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NOW OFFERING A $20,000 SIGN ON BONUS FOR QUALIFIED CANDIDATES! Introduction Do you have the career opportunities as a Medical Technologist Lead you want with your current employer? We have an exciting opportunity for you to join Research Medical Center which is part of the nation's leading provider of healthcare services, HCA Healthcare. Benefits Research Medical Center offers a total rewards package that supports the health, life, career and retirement of our colleagues. The available plans and programs include: • Comprehensive medical coverage that covers many common services at no cost or for a low copay. Plans include prescription drug and behavioral health coverage as well as free telemedicine services and free AirMed medical transportation., • Additional options for dental and vision benefits, life and disability coverage, flexible spending accounts, supplemental health protection plans (accident, critical illness, hospital indemnity), auto and home insurance, identity theft protection, legal counseling, long-term care coverage, moving assistance, pet insurance and more., • Free counseling services and resources for emotional, physical and financial wellbeing, • 401(k) Plan with a 100% match on 3% to 9% of pay (based on years of service), • Employee Stock Purchase Plan with 10% off HCA Healthcare stock, • Family support through fertility and family building benefits with Progyny and adoption assistance., • Referral services for child, elder and pet care, home and auto repair, event planning and more, • Consumer discounts through Abenity and Consumer Discounts, • Retirement readiness, rollover assistance services and preferred banking partnerships, • Education assistance (tuition, student loan, certification support, dependent scholarships), • Colleague recognition program, • Time Away From Work Program (paid time off, paid family leave, long- and short-term disability coverage and leaves of absence), • Employee Health Assistance Fund that offers free employee-only coverage to full-time and part-time colleagues based on income. Note: Eligibility for benefits may vary by location. Our teams are a committed, caring group of colleagues. Do you want to work as a Medical Technologist Lead where your passion for creating positive patient interactions is valued? If you are dedicated to caring for the well-being of others, this could be your next opportunity. We want your knowledge and expertise! Job Summary and Qualifications Under the general supervision of the Blood Bank Section Manager provides technical leadership and oversight for the personnel in the section/laboratory. Plans and coordinates daily activities for laboratory personnel. Provides documentation and makes recommendations to the manager for performance evaluations and/or disciplinary action of section/laboratory employees. Performs preanalytic, analytic, and post-analytic biochemical/hematologic testing responsibilities. Investigates technical, instrumental, and/or physiologic causes of unexpected test results. Monitors quality control and inventory of supplies and reagents. Maintains a safe work area. Demonstrates professional work habits and interpersonal skills. Participates in performance improvement activities, evaluation of new test methodologies/instrumentation, and management of laboratory data. Correlates abnormal laboratory data with pathologic states to determine validity and/or whether follow-up tests should be performed; teaches theory and procedures using educational methodology to clinical laboratory science (medical technology) students; assists with the orientation and training of MLT/CLT, Non-registered MT/CLS, and Registered MT/CLS employees. The primary analytic testing responsibilities for the employee will be in the Chemistry (includes Hematology, Urinalysis, Chemistry, Special Chemistry) section of the Laboratory. What qualifications you will need: • Bachelors Degree as a (MT-AAB) Medical Technologist, or (MLS) Medical Laboratory Scientist, • 3 years experience in an accredited laboratory required, • 2 years experience in the technical area preferred ___ is a 95+ bed facility. We offer acute inpatient, day treatment, and community-based outpatient behavioral healthcare. We treat adolescents, adults, and senior adults for emotional disorders, mental illness, and substance abuse. Our professional staff includes psychiatrists, psychologists, social workers, and licensed professional counselors. We are committed to delivering our patients skilled compassionate care regardless of age or circumstance. HCA Healthcare has been recognized as one of the World’s Most Ethical Companies® by the Ethisphere Institute more than ten times. In recent years, HCA Healthcare spent an estimated $3.7 billion in cost for the delivery of charitable care, uninsured discounts, and other uncompensated expenses. "Bricks and mortar do not make a hospital. People do."- Dr. Thomas Frist, Sr. HCA Healthcare Co-Founder If you are looking for an opportunity that provides satisfaction and personal growth, we encourage you to apply for our Medical Technologist Lead opening. We promptly review all applications. Highly qualified candidates will be contacted for interviews. Unlock the possibilities and apply today! We are an equal opportunity employer. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

