Senior principal scientist jobs in Springdale, AR - 445 jobs

Current University of Arkansas System employees, including student employees and graduate assistants, need to log in to Workday via MyApps.Microsoft.com, then access Find Jobs from the Workday search bar to view and apply for open positions. Students at all University of Arkansas institutions will view open positions and apply within Workday by searching for "Find Jobs for Students." University of Arkansas, Fayetteville students will view open positions and apply within Workday by searching for "Find Student Jobs at UAF." All Job Postings will close at 12:01 a.m. CT on the specified Closing Date (if designated). If you close the browser or exit your application prior to submitting, the application process will be saved as a draft. You will be able to access and complete the application through "My Draft Applications" located on your Candidate Home page. Closing Date: 01/23/2026 Type of Position: Researchers and Scientists Workstudy Position: No Job Type: Fixed Duration of Project/Grant (Fixed Term) Work Shift: Sponsorship Available: No Institution Name: University of Arkansas, Fayetteville Founded in 1871, the University of Arkansas is a land grant institution, classified by the Carnegie Foundation among the nation's top 2 percent of universities with the highest level of research activity. The University of Arkansas works to advance the state and build a better world through education, research, and outreach by providing transformational opportunities and skills, fostering a welcoming climate, and nurturing creativity, discovery, and the spread of new ideas and innovations. The University of Arkansas campus is located in Fayetteville, a welcoming community ranked as one of the best places to live in the U.S. The growing region surrounding Fayetteville is home to numerous Fortune 500 companies and one of the nation's strongest economies. Northwest Arkansas is also quickly gaining a national reputation for its focus on the arts and overall quality of life. As an employer, the University of Arkansas offers a vibrant work environment and a workplace culture that promotes a healthy work-life balance. The benefits package includes university contributions to health, dental, life and disability insurance, tuition waivers for employees and their families, 12 official holidays, immediate leave accrual, and a choice of retirement programs with university contributions ranging from 5 to 10% of employee salary. Below you will find the details for the position including any supplementary documentation and questions, you should review before applying for the opening. If you have a disability and need assistance with the hiring process, please submit a request via the Disability Accommodations | OEOC | University of Arkansas (uark.edu) : Request an Accommodation. Applicants are required to submit a request for each position of which they have applied. For general application assistance or if you have questions about a job posting, please contact Human Resources at ************. Department: Executive Director I3R Department's Website: i3r.uark.edu Summary of Job Duties: ABOUT THE INSTITUTE FOR INTEGRATIVE & INNOVATIVE RESEARCH (I³R): Established through a transformative gift from the Walton Family Charitable Support Foundation, the Institute for Integrative and Innovative Research (I3R) at University of Arkansas pioneers solutions to wicked problems through convergence research across academic, industry, government, and non-profit sectors to make a positive societal impact by creating and deploying innovations at scale. You will have the opportunity to collaborate with purpose-driven coworkers in one of the fastest-growing and most naturally beautiful regions in the U.S. You will join a growing team of visionary researchers and thought leaders dedicated to working with a thriving entrepreneurial ecosystem to deliver innovative solutions. I³R is committed to building a diverse, collaborative, and inclusive team and cultivating a welcoming atmosphere where all opinions are valued, all voices are heard, and ideas become reality. The I3R MRI facility houses a 3-Tesla Siemens Magnetom Cima.X to support academic and clinical research and care. This state-of-the-art system is designed with several technical advances to enhance imaging capabilities, workflow efficiency, and MRI recipient experience. It has a fast gradient system capable of high-speed structural and functional imaging, and a 64-receiver channel data acquisition system for parallel imaging with acceleration, which permits faster temporal resolution for functional MRI scans. The scanner has industry-leading gradients for human MRI scanning (i.e., gradient rise time = 200 T/m/s on each of the three gradient axes; peak gradient strength = 80 mT/m per axis). Its high performance driven by superior signal-to-noise ratio and AI powered advanced technology delivers high-quality images with faster acquisition time. It has advanced coil technology with a range of options that can be adapted for various anatomical regions and imaging needs and offers sophisticated imaging sequences that support specialized applications such as functional MRI and diffusion tensor imaging. An intuitive user-friendly interface simplifies operation and offers quieter operation and comfortable design to enhance MRI recipient's comfort during scans. A mock-MRI setup is also in the facility as are adjacent rooms to conduct other human health related studies including use of EEG, and fNIRS. Besides the support potential for advanced clinical scanning, the Magnetom Cima.X offers university researchers opportunities to establish stronger collaborations with the Arkansas Children's Research Institute, the University of Arkansas for Medical Sciences, and the Laureate Institute for Brain Research, for MRI in both adult and pediatric populations. Additionally, I3R researchers conducting medical robotics and mixed reality research seek MRI imaging of various anatomical regions. POSITION DESCRIPTION: A full-time MRI Senior Research Scientist position is available at the Institute for Integrative and Innovative Research (I3R) at University of Arkansas. We are looking for a researcher who can engage in state-of-the-art, multi-modal imaging research and in the application and development of novel, advanced imaging methods and data analytic strategies and their applications. The Magnetom Cima.X offers an unprecedented opportunity to be at the forefront of establishing an outstanding research program in multimodal imaging in the Northwest Arkansas region. In addition, there is a tremendous interest and need for support of clinical imaging. Some of the areas of research interest include: 1) development and implementation of novel real-time multimodal EEG and fMRI techniques; 2) development and implementation of quantitative MRI and fMRI protocols and MRS techniques; and 3) development and implementation of techniques for analyzing large and complex data sets involving data from multiple sources (e.g., structural MRI, fMRI, DTI, EEG, bio- and behavioral data). Additional areas of research related to the candidate's expertise are welcome. This position involves supervising and supporting all aspects of the MRI facility daily operations, ongoing clinical imaging research, and scientific collaboration within the I3R and across the University of Arkansas. It is also anticipated that, through partnerships with healthcare providers, the facility will support the advanced MRI needs for the clinical patient population in Northwest Arkansas and neighboring regions. The position offers excellent opportunities in all aspects of MRI technology development, clinical applications, and data analysis in a dynamic, interactive, and transdisciplinary research environment with a diverse team of researchers that include physicists, psychologists, neuroscientists, engineers, and data scientists. The successful applicant will have the ability to work effectively on interdisciplinary teams in a fast-paced environment, work independently and collaboratively with clinical and industry partners, and have excellent communication skills. A professional demeanor and the ability to establish effective working relationships are crucial in building trust and influence to accomplish work within a setting that includes a wide array of individuals, groups, policies, and processes. SUMMARY OF JOB DUTIES: * Manage the I3R MRI facility for safe access and use under federal and state required guidelines. * Supervise MRI technologist and other MRI facility personnel. * Lead cross-functional projects with internal research and clinical (medical, operations, statistics, regulatory) teams as well as external partners. * Design and implement customized MRI (structural, functional, diffusion) image analysis methods, leveraging novel and standard methodologies. * Develop and maintain excellent direct relationships with clinical and research partners, supporting them on site or remotely such as setting parameters for MRIs, developing and updating field-specific protocols, adapting and optimizing equipment to their needs. * Maintain accurate research records and documentation of procedures. * Pursue funding to support the development and evaluation of medical imaging as a lead investigator and as collaborator. * Provide technical guidance and mentorship to researchers and graduate students. * Additional duties as assigned. Regular, reliable, and non-disruptive attendance is an essential job duty, as is the ability to create and maintain collegial, harmonious working relationships with others. Qualifications: Minimum Qualifications: * PhD or MD in Medical Physics, Engineering, Neuroscience or a relevant field with specific experience in MRI research * More than three years of postdoctoral experience * Experience in designing and executing clinical MRI studies with human participants * Evidence of direct role and contribution to the medical imaging field (publications in peer-reviewed scientific journals, presentations at imaging-related conferences and/or developed software codes) * Experience in managing multi-faceted and complex data sets and in performing statistical analysis Preferred Qualifications: * Experience with managing an MRI facility * Experience with high-field Siemens MRI systems * MRI Certified by the American Board of Medical Physics and/or certified by the American Board of MR Safety as an MR Safety Expert * Participation in clinical trials and implementation of MRI biomarkers Knowledge, Skills and Abilities: * Knowledge of structural, diffusion, functional MRI procedures and acquisition protocols * Proven expertise in programming and medical imaging & statistical software * Proven leadership, organizational, and communication skills * Highly creative with exceptional abstract problem-solving abilities and attention to detail * Excellent written and verbal communication skills, particularly the ability to present and publish complex scientific approaches and results in an interdisciplinary field as well as to maintain clear and concise documentation * Excellent ability to work effectively in a team environment, across multiple clinical sites Additional Information: This position is renewable annually based on continued need for the position, availability of funding, and satisfactory job performance. Salary Information: A minimum of $150,000 - Commensurate with education and experience. Required Documents to Apply: Cover Letter/Letter of Application, List of three Professional References (name, email, business title), Resume Optional Documents: Proof of Veteran Status Recruitment Contact Information: Julia Menke, *************** - Sr. HR Partner Crystal Ellis, Strategic Talent Acquisition Specialist, ************** All application materials must be uploaded to the University of Arkansas System Career Site ***************************************** Please do not send to listed recruitment contact. Special Instructions to Applicants: Pre-employment Screening Requirements: Criminal Background Check, Sex Offender Registry The University of Arkansas is committed to providing a safe campus community. We conduct background checks for applicants being considered for employment. Background checks include a criminal background check and a sex offender registry check. For certain positions, there may also be a financial (credit) background check, a Motor Vehicle Registry (MVR) check, and/or drug screening. Required checks are identified in the position listing. A criminal conviction or arrest pending adjudication or adverse financial history information alone shall not disqualify an applicant in the absence of a relationship to the requirements of the position. Background check information will be used in a confidential, non-discriminatory manner consistent with state and federal law. The University of Arkansas seeks to attract, develop and retain high quality faculty, staff and administrators that consistently display practices and behaviors to advance a culture that embeds equal opportunity, educational excellence and unparalleled access for all. The University of Arkansas is an equal opportunity institution. The University does not discriminate in its education programs or activities (including in admission and employment) on the basis of any category or status protected by law, including age, race, color, national origin, disability, religion, protected veteran status, military service, genetic information, sex, sexual orientation, or pregnancy. Questions or concerns about the application of Title IX, which prohibits discrimination on the basis of sex, may be sent to the University's Title IX Coordinator and to the U.S. Department of Education Office for Civil Rights. Persons must have proof of legal authority to work in the United States on the first day of employment. All Application information is subject to public disclosure under the Arkansas Freedom of Information Act. Constant Physical Activity: N/A Frequent Physical Activity: N/A Occasional Physical Activity: N/A Benefits Eligible: Yes

