Laboratory Scientist jobs at Alverno Laboratories - 274 jobs

LeaderStat is seeking a travel Cath Lab Technologist for a travel job in Mattoon, Illinois. Job Description & Requirements Specialty: Cath Lab Technologist Discipline: Allied Health Professional Duration: 13 weeks 40 hours per week Shift: 8 hours Employment Type: Travel Estimated Pay Package : Up to $ 3319.20 per week *The above pay package is an estimate, please contact our team to put together your personalized pay package, as a variety of factors can influence your total pay.* Temp - Technologist - Cath Lab (Days) Mattoon, IL in Mattoon, IL LeaderStat is currently seeking a Temp - Technologist - Cath Lab (Days) Mattoon, IL for a(n) 13 week contract in IL. Start Date: 2/16/2026 End Date: 5/18/2026 Shift: Days, 40 Hour Guarantee 1 year of experience working as a full-time Technologist Clinical experience within the last 2 years Current State Licensure Current Relevant Certifications (BLS, ACLS, etc) The LeaderStat Difference Our LeaderStat recruiters are experts in travel healthcare! We work hard to find the best assignments for each candidate. However, our service doesn't end at placement. We set you up for success by providing support throughout your contract... from start to finish! Our goal is to find the best travel healthcare assignments to fit your individual needs. While you focus on providing top-notch care to your patients, we'll handle the rest. LeaderStat Perks & Benefits As a traveling healthcare professional with LeaderStat you receive excellent benefits: Weekly Pay & Direct Deposit W2 Employee Status 401(k) Retirement Plan Medical, Dental and Vision Insurance Referral Bonuses Dedicated Support Team To learn more about LeaderStat visit ************************* -nursing Equal Employment Opportunity: LeaderStat, Ltd. prohibits discrimination with respect to the hiring or promotion of individuals, conditions of employment, disciplinary and discharge practices or any other aspect of employment on the basis of sex, race, color, age, national origin, religion, disability, marital status, sexual orientation, gender identity, pregnancy or veteran status. LeaderStat Job ID #289771. Pay package is based on 8 hour shifts and 40 hours per week (subject to confirmation) with tax-free stipend amount to be determined. Posted job title: Catheterization Laboratory - Technologist About LeaderStat LeaderStat is a National staffing, recruiting, and consulting firm dedicated to the healthcare industry. For 20 years, LeaderStat has been dedicated to partnering with exceptional healthcare providers to find them the very best assignments throughout the country. Specializing in Travel Nursing, Interim Leadership, Executive Search, and Consulting. When you work with the LeaderStat team, you work with a recruiter who is dedicated to finding you the perfect assignment. Why would you settle for less? Benefits Referral bonus License and certification reimbursement Medical benefits Holiday Pay Weekly pay 401k retirement plan

is $34.50 - $46.58 (Hourly Rate) Placement within the salary range is dependent on several factors such as relevant work experience and internal equity. For positions represented by a labor union, placement within the salary range is guided by the rules outlined in the collective bargaining agreement. We offer a wide range of benefits that provide employees with tools and resources to improve their physical, emotional, and financial well-being while providing protection for unexpected life events. Please visit our Benefits section located at jobs.nm.org/benefits to learn more. Northwestern Medicine is powered by a community of colleagues who are purpose-driven and committed to our mission to deliver world-class care. Here, you'll work alongside some of the best clinical talent in the nation leading the way in medical innovation and breakthrough research with Northwestern University Feinberg School of Medicine. We recognize where you've been, and we support where you're headed. We celebrate diverse perspectives and experiences, which fuel our commitment to equity and culture of service. Grow your career with comprehensive training and development opportunities, mentorship programs, educational support and student loan repayment. Create the life you envision for yourself with flexible work options, a Reimbursable Well-Being Fund and a Total Rewards package that support your physical, mental, emotional, and financial well-being. Make a difference through volunteer opportunities we offer in local communities and drive inclusive change through our workforce-led resource groups. From discovery to delivery, come help us shape the future of medicine. Benefits: * $10,000 Tuition Reimbursement per year ($5,700 part-time) * $10,000 Student Loan Repayment ($5,000 part-time) * $1,000 Professional Development per year ($500 part-time) * $250 Wellbeing Fund per year ($125 for part-time) * Matching 401(k) * Excellent medical, dental and vision coverage * Life insurance * Annual Employee Salary Increase and Incentive Bonus * Paid time off and Holiday pay Description The Cellular Therapy Scientist reflects the mission, vision, and values of NM, adheres to the organization's Code of Ethics and Corporate Compliance Program, and complies with all relevant policies, procedures, guidelines and all other regulatory and accreditation standards. The incumbent will perform process development, assay development and validations under supervision of the laboratory Director as well as manufacture cellular therapy products for treatments of patients on clinical trials and standard of care plans. Responsibilities: Technical: * Responsible for manufacturing of autologous and allogeneic cell and gene therapy products according to standard operating procedures, and