🚀 NOW HIRING: Associate Scientist II – Biochemical Analysis | Kansas City, MO Are you passionate about science, precision, and making a real impact in the pharmaceutical industry? We’re looking for a driven Associate Scientist II to join a leading global company in biologics and pharmaceutical development. If you thrive in a lab environment and want hands-on experience with cutting-edge analytical techniques—this is your opportunity. * Location: Kansas City, MO (Onsite) * Schedule: Monday – Friday | 8:00 AM – 4:00 PM * Pay Rate: $26.00/hr * Type: Temp-to-Hire (6 months) As an Associate Scientist II, you will play a key role in supporting biologics development through laboratory testing and data analysis under strict cGMP guidelines. Core Responsibilities: * Perform analytical testing for biologics using techniques such as: * HPLC/UPLC (SEC, IEX, RP-HPLC, HIC) * UV-Vis, Karl Fischer * Electrophoresis (CE-SDS, SDS-PAGE, Western Blot, icIEF) * Aggregation methods (MFI, AUC, SEC-MALS) * FTIR, DSC, Fluorescence, CD * Execute compendial assays (pH, osmolality, viscosity, particulates, etc.) * Follow and interpret Standard Operating Procedures (SOPs) with precision * Accurately document results in compliance with cGMP regulations * Support method development, reports, and technical documentation * Maintain lab equipment and ensure safe, compliant operations * Bachelor’s degree in Biology, Chemistry, Biochemistry, or related field * Strong understanding of scientific principles and lab techniques * High attention to detail and critical thinking skills * Ability to multitask and meet deadlines in a fast-paced environment * Strong communication and organizational skills * Comfortable working under cGMP regulations * Hands-on experience with advanced analytical technologies * Opportunity to grow within a leading pharmaceutical environment * Collaborative and quality-driven culture * Clear pathway to permanent employment Apply now and a recruiter will connect with you to discuss this exciting opportunity. Don’t miss your chance to grow your scientific career in a high-impact role! ManpowerGroup® (NYSE: MAN), the leading global workforce solutions company, helps organizations transform in a fast-changing world of work by sourcing, assessing, developing, and managing the talent that enables them to win. We develop innovative solutions for hundreds of thousands of organizations every year, providing them with skilled talent while finding meaningful, sustainable employment for millions of people across a wide range of industries and skills. Our expert family of brands – Manpower, Experis, Talent Solutions, and Jefferson Wells – creates substantial value for candidates and clients across more than 75 countries and territories and has done so for over 70 years. We are recognized consistently for our diversity - as a best place to work for Women, Inclusion, Equality and Disability and in 2023 ManpowerGroup was named one of the World's Most Ethical Companies for the 14th year - all confirming our position as the brand of choice for in-demand talent.

Job Title – Associate Scientist II - Molecular & Cellular Biology Location – Kansas City MO 64137 Duration – 6+ months contract position, with the possibility of extension Shift Time – Mon – Fri 8AM – 4PM Position Summary: • Associate Scientist II is primarily responsible for testing samples, drafting methods and reporting data under cGMP regulatory guidance for Large Molecules/Biologics product development and related stability studies., • In support of Large Molecules/Biologics Therapeutics, will execute laboratory testing using the following techniques as required:, • Mammalian cell culture, • Sterile technique, • In vitro cell based assays (e.g., reporter gene bioassay, cell titer glo proliferation bioassay, etc.), • ELISA assays, quantitative and potency (fluorescence, luminescence, colorimetric, MSD), • Molecular biology (e.g., qPCR, PCR, etc.), • Kinetic binding assessment (e.g., BLI or SPR), • Flow cytometry, • Other technologies/methodologies as required by management Essential Functions: • Reads and follows Standard Operating procedures with attention to details, • Successfully trains on 1-2 methods and/or techniques mentioned above and performs adhoc sample testing activities under cGMP as required, • Applies basic scientific and laboratory concepts and theories related to specific testing in the group, • Follow cGMP requirements for legible, accurate and thorough documentation to meet regulatory compliance. Supports drafting of simple methods, method forms and result reports., • Adheres to policies, processes, and procedures for operating laboratory equipment in a safe and compliant manner, • Understands the Catalent culture, programs, and communication processes regarding quality, safety, and ethical practices, • All other duties as assigned III. Position Requirements Education and Experience: • Bachelor’s Degree in Life Sciences or Physical Science field. No work experience required, Knowledge/Skills Requirements: • High Proficiency in Microsoft Office, Word, Excel, Outlook, • Maintain high quality documentation in accordance with applicable regulatory guidance and Site SOPs., • Ability to learn and retain technical information., • Proactively address work issues at both an individual level and a team level., • Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form., • Mathematical and scientific reasoning ability., • Excellent written and verbal communications skills with internal and external customers., • Lead by example according to Catalent's values and culture., • Strategy is focused on personal time management and efficiency., • Well organized with ability to multitask., • Ability to work effectively under pressure to meet deadlines. Company Overview: • Infojini Consulting is a Staffing and Recruitment company and incorporated in Baltimore, MD., • Infojini caters various hospitals, health & wellness centers, pharmacy, and medical facilities over fifty states across the United States

CONTRACT-TO-HIRE: 6 months MUST HAVES: • Bachelor’s Degree in Life Sciences or Physical Science field. No work experience required., • Basic knowledge of the principles and concepts of a discipline (e.g., Biology, Chemistry, Biochemistry), • Experience with a few of the following laboratory techniques: mammalian cell culture, qPCR, PCR, ELISA, MSD, and In vitro cell based assays Position Overview Associate Scientist II is primarily responsible for testing samples, drafting methods and reporting data under cGMP regulatory guidance for Large Molecules/Biologics product development and related stability studies. In support of Large Molecules/Biologics Therapeutics, will execute laboratory testing using the following techniques as required: • Mammalian cell culture, • Sterile technique, • In vitro cell based assays (e.g., reporter gene bioassay, cell titer glo proliferation bioassay, etc.), • ELISA assays, quantitative and potency (fluorescence, luminescence, colorimetric, MSD), • Molecular biology (e.g., qPCR, PCR, etc.), • Kinetic binding assessment (e.g., BLI or SPR), • Flow cytometry, • Other technologies/methodologies as required by management Essential Functions: • Reads and follows Standard Operating procedures with attention to details, • Successfully trains on 1-2 methods and/or techniques mentioned above and performs adhoc sample testing activities under cGMP as required, • Applies basic scientific and laboratory concepts and theories related to specific testing in the group, • Follow cGMP requirements for legible, accurate and thorough documentation to meet regulatory compliance. Supports drafting of simple methods, method forms and result reports., • Adheres to policies, processes, and procedures for operating laboratory equipment in a safe and compliant manner, • Understands the Catalent culture, programs, and communication processes regarding quality, safety, and ethical practices, • All other duties as assigned Position Requirements Education and Experience: • Bachelor’s Degree in Life Sciences or Physical Science field. No work experience required Knowledge/Skills Requirements: • Has basic knowledge of the principles and concepts of a discipline (e.g., Biology, Chemistry, Biochemistry)., • Excellent written and verbal communications skills with internal customers, colleagues, and supervisor, • Well organized with ability to multitask and be flexible with daily work schedule, • Ability to work effectively under pressure to meet deadlines, • Ability to pay attention to detail and exhibit critical thinking