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!

At Sensient Technologies, we are experts in the science, art and innovation of color and flavor. We are market savvy and visionary. We are problem solvers. And we will be better with you. Are you a recent graduate or early-career scientist looking to turn your toxicology education into hands-on experience? This is a great opportunity to learn on the job, build practical regulatory skills, and work with ingredients used in everyday consumer and food-related products. You don't need years of experience, just curiosity, organization, and a willingness to learn. This role is ideal if you're self-motivated, enjoy working with data and documentation, and want to grow into a career in toxicology, regulatory affairs, or product safety. This opportunity is 100% office based in St Louis, MO. What you'll do: Conduct and support safety assessments of raw materials and ingredients, including actives, impurities, carryovers, and formulations. Assist with toxicological evaluations such as hazard identification, exposure assessment, risk characterization, and derivation of safety/risk values. Perform literature searches and data reviews to evaluate toxicological information in line with regulatory guidance. Support the preparation and maintenance of regulatory and safety documentation, including dossiers, safety summaries, and responses to regulatory or customer inquiries. Maintain toxicology databases and documentation, collaborate with cross-functional teams, and stay up to date on global chemical and food regulatory requirements. What you'll bring: Bachelor's or Master's degree in Toxicology, Pharmacology, Chemistry, Biochemistry, or a related scientific discipline. 0-2 years of relevant experience in toxicology, regulatory affairs, product stewardship, or related areas (including academic projects or internships). Foundational knowledge of toxicology and toxicokinetics (ADME) and exposure-based risk assessment across key endpoints (e.g., acute and repeated dose toxicity, genotoxicity, carcinogenicity, reproductive and developmental toxicity). Basic understanding of food ingredient and chemical regulations, such as EU REACH, CLP, Cosmetics Regulation, Food Contact Materials, or similar global frameworks. Strong organizational and project management skills, with the ability to manage data, work with regulatory databases, and communicate effectively across teams. What you'll get: Opportunity to collaborate with your colleagues, onsite 5 days per week An excellent salary, benefit offering and development opportunities A thorough and effective training experience during onboarding and beyond About Sensient: Sensient Technologies Corporation is a leading global manufacturer and marketer of colors, flavors, and extracts. Sensient employs advanced technologies at facilities around the world to develop specialty food and beverage systems, cosmetic and pharmaceutical systems, specialty colors, and other specialty and fine chemicals. The Company's customers include major international manufacturers representing most of the world's best-known brands. About Sensient Colors: Sensient Colors is a leading developer, producer, and supplier of natural and synthetic color systems for customers around the globe. The Company's high-performance products play a vital role in the manufacture of foods and beverages, cosmetic and pharmaceutical colors and coatings, and colors for agricultural uses, household cleaners and paper products. SPONSORSHIP: Due to our inability to offer visa sponsorship, we can only consider candidates who are authorized to work in (country) without the need for employment visa sponsorship. RELOCATION: We are unable to offer relocation assistance. The successful candidate will be expected to work at (location) and must reside in area or be willing to commute. THIRD PARTY AGENCY: Any unsolicited submissions received from recruitment agencies will be considered property of Sensient Technologies, and we will not be liable for any fees or obligations related to those submissions. Sensient is an Equal Opportunity Employer, headquartered in Milwaukee, Wisconsin, USA. #LI-MM1 #LI-onsite

