Microbiologist jobs in Madison, WI - 24 jobs

Scientist I Department: Microbiology Shift: Full-Time; Monday - Friday 2pm-10pm This is a fully onsite role based at our GMP Laboratory in Middleton, WI. We welcome applicants from all locations within the U.S. Please note that relocation assistance is not provided for this position, and any relocation costs will be the responsibility of the candidate. Must be legally authorized to work in the United States without sponsorship. Must be able to pass a comprehensive background check, which includes a drug screening. At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future. Our PPD Laboratory Services team has a direct impact on improving patient health through the expertise of scientists, industry thought leaders and therapeutic experts. As the world leader in serving science, our laboratory professionals bring their commitment to accuracy and quality to deliver groundbreaking innovations. Discover Impactful Work: As a Scientist I, you will use innovative technologies to perform high-quality sample testing for key pharmaceutical clients across the industry. Your sample preparation and analysis serve as an integral piece in helping PPD accomplish our goal of helping bring life-changing therapies to market. A day in the Life: * Possesses an understanding of laboratory procedures and under general supervision can conduct complex analysis. * Performs a variety of routine sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices for stability and analytical testing. * Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory guidelines. * Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. Education * Bachelor's degree (Life Sciences degree preferred) or equivalent and relevant formal academic / vocational qualification Experience * Previous experience that provides the knowledge, skills, and abilities to perform the job * Previous work experience which is comparable to 0-2 years, or equivalent combination of education, training, and experience. * In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role. Knowledge, Skills, Abilities * Knowledge of routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory guidelines * Knowledge of applicable regulatory authority, compendia and ICH guidelines * Excellent manual dexterity skills * Good written and oral communication skills * Time management and project management skills * Proven solving and troubleshooting abilities * Ability to cross-train on sample preparation techniques with another laboratory group * Ability to work in a collaborative work environment with a team * Manual dexterity and can follow detailed written and verbal instruction * Cooperate with coworkers within an organized team environment or work alone with supervision * Manage time effectively to complete assignments in expected time frame Working Environment Thermo Fisher Scientific values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role: * Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner. * Able to work upright and stationary and/or standing for typical working hours. * Able to lift and move objects up to 25 pounds. * Able to work in non-traditional work environments. * Able to use and learn standard office equipment and technology with proficiency. * May have exposure to potentially hazardous elements, including infectious agents, typically found in healthcare or laboratory environments. * Able to perform successfully under pressure while prioritizing and handling multiple projects or activities. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued. Apply today! **************************** Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status. Accessibility/Disability Access Job Seekers with a Disability: Thermo Fisher Scientific offers accessibility service for job seekers requiring accommodations in the job application process. For example, this may include individuals requiring assistance because of hearing, vision, mobility, or cognitive impairments. If you are a job seeker with a disability, or assisting a person with a disability, and require accessibility assistance or an accommodation to apply for one of our jobs, please submit a request by telephone at ***************. Please include your contact information and specific details about your required accommodation to support you during the job application process. This telephone line is reserved solely for job seekers with disabilities requiring accessibility assistance or an accommodation in the job application process. Messages left for other purposes, such as not being able to get into the career website, following up on an application, or other non-disability related technical issues will not receive a response.

Laboratory bench work individually or in a team setting to accomplish daily Quality Control lab tasks. Active participation as a member of the Quality Control team in testing and release of production materials. Working in a lab setting to supporting fermentation facility that produces probiotics and dairy cultures. ESSENTIAL DUTIES AND RESPONSIBILITIES The essential functions of this position include, but are not limited to, the following: · Adhere to all quality systems including, but not limited to, ISO 22000, NSF, and GLP guide-lines, with an understanding of IFF's Quality Policy and procedures. · Perform routine lab testing with accurate and timely recording of test results into the SAP Quality Management module and utilize lab reference materials for information regarding testing. · Understand and follow procedures of the department for the proper calibration and use of the department's equipment. · Understand and follow Good Manufacturing Practices for the care, handling, and storage of food and Dietary Supplement products. · Perform environmental sampling procedures. · Follow and enforce laboratory safety procedures. KNOWLEDGE, SKILLS AND ABILITIES · Must have bachelor's degree in chemistry, Microbiology, Biology or similar field, or associate degree with at least 1 year relevant experience. · Must be knowledgeable about the analyses and tests performed in the Quality Control de-partment. · Must have the ability to work as an active team member as well as independently. · Must have strong math and good communication skills (both verbal and written). WORKING CONDITIONS This position operates in a laboratory environment 95-100% of the time. Exposure to hazardous materials training is required. Must wear Personal Protective Equipment (PPE) as appropriate in accordance with plant policy. SCOPE OF POSITION This position reports directly to the Quality Control Supervisor and has no direct supervisory responsibilities. Must be able to work overtime as needed. Management retains the discretion to add or change the duties and responsibilities of this position at any time. We are a global leader in taste, scent, and nutrition, offering our customers a broader range of natural solutions and accelerating our growth strategy. At IFF, we believe that your uniqueness unleashes our potential. We value the diverse mosaic of the ethnicity, national origin, race, age, sex, or veteran status. We strive for an inclusive workplace that allows each of our colleagues to bring their authentic self to work regardless of their religion, gender identity & expression, sexual orientation, or disability. Visit IFF.com/careers/workplace-diversity-and-inclusion to learn more

Laboratory bench work individually or in a team setting to accomplish daily Quality Control lab tasks. Active participation as a member of the Quality Control team in testing and release of production materials. Working in a lab setting to supporting fermentation facility that produces probiotics and dairy cultures. ESSENTIAL DUTIES AND RESPONSIBILITIES The essential functions of this position include, but are not limited to, the following: * Adhere to all quality systems including, but not limited to, ISO 22000, NSF, and GLP guide-lines, with an understanding of IFF's Quality Policy and procedures. * Perform routine lab testing with accurate and timely recording of test results into the SAP Quality Management module and utilize lab reference materials for information regarding testing. * Understand and follow procedures of the department for the proper calibration and use of the department's equipment. * Understand and follow Good Manufacturing Practices for the care, handling, and storage of food and Dietary Supplement products. * Perform environmental sampling procedures. * Follow and enforce laboratory safety procedures. KNOWLEDGE, SKILLS AND ABILITIES * Must have bachelor's degree in chemistry, Microbiology, Biology or similar field, or associate degree with at least 1 year relevant experience. * Must be knowledgeable about the analyses and tests performed in the Quality Control de-partment. * Must have the ability to work as an active team member as well as independently. * Must have strong math and good communication skills (both verbal and written). WORKING CONDITIONS This position operates in a laboratory environment 95-100% of the time. Exposure to hazardous materials training is required. Must wear Personal Protective Equipment (PPE) as appropriate in accordance with plant policy. SCOPE OF POSITION This position reports directly to the Quality Control Supervisor and has no direct supervisory responsibilities. Must be able to work overtime as needed. Management retains the discretion to add or change the duties and responsibilities of this position at any time. We are a global leader in taste, scent, and nutrition, offering our customers a broader range of natural solutions and accelerating our growth strategy. At IFF, we believe that your uniqueness unleashes our potential. We value the diverse mosaic of the ethnicity, national origin, race, age, sex, or veteran status. We strive for an inclusive workplace that allows each of our colleagues to bring their authentic self to work regardless of their religion, gender identity & expression, sexual orientation, or disability. Visit IFF.com/careers/workplace-diversity-and-inclusion to learn more