• TEMP TO HIRE, • DURATION - 6 MONTHS, • SHIFT - MON-FRI 8AM-4PM, • ONSITE POSITION Position Overview Associate Scientist II is primarily responsible for testing samples, drafting methods and reporting data under cGMP regulatory guidance for Large Molecules/Biologics product development and related stability studies. In support of Large Molecules/Biologics Therapeutics, will execute laboratory testing using the following techniques as required: • Mammalian cell culture, • Sterile technique, • In vitro cell based assays (e.g., reporter gene bioassay, cell titer glo proliferation bioassay, etc.), • ELISA assays, quantitative and potency (fluorescence, luminescence, colorimetric, MSD), • Molecular biology (e.g., qPCR, PCR, etc.), • Kinetic binding assessment (e.g., BLI or SPR), • Flow cytometry, • Other technologies/methodologies as required by management II. Essential Functions • Reads and follows Standard Operating procedures with attention to details, • Successfully trains on 1-2 methods and/or techniques mentioned above and performs ad-hoc sample testing activities under cGMP as required, • Applies basic scientific and laboratory concepts and theories related to specific testing in the group, • Follow cGMP requirements for legible, accurate and thorough documentation to meet regulatory compliance. Supports drafting of simple methods, method forms and result reports., • Adheres to policies, processes, and procedures for operating laboratory equipment in a safe and compliant manner, • Understands the culture, programs, and communication processes regarding quality, safety, and ethical practices, • All other duties as assigned III. Position Requirements Education and Experience: • Bachelor’s Degree in Life Sciences or Physical Science field. No work experience required. Knowledge/Skills Requirements: • Has basic knowledge of the principles and concepts of a discipline (e.g., Biology, Chemistry, Biochemistry)., • Excellent written and verbal communications skills with internal customers, colleagues, and supervisor, • Well organized with ability to multitask and be flexible with daily work schedule, • Ability to work effectively under pressure to meet deadlines, • Ability to pay attention to detail and exhibit critical thinking

Title: Associate Scientist II - Molecular & Cellular Biology Location: Kansas City MO 64137 Duration: 6 Months Shift - Mon-Fri 8AM - 4PM I. Position Overview Associate Scientist II is primarily responsible for testing samples, drafting methods and reporting data under cGMP regulatory guidance for Large Molecules/Biologics product development and related stability studies. In support of Large Molecules/Biologics Therapeutics, will execute laboratory testing using the following techniques as required: • Mammalian cell culture, • Sterile technique, • In vitro cell based assays (e.g., reporter gene bioassay, cell titer glo proliferation bioassay, etc.), • ELISA assays, quantitative and potency (fluorescence, luminescence, colorimetric, MSD), • Molecular biology (e.g., qPCR, PCR, etc.), • Kinetic binding assessment (e.g., BLI or SPR), • Flow cytometry, • Other technologies/methodologies as required by management

Associate Scientist II is primarily responsible for testing samples, drafting methods and reporting data under cGMP regulatory guidance for Large Molecules/Biologics product development and related stability studies. In support of Large Molecules/Biologics Therapeutics, will execute laboratory testing using the following techniques as required: • Mammalian cell culture, • Sterile technique, • In vitro cell based assays (e.g., reporter gene bioassay, cell titer glo proliferation bioassay, etc.), • ELISA assays, quantitative and potency (fluorescence, luminescence, colorimetric, MSD), • Molecular biology (e.g., qPCR, PCR, etc.), • Kinetic binding assessment (e.g., BLI or SPR), • Flow cytometry, • Other technologies/methodologies as required by management II. Essential Functions • Reads and follows Standard Operating procedures with attention to details, • Successfully trains on 1-2 methods and/or techniques mentioned above and performs adhoc sample testing activities under cGMP as required, • Applies basic scientific and laboratory concepts and theories related to specific testing in the group, • Follow cGMP requirements for legible, accurate and thorough documentation to meet regulatory compliance. Supports drafting of simple methods, method forms and result reports., • Adheres to policies, processes, and procedures for operating laboratory equipment in a safe and compliant manner, • All other duties as assigned III. Position Requirements Education and Experience: • Bachelor’s Degree in Life Sciences or Physical Science field. No work experience required Knowledge/Skills Requirements: • Has basic knowledge of the principles and concepts of a discipline (e.g., Biology, Chemistry, Biochemistry)., • Excellent written and verbal communications skills with internal customers, colleagues, and supervisor, • Well organized with ability to multitask and be flexible with daily work schedule, • Ability to work effectively under pressure to meet deadlines, • Ability to pay attention to detail and exhibit critical thinking