Requisition ID 62101 Position Type (US) Full Time Workplace Arrangement About Kerry Kerry is the world's leading taste and nutrition company for the food, beverage and pharmaceutical industries. Every day we partner with customers to create healthier, tastier and more sustainable products that are consumed by billions of people across the world. Our vision is to be our customers' most valued partner, creating a world of sustainable nutrition. A career with Kerry offers you an opportunity to shape the future of food while providing you opportunities to explore and grow in a truly global environment. About the role We are seeking a highly motivated and technically skilled Associate Scientist to join our team. In this role, you will support customer requests-both internal and external-from concept development through troubleshooting and commercialization. You will collaborate with cross-functional teams to deliver innovative solutions that meet customer needs and uphold our commitment to quality, taste, and nutrition. Key responsibilities * Support customer projects from ideation to commercialization, including troubleshooting technical challenges. * Participate in brainstorming sessions and develop gold standards in collaboration with Culinary and Subject Matter Experts (SMEs). * Conduct competitive product matching and formulation optimization. * Understand and navigate internal processes to provide effective project support. * Troubleshoot customer processes and provide technical solutions. * Act as a strong customer-facing representative to deliver solutions that "Nourish and Delight." * Assist sales and senior R&D representatives during customer calls with technical and culinary presentations. * Collaborate with cross-functional teams to leverage company strengths and deliver superior taste and nutrition experiences. * Research and apply methods to improve food quality, including flavor, color, texture, nutritional value, and convenience. * Complete project requests as required by customers and manage time efficiently. * Provide technical assistance to customers and internal teams as needed. * Work effectively in team environments. * Ability to taste and smell chemicals, flavors, and food products. * Ability to stand for extended periods in a lab setting and lift up to 50 lbs. Qualifications and skills * Education Bachelor's degree in Food Science, Dairy Science, Microbiology, Chemical Engineering, or related field (Master's preferred). * Experience 3+ years in food product development or applications (internships/co-ops considered). * Strong knowledge of food processing technologies, HACCP, and regulatory standards. * Hands-on experience with pilot plant equipment and laboratory analysis. * Excellent problem-solving skills and attention to detail. * Strong communication and teamwork abilities. * Ability to manage multiple projects and adapt to changing priorities. * Willingness to travel up to 20%. The pay range for this position is $75,602 - $123,432 in Annual Salary. Kerry typically does not hire an individual at the top or near the top of the range, as we are a pay-for-performance company, and this range is set to continue to reward performance annually while in role. Compensation decisions are dependent on the facts and circumstances of each case. The specific compensation offered to a candidate within the above range may be influenced by a variety of factors including skills, qualifications, experience, and internal equity. Kerry offers a competitive benefits package, including medical, dental, vision, paid time off, a 401(k) plan with employee and company contribution opportunities, Employee Share Plan, Life, disability, and accident insurance, and tuition reimbursement. This job posting is anticipated to expire on Feb 28th, 2026. Kerry is an equal opportunity employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age disability, protected veteran status or other characteristics protected by law. Kerry will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditional upon the successful completion of a background investigation and drug screen. Additional information can be found at Know Your Rights Workplace Discrimination is Illegal (dol.gov). Beware of scams online or from individuals claiming to represent us. A Kerry employee will not solicit candidates through a non-Kerry email address or phone number. In addition, Kerry does not currently utilise video chat rooms (e.g., Google Hangouts) to conduct interviews. Refuse any request that asks you to provide payment to participate in the hiring process (e.g., purchasing a "starter kit," investing in training, or something similar). Kerry will not ask you to pay any money at any point in the hiring process with the exception of reimbursable travel expenses. In addition, any payments made by Kerry will be from official firm accounts bearing the Kerry name. Recruiter Posting Type DNI

Requisition ID 62101 Position Type (US) Full Time Workplace Arrangement Kerry is the world's leading taste and nutrition company for the food, beverage and pharmaceutical industries. Every day we partner with customers to create healthier, tastier and more sustainable products that are consumed by billions of people across the world. Our vision is to be our customers' most valued partner, creating a world of sustainable nutrition. A career with Kerry offers you an opportunity to shape the future of food while providing you opportunities to explore and grow in a truly global environment. About the role We are seeking a highly motivated and technically skilled Associate Scientist to join our team. In this role, you will support customer requests-both internal and external-from concept development through troubleshooting and commercialization. You will collaborate with cross-functional teams to deliver innovative solutions that meet customer needs and uphold our commitment to quality, taste, and nutrition. Key responsibilities + Support customer projects from ideation to commercialization, including troubleshooting technical challenges. + Participate in brainstorming sessions and develop gold standards in collaboration with Culinary and Subject Matter Experts (SMEs). + Conduct competitive product matching and formulation optimization. + Understand and navigate internal processes to provide effective project support. + Troubleshoot customer processes and provide technical solutions. + Act as a strong customer-facing representative to deliver solutions that "Nourish and Delight." + Assist sales and senior R&D representatives during customer calls with technical and culinary presentations. + Collaborate with cross-functional teams to leverage company strengths and deliver superior taste and nutrition experiences. + Research and apply methods to improve food quality, including flavor, color, texture, nutritional value, and convenience. + Complete project requests as required by customers and manage time efficiently. + Provide technical assistance to customers and internal teams as needed. + Work effectively in team environments. + Ability to taste and smell chemicals, flavors, and food products. + Ability to stand for extended periods in a lab setting and lift up to 50 lbs. Qualifications and skills + Education Bachelor's degree in Food Science, Dairy Science, Microbiology, Chemical Engineering, or related field (Master's preferred). + Experience 3+ years in food product development or applications (internships/co-ops considered). + Strong knowledge of food processing technologies, HACCP, and regulatory standards. + Hands-on experience with pilot plant equipment and laboratory analysis. + Excellent problem-solving skills and attention to detail. + Strong communication and teamwork abilities. + Ability to manage multiple projects and adapt to changing priorities. + Willingness to travel up to 20%. The pay range for this position is $75,602 - $123,432 in Annual Salary. Kerry typically does not hire an individual at the top or near the top of the range, as we are a pay-for-performance company, and this range is set to continue to reward performance annually while in role. Compensation decisions are dependent on the facts and circumstances of each case. The specific compensation offered to a candidate within the above range may be influenced by a variety of factors including skills, qualifications, experience, and internal equity. Kerry offers a competitive benefits package, including medical, dental, vision, paid time off, a 401(k) plan with employee and company contribution opportunities, Employee Share Plan, Life, disability, and accident insurance, and tuition reimbursement. This job posting is anticipated to expire on Feb 28th, 2026. Kerry is an equal opportunity employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age disability, protected veteran status or other characteristics protected by law. Kerry will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditional upon the successful completion of a background investigation and drug screen. Additional information can be found at Know Your Rights Workplace Discrimination is Illegal (dol.gov). Beware of scams online or from individuals claiming to represent us. A Kerry employee will not solicit candidates through a non-Kerry email address or phone number. In addition, Kerry does not currently utilise video chat rooms (e.g., Google Hangouts) to conduct interviews. Refuse any request that asks you to provide payment to participate in the hiring process (e.g., purchasing a "starter kit," investing in training, or something similar). Kerry will not ask you to pay any money at any point in the hiring process with the exception of reimbursable travel expenses. In addition, any payments made by Kerry will be from official firm accounts bearing the Kerry name. Recruiter Posting Type DNI