Scientist I Department: Microbiology Shift: Full-Time; Monday - Friday 2pm-10pm This is a fully onsite role based at our GMP Laboratory in Middleton, WI. We welcome applicants from all locations within the U.S. Please note that relocation assistance is not provided for this position, and any relocation costs will be the responsibility of the candidate. Must be legally authorized to work in the United States without sponsorship. Must be able to pass a comprehensive background check, which includes a drug screening. At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future. Our PPD Laboratory Services team has a direct impact on improving patient health through the expertise of scientists, industry thought leaders and therapeutic experts. As the world leader in serving science, our laboratory professionals bring their commitment to accuracy and quality to deliver groundbreaking innovations. Discover Impactful Work: As a Scientist I, you will use innovative technologies to perform high-quality sample testing for key pharmaceutical clients across the industry. Your sample preparation and analysis serve as an integral piece in helping PPD accomplish our goal of helping bring life-changing therapies to market. A day in the Life: Possesses an understanding of laboratory procedures and under general supervision can conduct complex analysis. Performs a variety of routine sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices for stability and analytical testing. Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory guidelines. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. Education Bachelor's degree (Life Sciences degree preferred) or equivalent and relevant formal academic / vocational qualification Experience Previous experience that provides the knowledge, skills, and abilities to perform the job Previous work experience which is comparable to 0-2 years, or equivalent combination of education, training, and experience. In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role. Knowledge, Skills, Abilities Knowledge of routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory guidelines Knowledge of applicable regulatory authority, compendia and ICH guidelines Excellent manual dexterity skills Good written and oral communication skills Time management and project management skills Proven solving and troubleshooting abilities Ability to cross-train on sample preparation techniques with another laboratory group Ability to work in a collaborative work environment with a team Manual dexterity and can follow detailed written and verbal instruction Cooperate with coworkers within an organized team environment or work alone with supervision Manage time effectively to complete assignments in expected time frame Working Environment Thermo Fisher Scientific values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role: Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner. Able to work upright and stationary and/or standing for typical working hours. Able to lift and move objects up to 25 pounds. Able to work in non-traditional work environments. Able to use and learn standard office equipment and technology with proficiency. May have exposure to potentially hazardous elements, including infectious agents, typically found in healthcare or laboratory environments. Able to perform successfully under pressure while prioritizing and handling multiple projects or activities. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued. Apply today! **************************** Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status. Accessibility/Disability Access Job Seekers with a Disability: Thermo Fisher Scientific offers accessibility service for job seekers requiring accommodations in the job application process. For example, this may include individuals requiring assistance because of hearing, vision, mobility, or cognitive impairments. If you are a job seeker with a disability, or assisting a person with a disability, and require accessibility assistance or an accommodation to apply for one of our jobs, please submit a request by telephone at ***************. Please include your contact information and specific details about your required accommodation to support you during the job application process. This telephone line is reserved solely for job seekers with disabilities requiring accessibility assistance or an accommodation in the job application process. Messages left for other purposes, such as not being able to get into the career website, following up on an application, or other non-disability related technical issues will not receive a response.

**Why Choose Labcorp?** At Labcorp, our people are the heart of everything we do. We're not just a global life sciences company - we're a team of passionate individuals working together to improve health and change lives. Whether you're just starting out or looking to grow your career, you'll collaborate with brilliant minds, explore your potential, and make a real impact on the future of medicine. **Step Into a Role That Moves Your Career Forward** We're looking for a Research Technician to join our Dose Formulation team in Madison, WI. In this hands-on lab role, you'll help prepare materials that support groundbreaking research and drug development. **What You'll Do** As a Study Technician, you'll learn and perform essential lab techniques to prepare test materials for preclinical studies. Your day-to-day will include: + Preparing lab reagents, solutions, suspensions, and capsules per study protocols + Recording data accurately in both digital and written formats + Learning formulation verification, sample disposition, and safe handling procedures + Collaborating with scientists and technicians to ensure study integrity + Maintaining a clean, safe, and GLP-compliant lab environment + Developing skills in study setup, data organization, and client communication **Education/Experience** + A Bachelor's degree in Chemistry or a related scientific field + A strong attention to detail and eagerness to learn + A passion for science and a desire to contribute to life-changing research **Work Schedule** + 3rd Shift: 3:00am - 11:45am (includes a 12% shift differential) **Pay:** $23/hour **Why You'll Love Working Here** + Be part of a mission-driven company that's improving lives + Gain hands-on lab experience in a regulated, high-impact environment + Grow your career with mentorship, training, and advancement opportunities **Benefits:** Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO), Tuition Reimbursement and Employee Stock Purchase Plan. Casual, PRN & Part Time employees regularly scheduled to work less than 20 hours are eligible to participate in the 401(k) Plan only. For more detailed information, please click here (************************************************************** . ** ** **Labcorp is proud to be an Equal Opportunity Employer:** Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. **We encourage all to apply** If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site (**************************************************** or contact us at Labcorp Accessibility. (Disability_*****************) For more information about how we collect and store your personal data, please see our Privacy Statement (************************************************* .