Job Details: Job Title: Associate Scientist II Location: Kansas City MO Duration - 06 Months - Temp to Hire Onsite Position - Shift - Mon-Fri 8am - 4:30pm ( Open for recent grads to apply ) Job Description: Associate Scientist II is primarily responsible for testing samples, drafting methods and reporting data under cGMP regulatory guidance for Large Molecules/Biologics product development and related stability studies. In support of Large Molecules/Biologics Therapeutics, will execute laboratory testing using the following techniques as required: • Mammalian cell culture, • Sterile technique, • In vitro cell based assays (e.g., reporter gene bioassay, cell titer glo proliferation bioassay, etc.), • ELISA assays, quantitative and potency (fluorescence, luminescence, colorimetric, MSD), • Molecular biology (e.g., qPCR, PCR, etc.), • Kinetic binding assessment (e.g., BLI or SPR), Flow cytometry, • Other technologies/methodologies as required by management II. Essential Functions • Reads and follows Standard Operating procedures with attention to details, • Successfully trains on 1-2 methods and/or techniques mentioned above and performs adhoc sample testing activities under cGMP as required, • Applies basic scientific and laboratory concepts and theories related to specific testing in the group, • Follow cGMP requirements for legible, accurate and thorough documentation to meet regulatory compliance. Supports drafting of simple methods, method forms and result reports., • Adheres to policies, processes, and procedures for operating laboratory equipment in a safe and compliant manner, • Understands the culture, programs, and communication processes regarding quality, safety, and ethical practices, • All other duties as assigned Education and Experience: • Bachelor’s Degree in Life Sciences or Physical Science field. No work experience required Knowledge/Skills Requirements: • Has basic knowledge of the principles and concepts of a discipline (e.g., Biology, Chemistry, Biochemistry)., • Excellent written and verbal communications skills with internal customers, colleagues, and supervisor, • Well organized with ability to multitask and be flexible with daily work schedule, • Ability to work effectively under pressure to meet deadlines, • Ability to pay attention to detail and exhibit critical thinking EEO: “Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of – Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans.”

Job Description Open position in RADaR office locations, including Kansas City, MO, Columbia, MO, and St. Louis, MO; Hybrid work schedule: 3 days in the office, 2 days working from home Visa sponsorship is not available for this position, now or in the future. Applicants must be legally authorized to work in the United States on a permanent basis without requiring employer sponsorship. We're seeking a Data Scientist with exceptional statistical expertise to join our team. In this role, you'll work directly with advertising agencies and brands to analyze customer behavior patterns and advertising performance, developing sophisticated machine learning models that inform strategic marketing decisions. Essential Duties and Responsibilities (Other duties may be assigned) • Conduct deep statistical analysis of customer behavior data and advertising performance metrics across multiple channels and campaigns, • Design, develop, and deploy machine learning models to predict customer responses, optimize advertising spend, and identify high-value audience segments, • Perform advanced statistical modeling including regression analysis, hypothesis testing, time series analysis, and causal inference, • Build predictive models for customer lifetime value, churn prediction, attribution modeling, and campaign optimization, • Communicate complex analytical findings to both technical and non-technical stakeholders through compelling data visualizations and presentations, • Develop automated reporting solutions and dashboards that enable clients to monitor campaign performance in real-time, • Collaborate with cross-functional teams to ensure data quality and integrity across all analytics initiatives, • 3+ years of professional experience applying statistical methods and machine learning to business problems, • Strong foundation in statistical theory including probability, inference, experimental design, and multivariate analysis, • Demonstrated expertise in machine learning algorithms (e.g., random forests, gradient boosting, neural networks, clustering methods), • Proficiency in Python or R for statistical analysis and machine learning, including libraries such as scikit-learn, pandas, NumPy, statsmodels, • Experience with SQL and working with large-scale databases, • Proven ability to design and analyze A/B tests and controlled experiments, • Track record of translating complex analytical insights into clear, actionable business recommendations, • Experience working with advertising agencies, marketing teams, or in the ad tech industry, • Knowledge of digital advertising platforms (Google Ads, Facebook Ads, programmatic platforms), • Familiarity with marketing attribution models and multi-touch attribution methods, • Experience with cloud computing platforms (AWS, GCP, or Azure), • Knowledge of causal inference methods and their application to marketing effectiveness, • The chance to be a part of a growing company and the next success story, • Amazing opportunities for career development, • Recognition programs, • Employee referral bonus, • Hybrid work schedule; 3 days in the office, 2 days working from home, • Fun and collaborative work environment, • Casual dress code, • Insurance Coverage (medical, dental, vision, life, and disability), • 401(k) retirement plan, with employer 4% match, • Work/life benefits, including mental health and wellbeing support, • Flexible Time Off Policy, • Paid holidays, including agency closing Christmas Eve-New Year's Day