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description • The qualified candidate will join the Bioassay and Impurities Testing group, which is part of the Analytical R&D organization located in Chesterfield to enable the development of biological therapeutics at Pharmaceutical. • The position will be part of a highly matrixed team responsible for developing analytical methodologies (, ELISA, qPCR) and strategies needed to progress biotherapeutic products through the pipeline. • The scientist filling this position will work within a highly- matrixed team setting on a variety of modalities including vaccines, viral constructs, therapeutic proteins, and monoclonal antibodies. • The contractor will work in a cGMP testing environment performing sample testing, method development, and method qualification. Work skills required: • Experience with ELISA, and DNA techniques (qPCR). Intermediate proficiency in Microsoft Office (Excel, Word, and Outlook) is required. • Must be able to understand and follow standard operating procedures. Qualifications Required/Intermediate/1-3 years: • ELISA • PCR • MS Office • SOP Requied/Advanced Desired/Entry Level: • GMP • LIMS Additional Skills: • 1 - 3 years experience • ELISA experience is required • Advanced experience with SOP Additional Information For more information, please contact, Atul Soni ************** Ext.4554 Morristown, NJ 07960

Duration: 18+ Month (With possible extension) Minimum education experience required: Associates degree with 5 years of experience/ Bachelor's degree with 1 year of experience Experience required: 0-3 years Top 3 critical skills: Buffer preparation; Concentration by UV; pH Job Description: Proficient with wet chemistry and analytical instrumentation (emphasis on proteins desired). Primary roles include SDS-PAGE analysis, buffer preparation and routine testing (appearance, pH, moisture, concentration by UV, colorimetric assay, etc.) for a high throughput Protein Analytics laboratory. Responsible for general laboratory and operational support, including assisting scientific staff with lab maintenance activities. Proficiency with Excel spreadsheets is required. Basic laboratory skills including use of balances and adjustable pipets, ability to work with Excel spreadsheets, and attention to detail are required Qualifications Minimum education experience required: Associates degree with 5 years of experience/ Bachelor's degree with 1 year of experience Experience required: 0-3 years Top 3 critical skills: Buffer preparation; Concentration by UV; pH Additional Information All your information will be kept confidential according to EEO guidelines.

PK Scientist- Full-Time, Remote ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients' lives. Our 'Own It' culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development. That's our vision. We're driven by it. And we need talented people who share it. If you're as driven as we are, join us. You'll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you'll be helping shape an industry. What will you be doing? This position can be done remotely worldwide, or Kansas City based in the office. * Prepare model-based strategies to support clinical development programs * Design, conduct, interpret and prepare appropriate study and regulatory summaries of quantitative pharmacology and pharmacometric activities * Build and sustain great relationships with clients * Prepare and present scientific publications; Excellent understanding of the integration of quantitative pharmacology and pharmacometrics into clinical drug development * Excellent written and verbal communications skills. Qualifications * Pharm.D. or Ph.D. preferred, but not required. * Clinical Pharmacology Experience * Candidate should have ideally at least 3-5 years of experience in Quantitative Pharmacology and Pharmacometrics. * Excellent organizational and communication skills. * Working knowledge in WinNonlin, NONMEM (or equivalent software) and R,. Benefits of Working in ICON: Our success depends on the quality of our people. That's why we've made it a priority to build a culture that rewards high performance and nurtures talent. We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals - both ours and yours. We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead. But beyond the competitive salaries and comprehensive benefits, you'll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change. ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below. #LI-HP1 #LI- REMOTE 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

The Medical Toxicologist at CTEH provides support in the areas of litigation support, occupational health, toxicology, risk assessment, industrial hygiene, and emergency response and may participate as a member of an emergency response team, either in person or remotely. The successful candidate will also perform in the role of project technical director in these same areas, providing expert consultation services to clients. An individual in this role will assemble, prepare, and analyze data concerning toxicological, environmental, and human health risk assessments while supervising nursing and health scientist staff on assigned projects. Utilizing a knowledge of various scientific disciplines, the Medical Toxicologist may oversee sampling, monitoring, and information collection and assist in CTEH's Toxicology and Emergency Response Program (TERP), will help administer the Workers Exposure Response Program (WERP), and assist with the administration of the CTEH employee health program, as well as the Montrose employee health program, and potentially health programs for other companies. Additionally, the Medical Toxicologist is expected to prepare, present, and promote scientific articles and publications in relevant journals as well as presentation before professional associations. This position will report to the Business Development Manager. Job Type: Part-Time Salary: Commensurate with experience ACTIVITIES Provide expert consultation services (including support to counsel) in the area of occupational/emergency medicine and toxicology Evaluate client projects related to toxicology, occupational health, and emergency response and develop strategies to address issues related to each project; Participate as a leader, project manager, or member of occupational health, toxicology, risk assessment, and/or emergency response; Act as a point of contact for CTEH clients in the TERP/WERP programs; Prepare written reports summarizing scientific data and findings; Participate in marketing and business development activities, including the development of articles and presentations; Compile, critically review, and summarize scientific/technical data and literature; and, Performs such other duties as are assigned EDUCATION, EXPERIENCE, & CREDENTIALS Degree of Doctor of Medicine (M.D.) from a U.S. accredited institution Active medical license in one or more US state Prior experience and Board certification in medical toxicology Prior experience and Board certification (preferred) in occupational medicine Masters' of Public Health (MPH) with experience in epidemiology (preferred) KNOWLEDGE, SKILLS, & ABILITIES Current driver's license (required) Ability to obtain a passport (required) Able to use Microsoft Office Able to work independently with minimal supervision Strong verbal and written communication skills in the English language WORK ENVIRONMENT & PHYSICAL DEMANDS The physical demands described below are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Sitting, standing, and walking Lifting up to 50 pounds several times a day Overhead lifting of over 20 pounds Bending, stooping, climbing ladders and crawling Long hours involving overtime and weekends as necessary Keyboarding/typing Ability to read effectively from a computer screen, sampling device and/or a paper copy Ability to handle a large volume of work and perform multiple tasks in a fast-paced environment Frequent, unscheduled travel for extended periods of time Ability to drive noncommercial vehicles Rarely may work shifts of up to 24 hours in duration Dress out in physically demanding personal protective equipment (PPE) for site entry at HAZWOPER sites as required under 29CFR 1910.120 Wear half-face and full-face air purifying respirator (APR) as well as supplied air respirators in the form of Self-Contained Breathing Apparatus (SCBA) and hose supplied respirator with medical clearance as required under 29CFR 1910.134 Wear partially or totally encapsulating personal protective equipment The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Works in an office environment when not deployed on an emergency response Often works outdoors and may be exposed to hot and cold environments and extreme weather conditions, including sunlit, rainy and windy conditions May occasionally work shifts up to 24 hours in duration Encounter environments presenting physical hazards of uneven ground, standing water, ditches, dusty conditions, rapidly moving transportation and remediation equipment, and physical stress associated with the wear of personal protective equipment May work at altitudes greater than 5000 feet above sea level May work on land, sea or air May work in a setting with potential physical and chemical hazards; and Frequent, extended travel

