, Chemical Engineering, or other Life Science or Engineering discipline.
* 3+ years hands-on LC-MS experience
OR
* PhD in Microbiology, Chemistry, Biomedical Engineering, Chemical Engineering, or other Life Science or Engineering discipline
* 1+ years hands-on LC-MS experience
Preferred Qualifications:
* Strong understanding of mass spectrometric principles and procedures for LC-MS method development and characterization of small molecules or biologics.
* Hands-on experience using LC-MS instrumentation (e.g., QTOF, Orbitrap, triple quadrupole) to analyze complex biological matrices such as cell culture media and fermentation broths is highly desirable.
* Strong critical thinking skills, problem-solving skills, attention to detail, and ability to manage multiple priorities.
* Good oral and written communication skills
* Laboratory experience performing small or large molecule characterization using LC or LC-MS.
* Experience using one or more of the following instruments is a plus: Waters, Sciex, and Thermo LC-MS systems.
* Knowledge or experience using data analytics or programming skills for analysis of LC-MS data is a plus.
* Experience with metabolomics workflows.
Pay Range for this position: $76,600-$137,900.
The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here.
What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!
Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!
$76.6k-137.9k yearly 5d ago
AI Research Scientist
Propio 4.1
Research associate job in Overland Park, KS
Job DescriptionDescription:
Propio is on a mission to make communication accessible to everyone. As a leader in real-time interpretation and multilingual language services, we connect people with the information they need across language, culture, and modality. We're committed to building AI-powered tools to enhance interpreter workflows, automate multilingual insights, and scale communication quality across industries.
We are seeking an AI Research Scientist that will conduct groundbreaking research in machine learning and natural language technologies to drive innovation at Propio. This role focuses on exploring novel algorithms, improving existing models for interpretation and speech tasks, and publishing high-impact research to strengthen Propio's position as an AI leader in language services.
Key Responsibilities:
Conduct research in NLP, speech, and machine learning, with focus on translation, interpretation, bidirectional communication, and low-resource language challenges
Develop and prototype novel architectures and algorithms for real-world applications in Propio's core domains
Publish in top AI and NLP conferences and journals (NeurIPS, ACL, ICML, EMNLP, Interspeech)
Collaborate with engineering teams to transition research into production systems, ensuring research advances translate to product improvements
Advise leadership on emerging technologies, research trends, and their applicability to Propio's roadmap
Mentor junior researchers and foster a strong internal research culture within the expanded team
Identify and explore emerging challenges in speech-to-speech systems, multilingual interpretation, and agentic AI
Requirements:
Qualifications:
Master's Degree in Engineering, preferably in Computer Science, Statistics, or Data Science or equivalent work experience
2-3+ years of experience working with NLP or large-scale ML models in production
Proven publication record in leading AI/NLP venues (NeurIPS, ACL, ICML, EMNLP, Interspeech)
Expertise in ML, deep learning, NLP, or speech processing methods
Proficiency in Python and research tooling (PyTorch, JAX, Transformers)
Ph.D. in Computer Science, AI, or related field (or equivalent research experience)
Strong problem-solving and scientific communication skills
Interest in applied research with real-world impact; experience in production ML systems a plus
#LI-JS1
$61k-83k yearly est. 16d ago
Research Assistant
Alliance for Multispecialty Research
Research associate job in Newton, KS
The role of the Research Assistant is responsible for performing a wide variety of administrative and clinical tasks to support the study site. The Research Assistant supports all study related activities to ensure that the study is completed accurately per study protocol. The Research Assistant is an integral role to assist with the flow of the clinic.
To consistently embody AMR Clinical's Core Values:
United We Achieve
Celebrate Diverse Perspectives
Do the Right Thing
Adapt and Persevere
The Research Assistant reports to the Site Manager/Team Lead.
Classification: Non-Exempt
Primary Responsibilities:
Effectively prioritize tasks and meet deadlines in a fast-paced environment.
Maintain a strong emphasis on compliance responsibilities, including timely identification and reporting of protocol deviations, serious adverse events (SAEs), and adherence to regulatory and site-specific requirements.
Monitor & Report Adverse Events - Recognize and promptly report AEs, protocol deviations, and safety concerns to the clinical team. Document AEs and Serious Adverse Event reporting in compliance with FDA, IRB, and sponsor requirements, ensuring timely follow-up and resolution.
Ensure Compliance with Study Protocols & Regulatory Guidelines - Adhere to Good Clinical Practice (GCP), FDA regulations, and site SOPs when conducting study-related activities.
Assist in Subject Retention Efforts - Support ongoing engagement, communication, and compliance to enhance subject retention throughout the study.