specific guidance for clinical trials/commercial products, using aseptic technique * Performs cell and gene therapy product manufacturing under GXP (GLP, GTP, GMP, GDP) guidelines and protocols to ensure the quality of cellular therapy products and regulatory compliance * Performs various quality control testing of cellular therapy products and components with immunological and cell biological techniques required for the quality of cellular therapy products * Performs cellular therapy product infusion preparation and product transport under established procedures * Accurately document processing records, generate and review processing reports and charts * Assist in inspections and audits to ensure compliance with regulations from Federal Drug Administration (FDA) and other regulatory agencies * Required to wear pager to respond promptly to emergency calls and for critical equipment failure. * Performs cell and gene therapy manufacturing process development, assay development, optimization, validation, and verification for cellular therapy investigational new drug applications * Ability to troubleshoot issues in process and assay development, analyze results and compile reports. * Performs technology transfer from lab bench to clinical manufacturing * Performs preventative maintenance on facility and instruments/equipment in a timely fashion according to defined procedures and schedule * Assists in equipment installation/operation/performance qualifications (IQ/OQ/PQ) * Verifies reagents and supplies meet defined acceptability criteria upon receipt and prior to use; take action to ensure unacceptable items are removed from use; ensures that sufficient reagents and supplies necessary for manufacturing are available * Performs and records all necessary quality control (QC) required for product manufacture, evaluate QC results and take necessary corrective actions according to established protocol * Writes or assist in writing standard operating procedures * Reviews results for completeness, correctness, and consistency * Participate in training and competency assessment. Keep up with current knowledge of cellular therapy product manufacturing and analytical techniques and industry practices Universal responsibilities: * Ensures quality of operations: * Follows written standard operating procedures (SOP) * Operates instruments/equipment according to protocol * Uses computers according to established protocol; follows downtime procedures as required * Performs required quality system responsibilities * Participates in the training of new employees, fellows and students * Attends at least one personal development session per year * Performs other duties as assigned, or as needed, to ensure continued quality operations * Ensures safety of operations: * Follows all required safety procedures, uses personal protective equipment (PPE) appropriate for tasks performed, and assumes a proactive role in laboratory safety * Maintains clean and organized work area * Provides service excellence: * Answers telephone when needed, using NM telephone etiquette * Maintains patient confidentiality including protected health information (PHI) * Assists patients, visitors and other contacts whenever need occurs Qualifications Required: * Bachelor's degree in Medical Technology, Medical Laboratory Science, Clinical Laboratory Science, Chemistry, Biology, immunology, Molecular Biology and other related field. * Minimum of 1~2 years of relevant laboratory experience including training in a technical specialty. Preferred: * Master's degree or higher in Chemistry, Biology, immunology, Molecular Biology and other related field. * Working Experience in a cellular therapy laboratory or in clinical hematology or blood bank setting preferred. Bone marrow and/or stem cell processing, blood banking, hematology, cell culture and apheresis. * Experience with processing of either mammalian cells for upstream and downstream processing of viral vectors, or primary tissue and human blood for the isolation and expansion of immune cell populations (e.g. T-cells, NK cells, T-regs, monocytes, dendritic cells, etc.) and also characterization assays for cells and proteins (flow cytometry, ELISA, functional assays, etc.). Equal Opportunity Northwestern Medicine is an equal opportunity employer (disability, VETS) and does not discriminate in hiring or employment on the basis of age, sex, race, color, religion, national origin, gender identity, veteran status, disability, sexual orientation or any other protected status. Background Check Northwestern Medicine conducts a background check that includes criminal history on newly hired team members and, at times, internal transfers. If you are offered a position with us, you will be required to complete an authorization and disclosure form that gives Northwestern Medicine permission to run the background check. Results are evaluated on a case-by-case basis, and we follow all local, state, and federal laws, including the Illinois Health Care Worker Background Check Act. Artificial Intelligence Disclosure Artificial Intelligence (AI) tools may be used in some portions of the candidate review process for this position, however, all employment decisions will be made by a person. Benefits We offer a wide range of benefits that provide employees with tools and resources to improve their physical, emotional, and financial well-being while providing protection for unexpected life events. Please visit our Benefits section to learn more. Sign-on Bonus Eligibility: Internal employees and rehires who left Northwestern Medicine within 1 year are not eligible for the sign on bonus. Exception: New graduate internal employees seeking their first licensed clinical position at NM may be eligible depending upon the job family.