Current University of Arkansas System employees, including student employees and graduate assistants, need to log in to Workday via MyApps.Microsoft.com, then access Find Jobs from the Workday search bar to view and apply for open positions. Students at all University of Arkansas institutions will view open positions and apply within Workday by searching for “Find Jobs for Students.” University of Arkansas, Fayetteville students will view open positions and apply within Workday by searching for “Find Student Jobs at UAF.” All Job Postings will close at 12:01 a.m. CT on the specified Closing Date (if designated). If you close the browser or exit your application prior to submitting, the application process will be saved as a draft. You will be able to access and complete the application through “My Draft Applications” located on your Candidate Home page. Closing Date: 01/23/2026 Type of Position:Researchers and Scientists Workstudy Position: No Job Type:Fixed Duration of Project/Grant (Fixed Term) Work Shift: Sponsorship Available: No Institution Name: University of Arkansas, Fayetteville Founded in 1871, the University of Arkansas is a land grant institution, classified by the Carnegie Foundation among the nation's top 2 percent of universities with the highest level of research activity. The University of Arkansas works to advance the state and build a better world through education, research, and outreach by providing transformational opportunities and skills, fostering a welcoming climate, and nurturing creativity, discovery, and the spread of new ideas and innovations. The University of Arkansas campus is located in Fayetteville, a welcoming community ranked as one of the best places to live in the U.S. The growing region surrounding Fayetteville is home to numerous Fortune 500 companies and one of the nation's strongest economies. Northwest Arkansas is also quickly gaining a national reputation for its focus on the arts and overall quality of life. As an employer, the University of Arkansas offers a vibrant work environment and a workplace culture that promotes a healthy work-life balance. The benefits package includes university contributions to health, dental, life and disability insurance, tuition waivers for employees and their families, 12 official holidays, immediate leave accrual, and a choice of retirement programs with university contributions ranging from 5 to 10% of employee salary. Below you will find the details for the position including any supplementary documentation and questions, you should review before applying for the opening. If you have a disability and need assistance with the hiring process, please submit a request via the Disability Accommodations | OEOC | University of Arkansas (uark.edu) : Request an Accommodation. Appli cants are required to submit a request for each position of which they have applied. For general application assistance or if you have questions about a job posting, please contact Human Resources at ************. Department:Executive Director I3R Department's Website: i3r.uark.edu Summary of Job Duties:ABOUT THE INSTITUTE FOR INTEGRATIVE & INNOVATIVE RESEARCH (I³R): Established through a transformative gift from the Walton Family Charitable Support Foundation, the Institute for Integrative and Innovative Research (I3R) at University of Arkansas pioneers solutions to wicked problems through convergence research across academic, industry, government, and non-profit sectors to make a positive societal impact by creating and deploying innovations at scale. You will have the opportunity to collaborate with purpose-driven coworkers in one of the fastest-growing and most naturally beautiful regions in the U.S. You will join a growing team of visionary researchers and thought leaders dedicated to working with a thriving entrepreneurial ecosystem to deliver innovative solutions. I³R is committed to building a diverse, collaborative, and inclusive team and cultivating a welcoming atmosphere where all opinions are valued, all voices are heard, and ideas become reality. The I3R MRI facility houses a 3-Tesla Siemens Magnetom Cima.X to support academic and clinical research and care. This state-of-the-art system is designed with several technical advances to enhance imaging capabilities, workflow efficiency, and MRI recipient experience. It has a fast gradient system capable of high-speed structural and functional imaging, and a 64-receiver channel data acquisition system for parallel imaging with acceleration, which permits faster temporal resolution for functional MRI scans. The scanner has industry-leading gradients for human MRI scanning (i.e., gradient rise time = 200 T/m/s on each of the three gradient axes; peak gradient strength = 80 mT/m per axis). Its high performance driven by superior signal-to-noise ratio and AI powered advanced technology delivers high-quality images with faster acquisition time. It has advanced coil technology with a range of options that can be adapted for various anatomical regions and imaging needs and offers sophisticated imaging sequences that support specialized applications such as functional MRI and diffusion tensor imaging. An intuitive user-friendly interface simplifies operation and offers quieter operation and comfortable design to enhance MRI recipient's comfort during scans. A mock-MRI setup is also in the facility as are adjacent rooms to conduct other human health related studies including use of EEG, and fNIRS. Besides the support potential for advanced clinical scanning, the Magnetom Cima.X offers university researchers opportunities to establish stronger collaborations with the Arkansas Children's Research Institute, the University of Arkansas for Medical Sciences, and the Laureate Institute for Brain Research, for MRI in both adult and pediatric populations. Additionally, I3R researchers conducting medical robotics and mixed reality research seek MRI imaging of various anatomical regions. POSITION DESCRIPTION: A full-time MRI Senior Research Scientist position is available at the Institute for Integrative and Innovative Research (I3R) at University of Arkansas. We are looking for a researcher who can engage in state-of-the-art, multi-modal imaging research and in the application and development of novel, advanced imaging methods and data analytic strategies and their applications. The Magnetom Cima.X offers an unprecedented opportunity to be at the forefront of establishing an outstanding research program in multimodal imaging in the Northwest Arkansas region. In addition, there is a tremendous interest and need for support of clinical imaging. Some of the areas of research interest include: 1) development and implementation of novel real-time multimodal EEG and fMRI techniques; 2) development and implementation of quantitative MRI and fMRI protocols and MRS techniques; and 3) development and implementation of techniques for analyzing large and complex data sets involving data from multiple sources (e.g., structural MRI, fMRI, DTI, EEG, bio- and behavioral data). Additional areas of research related to the candidate's expertise are welcome. This position involves supervising and supporting all aspects of the MRI facility daily operations, ongoing clinical imaging research, and scientific collaboration within the I3R and across the University of Arkansas. It is also anticipated that, through partnerships with healthcare providers, the facility will support the advanced MRI needs for the clinical patient population in Northwest Arkansas and neighboring regions. The position offers excellent opportunities in all aspects of MRI technology development, clinical applications, and data analysis in a dynamic, interactive, and transdisciplinary research environment with a diverse team of researchers that include physicists, psychologists, neuroscientists, engineers, and data scientists. The successful applicant will have the ability to work effectively on interdisciplinary teams in a fast-paced environment, work independently and collaboratively with clinical and industry partners, and have excellent communication skills. A professional demeanor and the ability to establish effective working relationships are crucial in building trust and influence to accomplish work within a setting that includes a wide array of individuals, groups, policies, and processes. SUMMARY OF JOB DUTIES: · Manage the I3R MRI facility for safe access and use under federal and state required guidelines. · Supervise MRI technologist and other MRI facility personnel. · Lead cross-functional projects with internal research and clinical (medical, operations, statistics, regulatory) teams as well as external partners. · Design and implement customized MRI (structural, functional, diffusion) image analysis methods, leveraging novel and standard methodologies. · Develop and maintain excellent direct relationships with clinical and research partners, supporting them on site or remotely such as setting parameters for MRIs, developing and updating field-specific protocols, adapting and optimizing equipment to their needs. · Maintain accurate research records and documentation of procedures. · Pursue funding to support the development and evaluation of medical imaging as a lead investigator and as collaborator. · Provide technical guidance and mentorship to researchers and graduate students. · Additional duties as assigned. Regular, reliable, and non-disruptive attendance is an essential job duty, as is the ability to create and maintain collegial, harmonious working relationships with others. Qualifications: Minimum Qualifications: PhD or MD in Medical Physics, Engineering, Neuroscience or a relevant field with specific experience in MRI research More than three years of postdoctoral experience Experience in designing and executing clinical MRI studies with human participants Evidence of direct role and contribution to the medical imaging field (publications in peer-reviewed scientific journals, presentations at imaging-related conferences and/or developed software codes) Experience in managing multi-faceted and complex data sets and in performing statistical analysis Preferred Qualifications: Experience with managing an MRI facility Experience with high-field Siemens MRI systems MRI Certified by the American Board of Medical Physics and/or certified by the American Board of MR Safety as an MR Safety Expert Participation in clinical trials and implementation of MRI biomarkers Knowledge, Skills and Abilities: Knowledge of structural, diffusion, functional MRI procedures and acquisition protocols Proven expertise in programming and medical imaging & statistical software Proven leadership, organizational, and communication skills Highly creative with exceptional abstract problem-solving abilities and attention to detail Excellent written and verbal communication skills, particularly the ability to present and publish complex scientific approaches and results in an interdisciplinary field as well as to maintain clear and concise documentation Excellent ability to work effectively in a team environment, across multiple clinical sites Additional Information: This position is renewable annually based on continued need for the position, availability of funding, and satisfactory job performance. Salary Information: A minimum of $150,000 - Commensurate with education and experience. Required Documents to Apply: Cover Letter/Letter of Application, List of three Professional References (name, email, business title), Resume Optional Documents: Proof of Veteran Status Recruitment Contact Information: Julia Menke, *************** - Sr. HR Partner Crystal Ellis, Strategic Talent Acquisition Specialist, ************** All application materials must be uploaded to the University of Arkansas System Career Site ***************************************** Please do not send to listed recruitment contact. Special Instructions to Applicants: Pre-employment Screening Requirements:Criminal Background Check, Sex Offender Registry The University of Arkansas is committed to providing a safe campus community. We conduct background checks for applicants being considered for employment. Background checks include a criminal background check and a sex offender registry check. For certain positions, there may also be a financial (credit) background check, a Motor Vehicle Registry (MVR) check, and/or drug screening. Required checks are identified in the position listing. A criminal conviction or arrest pending adjudication or adverse financial history information alone shall not disqualify an applicant in the absence of a relationship to the requirements of the position. Background check information will be used in a confidential, non-discriminatory manner consistent with state and federal law. The University of Arkansas seeks to attract, develop and retain high quality faculty, staff and administrators that consistently display practices and behaviors to advance a culture that embeds equal opportunity, educational excellence and unparalleled access for all. The University of Arkansas is an equal opportunity institution. The University does not discriminate in its education programs or activities (including in admission and employment) on the basis of any category or status protected by law, including age, race, color, national origin, disability, religion, protected veteran status, military service, genetic information, sex, sexual orientation, or pregnancy. Questions or concerns about the application of Title IX, which prohibits discrimination on the basis of sex, may be sent to the University's Title IX Coordinator and to the U.S. Department of Education Office for Civil Rights. Persons must have proof of legal authority to work in the United States on the first day of employment. All Application information is subject to public disclosure under the Arkansas Freedom of Information Act. Constant Physical Activity:N/A Frequent Physical Activity:N/A Occasional Physical Activity:N/A Benefits Eligible:Yes