Perform Inventory Management - Track and manage study supplies, lab kits, and investigational products (if applicable) to ensure readiness for study visits.
Assist in maintaining accurate, timely, and audit-ready documentation of all study-related activities.
Perform Laboratory Responsibilities with Accuracy - Ensure proper labeling, handling, storage and shipment of specimens per protocol and regulatory requirements.
Strong problem-solving skills and ability to adapt to evolving study requirements.
Ability to handle confidential and sensitive information with discretion.
Ability to follow detailed instructions and maintain high levels of accuracy.
Establish and maintain patient rapport during clinical drug trials to include management of subjects
Clinical data collection such as vital signs, EKG recording, subject weights, etc.
Medical record retrieval and review when required
Subject interviews
Phlebotomy
Filing and pulling study records
Answering and triage of research office calls
Subject check in and out process
Study preparation, such as screening packets, preparing informed consents, pulling charts for the next business day, etc.
Filing study documents in the subject's chart.
Develop rapport with study sponsors, monitors, study participants, etc.
Assist monitors during onsite visits
Maintain accurate enrollment/ICF logs
Assist the clinical team to complete study activities. The clinical team includes but is not limited to CRCs, Laboratory, Data management, etc
Educate subjects on diaries as studies require.
Accurate and timely documentation
Unblinded duties as assigned.
Position may require occasional weekend and/or overtime hours.
Other duties as assigned
Desired Skills and Qualifications:
Medical office experience, medical certificate, or equivalent work experience preferred.
Phlebotomy skills are preferred
Excellent attention to detail
Strong listening, verbal and written communication skills
Excellent task management and organizational skills
Ability to multi-task in an always evolving fast paced environment.
Demonstrate proficient knowledge of operating office equipment and software.
Ability to be ambulatory most of the workday.
Ability to lift/transfer/push/manipulate equipment and patients, which requires strength, gross motor and fine motor coordination.
AMR Clinical does not discriminate in employment on the basis of race, color, religion, sex (including pregnancy and gender identity), national origin, political affiliation, sexual orientation, marital status, disability, genetic information, age, retaliation, parental status, military service, or other non-merit factor.
** This job description is intended to be a representative summary of the major responsibilities and accountabilities of the staff holding this position. The staff may be requested to perform job-related tasks other than those stated in this description.
$27k-41k yearly est. Auto-Apply 60d+ ago
Research Assistant
Univer. of Kansas Schoo
Research associate job in Wichita, KS
The Research Assistant in the Department of Psychiatry & Behavioral Sciences will contribute to a HRSA funded project by collecting and analyzing data, assisting with the preparation of the annual HRSA report, and drafting publications. This position provides hands-on experience with a HRSA training grant that aims to increase the supply of highly trained child and adolescent psychiatrists and psychologists prepared to provide integrated mental health care for children, adolescents, and young adults, with particular focus on under-served communities. This position requires approx. 8 hours per month for 10 months of the year, and 20 hours per week through June and July to compile and submit the annual HRSA report.
ESSENTIAL FUNCTIONS
Data Entry & Reporting
Collect, enter, and maintain data in electronic systems
Assist the grant coordinator with creating and submitting reports through HRSA Grant Solutions
Compile and submit annual HRSA report, due each July
Administration
Participate in research team meetings and support grant related activities
May participate in relevant committees, task force, or other similar activities
Reliable Attendance and Punctuality.
Other duties as assigned.
Education: Two (2) years of experience navigating complex databases, government forms, data collection, report writing, or similar detail-oriented work. Education may be substituted for experience on a year for year basis.
Experience : Two (2) years of experience navigating complex databases, government forms, data collection, report writing, or similar detail-oriented work. Education may be substituted for experience on a year for year basis.
Microbiology Tech or Microbiology Technologist in Kansas for Permanent Hire
K.A. Recruiting
Research associate job in Kansas
I have a Microbiology Med Tech role available near New Century, Kansas!
Details - Full-time and permanent - Shift: Evenings - Opportunities for growth
- Full, comprehensive benefits package (PTO, health insurance, life insurance, 401k, etc)
Requirements
- College degree
- ASCP cert
- Prior experience, including microbiology
Click apply or email your resume to leah@ka-recruiting.com/call or text 617-746-2751! You can also schedule a time to chat here -https://calendly.com/leahkarecruiting/10min.