Evergen is a global industry-leading contract development and manufacturing organization (CDMO) in regenerative medicine. As the only regenerative medicine company that offers a differentiated portfolio of allograft and xenograft biomaterials at scale, Evergen is headquartered in Alachua, FL, and has manufacturing facilities in West Lafayette, IN., Eden Prairie and Glencoe, MN., Neunkirchen, DE., Glasgow, UK., and Marton, NZ. Read more about this change and Evergen's commitment to advancing regenerative medicine here: ************************ ; RESPONSIBILITIES Perform quality control routine testing for raw material/ Intermediate/ Release and Stability testing Perform Method development and method validation execution, including writing protocols and reports Must have good communication skills and be able to, coordinate, and communicate with clients, both internal and external Working knowledge of instrument qualification (e.g. IQ, OQ, PQ, calibration) Meet internal timelines Meet client expectations Perform investigations Ability to use good judgment, diplomacy, maintain confidentiality, and exercise discretion regarding various operational matters and customer service.. Other duties as assigned REQUIREMENTS Education Bachelor's degree in Chemistry Experience 0 to 2 years of lab experience (entry level). Skills Familiarity with the company and CFR 21-part 11 compliance Familiarity with pharmaceutical testing requirements in a company laboratory environment Experienced with HPLC preferred Empower experience is preferred, but not required Experienced or familiar with UV-Vis, Dissolution, FTIR, and general lab equipment. Travel N/A SAFETY Physical Requirement Move or lift objects up to 25 pounds Frequent (>75%) stationary position (standing or sitting) while utilizing digital displays Frequent (>75%) fine manipulation using hands and fingers (typing, opening, writing, clicking, paper sorting, etc.) Working Environment Onsite: Office environment with assigned workstation Remote positions only: Home office environment with minimum distractions More about Evergen: Evergen provides customers across a diverse set of market segments with leading-edge expertise, scale, and flexibility across end-to-end services including design, development, regulatory support, verification and validation, manufacturing, and supply chain management. Evergen is rooted in a steadfast commitment to quality, integrity, and patient safety with a focus on five key values: Accountable: We own our actions and decisions. Agile: We embrace change to stay ahead of the curve and evolve to drive innovation and growth. Growth Mindset: We embrace challenges as opportunities for continuous learning. Customer-Centric: We prioritize customers at every touch point. Inclusive: We thrive on the richness of our diversity and ensure every voice is heard, respected, and celebrated. At Evergen, we are committed to fostering an inclusive workplace where we embrace the richness of our diversity and ensure that every voice is heard, respected, and celebrated. We believe that by embracing diversity and promoting inclusivity, we not only uphold our values but also strengthen our position as the CDMO of Choice in regenerative medicine solutions. We recognize that cultivating a growth mindset is essential to our success, and we are dedicated to continuous learning and improvement in our diversity, equity, and inclusion efforts. Through accountability and action, we strive to create an environment where individuals can thrive, innovate, and contribute their unique perspectives to drive our collective success. Montagu Private Equity (“Montagu”), a leading European private equity firm, acquired RTI in 2020 and has supported the transformation of the company to its next level of potential. #LI-Onsite

Job Title: Embryologist Trainee The Embryologist Trainee will assist in day-to-day laboratory operations, including specimen collection, processing, and test performance. The role involves training in IVF equipment maintenance, andrology functions, endocrine testing, and phlebotomy, while ensuring compliance with safety, regulatory, and quality control standards. Key Responsibilities: * Follow lab procedures for specimen collection, processing, and reporting results. * Maintain lab equipment and ensure quality control. * Adhere to safety and regulatory standards (FDA, CAP). * Assist in inventory management and quality assurance data entry. * Provide support for gametes, tissue, and embryo preservation. Explore All Benefits: ******************************************************************************** Qualifications: * Bachelor's degree in Biological Sciences or related field. * Minimum one year of relevant laboratory experience. * High school diploma required.

Passionate about precision medicine and advancing the healthcare industry? Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way. Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time. Tempus' proprietary data and platform connect an entire ecosystem of real-world data to deliver real-time, actionable insights to physicians. Our data empowers researchers to better characterize and understand disease, and to drive better outcomes through precise, individualized care. The Computational Biologist II - Translational Research will execute research projects for early stage biopharmaceutical partners. This role involves performing complex computational analyses, and providing interpreted insights to guide decision-making for biopharma clients. The ideal candidate will possess strong genomic analytical skills and the ability to communicate complex scientific findings to various stakeholders. Key Responsibilities: Independent Contribution: Independently execute complex translational research projects integrating molecular and clinical data from Tempus multimodal data platform to derive real-world insights for biopharma partners Scientific Communication: Present scientific findings clearly and meaningfully to diverse sets of external stakeholders Continuous Improvement: Stay current with industry trends, best practices, and advancements in computational oncology research. Apply this knowledge to enhance research methodologies and improve overall research quality on team Qualifications: Education: PhD degree in a quantitative discipline (e.g. Biostatistics/Statistical Genetics, Cancer Genetics, Bioinformatics, Computational Biology, Computational Immunology or similar) or, a PhD in Molecular Biology or Immunology combined with a very strong record of computational biology. Alternatively an MSc degree with 4+ years of industry experience. Technical/Scientific Skills: Highly proficient in R (ideally Rmd and/or RShiny) Communication Skills: Excellent written and verbal communication skills, with the ability to present complex information clearly and persuasively to diverse audiences. Preferred Skillsets/Background: Strong understanding of molecular data and artificial intelligence in drug discovery with experience in integrative modeling of multi-modal clinical and omics data. Previous experience working with large transcriptome and NGS data sets. Prior consulting and/or client facing experience is highly desirable Ability to work collaboratively in a team environment Thrive in a fast-paced environment and willing to shift priorities seamlessly. Experience with R package development. Strong peer-reviewed publication record. Experience with: Pandas, NumPy, SciPy, Scikit-learn, Jupyter Notebooks, RStudio, R Package development, tidyverse, ggplot, Git, matplotlib, seaborn, HTML5, CSS3, JavaScript, D3, Plot.ly, Flask, Dask, Docker, AWS. Goal orientation, self motivation, and drive to make a positive impact in healthcare. CHI: $90,000-$135,000 USD NYC/SF: $100,000-$150,000 USD The expected salary range above is applicable if the role is performed from California and may vary for other locations (Colorado, Illinois, New York). Actual salary may vary based on qualifications and experience. Tempus offers a full range of benefits, which may include incentive compensation, restricted stock units, medical and other benefits depending on the position. Additionally, for remote roles open to individuals in unincorporated Los Angeles - including remote roles- Tempus reasonably believes that criminal history may have a direct, adverse and negative relationship on the following job duties, potentially resulting in the withdrawal of the conditional offer of employment: engaging positively with customers and other employees; accessing confidential information, including intellectual property, trade secrets, and protected health information; and appropriately handling such information in accordance with legal and ethical standards. Qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law, including the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. We are an equal opportunity employer. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