PK Scientist- Full-Time, Remote ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. **At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients' lives.** **Our 'Own It' culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.** **That's our vision. We're driven by it. And we need talented people who share it.** **If you're as driven as we are, join us. You'll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you'll be helping shape an industry.** **What will you be doing?** **This position can be done remotely worldwide, or Kansas City based in the office.** **Prepare model-based strategies to support clinical development programs** **Design, conduct, interpret and prepare appropriate study and regulatory summaries of quantitative pharmacology and pharmacometric activities** **Build and sustain great relationships with clients** **Prepare and present scientific publications; Excellent understanding of the integration of quantitative pharmacology and pharmacometrics into clinical drug development** **E** **xcellent written and verbal communications skills.** **Qualifications** **Pharm.D. or Ph.D. preferred, but not required.** + **Clinical Pharmacology Experience** **Candidate should have ideally at least 3-5 years of experience in Quantitative Pharmacology and Pharmacometrics.** **Excellent organizational and communication skills.** **Working knowledge in WinNonlin, NONMEM (or equivalent software) and R,.** **Benefits of Working in ICON:** **Our success depends on the quality of our people. That's why we've made it a priority to build a culture that rewards high performance and nurtures talent.** **We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals - both ours and yours.** **We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead.** **But beyond the competitive salaries and comprehensive benefits, you'll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.** **ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.** **If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.** \#LI-HP1 \#LI- REMOTE **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

Your New Company! At Altasciences we all move in unison to assist and work in the discovery, development, and manufacturing of new drug therapies to get them faster to people who need them. No matter your role, we all play an important part and you will have a significant impact on the health and well-being of people across the globe. By living our values of Employee Development, Customer Focus, Quality and Excellence, Respect and Integrity, we look to foster a passionate and collaborative work environment and we are looking for talented and enthusiastic people, like you, to join our growing team! Whether you're a recent college graduate or seeking your next career opportunity, it's time to discover your future at Altasciences. We are better together and together We Are Altasciences. About The Role You will assist in daily activities and operation of the Laboratory Sciences department including equipment maintenance, stocking supplies and general cleaning. You will also support and perform data collection activities including primarily focused on mass-spectrometry. What You'll Do Here Prepare materials, including animal blood and tissues, for analytical assays (e.g., ligand binding assays, flow cytometry, cell-based assays, mass-spectrometry, as assigned) and perform the assays according to Protocol or other guiding documents with accurate documentation. Maintain and document chain of custody for specimens, reagents, controls, and samples in the laboratory. Maintain and update facility records related to the laboratory and its analyses. Review laboratory records, procedures and study data for completeness and accuracy. Document deviations to laboratory procedures and study protocols and unforeseen circumstances in a timely manner and provide input for corrective actions. Assist in calibration, optimization, maintenance, and collection of data from analytical instruments. Follow Alta's Standard Operating Procedures (SOPs), ensure compliance with GLP, ALCOA+, USDA, and AAALAC guidelines, and can identify areas for improvement. Perform routine laboratory maintenance (including cleaning, stocking supplies, equipment maintenance tasks, etc.). What You'll Need to Succeed Associates/Bachelor's degree in Immunology/ Biology/ Chemistry or equivalent discipline plus a minimum of 6 months relevant laboratory experience, or an equivalent combination of education and experience. Problem solving and analysis Time management and organizational skills What We Offer Altasciences offers a wide variety of benefits to help our employees live healthy and fulfilling lives both at and outside of work. Altasciences' Benefits Package Includes: Health/Dental/Vision Insurance Plans 401(k)/RRSP with Employer Match Paid Vacation and Holidays Paid Sick and Bereavement Leave Employee Assistance & Telehealth Programs Altasciences' Incentive Programs Include: Training & Development Programs Employee Referral Bonus Program Annual Performance Review #LI-TA1 MOVING IN UNISON TO DELIVER A BIG IMPACT WITH A PERSONAL TOUCH Altasciences is an equal opportunity employer committed to diversity and inclusion. Our goal is to attract, develop and retain highly talented employees from diverse backgrounds, allowing us to benefit from a wide variety of experiences and perspectives. All qualified applicants will receive consideration for employment without regard to age, race, color, religion, creed, sex, sexual orientation, gender identity, national origin, disability or any other protected grounds under applicable legislation. Reasonable accommodations for persons with disabilities during the recruitment process are available upon request. Join us at Altasciences!