Job Description Duration: 6 months Contract (Temp To Hire) SHIFT - MON-FRI 8AM - 4PM - ONSITE POSITION. Education and Experience: • Bachelor’s Degree in Life Sciences or Physical Science field. No work experience required, Knowledge/Skills Requirements: • High Proficiency in Microsoft Office, Word, Excel, Outlook, • Maintain high quality documentation in accordance with applicable regulatory guidance and Site SOPs., • Ability to learn and retain technical information., • Proactively address work issues at both an individual level and a team level., • Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form., • Mathematical and scientific reasoning ability., • Excellent written and verbal communications skills with internal and external customers., • Lead by example according to client's values and culture., • Strategy is focused on personal time management and efficiency., • Well organized with ability to multitask., • Ability to work effectively under pressure to meet deadlines. Position 2: Position Overview Associate Scientist II is primarily responsible for testing samples, drafting methods and reporting data under cGMP regulatory guidance for Large Molecules/Biologics product development and related stability studies. In support of Large Molecules/Biologics Therapeutics, will execute laboratory testing using the following techniques as required: • Mammalian cell culture, • Sterile technique, • In vitro cell based assays (e.g., reporter gene bioassay, cell titer glo proliferation bioassay, etc.), • ELISA assays, quantitative and potency (fluorescence, luminescence, colorimetric, MSD), • Molecular biology (e.g., qPCR, PCR, etc.), • Kinetic binding assessment (e.g., BLI or SPR), • Flow cytometry, • Other technologies/methodologies as required by management II. Essential Functions • Reads and follows Standard Operating procedures with attention to details, • Successfully trains on 1-2 methods and/or techniques mentioned above and performs adhoc sample testing activities under cGMP as required, • Applies basic scientific and laboratory concepts and theories related to specific testing in the group, • Follow cGMP requirements for legible, accurate and thorough documentation to meet regulatory compliance. Supports drafting of simple methods, method forms and result reports., • Adheres to policies, processes, and procedures for operating laboratory equipment in a safe and compliant manner, • Understands the client culture, programs, and communication processes regarding quality, safety, and ethical practices, • All other duties as assigned III. Position Requirements Education and Experience: • Bachelor’s Degree in Life Sciences or Physical Science field. No work experience required Knowledge/Skills Requirements: • Has basic knowledge of the principles and concepts of a discipline (e.g., Biology, Chemistry, Biochemistry)., • Excellent written and verbal communications skills with internal customers, colleagues, and supervisor, • Well organized with ability to multitask and be flexible with daily work schedule, • Ability to work effectively under pressure to meet deadlines, • Ability to pay attention to detail and exhibit critical thinking Company DescriptionWith almost four decades of experience as a proven industry leader, Acro continues to be consistently recognized among the Best & Brightest Companies to Work for in the United States. As an international professional services firm with deep expertise in consulting and staff augmentation offering a variety of solutions including MSP, VMS, RPO, HRO (and more), Acro operates across North America, Europe, and Asia from over 30 locations. Acro’s client portfolio includes some of the most well-known names in business and provides services across all verticals including technology, aerospace, energy, automotive, government, and manufacturing. To learn more, please visit almost four decades of experience as a proven industry leader, Acro continues to be consistently recognized among the Best & Brightest Companies to Work for in the United States. As an international professional services firm with deep expertise in consulting and staff augmentation offering a variety of solutions including MSP, VMS, RPO, HRO (and more), Acro operates across North America, Europe, and Asia from over 30 locations. Acro’s client portfolio includes some of the most well-known names in business and provides services across all verticals including technology, aerospace, energy, automotive, government, and manufacturing. To learn more, please visit .

Job Description ASSOCIATE SCIENTIST - COMPLIANCE | ESSENTIAL FUNCTIONS: Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. • Ability to understand and implement permit parameters effectively for sampling or other requirements for several different industries., • Perform Spill Prevention, Control, and Countermeasure (SPCC) and Stormwater Pollution Prevention Plan (SWPPP) Resource Conservation and Recovery Act (RCRA) inspections of regulated areas and outfalls as required by state-specific or site-specific permits., • Inspections include visual monitoring of stormwater Best Management Practices (BMPs) and escalation of required corrective actions to be implemented including significant new materials or regulated activities that drive plan/permit changes, non-stormwater discharge evaluations, stormwater discharge visual assessment., • Complete sampling requirements (visual or analytical sampling requirements) on-time in a safe and time-efficient manner., • Ability to review the analytical data from the sampling results and notify the project or program manager(s) of any exceedances or overages., • Track inspections and sampling requirements, corrective actions/corrective actions reports (CARs), and communication with project/program managers., • Request information and communicate with various governmental and regulatory organizations., • Develop and maintain relationships with employees at all locations., • Conduct activities in a safe and healthy manner and work in accordance with established OSHA and internal requirements., • Required to follow safety standards. Required to wear all personal protective equipment (PPE) in designated areas., • Promote a positive working environment in order to achieve the organization's goals., • Help project manager perform environmental audits, as assigned, for ISO 14001 program, other regulatory programs, or as requested by clients., • Perform other duties as assigned ASSOCIATE SCIENTIST - COMPLIANCE | COMPETENCIES: • Excellent communication skills, both oral and written., • High level of attention to detail., • Ability to read and interpret a variety of maps and aerial photography., • Capable of managing deadline-driven projects and workload., • Ability to work in both a field and office environment., • Understand and interpret regulatory guidelines., • Analyze numerical and graphic data., • Strong organizational skills., • Requires effective time management skills, personal conduct, and change management abilities with the ability to multi-task., • Must be extremely reliable, have a curiosity for problem solving, a desire to learn and succeed and a high level of energy., • Ability to meet deadlines and communicate effectively., • Ability to work independently and efficiently., • For insurability purposes a valid Driver's License is required., • Must be able to attain Class E Driver’s License within first week of employment., • Must complete 40-hour HAZWOPER training within the first 2 weeks of employment., • Must be able to pass a DOT and Hazmat Physical., • One (1) - three (3) year experience in and/ or exposure to environmental consulting, compliance., • This is a full-time position. Ability to work flexible hours required. Work is performed mostly in an uncontrolled atmosphere. Exposure to harsh conditions such as: dust, fumes, chemicals, hazardous materials, noise, and varying weather and temperatures for long periods of time is possible. All employees are required to follow safety standards and wear all personal protective equipment in designated areas. Work in diverse environments such as confined spaces, various heights, and storage tanks. Work outdoors in all weather conditions; extreme heat, cold, dry or wet environment. ASSOCIATE SCIENTIST - COMPLIANCE | PHYSICAL DEMANDS: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. While performing the duties of this position, the employee is regularly required to walk, stand, use hands and fingers, grip, handle or feel; reach with hands and arms; climb or balance; stoop, kneel, crouch or crawl; and talk and hear. Ability to regularly lift and carry 50 pounds. Sitting 30%, standing/walking 70%. SALARY RANGE: $55,000 to $70,000 BENEFITS • 1700/3400 Deductible Health Insurance Plans Available, • 3400 includes Health Savings Plan (HSA) Company Contribution with Employee Contribution, • Dental, • Vision, • Health Savings Account (HSA), • 401k | Up to 4% Company Match ADDITIONAL BENEFITS • Tuition Reimbursement, • Career and Personal Development Resources and Training, • Safety Boot Reimbursement, • Gym Membership Reimbursement, • Company Cell Phone, • Company paid lodging and per diem, • Quarterly Bonus when eligible EEO: Environmental Works, Inc. is committed to maintaining a workplace that is free from discrimination on the basis of race, gender, religion, color, national origin, sexual orientation, age, marital status, veteran status, disability status, or any other characteristic protected by federal, state, or local laws. We strive to create a diverse and inclusive work environment where all employees are treated with kindness and respect. #IND