A Research Scientist performs relevant background research on a topic and develops pertinent questions and experimental designs with general guidance. This role conducts and analyzes experiments on complex biological topics with limited supervision while assisting with laboratory maintenance. This role is part of a team investigating potential new product areas while also assisting with informal training, trouble-shooting of methods or equipment, and connecting with others in R&D through excellent written and verbal communication. We are looking for self-motivated candidates who are eager to contribute creative ideas and quickly generate and analyze high quality data supporting the design and testing of novel therapeutic agents and materials. Responsibilities Contribute ideas for new experiments. Set own objectives to achieve larger project goals. Conduct and analyze experiments. Own the writing of experiment documentation including methods, reports and validation protocols. Contribute to laboratory maintenance including equipment calibrations. Initiate problem-solving of equipment or methodological issues. Generate project reports and assist with writing manuscripts or IP for external review. Present data internally within team or department. Assist in technology transfer to development by providing technical support, generating development reports, and data analysis. Assist in identifying new materials or methods for achieving project goals and determining best practices for their use and testing. Provide occasional guidance to others within the team. Qualifications BS degree life science/engineering with 3 years relevant experience Previous experience with biology/biotechnology industries preferred Experience with advanced cell culture models and quantitative molecular or biological assays Operation and validation of specialty instrumentation Experience with sourcing and testing of new materials Must be able to work independently and as part of a multi-disciplinary team and committed to high quality work Must be highly motivated, have excellent organizational and communication skills Physical Requirements: Position requires training in blood borne pathogen safety measures New hires will be given the option of Hepatitis B vaccination Position requires use of cryogenic substances (liquid nitrogen) and in handling potentially pathogenic agents. Training will be required as part of role. Applications must be able to work in a controlled laboratory environment All procedures in which infectious aerosols or splashes may be created are conducted in biosafety cabinets (BSCs) or other physical containment equipment. This position requires work in a Biosafety Level 2 environment involving agents that pose moderate hazards to personnel and the environment

A Research Scientist performs relevant background research on a topic and develops pertinent questions and experimental designs with general guidance. This role conducts and analyzes experiments on complex biological topics with limited supervision while assisting with laboratory maintenance. This role is part of a team investigating potential new product areas while also assisting with informal training, trouble-shooting of methods or equipment, and connecting with others in R&D through excellent written and verbal communication. We are looking for self-motivated candidates who are eager to contribute creative ideas and quickly generate and analyze high quality data supporting the design and testing of novel therapeutic agents and materials. Responsibilities * Contribute ideas for new experiments. * Set own objectives to achieve larger project goals. * Conduct and analyze experiments. * Own the writing of experiment documentation including methods, reports and validation protocols. * Contribute to laboratory maintenance including equipment calibrations. * Initiate problem-solving of equipment or methodological issues. * Generate project reports and assist with writing manuscripts or IP for external review. * Present data internally within team or department. * Assist in technology transfer to development by providing technical support, generating development reports, and data analysis. * Assist in identifying new materials or methods for achieving project goals and determining best practices for their use and testing. * Provide occasional guidance to others within the team. Qualifications * BS degree life science/engineering with 3 years relevant experience * Previous experience with biology/biotechnology industries preferred * Experience with advanced cell culture models and quantitative molecular or biological assays * Operation and validation of specialty instrumentation * Experience with sourcing and testing of new materials * Must be able to work independently and as part of a multi-disciplinary team and committed to high quality work * Must be highly motivated, have excellent organizational and communication skills Physical Requirements: * Position requires training in blood borne pathogen safety measures * New hires will be given the option of Hepatitis B vaccination * Position requires use of cryogenic substances (liquid nitrogen) and in handling potentially pathogenic agents. Training will be required as part of role. * Applications must be able to work in a controlled laboratory environment * All procedures in which infectious aerosols or splashes may be created are conducted in biosafety cabinets (BSCs) or other physical containment equipment. * This position requires work in a Biosafety Level 2 environment involving agents that pose moderate hazards to personnel and the environment