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies. In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to over 50,000 staff across a network of more than 900 independent companies in over 50 countries and operating more than 800 laboratories. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialized clinical diagnostics testing. In 2021, Eurofins generated total revenues of EUR € 6.7 billion, and has been among the best performing stocks in Europe over the past 20 years. Job Description We are seeking a highly motivated Antibody Discovery Scientist to join Biotherapeutics team at Eurofins. This role requires demonstrated experience in immunization, antibody generation and characterization, and preclinical pharmacology. The position will provide service for clients, including discovery and development of therapeutic antibodies, and collaborate with internal and external stakeholders to advance projects. Essential Duties and Responsibilities: Performs work in a laboratory setting, meeting the physical job requirements of a lab role. May be required to conduct production assays in other Biotherapeutic Services areas, based on business needs. Completes required training and supports 100% of Employee Health and Safety requirements Demonstrates proficiency, care and maintenance of lab equipment and department assets Conducts responsible use of confidential IT and business systems as required Maintains accurate data management and data reporting Supports unit goals and demonstrates Eurofins competencies as defined in the job plan Contributes to scientific community and site research and development objectives Works effectively in team environment, under minimum direction to achieve business production, project timelines and quality objectives. Supports site goals and demonstrates Eurofins' competencies, as defined in the job plan Performs other duties, as assigned . Adjusts work hours and provide cross-functional support to other departments as required and maintains accountability in delivering to client needs/timelines. Qualifications PhD in a relevant field (Immunology preferred) with 3 years relevant experience or Master's Degree or equivalent education with about 5 years of experience or Bachelor's Degree with 7 years of experience Hands-on experience with antibody discovery techniques. Execute a range of experiments independently including antibody characterization assays (octet, binding, SEC/HPLC, etc), imaging, etc. for antibody screening and function evaluation. Demonstrated flow cytometry skills (including cell sorting). Proficiency in molecular biology/cloning and mammalian cell expression systems - with previous experience working with antibody-based therapeutics. Familiarity with display technologies (e.g., phage display, yeast display) desired. Strong analytical skills and experience with data analysis software. Excellent communication skills and teamwork spirit. Knowledge of antibody engineering and optimization strategies is a plus. Data Analysis: Analyze experimental data, interpret results, and contribute to scientific publications, presentations, and project reports Experience supporting technical correspondence, compiling and presenting scientific data QC review of data and project reports Adhere to department SOP's and documentation requirements, maintain accurate data management and reporting. Ability to read, write, and interpret documents, such as standard operating procedures and technical reports Ability to solve practical problems and troubleshooting skills Ability to work in a laboratory setting, according to physical requirements of a laboratory role Lab equipment and office computer/software proficiency Demonstrates a positive attitude, capacity for team environment, and exhibits a genuine interest in drug discovery in support of advancing human health Ability to develop new methods, and lead research and development projects Ability to review and QC release data/reports Ability to contribute to establishment of new service lines, equipment, and data management systems Ability to support cross-functional demands Additional Information The position is full-time, Monday-Friday, 8 a.m.-5 p.m., with overtime as needed. Candidates within a commutable distance of St. Charles, MO area are encouraged to apply. Excellent full time benefits including comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays #LI-EB1 All your information will be kept confidential according to EEO guidelines. Eurofins USA Discovery Services is a Disabled and Veteran Equal Employment Opportunity employer.

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.

Biology Posted 11/18/2025 Full-Time John Brown University seeks a full-time faculty member to teach in the department of Biology beginning Fall of 2026. Primary teaching responsibilities will include multiple sections of non-major's biology lecture and laboratories. This course is an integral part of the University's Core Curriculum. Additional courses could include lectures and/or labs in cell biology, bioethics, human anatomy & physiology, and/or environmental science. Additional responsibilities include, but are not limited to, advising and recruitment of students, participation in departmental governance, attendance and participation at public events, as appropriate, and service on college and university committees. Program The Department of Biology offers courses designed to give students a broad foundation in the principles of biology as well as preparation in specific subdisciplines of biology. The approach taken by the department is to help students understand scientific methods and the key scientific facts, concepts, and theories of life processes, while emphasizing harmony with a biblically-based worldview. Students majoring in Biology are well-prepared for graduate training or careers in a wide range of health-related areas, such as medicine, dentistry, veterinary medicine, nursing, optometry, pharmacy, physical therapy, occupational therapy, physician assistance, and public health. Additionally, the department offers courses that fulfill the Natural Science component of the university Core Curriculum. Institution John Brown University's mission is to provide Christ-centered education that prepares people to honor God and serve others by developing their intellectual, spiritual, and professional lives. Founded in 1919, JBU is a Christ-centered, Biblically-faithful, interdenominational university that represents the best of Protestant evangelicalism in our commitment to the following theological principles: the fundamental human need for conversion and lifelong discipleship; the centrality of Jesus Christ's death and resurrection for the redemption of human beings; high regard for, and obedience to, the Bible as our authority; and active involvement in a local church, in missions and in ministries that work for Biblical justice and serve people in need. At JBU, we seek to integrate faith and learning, foster holistic Christian formation, promote pragmatic liberal arts education, and prepare people to follow Christ's call to serve others in all areas of life. All employees must affirm JBU's Employee Expectations and Articles of Faith. With more than 2,250 students from 37 states and 42 countries, JBU offers approximately 50 undergraduate programs, seven fully online bachelor's degrees, and 12 graduate degrees in business, education, cybersecurity, and counseling. JBU is accredited by the Higher Learning Commission and holds program-specific accreditations from various agencies." More information is available at jbu.edu/accreditation. JBU has benefited from stable and excellent leadership throughout the organization. President Chip Pollard started in 2004 and has led the organization in consistently meeting enrollment goals, completing two capital campaigns and launching a third, completing two strategic plans and launching a third, 17 major building projects, encouraging efforts to recruit and retain diverse faculty, staff, and students, and navigating the educational and financial challenges of the pandemic successfully. He served on the Council for Christian Colleges and Universities (CCCU) board for thirteen years and as chair for five years. Most of the president's cabinet has served for over 20 years, and all cabinet members have held volunteer leadership positions in the CCCU, ACSD, CIC, NACUBO, and other higher education associations. JBU's board of trustees are people of deep Christian faith, generous spirit, and professional expertise, with an average length of service of 11 years. They are deeply committed to maintaining JBU's mission to educate students to honor God and serve others. JBU has experienced a season of God's favor and blessing, for which we are grateful. In the last 20 years, JBU has received over $300 million in gifts and grants and has built or renovated over 90% of the university's facilities. JBU has only about $4 million of debt on over $220 million of assets. During that same time, JBU's endowment has grown from about $50 million to over $150 million, much of it dedicated to scholarships and academic programs and to support maintenance costs for new facilities. This financial strength has enabled JBU to retain excellent faculty and staff with consistent compensation increases and funds for faculty and staff development. JBU has not been not immune to the economic and cultural challenges facing higher education, but it is positioned better than many institutions to respond. JBU has received national recognition from many national newspapers and industry journals. For instance, in eight out of the last nine years, the Chronicle of Higher Education has named JBU on its "high honor roll" in its "Great Place to Work" survey. The Wall Street Journal has named JBU to its Best Colleges list since 2019, ranking us the top private school in Arkansas (2020) and top Arkansas university overall (2022, 2024). We are typically in the top 10% in our category (master's level universities in the South) in U.S. News and World Report rankings. JBU is located in Northwest Arkansas, a region predicted to have the third fastest job growth rate in the country behind only Austin, Texas and Charlotte, North Carolina. Three of the largest corporations in the world are located here-Walmart, Tyson Foods, and JB Hunt-and there is a growing technology, entrepreneurial, and art business ecosystem in the region. The quality of life is enhanced with a world-class art museum, Crystal Bridges, 25 miles from campus, over 400 miles of mountain biking trails, several state and national historic sites, parks, and large lakes, and a new $33 million whitewater rafting park just five miles south of campus. Siloam Springs has approximately 18,350 people with affordable housing and good private and public schools. Required Qualifications * A Master's degree in a field closely related to Biology * A committed follower of Jesus Christ * Ability to teach undergraduate courses including Biological Science (a non-major's lecture and lab course) * A commitment supporting teaching-related efforts * Ability to contribute to the mission and vision of the institution in the department and more broadly at the institution * A commitment to the integration of the Christian faith and teaching * A commitment to supporting and collaborating with students, faculty, and staff from varied academic and cultural backgrounds Preferred Qualifications * A doctorate degree in a field closely related to Biology * Experience teaching undergraduate courses, especially human anatomy & physiology, bioethics, and/or environmental science * Demonstrated evidence of scholarly potential * Evidence of successfully teaching, mentoring, or working with people who have different perspectives, life experiences, and cultural expressions Important Dates Position begins July 1, 2026. The screening process begins December 17, 2025 and continues until the position is filled. Salary A competitive salary exists which will be commensurate with training and/or experience. In addition, JBU offers a comprehensive benefits package, including 403(b) retirement plan, medical and dental insurance, tuition remission, leave related to the birth of a child, adoption leave, and moving expenses. More information about JBU A summary describing the university is available online. Applications Please upload the following documents to the "Upload Your Documents" page: * Letter of Interest * Your resume or CV * Faculty application (completed and signed) * Statement of Christian Commitment - regarding your relationship with Jesus Christ and your Christian Commitment (integration of faith and learning) related to your teaching, scholarship and/or service. (Please Note: This is not the same as answering the faith questions on the application, although there may be some overlap. The search committee will be expecting to see a separate document regarding the integration of faith and learning related to your teaching, scholarship and/or service.) The employee is expected to adhere to all University policies. Contact Information: Office of Human Resources John Brown University 2000 West University Street Siloam Springs, AR 72761 Phone: ************ e-mail: ************