Job Description Title: Associate Scientist II - Molecular & Cellular Biology Location: Kansas City MO 64137 Duration: 6 Months Shift - Mon-Fri 8AM - 4PM I. Position Overview Associate Scientist II is primarily responsible for testing samples, drafting methods and reporting data under cGMP regulatory guidance for Large Molecules/Biologics product development and related stability studies. In support of Large Molecules/Biologics Therapeutics, will execute laboratory testing using the following techniques as required: • Mammalian cell culture, • Sterile technique, • In vitro cell based assays (e.g., reporter gene bioassay, cell titer glo proliferation bioassay, etc.), • ELISA assays, quantitative and potency (fluorescence, luminescence, colorimetric, MSD), • Molecular biology (e.g., qPCR, PCR, etc.), • Kinetic binding assessment (e.g., BLI or SPR), • Flow cytometry, • Other technologies/methodologies as required by management II. Essential Functions • Reads and follows Standard Operating procedures with attention to details, • Successfully trains on 1-2 methods and/or techniques mentioned above and performs adhoc sample testing activities under cGMP as required, • Applies basic scientific and laboratory concepts and theories related to specific testing in the group, • Follow cGMP requirements for legible, accurate and thorough documentation to meet regulatory compliance. Supports drafting of simple methods, method forms and result reports., • Adheres to policies, processes, and procedures for operating laboratory equipment in a safe and compliant manner, • Understands the client culture, programs, and communication processes regarding quality, safety, and ethical practices, • All other duties as assigned III. Position Requirements Education and Experience: • Bachelor’s Degree in Life Sciences or Physical Science field. No work experience required Knowledge/Skills Requirements: • Has basic knowledge of the principles and concepts of a discipline (e.g., Biology, Chemistry, Biochemistry)., • Excellent written and verbal communications skills with internal customers, colleagues, and supervisor, • Well organized with ability to multitask and be flexible with daily work schedule, • Ability to work effectively under pressure to meet deadlines, • Ability to pay attention to detail and exhibit critical thinking

Job DescriptionPerforming critical work that impacts our industry and our world’s health while problem solving and innovating in the field – that is what Principal Scientists at KCAS Bio get to do every day. If that gets you excited too, then maybe working as a Principal Scientist at KCAS Bio is the role for you. As a Principal Scientist on the KCAS BioPharma services team, you get to further our mission as a core technical expert in quantifying proteins and anti-drug antibodies. You will provide oversight in the areas of early drug discovery, preclinical toxicology work, and clinical studies, including multiplexing by LBA (ligand binding assays) platforms, LCMS (liquid chromatography mass spectrometry), and flow cytometry. In this role, we will rely on you to: • Function independently as a Principal Scientist and technical expert in the direction and execution of bioanalytical validations and biostudies as required., • Provide oversight of the laboratory and mentor research staff in areas such as protocol interpretation, method development and refinement, study-related problem resolution, and technique validation, as well as providing scientific expertise in study design, conduct, and interpretation., • Independently review, interpret, analyze, evaluate, and discuss study results with research staff and Sponsors., • Prepare high-quality final reports appropriate for the study, including integration of supporting subcontractor(s)’ reports into final reports as required., • Supervise research and scientific staff within the function., • Direct activities of assigned group(s), to ensure effective performance of function., • Review protocols, reports, and scientific documents of direct reports as required., • Provide scientific and technical leadership within the designated business unit to resolve analytical challenges in a timely fashion, and to evaluate new technologies for potential integration into the existing portfolio of services., • Provide direct daily supervision and review the work of assigned departmental employees, to ensure scientific accuracy and adherence to departmental policies, practices, and procedures. Schedule and prioritize direct reports' workload., • Ensure effective communication within departmental groups, to provide overlap of diverse expertise. Implement techniques to improve productivity, increase efficiencies, and maintain state-of-the-art practices., • Monitor and increase the technical performance and expertise of departmental direct reports through coaching and mentoring. Prepare and deliver salary and performance reviews; review and approve salary appraisals initiated by direct reports., • Attend scientific meetings, conferences, and training courses to enhance job and professional skills. Present abstracts/posters at national meetings, when appropriate, to maintain a scientific presence and visibility in areas of individual expertise., • Ensure that reports, raw data specimens, and supporting study documentation are transferred to the archives at the close of each study., • Ensure effective communication within departmental groups to provide expertise in Sponsor calls, presentation materials, and pricing information., • Perform other related duties as assigned.To qualify specifically for this role, you will have:, • At least six years of relevant experience within contract research, academic or pharmaceutical industry, including expertise in the core competencies of validation and bioanalysis of study samples. Also requires a full understanding of GLPs, and departmental/company SOPs., • Experience designing, planning, and executing bioanalytical assays (ADA, PK, Biomarker and Nab), method development and validation., • Proficient in using common immunoassay platforms (ELISA, MSD, Luminex, etc.), • Experience designing complex experiments & evaluating outcome vs. regulatory guidelines, white papers, and current industry practices., • Experience troubleshooting problems and actively participating in the life cycle management of assays., • Ability to manage multiple moderate to highly complex projects, prioritizes work, and meets deadlines., • Capable of anticipating and recognizing potential problems within programs and effectively communicate alternatives to clients in a meaningful fashion., • Must have proven record of delivering quality service to customers on time and on budget., • Expert knowledge of applicable lab techniques., • Familiarity with current industry trends and expectations.