Current Employees: If you are currently employed at any of the Universities of Wisconsin, log in to Workday to apply through the internal application process. The Scientist I position is a full-time appointment in the laboratory of Dr. Alexey Glukhov within the Division of Cardiovascular Medicine, Department of Medicine, at the University of Wisconsin-Madison. The University of Wisconsin-Madison is a leading public research institution with a strong commitment to biomedical research, education, and clinical innovation. The Department of Medicine supports a broad range of basic and translational research programs aimed at improving human health. Dr. Glukhov's laboratory is part of the Division of Cardiovascular Medicine and focuses on understanding mechanisms of heart rhythm disorders and regulation of cardiac function. The primary purpose of the Scientist I position is to support ongoing cardiovascular research projects by conducting laboratory-based experiments, analyzing data, and contributing to the communication of research findings. The Scientist I will perform electrophysiological studies and pharmacological testing on isolated, Langendorff-perfused mouse and rat hearts, as well as isolated mouse and rat atrial preparations, under various physiological conditions, including neurohormonal, mechanical, and drug-based stimulation. These studies are conducted using established experimental methods to evaluate heart electrical activity, calcium signaling, and mechanical function. The Scientist I will collect, organize, analyze, and document research data in accordance with established policies and procedures, working under general supervision. The position includes preparing research summaries, reports, and manuscripts for submission to peer-reviewed journals, presenting research findings at local and national scientific meetings, and conducting reviews of relevant scientific literature. The Scientist I will also assist with the preparation of research grant applications, support collaborative research projects within and outside the University of Wisconsin-Madison, and provide day-to-day supervision and guidance to undergraduate and graduate students. Participation in seminars, meetings, and scholarly events organized by the Cardiovascular Research Center, Division of Cardiovascular Medicine, and Department of Medicine is also expected. This position requires work to be completed onsite, at a designated campus work location. Terminal, 24 month appointment This position has the possibility to be extended or converted to an ongoing appointment based on need and/or funding. Key Job Responsibilities: Conducts literature reviews, prepares reports and materials, and disseminates information to appropriate entities Writes or assists in developing grant applications and proposals to secure research funding Collects and analyzes research data, conducts experiments and interviews, and documents results according to established policies and procedures under general supervision and limited responsibility Attends and assists with the facilitation of scholarly events and presentations in support of continued professional development and the dissemination of research information Assists with the identification of research problems and the development of research methodologies and procedures Serves as a main point of contact and liaison with internal and external stakeholders providing information and representing the interests of a specialized research area Department: School of Medicine and Public Health, Department of Medicine, Division of Cardiovascular Medicine, In the Operational Area of Glukhov Lab Fueled by innovation yet grounded in kindness, the Department of Medicine empowers leaders to transform medicine and improve lives everywhere. We are committed to professional fulfillment and health equity. We strive to ensure that everyone in our department understands the importance of social impact and belonging-and is empowered to champion it in all they do. Join us and be a part of supporting our nationally recognized faculty, innovative medical education programs and exceptional clinical care as we work towards our vision of healthy people and healthy communities! At the Division of Cardiovascular Medicine, we help people live their healthiest lives through prevention and state-of-the-art care for complex heart disease. We lead comprehensive education, research and clinical programs-in partnership with our world-class university and remarkable health system. We are innovative, collaborative and kind. We strive for excellence and equity. And we make an impact in Wisconsin and beyond. Compensation: The starting salary for the position is $65,000 annually; but is negotiable based on experience and qualifications. Employees in this position can expect to receive benefits such as generous vacation, holidays, and sick leave; competitive insurances and savings accounts; retirement benefits. For more information, refer to the campus benefits webpage. SMPH Academic Staff Benefits Flyer Required Qualifications: Demonstrated expertise in cardiac electrophysiology, cardiac mechanics, and cell biophysics Experience conducting research involving animal models Experience working with isolated cardiac preparations, including Langendorff-perfused hearts and isolated atrial and sinoatrial node preparations from mouse and rat models Experience with electrophysiological measurement techniques, such as electrocardiography (ECG), optical mapping, and related electrical recording method Knowledge of cardiac pharmacology and neurohormonal regulation of heart function Preferred Qualifications: Experience in mechanobiology and mechanical regulation of cardiac function Experience with basic molecular biology techniques Experience working with isolated single cardiac muscle cells Experience using fluorescent microscopy and related imaging techniques Education: Ph.D. in Biophysics, or closely related discipline, is required by the start date of the position. How to Apply: To apply for this position, select either “I am a current employee” or “I am not a current employee” under Apply Now. You will then be prompted to upload your application materials. Important: There is only one attachment field. All required documents must be combined into a single file and uploaded in that field. Upload required documents: • Cover letter • Resume Your cover letter should address how your training and experience align with the required and preferred qualifications listed above. Application reviewers will rely on these written materials to determine which applicants move forward in the process. References will be requested from final candidates. All applicants will be notified once the search concludes and a candidate is selected. Contact Information: Alexey Glukhov, PhD, **************************, ************ Relay Access (WTRS): 7-1-1. See RELAY_SERVICE for further information. Institutional Statement on Diversity: Diversity is a source of strength, creativity, and innovation for UW-Madison. We value the contributions of each person and respect the profound ways their identity, culture, background, experience, status, abilities, and opinion enrich the university community. We commit ourselves to the pursuit of excellence in teaching, research, outreach, and diversity as inextricably linked goals. The University of Wisconsin-Madison fulfills its public mission by creating a welcoming and inclusive community for people from every background - people who as students, faculty, and staff serve Wisconsin and the world. The University of Wisconsin-Madison is an Equal Opportunity Employer. Qualified applicants will receive consideration for employment without regard to, including but not limited to, race, color, religion, sex, sexual orientation, national origin, age, pregnancy, disability, or status as a protected veteran and other bases as defined by federal regulations and UW System policies. We promote excellence by acknowledging skills and expertise from all backgrounds and encourage all qualified individuals to apply. For more information regarding applicant and employee rights and to view federal and state required postings, visit the Human Resources Workplace Poster website. To request a disability or pregnancy-related accommodation for any step in the hiring process (e.g., application, interview, pre-employment testing, etc.), please contact the Divisional Disability Representative (DDR) in the division you are applying to. Please make your request as soon as possible to help the university respond most effectively to you. Employment may require a criminal background check. It may also require your references to answer questions regarding misconduct, including sexual violence and sexual harassment. The University of Wisconsin System will not reveal the identities of applicants who request confidentiality in writing, except that the identity of the successful candidate will be released. See Wis. Stat. sec. 19.36(7). The Annual Security and Fire Safety Report contains current campus safety and disciplinary policies, crime statistics for the previous 3 calendar years, and on-campus student housing fire safety policies and fire statistics for the previous 3 calendar years. UW-Madison will provide a paper copy upon request; please contact the University of Wisconsin Police Department.