Passionate about precision medicine and advancing the healthcare industry? Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way. Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time. Focus: Contribute to the design of the core architecture of LMMs and building of the infrastructure for training it at scale. Responsibilities: You will contribute to the following activities: Design and definition of the architecture of the LMMs, considering different fusion strategies and modality-specific processing. Implement, refine, benchmark and optimize model architectures using deep learning frameworks such as PyTorch or TensorFlow. Develop and manage the end-to-end training pipelines, including data loading, preprocessing, and model training. Architect and deploy distributed training workflows, optimizing for performance across cloud GPU fleets. Implement distributed training strategies to handle large-scale datasets and models. Design and implement methods to fuse knowledge with the multimodal representations within the LMM. Experiment with different approaches to enhance the model's understanding and reasoning abilities through knowledge integration. Monitor and debug training processes, identifying and resolving performance bottlenecks. Collaborate with the knowledge integration engineer to ensure the architecture can accommodate knowledge injection mechanisms. Skills needed: Deep understanding of deep learning principles and architectures (especially transformers). Extensive experience with multimodal machine learning concepts and techniques (for example, different fusion methods for text and images). Solid understanding of optimization techniques for large-scale models. Strong proficiency in Python and deep learning frameworks (PyTorch/TensorFlow) and model management libraries like HF Transformers. Experience with training large multimodal models with distributed training frameworks (for example, Horovod, MosaicML) and GPU fleet management. Strong understanding of knowledge representation concepts (for example, knowledge graphs, ontologies). Experience with distributed training frameworks and cloud computing platforms (for example, GCP, Azure). #LI-SH1 New York Pay Range - $220,000 - $260,000 USD California Pay Range - $220,000 - $260,000 USD Illinois Pay Range - $200,000 - $240,000 USD Remote - USA Range - $200,000 - $240,000 USD The expected salary range above is applicable if the role is performed from California and may vary for other locations (Colorado, Illinois, New York). Actual salary may vary based on qualifications and experience. Tempus offers a full range of benefits, which may include incentive compensation, restricted stock units, medical and other benefits depending on the position. Additionally, for remote roles open to individuals in unincorporated Los Angeles - including remote roles- Tempus reasonably believes that criminal history may have a direct, adverse and negative relationship on the following job duties, potentially resulting in the withdrawal of the conditional offer of employment: engaging positively with customers and other employees; accessing confidential information, including intellectual property, trade secrets, and protected health information; and appropriately handling such information in accordance with legal and ethical standards. Qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law, including the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. We are an equal opportunity employer. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

fairlife, LLC is a Chicago-based nutrition company that creates great-tasting, nutrition-rich and dairy products to nourish consumers. With over $3B in annual retail sales, fairlife's portfolio of delicious, lactose-free, real dairy products includes: fairlife ultra-filtered milk; Core Power High Protein Shakes, a sports nutrition drink to support post-workout recovery; fairlife nutrition plan™, a nutrition shake to support the journey to better health. A wholly owned subsidiary of The Coca-Cola company, fairlife, LLC has been recognized by both Fast Company and Nielsen for its industry leading innovation. To learn more about fairlife and its complete line of products, please visit fairlife.com. job purpose: The Associate Scientist will be applying scientific principles, conducting research experiments, and producing reliable test results. The primary objectives of this position are to resolve technical challenges, develop new products, improve existing products, validate testing methods, or enhance efficiency. The candidate should be comfortable working with a team and should have a passion for creativity and innovation within a fast-paced environment. The successful candidate will learn to interpret and apply scientific findings to dairy systems, to translate findings into innovative manufacturing processes and products. responsibilities: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Design and conduct benchtop experiments and perform tests according to research plan. Up-scale trials from benchtop to pilot plant and perform tests according to research plan. Design and execute shelf-life studies on selected products including routine analysis and sensory evaluations. Keeping up to date with relevant scientific and technical developments. Analyzing and summarizing research data. Presenting scientific findings to the R&D team and to other functions when needed. Consistently deliver concise, accurate and complete reporting of work in the specified format (written and/or electronic). Operating benchtop and pilot plant equipment. Adhering to GMP and other safety regulations. Maintaining a safe, clean, and sanitary work area. Organizing, storing, and handling all chemical substances, fluids, and compressed gases according to safety instructions. Ensuring that safety guidelines are adhered to at all times within the laboratory. Cleaning, sterilizing, maintaining, and calibrating laboratory equipment. Providing technical support when necessary. Performing other duties assigned by supervisor. skills/qualifications required: BS or MS degree in food science with either a focus on dairy science or a working experience in dairy 0-1 years' experience in a lab/ pilot plant environment. Previous working knowledge related to at least one of the following: food science, product recipe/formulation, process research, experimental design and/or plant trials. Hands-on experience operating electrical and non-electrical laboratory equipment. In depth knowledge of QHSE management systems, preventative measures, and laboratory best practices. Ability to handle ambiguity and work in a fast paced, entrepreneurial environment. Working knowledge of MS Office Suite and database systems. Excellent verbal and written communication skills Strong analytical skills. Willingness to travel overnight, and to work night and weekend shifts for special projects working conditions and physical requirements: 8+ hours sitting/standing/walking Ability to lift up to 40 lbs. Exposure to hazards (machinery, flammable liquids, biohazards, etc.), etc.) position location: Chicago, IL reports to: Director, R&D travel requirements: 5-15% exempt/nonexempt: exempt #LI-Onsite #LI-BB1 *Base pay offered may vary depending on geography, job-related knowledge, skills, and experience. A full range of medical, financial, and/or other benefits, dependent on the position, is offered. Base pay range:$75,000-$90,000 USD fairlife, LLC is an equal opportunity employer. We do not discriminate on the basis of 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. All qualified applicants and employees will be given equal opportunity. Selection decisions are based on job-related factors. In addition to its nondiscrimination commitment, the Company will also provide reasonable accommodation of qualified individuals with known disabilities unless doing so would impose an undue hardship on the Company. If you have a disability and would like to request accommodation in order to apply for a position with us, please email ******************** . For Recruitment Agencies At fairlife, we manage the majority of our hiring internally through our dedicated Talent Acquisition team, which is actively engaged in direct candidate sourcing. Most of our roles are filled through applications submitted via our careers site or through direct outreach by our team. As our recruitment is primarily handled in-house, we work only occasionally with external agencies, and only those on our existing, pre-approved vendor list. At this time, we are not reviewing or expanding that list. Unsolicited resumes or submissions from external agencies not authorized by our Talent Acquisition team will be considered direct candidate applications. As such, fairlife will not assume responsibility for any placement fees associated with these submissions.