Job DescriptionSalary: commensurate with experience At Argenta, we partner with our customers to take animal health solutions from molecule to market. Our teams combine deep scientific expertise with world-class manufacturing capabilities to deliver innovative therapies that improve the lives of animals around the world. About the Role Argenta is seeking a Research & Development Analytical Scientist to join our Global CDO team at our Shawnee, KS facility. This role is an excellent opportunity for a motivated and driven individual to contribute to our Global CDO team and showcase their ability to muti-task. Key Responsibilities • Conduct qualitative and quantitative chemical analysis and experiments for active pharmaceutical ingredients and pharmaceutical products as per project requirements, • Assist in the development of new products and processes as per compliance and regulatory requirements, • Assist with the technology transfer (methods and products) from Argenta Research into Argenta Manufacturing, • Support the Research & Development efforts of the company by providing scientific and technical support for the development of new products., • Create and maintain activity plans for assigned projects, • Generate, document and review technical data for internal reports, client reports and CMC regulatory support documents. About You • Bachelors degree in science related field, • Previous experience in pharmaceutical industry, animal health industry or related field preferred, • Previous experience in analytical pharmaceutical development preferred, • Strong oral and written communication skills, • Ability to work independently and handle multiple projects and able to adapt to rapidly changing priorities, • Ability to work with outside customers and clients Why Join Argenta? At Argenta, we are building a culture of ownership where our people play a direct role in shaping the future of the organization. You will work alongside passionate experts across science, manufacturing and commercial functions to deliver life-changing outcomes for animals worldwide. We offer the opportunity to work within a growing, global business where your leadership and expertise will have a meaningful impact on performance, transformation, and long-term success. We areOne Argenta- working together across teams, disciplines and geographies to create meaningful impact.

Job Description Title: Associate Scientist II - BioChemical Analysis Location: Kansas City MO 64137 Duration: 6 Months I. Position Overview Associate Scientist II is primarily responsible for testing samples, drafting methods and reporting data under cGMP regulatory guidance for Large Molecules/Biologics product development and related stability studies. In support of Large Molecules/Biologics Therapeutics, will execute laboratory testing using the following techniques as required: ▪ Compendial assays, (i.e., appearance. pH, Osmolality, Particulate measurements, Viscosity etc.) ▪ Karl Fischer ▪ UV-Vis ▪ HPLC/UPLC techniques/methods (e.g., SEC, IEX, RP-HPLC, HIC, peptide map, glycan analysis, etc.) ▪ Aggregation techniques such as MFI, AUC, SEC-MALS ▪ Capillary and Gel Electrophoresis (e.g., CE-SDS, SDS-PAGE, icIEF, IEF, western blot, etc.) ▪ FTIR, CD, Intrinsic Fluorescence, DSC ▪ Other technologies/methodologies as required by management II. Essential Functions ▪ Reads and follows Standard Operating procedures with attention to details ▪ Successfully trains on 1-2 methods and/or techniques mentioned above and performs adhoc sample testing activities under cGMP as required ▪ Applies basic scientific and laboratory concepts and theories related to specific testing in the group ▪ Follow cGMP requirements for legible, accurate and thorough documentation to meet regulatory compliance. Supports drafting of simple methods, method forms and result reports. ▪ Adheres to policies, processes, and procedures for operating laboratory equipment in a safe and compliant manner ▪ Understands the Client culture, programs, and communication processes regarding quality, safety, and ethical practices ▪ All other duties as assigned III. Position Requirements Education and Experience: ▪ Bachelor’s Degree in Life Sciences or Physical Science field. No work experience required Knowledge/Skills Requirements: ▪ Has basic knowledge of the principles and concepts of a discipline (e.g., Biology, Chemistry, Biochemistry). ▪ Excellent written and verbal communications skills with internal customers, colleagues, and supervisor ▪ Well organized with ability to multitask and be flexible with daily work schedule ▪ Ability to work effectively under pressure to meet deadlines ▪ Ability to pay attention to detail and exhibit critical thinking