**Our Company** At Teradata, we believe that people thrive when empowered with better information. That's why we built the most complete cloud analytics and data platform for AI. By delivering harmonized data, trusted AI, and faster innovation, we uplift and empower our customers-and our customers' customers-to make better, more confident decisions. The world's top companies across every major industry trust Teradata to improve business performance, enrich customer experiences, and fully integrate data across the enterprise. **What you will do** We are seeking a Technology Researcher to evaluate emerging hardware and infrastructure technologies, conduct focused research spikes and proof-of-concepts, and identify optimization opportunities for our database and cloud platforms. You will collaborate with product engineering teams to advance innovations from research to production, leveraging AI-assisted development tools to accelerate your work. Key Responsibilities + Evaluate emerging technologies in compute hardware, storage, networking, GPUs, DPUs, and accelerators for potential platform integration + Evaluate technologies such as eBPF, DASK and other communication protocols that all for distributed and heterogeneous system designs + Design and execute targeted research spikes and proof-of-concept projects to validate technology value and measure performance impact + Collaborate with product engineering teams to scope, test, benchmark, and document technology enhancements + Research industry trends, academic innovations, and partner technologies to identify optimization opportunities + Build business cases and present technology recommendations through innovation reviews + Leverage AI-assisted coding tools to accelerate prototyping and development cycles **Who you will work with** On our team, you will have the opportunity to work with a dynamic group of professionals in Office of the CTO, Product Engineering, Product Management, Sales and other key departments. You will play a crucial role in helping Teradata better understand our customers' needs through dedicated technology research, proof-of-concepts and defining next generation infrastructure choices for our product portfolio. This position will report to the Engineering Fellow of Partner Technology Research and will reside within the Office of the CTO. **What makes you a qualified candidate** Technical Skills: + Distributed systems engineering background with multi-node architecture experience + CUDA X and NVIDIA GPU ecosystem experience + rocM/HIP and AMD GPU ecosystem experience + eBPF, DASK or Arrow experience + HPC or distributed application development background + Public cloud platform proficiency + Foundational database systems knowledge (Teradata experience a plus) + Backend software development or infrastructure engineering experience + Scripting/automation capabilities (Python, Bash, or similar) + Comfortable with modern AI-assisted coding tools and platforms Education & Experience: + Bachelor's degree in computer science (distributed systems focus), Computer Engineering, or IT with equivalent professional progression + 2-3+ years in backend development, systems engineering, or infrastructure engineering + DevOps or infrastructure automation experience **What you will bring** + Confident and resilient; comfortable navigating technical disagreements and feedback + Strong influencer with ability to persuade without direct authority or control of resources + Excellent communicator who articulates technical concepts and business value clearly + Collaborative, self-motivated, and intellectually curious + Thrives in ambiguous, fast-moving technology environments **Why We Think You'll Love Teradata** We prioritize a people-first culture because we know our people are at the very heart of our success. We embrace a flexible work model because we trust our people to make decisions about how, when, and where they work. We focus on well-being because we care about our people and their ability to thrive both personally and professionally. We are committed to actively working to foster an inclusive environment that celebrates people for all of who they are. \#LI-JR1 Teradata is proud to be an equal opportunity employer. We do not discriminate based upon race, color, ancestry, religion, creed, sex (including pregnancy, childbirth, breastfeeding, or related conditions), national origin, sexual orientation, age, citizenship, marital status, disability, medical condition, genetic information, gender identity or expression, military and veteran status, or any other legally protected status. We welcome and encourage individuals from all backgrounds to apply and join our team, bringing their unique perspectives and experiences to help us innovate and grow. Pay Rate: 84,000.00 - 105,000.00 - 126,000.00 Annually Starting pay for the successful applicant will depend on geographic location, internal equity, job-related knowledge, skills, and candidate experience. Sales roles will be eligible for commission payments tied to quota achievement. All other permanent roles will be eligible for one of our annual incentive plans, which are based on company financial attainment and individual performance. Employees in this position are also eligible to participate in the Company's comprehensive benefits programs, which include healthcare, life and disability insurance plans, a 401(k)-retirement savings plan, and time-off programs. Specific details of these benefits, including eligibility criteria and plan options, will be provided during the hiring process and can be reviewed here: **************************************************

Research Internships at Microsoft provide a dynamic environment for research careers with a network of world-class research labs led by globally-recognized scientists and engineers, who pursue innovation in a range of scientific and technical disciplines to help solve complex challenges in diverse fields, including computing, healthcare, economics, and the environment. Gray Systems Lab (GSL) is an applied research lab under Azure Data. We do research and development for databases, big-data, and cloud systems, working in close collaboration with product teams to design innovative solutions for real-world problems. We focus on a variety of exciting areas, including machine learning for systems, reinforcement learning finetuning and post-training techniques, natural language-to-query, agentic workflows, resource management, query optimization and execution. We also work on workload optimization, graph analytics, data storage formats and governance, modern/future hardware (e.g., GPU, NVM and FPGAs), program analysis, and data provenance. Our work covers both internal both Microsoft internal and open-source systems, such as Fabric, Spark, SQL Server, MySQL, Apache Iceberg, and more. We provide opportunities to work on ideas from internal collaborations, as well as external ones with partner universities, and to continue to be an active scholar in the research community. We are looking for highly motivated graduate students who are interested in cutting edge research in close collaboration with advanced industry product groups. Past Research Internships have resulted in a combination of impact on production systems and publications at top conferences. Applicants should demonstrate a track record in one or more systems, database, or data science topics and an aptitude for hands-on system building and design methodology to run and analyze experiments at scale. Responsibilities Research Interns put inquiry and theory into practice. Alongside fellow doctoral candidates and some of the world's best researchers, Research Interns learn, collaborate, and network for life. Research Interns not only advance their own careers, but they also contribute to exciting research and development strides. During the 12-week internship, Research Interns are paired with mentors and expected to collaborate with other Research Interns and researchers, present findings, and contribute to the vibrant life of the community. Research internships are available in all areas of research, and are offered year-round, though they typically begin in the summer. Qualifications Required Qualifications * Currently pursuing a PhD degree in computer science, statistics, mathematics, or related technical field. Other Requirements * Research Interns are expected to be physically located in their manager's Microsoft worksite location for the duration of their internship. * In addition to the qualifications below, you'll need to submit a minimum of two reference letters for this position as well as a cover letter and any relevant work or research samples. After you submit your application, a request for letters may be sent to your list of references on your behalf. Note that reference letters cannot be requested until after you have submitted your application, and furthermore, that they might not be automatically requested for all candidates. You may wish to alert your letter writers in advance, so they will be ready to submit your letter. Preferred Qualifications * Experience with one or more general purpose programming languages, such as Python, Java, C#, C++, Rust. * Experience with one of the following: PostgreSQL, MySQL, SQL Server, Spark, Apache Iceberg, CUDA, or other database or big data systems. * Experience contributing to research communities and/or efforts, including publishing papers (being listed as author) at academic conferences. * Take initiative but also follow a research/productization plan and work well as part of a team. * Critical thinking and communication skills. The base pay range for this internship is USD $6,710 - $13,270 per month. There is a different range applicable to specific work locations, within the San Francisco Bay area and New York City metropolitan area, and the base pay range for this role in those locations is USD $8,760 - $14,360 per month. Certain roles may be eligible for benefits and other compensation. Find additional benefits and pay information here: ************************************************* Benefits/perks listed below may vary depending on the nature of your employment with Microsoft and the country where you work. This position will be open for a minimum of 5 days, with applications accepted on an ongoing basis until the position is filled. Microsoft is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, citizenship, color, family or medical care leave, gender identity or expression, genetic information, immigration status, marital status, medical condition, national origin, physical or mental disability, political affiliation, protected veteran or military status, race, ethnicity, religion, sex (including pregnancy), sexual orientation, or any other characteristic protected by applicable local laws, regulations and ordinances. If you need assistance with religious accommodations and/or a reasonable accommodation due to a disability during the application process, read more about requesting accommodations.