Job Description fairlife, LLC is a Chicago-based nutrition company that creates great-tasting, nutrition-rich and dairy products to nourish consumers. With over $3B in annual retail sales, fairlife's portfolio of delicious, lactose-free, real dairy products includes: fairlife ultra-filtered milk; Core Power High Protein Shakes, a sports nutrition drink to support post-workout recovery; fairlife nutrition plan™, a nutrition shake to support the journey to better health. A wholly owned subsidiary of The Coca-Cola company, fairlife, LLC has been recognized by both Fast Company and Nielsen for its industry leading innovation. To learn more about fairlife and its complete line of products, please visit fairlife.com. job purpose:The Associate Scientist will be applying scientific principles, conducting research experiments, and producing reliable test results. The primary objectives of this position are to resolve technical challenges, develop new products, improve existing products, validate testing methods, or enhance efficiency. The candidate should be comfortable working with a team and should have a passion for creativity and innovation within a fast-paced environment. The successful candidate will learn to interpret and apply scientific findings to dairy systems, to translate findings into innovative manufacturing processes and products. responsibilities: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Design and conduct benchtop experiments and perform tests according to research plan. Up-scale trials from benchtop to pilot plant and perform tests according to research plan. Design and execute shelf-life studies on selected products including routine analysis and sensory evaluations. Keeping up to date with relevant scientific and technical developments. Analyzing and summarizing research data. Presenting scientific findings to the R&D team and to other functions when needed. Consistently deliver concise, accurate and complete reporting of work in the specified format (written and/or electronic). Operating benchtop and pilot plant equipment. Adhering to GMP and other safety regulations. Maintaining a safe, clean, and sanitary work area. Organizing, storing, and handling all chemical substances, fluids, and compressed gases according to safety instructions. Ensuring that safety guidelines are adhered to at all times within the laboratory. Cleaning, sterilizing, maintaining, and calibrating laboratory equipment. Providing technical support when necessary. Performing other duties assigned by supervisor. skills/qualifications required: BS or MS degree in food science with either a focus on dairy science or a working experience in dairy 0-1 years' experience in a lab/ pilot plant environment. Previous working knowledge related to at least one of the following: food science, product recipe/formulation, process research, experimental design and/or plant trials. Hands-on experience operating electrical and non-electrical laboratory equipment. In depth knowledge of QHSE management systems, preventative measures, and laboratory best practices. Ability to handle ambiguity and work in a fast paced, entrepreneurial environment. Working knowledge of MS Office Suite and database systems. Excellent verbal and written communication skills Strong analytical skills. Willingness to travel overnight, and to work night and weekend shifts for special projects working conditions and physical requirements: 8+ hours sitting/standing/walking Ability to lift up to 40 lbs. Exposure to hazards (machinery, flammable liquids, biohazards, etc.), etc.) position location: Chicago, IL reports to: Director, R&D travel requirements: 5-15% exempt/nonexempt: exempt #LI-Onsite #LI-BB1 *Base pay offered may vary depending on geography, job-related knowledge, skills, and experience. A full range of medical, financial, and/or other benefits, dependent on the position, is offered. Base pay range:$75,000-$90,000 USD fairlife, LLC is an equal opportunity employer. We do not discriminate on the basis of 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. All qualified applicants and employees will be given equal opportunity. Selection decisions are based on job-related factors. In addition to its nondiscrimination commitment, the Company will also provide reasonable accommodation of qualified individuals with known disabilities unless doing so would impose an undue hardship on the Company. If you have a disability and would like to request accommodation in order to apply for a position with us, please email ******************** . For Recruitment Agencies At fairlife, we manage the majority of our hiring internally through our dedicated Talent Acquisition team, which is actively engaged in direct candidate sourcing. Most of our roles are filled through applications submitted via our careers site or through direct outreach by our team. As our recruitment is primarily handled in-house, we work only occasionally with external agencies, and only those on our existing, pre-approved vendor list. At this time, we are not reviewing or expanding that list. Unsolicited resumes or submissions from external agencies not authorized by our Talent Acquisition team will be considered direct candidate applications. As such, fairlife will not assume responsibility for any placement fees associated with these submissions.