Job DescriptionPerforming critical work that impacts our industry and our world’s health while problem solving and innovating in the field – that is what we get to do every day at KCAS Bio. If that gets you excited too, then maybe working at KCAS Bio is for you. When you work as an Analyst at KCAS in the method development team, you get to further our mission by being part of a growing team that is responsible for helping to develop methods for both large and small molecule assays, utilizing skills including sample prep, instrumentation, and data analysis, with a focus on LC-MS/MS quantification or targeted proteomics. Our LC-MS/MS team uses LCMS (Liquid Chromatography Mass Spectrometry) techniques to conduct sophisticated sample preparation to meet bioanalytical needs for drug discovery, preclinical, and clinical studies, including bioanalysis of drugs and metabolites, biomarkers, and active endogenous compounds in biological fluids and tissues. In this roll, we will rely on you to: • Contribute to all phases of assigned projects including sample preparation (extractions, enrichments/affinity capture, digestions), method development and qualification for LCMS, troubleshooting, data analysis and report generation., • Work with a lead scientist to identify critical experiments and deliver results., • Able to setup and change instrument configurations for various LCMS methods., • Prepare data summaries for senior scientists to aid in client updates.To qualify for this roll, you will have:, • BS/BA degree in Chemistry, Biochemistry, chemical/biochemical engineering, or related field, • Experience with wet chemistry

Job Title: Associate Scientist II - BioChemical Analysis Location : Kansas City MO - ONSITE Duration: 6 months with possible extensions Pay: $26.00 / HR Shift: MON-FRI 8AM - 4:00PM Position Overview: The Associate Scientist II is primarily responsible for testing samples, drafting methods and reporting data under cGMP regulatory guidance for Large Molecules/Biologics product development and related stability studies. In support of Large Molecules/Biologics Therapeutics, will execute laboratory testing using the following techniques as required: Karl Fischer * UV-Vis * HPLC/UPLC techniques/methods (e.g., SEC, IEX, RP-HPLC, HIC, peptide map, glycan analysis, etc.) * Aggregation techniques such as MFI, AUC, SEC-MALS * Capillary and Gel Electrophoresis (e.g., CE-SDS, SDS-PAGE, icIEF, IEF, western blot, etc.) * FTIR, CD, Intrinsic Fluorescence, DSC * Other technologies/methodologies as required by management Essential Functions * Reads and follows Standard Operating procedures with attention to details * Successfully trains on 1-2 methods and/or techniques mentioned above and performs adhoc sample testing activities under cGMP as required Education and Experience: Well organized with ability to multitask and be flexible with daily work schedule * Ability to work effectively under pressure to meet deadlines * Ability to pay attention to detail and exhibit critical thinking Why Kelly? Kelly puts you in charge of your career, with access to cutting edge projects and technologies in industry leading organizations. Top companies throughout the world have trusted Kelly as a premier source of engineering & scientific talent and services since 1965. And Engineering & Scientific job seekers know Kelly as a firm with an unmatched reputation for quality, integrity and professionalism. Whether you seek the variety and flexibility of working on short-term project engagements or prefer contract-to-hire or direct hire placement with our clients, apply with Kelly to explore opportunities that suit your specific professional interests. 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As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here () for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community. Why Kelly Science & Clinical? Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world's most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals-it's the way we think job searching should be. 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Position Title Medical Lab Scientist - Core Lab 03/19/2026 03/19/2026, 2:07:25.658 PM R-48678 Medical Lab Scientist - Core Lab (Open), Edit Job Requisition Additional Data: Medical Lab Scientist - Core Lab Bell Hospital Position Summary / Career Interest: The Medical Lab Scientist provides comprehensive laboratory testing for patients. The position consists of ensuring patients' laboratory results are accurate, timely and with quality. Responsibilities and Essential Job Functions Analyzes patient, control and proficiency testing specimens and records results in a timely manner according to laboratory policy. Calibrates, maintains, operates and troubleshoots instrumentation issues and completes appropriate documentation. Completes continuing education and submits appropriate documentation where applicable. Follows regulatory, accreditation, safety and hospital standards, policies and procedures. Instructs, orients and mentors students, employees, residents, patients and other health care providers as applicable. Maintains an adequate inventory of all supplies. Accurately prepares, labels and stores reagents, standards, controls and specimens for analysis. Participates in quality assurance and quality improvement activities. Performs phlebotomy and sample collection as applicable. Reviews and correlates results of laboratory tests to each other and with the patient's condition, recognizing abnormal results and critical/alert values. Verifies accuracy of results and initiates corrective action when indicated. The employee may be required to float to other locations throughout the organization. Performs product preparations in compliance with FDA, cGMP, AABB standards and blood bank department procedures, if applicable. Uses personal protective equipment (PPE) as necessary to perform job duties safely and minimize risk. Must be able to perform the professional, clinical and or technical competencies of the assigned unit or department. These statements are intended to describe the essential functions of the job and are not intended to be an exhaustive list of all responsibilities. Skills and duties may vary dependent upon your department or unit. Other duties may be assigned as required. Required Education and Experience Bachelor of Science Biological, Physical, Chemical or Clinical Laboratory Science / Medical Technology from an accredited institution High School Graduate Required Licensure and Certification Medical Laboratory Scientist (MLS) - American Society for Clinical Pathology Board of Certification (ASCP) AMT or equivalent or eligible (must be completed within 6 months of hire) within 180 Days Knowledge Requirements Meets the CLIA requirements for high complexity testing. Time Type: Full time Job Requisition ID: R-48678 Important information for you to know as you apply: The health system is an equal employment opportunity employer. Qualified applicants are considered for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), national origin, ancestry, age, disability, veteran status, genetic information, or any other legally-protected status. See also Diversity, Equity & Inclusion . The health system provides reasonable accommodations to qualified individuals with disabilities. If you need to request reasonable accommodations for your disability as you navigate the recruitment process, please let our recruiters know by requesting an Accommodation Request form using this link . Employment with the health system is contingent upon, among other things, agreeing to the health-system-dispute-resolution-program.pdf and signing the agreement to the DRP. Need help finding the right job? We can recommend jobs specifically for you! Create a custom Job Alert by selecting criteria that suit your career interests.