Join the best radiopharmaceutical company in the world! If you're looking to make an impact while building a meaningful career in a specialized, fast-growing field, NorthStar Medical Radioisotopes is the place to do it. NorthStar Medical Radioisotopes is a growing, commercial-stage company focused on advancing patient care by providing therapeutic radioisotopes and novel radiopharmaceuticals to detect and treat cancer. At the forefront of NorthStar's technological innovation is scientific excellence, using first-in-kind electron accelerator technology and integrated campus capabilities to drive progress in radiopharmaceutical manufacturing. Our work is driven by a meaningful mission-advancing life-saving radiopharmaceutical development and ensuring a reliable supply of critical medical isotopes for patients in need. As a rapidly growing organization operating on the cutting edge of science, we offer exceptional career growth and professional development opportunities, supported by world-class facilities and a competitive benefits package. Position The Senior Microbiologist, Product Development will be a technical leader, bringing the science of microbiology in a pharmaceutical application to the development and maintenance of equipment, cleanrooms, and processes used in the manufacture of radioisotopes. This includes gathering technical information about engineering system/set up and managing the implementation of novel radioisotope manufacturing technologies. The Senior QAPD Microbiologist will develop and execute microbiological methods and validations from concept phase through design, planning, and execution, as well as coordinating with other departments. This person is also responsible for working with cross functional teams, including RA/QA and Engineering, to apply efficient cGMP processes, to preserve data integrity and quality of the drug product, and to ensure the safety of all production and non-production personnel. Responsibilities Drive the development of overall microbial validation strategy for pharmaceutical application to development of equipment used in the delivery of radioisotopes. This would include developing and executing methods and validations from concept phase through design, planning, and execution as well as coaching other team members. Assist lab management. Be the primary point of contact for microbiology laboratory supplies, instrumentation, and environmental monitoring program activities. Develop, plan, implement, and support microbiological development projects in collaboration with cross-functional teams with an overall focus on microbiological safety. Maintain laboratory procedures in accordance with Good Laboratory/Manufacturing Practice standards of the US FDA, 21 CFR Part 210 & 211 Follow good laboratory practice, good documentation, and good manufacturing practice when creating and executing advanced protocols to verify and/or validate product conformance in the area of microbiological testing and control. Early Development After 3 months: You will have completed all required training for new employees; for job-specific duties, and safety; and for access to restricted areas relevant to your job duties. You will have integrated into the quality unit, project, operations, and other cross-functional teams. You will understand the function and responsibilities of each group within other areas of the Quality department. After 6 months: You will understand the Quality Management Processes that support Aseptic Process Controls, Environmental Monitoring, and other contamination control strategies. You will have become qualified to train, qualify, and maintain operator status in all aspects of Aseptic Process Controls including: Aseptic Techniques, Aseptic Gowning, and Aseptic Process Operator Qualification. You will have engaged a cross-functional team to qualify, and maintain the qualification status of the systems in-place to maintain room classifications, (ISO 5, ISO 7, and ISO 8). Qualifications Master's Degree in biological science and five (5) or more years of experience in the pharmaceutical/medical device industry or equivalent combination of education and experience. Experience developing clear, concise, and adequate protocols, procedures, and work instructions required. Must possess a working knowledge of lab controls and general scientific equipment and should strictly adhere to written procedures and enforce it in others. Master's degree in microbiology preferred. Experience with Radiopharmaceuticals would be a strong asset in this position. Please note the company cannot provide immigration-related sponsorship (including H-1B status, O-1 status, Optional Practical Training support, etc.) for this position. Each successful applicant will be required to complete the Form I-9, Employment Eligibility Verification, demonstrating both identity and employment authorization, on or before the first day of employment. Under federal law, only truthful information may be provided on the Form I-9. Benefits Medical, dental, and vision insurance Healthcare Flex Spending Account (FSA) and Dependent Care FSA Company-paid short-term and long-term disability Company-paid life insurance & AD&D coverage Pet insurance 401(k) match Paid holidays and paid time off (PTO) Paid parental leave Bonus plan Equity Incentive Program Working Conditions This role may involve working in a controlled cleanroom environment, general office setting, or specific manufacturing areas. Conditions may include: Exposure to varying temperatures, both indoors (heated/air-conditioned spaces) and outdoors Noise levels range from quiet to loud, depending on the work area Specific vision abilities, including near vision, visual acuity, and color discrimination Personal Protective Equipment (PPE) is required and may include: Respirators, gloves, safety glasses, and full protective clothing Compliance with cleanroom gowning protocols (e.g., removal of all jewelry, including piercings) Prohibition of cosmetics, fragrances (perfume, aftershave), and nail products, including polish, artificial nails, or extensions As a radiopharmaceutical manufacturing site, radiation may be present in the laboratory and production areas. Employees in this role may be required to: Follow strict radiation safety procedures Participate in dosimetry monitoring and bioassay testing as part of the company protocol Inform leadership of any health conditions that may affect product integrity, by cleanroom standards Location NorthStar Medical Radioisotopes is proud to call Beloit, Wisconsin home. Our headquarters and primary manufacturing facility are located in this vibrant, growing community that combines the charm of a small city with the advantages of a central Midwest location. Beloit features a lively, revitalized downtown filled with local restaurants, shops, and cultural events, and is just a short drive from major metropolitan areas including Madison, Milwaukee, Chicago, and Rockford. Situated in the heart of the South Central Wisconsin and Northern Illinois region, Beloit offers a rare blend of urban amenities and scenic natural surroundings. Whether you're drawn to outdoor recreation, educational institutions, the arts, or historic landmarks, the area provides rich and diverse experiences for all interests. A variety of nearby communities, ranging from rural towns to suburban neighborhoods, offer flexible housing options and access to multiple school districts, making Beloit an excellent choice for individuals and families considering relocation. NorthStar Medical Radioisotopes 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.

Job Description Prairie Ridge Health is looking for a team member to join or Lab Department in the role of Certified Lab Scientist or Certified Lab Tech. This position is 0.2 FTE (8 hours per week) Day/PM shift Monday - Friday with an every 3rd weekend rotation. This position will be responsible for performing general laboratory testing in the areas of Hematology, Chemistry, Urinalysis, Transfusion Services, Coagulation, Microbiology, Serology, and Specimen processing with a high degree of accuracy and reliability...…. POSITION SUMMARY Lab Scientist The Medical Technologist performs general laboratory testing in the areas of Hematology, Chemistry, Urinalysis, Transfusion Services, Coagulation, Microbiology, Serology, and Specimen processing with a high degree of accuracy and reliability. The data obtained is used in the diagnosis and treatment of disease involving patient of all ages. The Medical Technologist develops and maintains test procedures and protocols, and troubleshoots both technology and sample related problems. (S)he exercises independent judgment and responsibility with minimal supervision. May supervise others in the absence of the Laboratory Supervisor. Makes decisions about the accuracy of test results, instrument operation, specimen suitability, and uses sound clinical judgment in setting the priority of tests/patients. OR Lab Tech I or II The Clinical Laboratory Technician I performs general laboratory testing in the areas of Hematology, Chemistry, Urinalysis, Transfusion Services, Coagulation, Microbiology, Serology, and Specimen processing with a high degree of accuracy and reliability. The data obtained is used in the diagnosis and treatment of disease involving patient of all ages. The Clinical Laboratory Technician II develops and maintains test procedures and protocols, and troubleshoots both technology and sample related problems. (S)he exercises independent judgment and responsibility with minimal supervision. Makes decisions about the accuracy of test results, instrument operation, specimen suitability, and uses sound clinical judgment in setting the priority of tests/patients. EDUCATION REQUIREMENTS/LICENSURE/CERTIFICATION/REGISTRATION Lab Scientist Bachelors' degree in Medical Technology and graduate of an accredited Medical Technology Program. Registered or eligible as a Medical Technologist (MT) or Clinical Laboratory Scientist (CLS) with a national accrediting agency (ASCP) or (AMT) or qualified as a MT/CLS having passed the Federal Equivalence Exam (HEW). Certification must be obtained within 9 months of employment. Meets the CLIA 88 requirements for individuals performing highly complex testing. CPR certification or obtained within 90 days of hire. OR Lab Tech I Associate degree and completion of a 2 year CLT / Medical Laboratory Technician (MLT) training program. Certified or eligible as a Clinical Laboratory Technician or Medical Laboratory Technician (MLT) with a national accrediting agency (ASCP) or (AMT). Certification must be obtained within 9 months of hire. Meets the CLIA 88 requirements for individuals performing highly complex testing. One year of experience in a clinical laboratory performing highly complex testing is preferred. CPR certification obtained within 90 days of hire. OR Lab Tech II Associate degree and completion of a 2 year CLT / Medical Laboratory Technician (MLT) training program. Certified or eligible as a Clinical Laboratory Technician or Medical Laboratory Technician (MLT) with a national accrediting agency (ASCP or AMT). Certification must be obtained within 9 months of hire. Meets the CLIA 88 requirements for individuals performing highly complex testing. A minimum of five years' experience as a CLT/MLT. CPR certification obtained within 90 days of hire FTE: 0.2 (8 hours per week) Shift: Monday-Friday Day/PM shift with every 3rd weekend rotation.