What You Will Do: * Perform quality assurance testing on various construction materials * Evaluate new products for specification conformance * Utilize instrumentation including XRD and XRF * Maintain lab organization with attention to detail Benefits to you: * Enjoy an excellent work/life balance. * Receive paid time off with vacation, sick and personal leave. * Receive 11 paid holidays per year. * Receive regular pay increases; 1st increase after 4 months. * Receive an extensive benefits package; including Medical and FREE Vision, Dental and Basic Life Insurance after completion of eligibility period. * Experience growth opportunities within organization. * Participate in employee tuition reimbursement programs. * Receive a pension plan with 14% employer contribution. For a list of all the State of Ohio benefits, please visit the Total Rewards website! 42 mos. pertinent laboratory experience commensurate with job duties to be performed as outlined per approved position description on file. * Or completion of undergraduate core coursework in a biological, chemical, natural or physical science; 12 mos. pertinent laboratory experience commensurate with job duties to be performed as outlined per approved position description on file. * Or completion of Master of Science core program in a biological, chemical, natural or physical science. * Or 12 mos. exp. as Laboratory Scientist 1, 83291. * Or positions in Department of Rehabilitation & Corrections & Department of Health must meet 1 of 5 options: (1) Associate's degree in a medical technology from accredited college or university (2) Medical Laboratory Technician (MLT) certification (3) Bachelor's degree in a chemical, physical, biological or clinical laboratory science, or medical technology; 12 mos. pertinent laboratory experience or training in the specialty or subspecialty in which the individual will be assigned. (4) Education &/or training equivalent to 60 semester hours, or equivalent, that included 24 semester hours of medical laboratory technology courses; 18 mos. pertinent laboratory experience commensurate with job duties to be performed as outlined per approved position description on file. (5) Education &/or training equivalent to 60 semester hours, or equivalent, that included 24 semester hours of science that included-- 6 semester hours of chemistry; 6 semester hours of biology; and 12 semester hours of chemistry, biology, or medical laboratory technology in any combination; 18 mos. documented laboratory exp. in each specialty in which the individual performs high complexity testing. * Or equivalent of Minimum Class Qualifications For Employment noted above. Job Skills: Laboratory

- Business Title: Molecular Biologist II Analyst II Division: Consumer Products Services Entity: ATL Reports to: Manager FLSA: Non-Exempt Hours Worked: Typically, Monday through Friday, forty-hours per week. However, must be flexible to meet the needs of the department and complete other projects as assigned. Position Summary: The Molecular Biologist II is responsible for efficient delivery of data from molecular, cellular, and molecular pharmacological biochemical assays. They are highly organized, able to execute and develop protocols for various laboratory techniques and adhere to good research practice (GRP) requirements. They are an detail-oriented laboratory scientist, conducting biochemical assays among other laboratory responsibilities independently or with little guidance from client scientists and can deliver and interpret data in a timely manner. They exhibit quality and compliance in their daily work. They are champions of and promote the organization's Values and Absolutes. The Molecular Biologist will complete their regular assigned daily work while meeting the expectations outlined below. Duties and Responsibilities: It is everyone's responsibility to live out our Values and Absolutes by Shaping a World of Trust while ensuring responsible progress. • Grow, treat, and transfect mammalian cells to isolate RNA, protein for use in biochemical assays. • Perform standard molecular/cellular techniques, such as BCA, Western blotting, ELISAs. • Perform in-vivo rodent tissue collections and subsequent processing of tissues for use in biochemical assays. • Monitor inventory of laboratory supplies and reagents and maintain clean, well-functioning laboratory environment. • Identify, troubleshoot and provide suggested technical solutions to clients and management. • Prepare written technical reports. • Perform basic data analysis as assigned. • Assist with training. • Comply with clients and Bureau Veritas Consumer Products Services, Inc management systems in accordance with appropriate regulatory agencies. • Follows the guidelines set forth by clients and the Bureau Veritas Consumer Products Services, Inc Quality Manual and Safety / Chemical Hygiene Plan. • Adhere to the requirements of the BV-CPS Quality System. • Other duties as defined by Manager, department needs and workload. Skills & Proficiencies: • Demonstrated ability to perform complex biochemical assays and deliver data in a timely and consistent manner • Extensive experience in molecular and biochemistry techniques • Ability to think critically about data and troubleshoot assays as needed • Written and verbal communication skills including the ability to communicate effectively in a group setting, with colleagues and clients • Organizational and time management skills • Ability to perform multiple tasks • Ability to organize and prioritize workload to meet or exceed deadlines • Individual and Team work ethic • Proficiency with Windows, Word & Excel • Attention to detail • Positive attitude, self-motivated, high level of engagement • Champions company values including team engagement • Ability to present both facts and recommendations effectively • Technical problem solving and process improvement skills Education and Experience: • Master's or Bachelor's in Biology, Molecular Biology, Neuroscience, or closely related field. • Minimum of one (1) year of experience with biochemical techniques including but not limited to qPCR, FLIPR kinase assays, and mammalian cell culture. • Minimum of one (1) year of experience with data analysis. • Experience with or willingness to learn/perform in-vivo rodent tissue collection. An equivalent combination of education and experience may be accepted in lieu of above. Compensation Range: $27.00 - $29.00 per hour (e.g., the job posting is not necessarily reflective of actual compensation that may be earned, and actual compensation is subject to variation due to such factors as locations, education, experience, and skillset).