REF#LM4193
$28k-38k yearly est. 6d ago
Research Scientist: Specialized in Polymer Science
Pittsburg State University 4.0
Research associate job in Pittsburg, KS
Pittsburg State University is accepting applications for a Research Scientist Specialized in Polymer Science in the Department of National Institute for Materials Advancement that is responsible for participating in ongoing projects within the division, focusing on the design, synthesis, and characterization of novel organic materials, monomers, and polymers for diverse applications. The successful candidate will be responsible for performing all stages of material development, including synthesis, testing, and analysis of prepared samples, as well as documenting results through detailed reports and scientific manuscripts. Additionally, the Research Scientist will contribute to propose development for external funding opportunities and may be assigned to teach relevant undergraduate (BS) and graduate (MS) courses as needed.
Duties and Responsibilities
50% - Research and Development
Design and conduct advanced research focused on the synthesis, purification, and characterization of new monomers, polymers, and polymer-based materials for various applications
Execute experiments, including sample preparation, materials testing, data collection, analysis, and interpretation, followed by preparation of comprehensive technical reports.
Maintain and calibrate laboratory instruments; develop and implement standard operating procedures (SOPs) to ensure consistency and safety in research practices.
Teach one or two undergraduate or graduate-level courses per semester as required.
Supervise and mentor students, research assistants, and junior scientists; review experimental data, evaluate progress, and provide technical guidance.
Prepare written reports, manuscripts, and presentations for internal and external stakeholders, conferences, and peer-reviewed journals.
Collaborate with the Associate Vice President and Executive Directors to oversee the activities of technical staff, students, and research personnel within the division.
40% - Business and Technical Management
Identify, develop, and manage externally funded research projects from federal, state, and industrial partners in alignment with the division's strategic objectives.
Write competitive research proposals, technical reports, patents, and scientific publications to support new funding and commercialization efforts.
Engage and collaborate with external partners to advance technology transfer, licensing, and commercialization opportunities in consultation with the supervisor.
Conduct literature reviews and identify emerging research areas and fundable topics in polymer and materials science.
Represent the division at conferences, trade shows, and recruitment events; manage exhibition booths, network with potential collaborators, and serve on institutional committees as needed.
Maintain active communication with the polymer and bio-based materials communities and establish relationships with new industrial and academic partners.
10% - Other Duties as Assigned
Perform additional responsibilities as delegated to support the mission and strategic goals of the division and university.
Education and Experience
Required Education and Experience - Time of Hire
Ph.D. in Polymer Science or related discipline
2 years of experience with monomer and polymer synthesis, design of new synthesis procedures, characterization, analysis, and writing reports/manuscripts
2 years of experience in applied polymer science
3+ Publications and presentations in polymers-related areas
Candidates must hold a doctoral degree in Polymer Science or a related field. This degree requirement ensures candidates possess the advanced theoretical knowledge, highly specialized methodologies, and critical problem-solving skills fundamental to this work. These competencies are typically developed and rigorously validated only through the comprehensive curriculum and intensive experiential experience inherent in a formal degree program.
Preferred Education and Experience
2 years of experience in operating analytical/testing instruments
1 year of experience in teaching BS and MS-level classes
2 years of supervisory experience
Screening Services (Background Checks): Your employment with Pittsburg State University is contingent on a satisfactory criminal background check and sex offender check.
Salary Range: Commensurate with Experience
Job Type: Unclassified
Appointment Duration: 12 months
Work Schedule: Full Time, Monday - Friday, 8:00 AM - 4:30 PM, nights and weekends as needed
Application Documents Required*:
Resume
Cover Letter
Names and Contact Details for three (3) Professional References
Transcript
*Consolidate into two documents to upload.
Open Until Filled with a first consideration date of January 23, 2026.
Search Committee Chair: Mary Louise Widmar, *********************
Visa Sponsorship is not available for this position.
PSU will only accept applications submitted through this process.
Pittsburg State University is an Equal Opportunity and Affirmative Action Employer. We are committed to creating an inclusive environment for all employees.
$44k-70k yearly est. Auto-Apply 12d ago
Scientist
Actalent
Research associate job in Wichita, KS
We are seeking a dedicated Quality Improvement Lead to join our team in a pivotal role within our department. This position focuses on ensuring the highest standards of quality improvement by managing various monthly activities and overseeing compliance with standard operating procedures (SOPs).
Responsibilities
* Manage and implement the monthly quality improvement activities as outlined in the department's calendar.
* Ensure adherence to SOPs and maintain accurate temperature logs.
* Conduct scheduled performance testing and distribute samples to various departments, overseeing their reporting to the state.
* Facilitate onboarding and training for new hires, emphasizing quality assurance.
* Collaborate with environmental services and quality assurance teams.
Essential Skills
* A degree in Sciences with a minimum of 1.5 years of experience in an environmental lab.
* Exposure to quality assurance processes and practices.
* Proficiency in quality control and chemistry.