Our client, a leader in food chemistry testing, is seeking a Sample Prep Technician to join their team. As a Sample Prep Technician, you will be part of the Food Chemistry Testing Department supporting various teams. The ideal candidate will have attention to detail, strong communication skills, and a willingness to ask questions, which will align successfully in the organization. **Job Title:** Sample Prep Technician **Location:** Madison, WI **Pay Range: $18.50/hr plus shift differential ($20.17/hr)** **Shift:** 2pm - 10:30pm **What's the Job?** + Perform a variety of sample preparation tasks to ensure sample homogeneity, including labeling, transferring, and weighing samples. + Communicate sample information and discrepancies to appropriate personnel. + Handle internal customer inquiries and requests effectively. + Learn and apply critical thinking skills to solve problems quickly and efficiently. + Work collaboratively within a team to achieve departmental goals. **What's Needed?** + High School diploma or equivalent. + 1+ years working experience (not specific to industry) + Strong customer service skills, including attention to detail and effective communication. + Ability to learn new tasks and adapt to changing priorities. + Willingness to work in a fast-paced environment and maintain excellent attendance. **What's in it for me?** + Opportunity for growth and development within a reputable organization. + Engaging work environment with a focus on teamwork. + Hands-on experience in food chemistry testing. + Exposure to various sample preparation techniques and processes. + Potential for temp-to-hire transition based on performance. **Upon completion of waiting period associates are eligible for:** + Medical and Prescription Drug Plans + Dental Plan + Supplemental Life Insurance + Short Term Disability Insurance + 401(k) If this is a role that interests you and you'd like to learn more, click apply now and a recruiter will be in touch with you to discuss this great opportunity. We look forward to speaking with you! **About ManpowerGroup, Parent Company of: Manpower, Experis, Talent Solutions, and Jefferson Wells** _ManpowerGroup (NYSE: MAN), the leading global workforce solutions company, helps organizations transform in a fast-changing world of work by sourcing, assessing, developing, and managing the talent that enables them to win. We develop innovative solutions for hundreds of thousands of organizations every year, providing them with skilled talent while finding meaningful, sustainable employment for millions of people across a wide range of industries and skills. Our expert family of brands -_ **_Manpower, Experis, Talent Solutions, and Jefferson Wells_** _-_ creates substantial value for candidates and clients across more than 75 countries and territories and has done so for over 70 years. We are recognized consistently for our diversity - as a best place to work for Women, Inclusion, Equality and Disability and in 2023 ManpowerGroup was named one of the World's Most Ethical Companies for the 14th year - all confirming our position as the brand of choice for in-demand talent. ManpowerGroup is committed to providing equal employment opportunities in a professional, high quality work environment. It is the policy of ManpowerGroup and all of its subsidiaries to recruit, train, promote, transfer, pay and take all employment actions without regard to an employee's race, color, national origin, ancestry, sex, sexual orientation, gender identity, genetic information, religion, age, disability, protected veteran status, or any other basis protected by applicable law.

All Job Postings will close at 12:01a.m. CST (1:01a.m. EST) on the specified Closing Date (if designated).If you close the browser or exit your application prior to submitting, the application progress 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.Job Posting Title:Research Assistant - visiting Position Type:VisitorDepartment:LSUAG PL1 - SPESS - Plant Environmental and Soil Sciences (Brenda Tubana (00000851)) Work Location:Madison B. Sturgis (New Agronomy Bldg) Pay Grade:: The scholar will research the evaluation of silicon fertilization and application of silica solubilizing bacteria in improving crop tolerance to stress and productivity. Additional Job Description:Competencies:NoneSpecial Instructions:Visiting ScholarPosting Date:January 4, 2024Closing Date (Open Until Filled if No Date Specified):Additional Position Information: Background Check - An offer of employment is contingent on a satisfactory pre-employment background check. Benefits - The LSU AgCenter has an attractive benefits package with a wide variety of benefit options. Benefits offered include retirement, multiple medical insurance options, supplemental insurances (dental, life, long-term disability, accident, vision, long-term care, etc.), Tax Saver Flexible Benefits Plan (saves tax dollars on some childcare and medical expenses), university holidays (14 per year), generous annual (vacation) and sick leave benefits, Employee Assistance Program, and possible educational leave and tuition exemption for coursework at campuses of the LSU System. Specific benefits depend on job category, percent effort and length of employment. Positions approved to work outside the State of Louisiana shall be employed through Louisiana State University's partner, next Source Workforce Solutions, for Employer of Record Services including but not limited to employment, benefits, payroll, and tax compliance. Positions employed through Employer of Record Services will be offered benefits and retirement as applicable through their provider and will not be eligible for State of Louisiana benefits and retirement. Essential Position (Y/N):About the LSU Agricultural Center: The LSU AgCenter, is one of eight campuses within the broader LSU enterprise (LSU System). The LSU AgCenter includes the Louisiana Agricultural Experiment Station, which conducts agricultural-based research, and the Louisiana Cooperative Extension Service, which extends the knowledge derived from research to the people of the state. The AgCenter is headquartered in Baton Rouge and has 12 “on campus” academic departments and five regions which are made up of 15 branch research stations and an extension office in each parish. For more information, visit the AgCenter's website at ******************** The LSU Agricultural Center is an Equal Opportunity Employer and SAME Agency: The LSU Agricultural Center is a statewide campus of the LSU System and provides equal opportunities in programs and employment. The AgCenter is an Equal Opportunity/Affirmative Action Employer and is committed to fostering an environment of inclusion, respect, and appreciation of differences in individuals. To learn more, visit The AgCenter's Diversity, Inclusion and Opportunity site. The AgCenter is also designated as a State As a Model Employer (SAME) agency and provides assistance to persons needing accommodations or with the accessibility of materials. HCM Contact Information: Questions or concerns can be directed to the LSU AgCenter Human Resources Management Office at ************ or emailed ************************.