Global Channel Management is a technology company that specializes in various types of recruiting and staff augmentation. Our account managers and recruiters have over a decade of experience in various verticals. GCM understands the challenges companies face when it comes to the skills and experience needed to fill the void of the day to day function. Organizations need to reduce training and labor costs but at same requiring the best "talent " for the job. Qualifications Position Responsibilities: • Analytical testing by qPCR in a cGMP environment • Analysis and documentation of results • Routine lab duties (ex. reagent preparation, consumable stocking) Technical Skills: • qPCR (required) • Proficiency in Microsoft Office (Excel and Word) required • ELISA (preferred) • cGMP experience (preferred) • LIMS experience (preferred) Preferred education is a bachelor's degree with 1-3 years of experience in DNA techniques (qPCR). Position Responsibilities: • Analytical testing by qPCR in a cGMP environment • Analysis and documentation of results • Routine lab duties (ex. reagent preparation, consumable stocking) Additional Information $21/hr 18 months

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description • Canditate will work with fellow scientists to designing and executing experiments including small-scale studies, and pilot plant and manufacturing studies in a variety of types and scales of equipment from bench top to pilot-scale, and, as required, technology transfer and validation in commercial plants. • Based on the analyses of these studies, these positions will be expected to develop and test new hypotheses to improve fundamental understanding of the chemical and biochemical processes, including bio-conjugation or large and small molecule combinations. • This position will support process validation, quality by design, regulatory approaches, and quality systems. Qualifications • EDUCATION/EXPERIENCE: Required: B.S. degree in Chemical/Biochemical Engineering, or equivalent or related field with 0-5 years of industry experience. • Proven record of delivering results in a fast paced environment and effective communication to project teams. • Desirable: 2-3 years of experience in process development of biotherapeutics. • Experience in developing relevant purification processes for complex biologics. • SKILLS: Demonstrated ability to drive for results and drive innovative research programs independently. • Good understanding of chemical engineering/bio-chemical engineering, chemistry/biochemistry and macromolecule analytics. Familiarity with recent scientific literature is required. Applicants should be self-motivated, organized, and capable of working indendently, and in a collaborative environment. • The successful candidate will possess strong oral and written communication skills. Strong analytical and computer skills are required. • Skills Skills Skills:Category Name Required Experience Software Skills MS Office No Additional • Skills:Undergraduate Degree required. 2 - 3 years experience in purification processes. Additional Information Sneha Shrivastava Technical Recruiter (Clinical/Scientific) Artech Information Systems LLC 360 Mt. Kemble Avenue, Suite 2000 | Morristown, NJ 07960 Office: ************ | Fax: ************ Connect with us on - LinkedIn | Facebook | Twitter

Mindlance is a national recruiting company which partners with many of the leading employers across the country. Feel free to check us out at ************************* Duration: 18+ Month (With possible extension) Location: St. Louis, MO Minimum education experience required: Associates degree with 5 years of experience/ Bachelor's degree with 1 year of experience Experience required: 0-3 years Top 3 critical skills: Buffer preparation; Concentration by UV; pH Job Description: Proficient with wet chemistry and analytical instrumentation (emphasis on proteins desired). Primary roles include SDS-PAGE analysis, buffer preparation and routine testing (appearance, pH, moisture, concentration by UV, colorimetric assay, etc.) for a high throughput Protein Analytics laboratory. Responsible for general laboratory and operational support, including assisting scientific staff with lab maintenance activities. Proficiency with Excel spreadsheets is required. Basic laboratory skills including use of balances and adjustable pipets, ability to work with Excel spreadsheets, and attention to detail are required Qualifications Minimum education experience required: Associates degree with 5 years of experience/ Bachelor's degree with 1 year of experience Experience required: 0-3 years Top 3 critical skills: Buffer preparation; Concentration by UV; pH Additional Information All your information will be kept confidential according to EEO guidelines.

Global Channel Management is a technology company that specializes in various types of recruiting and staff augmentation. Our account managers and recruiters have over a decade of experience in various verticals. GCM understands the challenges companies face when it comes to the skills and experience needed to fill the void of the day to day function. Organizations need to reduce training and labor costs but at same requiring the best "talent " for the job. Qualifications Position Responsibilities: • Analytical testing by qPCR in a cGMP environment • Analysis and documentation of results • Routine lab duties (ex. reagent preparation, consumable stocking) Technical Skills: • qPCR (required) • Proficiency in Microsoft Office (Excel and Word) required • ELISA (preferred) • cGMP experience (preferred) • LIMS experience (preferred) Preferred education is a bachelor's degree with 1-3 years of experience in DNA techniques (qPCR). Position Responsibilities: • Analytical testing by qPCR in a cGMP environment • Analysis and documentation of results • Routine lab duties (ex. reagent preparation, consumable stocking) Additional Information $21/hr 18 months