* Experience with batch records and EPA standards.
Additional Skills & Qualifications
* Familiarity with The NELAC Institute (TNI) standards.
* Understanding of ISO standards.
Work Environment
The work schedule is from 7 am to 4 pm, Monday through Friday. The laboratory houses a team of 20 people. Employees enjoy 11 paid holidays annually, contributing to a stable and supportive work environment.
Job Type & Location
This is a Contract to Hire position based out of Wichita, KS.
Pay and Benefits
The pay range for this position is $24.00 - $24.00/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 Wichita,KS.
Application Deadline
This position is anticipated to close on Jan 27, 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.
$24-24 hourly 7d ago
Online Research Participant - Earn Cash for Sharing Your Views
Opinion Bureau
Research associate job in Kansas City, KS
Take quick online surveys and earn rewards for sharing your thoughts. Join today - it's free and easy!
$32k-58k yearly est. 1d ago
Research Assistant
Alliance for Multispecialty Research
Research associate job in Wichita, KS
The role of the Research Assistant is responsible for performing a wide variety of administrative and clinical tasks to support the study site. The Research Assistant supports all study related activities to ensure that the study is completed accurately per study protocol. The Research Assistant is an integral role to assist with the flow of the clinic.
To consistently embody AMR Clinical's Core Values:
United We Achieve
Celebrate Diverse Perspectives
Do the Right Thing
Adapt and Persevere
The Research Assistant reports to the Site Manager/Team Lead.
Classification: Non-Exempt
Primary Responsibilities:
Effectively prioritize tasks and meet deadlines in a fast-paced environment.
Maintain a strong emphasis on compliance responsibilities, including timely identification and reporting of protocol deviations, serious adverse events (SAEs), and adherence to regulatory and site-specific requirements.
Monitor & Report Adverse Events - Recognize and promptly report AEs, protocol deviations, and safety concerns to the clinical team. Document AEs and Serious Adverse Event reporting in compliance with FDA, IRB, and sponsor requirements, ensuring timely follow-up and resolution.
Ensure Compliance with Study Protocols & Regulatory Guidelines - Adhere to Good Clinical Practice (GCP), FDA regulations, and site SOPs when conducting study-related activities.
Assist in Subject Retention Efforts - Support ongoing engagement, communication, and compliance to enhance subject retention throughout the study.
Perform Inventory Management - Track and manage study supplies, lab kits, and investigational products (if applicable) to ensure readiness for study visits.
Assist in maintaining accurate, timely, and audit-ready documentation of all study-related activities.
Perform Laboratory Responsibilities with Accuracy - Ensure proper labeling, handling, storage and shipment of specimens per protocol and regulatory requirements.
Strong problem-solving skills and ability to adapt to evolving study requirements.
Ability to handle confidential and sensitive information with discretion.
Ability to follow detailed instructions and maintain high levels of accuracy.
Establish and maintain patient rapport during clinical drug trials to include management of subjects
Clinical data collection such as vital signs, EKG recording, subject weights, etc.
Medical record retrieval and review when required
Subject interviews
Phlebotomy
Filing and pulling study records
Answering and triage of research office calls
Subject check in and out process
Study preparation, such as screening packets, preparing informed consents, pulling charts for the next business day, etc.
Filing study documents in the subject's chart.
Develop rapport with study sponsors, monitors, study participants, etc.
Assist monitors during onsite visits
Maintain accurate enrollment/ICF logs
Assist the clinical team to complete study activities. The clinical team includes but is not limited to CRCs, Laboratory, Data management, etc
Educate subjects on diaries as studies require.
Accurate and timely documentation
Unblinded duties as assigned.
Position may require occasional weekend and/or overtime hours.
Other duties as assigned
Desired Skills and Qualifications:
Medical office experience, medical certificate, or equivalent work experience preferred.
Phlebotomy skills are preferred
Excellent attention to detail
Strong listening, verbal and written communication skills
Excellent task management and organizational skills
Ability to multi-task in an always evolving fast paced environment.
Demonstrate proficient knowledge of operating office equipment and software.
Ability to be ambulatory most of the workday.
Ability to lift/transfer/push/manipulate equipment and patients, which requires strength, gross motor and fine motor coordination.
Fluent in English.
AMR Clinical does not discriminate in employment on the basis of race, color, religion, sex (including pregnancy and gender identity), national origin, political affiliation, sexual orientation, marital status, disability, genetic information, age, retaliation, parental status, military service, or other non-merit factor.
** This job description is intended to be a representative summary of the major responsibilities and accountabilities of the staff holding this position. The staff may be requested to perform job-related tasks other than those stated in this description.