Since 1997, Truckstar has been an independent, family-owned and operated, heavy duty collision repair shop, helping to get our customers' vehicles back on the road. We pride ourselves in always doing the job right and work on all makes and models, so you never know what kind of vehicle is pulling in next! Truckstar takes pride in providing a fun and fulfilling environment for our employees. BENEFITS: Monthly incentives for work produced Weekly pay period Fun and family-like work environment Free coffee, donuts and pizza Company sponsored health insurance Company paid life insurance and group plan rates Company sponsored short term disability Paid vacation, holidays, and sick time 401k with up to 4% company match Dental and vision insurance Long-term disability, accident, and critical illness insurance Company sponsored and paid on-the-job training Company outings, potlucks, holiday parties, and a turkey or ham for Thanksgiving Overtime available ROLE AND RESPONSIBILITIES: Disassemble and assemble vehicles as needed Move and setup vehicles and equipment for blasting & painting Use hand and power tools to sand, prime and block Mask adjacent panels Wiping down and preparing for paint application Physical ability to work at a variety of heights and positions Read and understand work orders Wash vehicles and perform light detailing REQUIREMENTS: Work experience in collision repair industry Positive attitude Ability to read and understand work orders Ability to problem solve Willingness to learn Strong attention to detail Ability to work independently Be able to multitask Provide your own tools Be reliable We are an equal opportunity employer and prohibit discrimination/harassment without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity, or expression, or any other characteristic protected by federal, state or local laws.

Join our Phase I Clinical Research Unit and gain hands-on experience in clinical trials. Work closely with nurses and coordinators to support study procedures and ensure participant safety. Key Responsibilities: Perform vital signs, ECGs, and venipuncture. Collect, process, and distribute biological samples per protocol. Monitor participant meals for dietary compliance. Prepare rooms and equipment for study procedures. Accurately document research data and maintain confidentiality. Assist with screening and quality control of study documents. Ensure participant safety and respond to inquiries promptly. Requirements High School Diploma required; CNA, Medical Assistant, EMT, or Bachelor's in Science/Healthcare preferred. 0-2 years of experience in healthcare, science, or research. Phlebotomy experience strongly preferred. Knowledge of FDA, ICH, and GCP guidelines is a plus. Job Type & Location This is a Contract position based out of Madison, WI. Pay and Benefits The pay range for this position is $23.00 - $23.00/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 Madison,WI. Application Deadline This position is anticipated to close on Jan 23, 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.

Scientist I** **Department: Microbiology** **Shift: Full-Time; Monday - Friday 2pm-10pm** This is a fully onsite role based at our GMP Laboratory in Middleton, WI. We welcome applicants from all locations within the U.S. Please note that relocation assistance is not provided for this position, and any relocation costs will be the responsibility of the candidate. Must be legally authorized to work in the United States without sponsorship. Must be able to pass a comprehensive background check, which includes a drug screening. At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future. Our PPD Laboratory Services team has a direct impact on improving patient health through the expertise of scientists, industry thought leaders and therapeutic experts. As the world leader in serving science, our laboratory professionals bring their commitment to accuracy and quality to deliver groundbreaking innovations. **Discover Impactful Work:** As a Scientist I, you will use innovative technologies to perform high-quality sample testing for key pharmaceutical clients across the industry. Your sample preparation and analysis serve as an integral piece in helping PPD accomplish our goal of helping bring life-changing therapies to market. **A day in the Life:** + Possesses an understanding of laboratory procedures and under general supervision can conduct complex analysis. + Performs a variety of routine sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices for stability and analytical testing. + Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory guidelines. + Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. **Education** + Bachelor's degree (Life Sciences degree preferred) or equivalent and relevant formal academic / vocational qualification **Experience** + Previous experience that provides the knowledge, skills, and abilities to perform the job + Previous work experience which is comparable to 0-2 years, or equivalent combination of education, training, and experience. + In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role. **Knowledge, Skills, Abilities** + Knowledge of routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory guidelines + Knowledge of applicable regulatory authority, compendia and ICH guidelines + Excellent manual dexterity skills + Good written and oral communication skills + Time management and project management skills + Proven solving and troubleshooting abilities + Ability to cross-train on sample preparation techniques with another laboratory group + Ability to work in a collaborative work environment with a team + Manual dexterity and can follow detailed written and verbal instruction + Cooperate with coworkers within an organized team environment or work alone with supervision + Manage time effectively to complete assignments in expected time frame **Working Environment** Thermo Fisher Scientific values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role: + Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner. + Able to work upright and stationary and/or standing for typical working hours. + Able to lift and move objects up to 25 pounds. + Able to work in non-traditional work environments. + Able to use and learn standard office equipment and technology with proficiency. + May have exposure to potentially hazardous elements, including infectious agents, typically found in healthcare or laboratory environments. + Able to perform successfully under pressure while prioritizing and handling multiple projects or activities. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued. **Apply today! ****************************** Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status. **Accessibility/Disability Access** Job Seekers with a Disability: Thermo Fisher Scientific offers accessibility service for job seekers requiring accommodations in the job application process. For example, this may include individuals requiring assistance because of hearing, vision, mobility, or cognitive impairments. If you are a job seeker with a disability, or assisting a person with a disability, and require accessibility assistance or an accommodation to apply for one of our jobs, please submit a request by telephone at ***************. Please include your contact information and specific details about your required accommodation to support you during the job application process. This telephone line is reserved solely for job seekers with disabilities requiring accessibility assistance or an accommodation in the job application process. Messages left for other purposes, such as not being able to get into the career website, following up on an application, or other non-disability related technical issues will not receive a response. Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

Laboratory bench work individually or in a team setting to accomplish daily Quality Control lab tasks. Active participation as a member of the Quality Control team in testing and release of production materials. Working in a lab setting to supporting fermentation facility that produces probiotics and dairy cultures. ESSENTIAL DUTIES AND RESPONSIBILITIES The essential functions of this position include, but are not limited to, the following: · Adhere to all quality systems including, but not limited to, ISO 22000, NSF, and GLP guide-lines, with an understanding of IFF's Quality Policy and procedures. · Perform routine lab testing with accurate and timely recording of test results into the SAP Quality Management module and utilize lab reference materials for information regarding testing. · Understand and follow procedures of the department for the proper calibration and use of the department's equipment. · Understand and follow Good Manufacturing Practices for the care, handling, and storage of food and Dietary Supplement products. · Perform environmental sampling procedures. · Follow and enforce laboratory safety procedures. KNOWLEDGE, SKILLS AND ABILITIES · Must have bachelor's degree in chemistry, Microbiology, Biology or similar field, or associate degree with at least 1 year relevant experience. · Must be knowledgeable about the analyses and tests performed in the Quality Control de-partment. · Must have the ability to work as an active team member as well as independently. · Must have strong math and good communication skills (both verbal and written). WORKING CONDITIONS This position operates in a laboratory environment 95-100% of the time. Exposure to hazardous materials training is required. Must wear Personal Protective Equipment (PPE) as appropriate in accordance with plant policy. SCOPE OF POSITION This position reports directly to the Quality Control Supervisor and has no direct supervisory responsibilities. Must be able to work overtime as needed. Management retains the discretion to add or change the duties and responsibilities of this position at any time. We are a global leader in taste, scent, and nutrition, offering our customers a broader range of natural solutions and accelerating our growth strategy. At IFF, we believe that your uniqueness unleashes our potential. We value the diverse mosaic of the ethnicity, national origin, race, age, sex, or veteran status. We strive for an inclusive workplace that allows each of our colleagues to bring their authentic self to work regardless of their religion, gender identity & expression, sexual orientation, or disability. Visit IFF.com/careers/workplace-diversity-and-inclusion to learn more

Why Choose Labcorp? At Labcorp, our people are the heart of everything we do. We're not just a global life sciences company - we're a team of passionate individuals working together to improve health and change lives. Whether you're just starting out or looking to grow your career, you'll collaborate with brilliant minds, explore your potential, and make a real impact on the future of medicine. Step Into a Role That Moves Your Career Forward We're looking for a Research Technician to join our Dose Formulation team in Madison, WI. In this hands-on lab role, you'll help prepare materials that support groundbreaking research and drug development. What You'll Do As a Study Technician, you'll learn and perform essential lab techniques to prepare test materials for preclinical studies. Your day-to-day will include: Preparing lab reagents, solutions, suspensions, and capsules per study protocols Recording data accurately in both digital and written formats Learning formulation verification, sample disposition, and safe handling procedures Collaborating with scientists and technicians to ensure study integrity Maintaining a clean, safe, and GLP-compliant lab environment Developing skills in study setup, data organization, and client communication Education/Experience A Bachelor's degree in Chemistry or a related scientific field A strong attention to detail and eagerness to learn A passion for science and a desire to contribute to life-changing research Work Schedule 1st Shift: 7:30am - 4:15pm Pay: $23/hour Why You'll Love Working Here Be part of a mission-driven company that's improving lives Gain hands-on lab experience in a regulated, high-impact environment Grow your career with mentorship, training, and advancement opportunities Benefits: Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO), Tuition Reimbursement and Employee Stock Purchase Plan. Casual, PRN & Part Time employees regularly scheduled to work less than 20 hours are eligible to participate in the 401(k) Plan only. For more detailed information, please click here. Labcorp is proud to be an Equal Opportunity Employer: Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. We encourage all to apply If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site or contact us at Labcorp Accessibility. For more information about how we collect and store your personal data, please see our Privacy Statement.

All Job Postings will close at 12:01a.m. CST (1:01a.m. EST) on the specified Closing Date (if designated).If you close the browser or exit your application prior to submitting, the application progress 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.Job Posting Title:Research Assistant - visiting Position Type:VisitorDepartment:LSUAG PL1 - SPESS - Plant Environmental and Soil Sciences (Brenda Tubana (00000851)) Work Location:Madison B. Sturgis (New Agronomy Bldg) Pay Grade:: The scholar will work on silicon research in crop production and investigate the potential of silica solubilizing bacteria as biostimulant in improving crop productivity. Additional Job Description:Competencies:NoneSpecial Instructions:Visiting ScholarPosting Date:January 4, 2024Closing Date (Open Until Filled if No Date Specified):Additional Position Information: Background Check - An offer of employment is contingent on a satisfactory pre-employment background check. Benefits - The LSU AgCenter has an attractive benefits package with a wide variety of benefit options. Benefits offered include retirement, multiple medical insurance options, supplemental insurances (dental, life, long-term disability, accident, vision, long-term care, etc.), Tax Saver Flexible Benefits Plan (saves tax dollars on some childcare and medical expenses), university holidays (14 per year), generous annual (vacation) and sick leave benefits, Employee Assistance Program, and possible educational leave and tuition exemption for coursework at campuses of the LSU System. Specific benefits depend on job category, percent effort and length of employment. Positions approved to work outside the State of Louisiana shall be employed through Louisiana State University's partner, next Source Workforce Solutions, for Employer of Record Services including but not limited to employment, benefits, payroll, and tax compliance. Positions employed through Employer of Record Services will be offered benefits and retirement as applicable through their provider and will not be eligible for State of Louisiana benefits and retirement. Essential Position (Y/N):About the LSU Agricultural Center: The LSU AgCenter, is one of eight campuses within the broader LSU enterprise (LSU System). The LSU AgCenter includes the Louisiana Agricultural Experiment Station, which conducts agricultural-based research, and the Louisiana Cooperative Extension Service, which extends the knowledge derived from research to the people of the state. The AgCenter is headquartered in Baton Rouge and has 12 “on campus” academic departments and five regions which are made up of 15 branch research stations and an extension office in each parish. For more information, visit the AgCenter's website at ******************** The LSU Agricultural Center is an Equal Opportunity Employer and SAME Agency: The LSU Agricultural Center is a statewide campus of the LSU System and provides equal opportunities in programs and employment. The AgCenter is an Equal Opportunity/Affirmative Action Employer and is committed to fostering an environment of inclusion, respect, and appreciation of differences in individuals. To learn more, visit The AgCenter's Diversity, Inclusion and Opportunity site. The AgCenter is also designated as a State As a Model Employer (SAME) agency and provides assistance to persons needing accommodations or with the accessibility of materials. HCM Contact Information: Questions or concerns can be directed to the LSU AgCenter Human Resources Management Office at ************ or emailed ************************.

Join our Phase I Clinical Research Unit and gain hands-on experience in clinical trials. Work closely with nurses and coordinators to support study procedures and ensure participant safety. Key Responsibilities: + Perform vital signs, ECGs, and venipuncture. + Collect, process, and distribute biological samples per protocol. + Monitor participant meals for dietary compliance. + Prepare rooms and equipment for study procedures. + Accurately document research data and maintain confidentiality. + Assist with screening and quality control of study documents. + Ensure participant safety and respond to inquiries promptly. Requirements + High School Diploma required; CNA, Medical Assistant, EMT, or Bachelor's in Science/Healthcare preferred. + 0-2 years of experience in healthcare, science, or research. + Phlebotomy experience strongly preferred. + Knowledge of FDA, ICH, and GCP guidelines is a plus. Job Type & Location This is a Contract position based out of Madison, WI. Pay and Benefits The pay range for this position is $23.00 - $23.00/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 Madison,WI. Application Deadline This position is anticipated to close on Jan 23, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.