Ann & Robert H. Lurie Children's Hospital of Chicago provides superior pediatric care in a setting that offers the latest benefits and innovations in medical technology, research and family-friendly design. As the largest pediatric provider in the region with a 140-year legacy of excellence, kids and their families are at the center of all we do. Ann & Robert H. Lurie Children's Hospital of Chicago is ranked in all 10 specialties by the U.S. News & World Report. Location Simpson Querrey Biomedical Research Center Job Description General Summary: We are seeking a highly motivated research technician to work on projects related to pediatric brain tumors. The candidate will be primarily responsible for obtaining, organizing, and preparing samples for molecular testing. An ideal candidate would have experience working with tissue, RNA, and DNA and have mouse handling experience. These tasks may include breeding, genotyping, and collection of samples/data. Additionally, the candidate will be expected to participate in the general management and daily operation of the lab. Essential Job Functions: Support scientific research, analysis, and experimentation by performing various laboratory tasks. Following protocols, designs and sets-up and conducts basic experiments. Analyzes and troubleshoots protocols and data obtained from individual experiments and recommends alternatives and suggestions to improved processes, validity and accuracy. Maintains detailed records of results which may include collecting, extracting and entering data. Manipulates, interprest and/or presents results. Prepares charts and graphs for presentations and publications. Performs scientific literature searches in support of research. Completes portions of grant applications, manuscripts and publications. Tracks and summarizes lab supply expenses. Verifies accuracy of invoices. Orders and maintains inventory of reagent, mice and/or lab supplies. Calibrate and validate laboratory equipment to ensure accuracy and precision in testing. Record and analyze data and report findings to senior laboratory staff. Maintain an organized and well-stocked laboratory by managing supplies, reagents, and equipment inventory. Place orders for necessary materials. Other job functions as assigned. Education and Experience: Successful completion of a full 4-year course of study in an accredited college or university leading to a bachelor's or higher degree in a scientific major or related; OR appropriate combination of education and experience. Minimum of 1 year of experience working with diverse groups of people. Working knowledge of computers, ability to troubleshoot, work independently, and function as a team member is essential. Therefore, experience in regular interaction with outside groups is highly desirable. Excellent command of the English language and the ability to communicate effectively. Strong organizational skills including the ability to establish priorities, react promptly to a large variety of requests, and the ability to keep the workplace clean and organized. Education Pay Range $40,560.00-$62,878.40 Salary At Lurie Children's, we are committed to competitive and fair compensation aligned with market rates and internal equity, reflecting individual contributions, experience, and expertise. The pay range for this job indicates minimum and maximum targets for the position. Ranges are regularly reviewed to stay aligned with market conditions. In addition to base salary, Lurie Children's offer a comprehensive rewards package that may include differentials for some hourly employees, leadership incentives for select roles, health and retirement benefits, and wellbeing programs. For more details on other compensation, consult your recruiter or click the following link to learn more about our benefits. Benefit Statement For full time and part time employees who work 20 or more hours per week we offer a generous benefits package that includes: Medical, dental and vision insurance Employer paid group term life and disability Employer contribution toward Health Savings Account Flexible Spending Accounts Paid Time Off (PTO), Paid Holidays and Paid Parental Leave 403(b) with a 5% employer match Various voluntary benefits: Supplemental Life, AD&D and Disability Critical Illness, Accident and Hospital Indemnity coverage Tuition assistance Student loan servicing and support Adoption benefits Backup Childcare and Eldercare Employee Assistance Program, and other specialized behavioral health services and resources for employees and family members Discount on services at Lurie Children's facilities Discount purchasing program There's a Place for You with Us At Lurie Children's, we embrace and celebrate building a team with a variety of backgrounds, skills, and viewpoints - recognizing that different life experiences strengthen our workplace and the care we provide to the Chicago community and beyond. We treat everyone fairly, appreciate differences, and make meaningful connections that foster belonging. This is a place where you can be your best, so we can give our best to the patients and families who trust us with their care. Lurie Children's and its affiliates are equal employment opportunity employers. All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity or expression, religion, national origin, ancestry, age, disability, marital status, pregnancy, protected veteran status, order of protection status, protected genetic information, or any other characteristic protected by law. Support email: ***********************************

This is where your work makes a difference. At Baxter, we believe every person-regardless of who they are or where they are from-deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond. Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results. Here, you will find more than just a job-you will find purpose and pride. Your Role at Baxter This is where your creativity addresses challenges Night shift: 6:00 PM - 6:30 AM on a rotating 2-2-3 schedule (including weekends). You are creative, thorough, and a heads-down do-er. You embrace a challenge and truly apply the collaborative powers of your team to produce great results. You are motivated by work that is never the same from one day to the next. The Position encompasses biological, chemical and physical analyses on pharmaceutical products (biologics and drugs) through all stages of the manufacturing process from incoming raw materials to finished goods, and environmental monitoring programs. A candidate must not be allergic to Penicillin and Cephalosporin or their related products and /or materials. Your Team at Baxter Within Quality, every role makes a difference. Products that Baxter makes are shipped worldwide for patients in need. Whether it's building a new process from scratch or facing a never-before-seen production hurdle, individuals within Quality are given the trust and opportunity to bring creativity to the table. Regardless of your specific role with a product, it is sure to touch a portion of our global operation. The mission of Baxter is to save and sustain lives. This mission is embedded into everything we do. This means if there is a decision to be made where quantity and quality are at odds, we will always choose quality. Our patients come first, always. The Quality function values both working together as a team and independently. We draw energy from working in a plant or an office where there are opportunities to collaborate. As the company evolves, so does the way our team approaches work as it strives to create top-of-the-line products. We build relationships with each other to get work done. Building these relationships is easy because we all share common traits of being reliable, ethical, and caring. We lean on our colleagues for their expertise and hold each other accountable. We feel empowered to speak up when there's a new insight or opportunity to improve something. This open dialog builds trust within the team and helps create a better product for our customers. What you'll be doing Conduct critical chemical and physical analysis on raw materials, initial, in-process and final products, and samples collected from the environmental monitoring programs at the Round Lake manufacturing facility. Work under minimum supervision. Serve as mentor to Quality Laboratory Associate (QLA) I positions. Provide training and work direction for QLA I positions as required. Perform review of test data, which includes overall documentation practices. Perform release functions in LIMS or other computerized systems. Use sophisticated laboratory instrumentation (e.g., HPLC, GC) and computer systems to collect and record data. Perform advanced chemical assays requiring precise analytical skills and understanding of biology and chemistry principles. Complete all testing, including special project / protocol testing in a timely and appropriate manner. Maintain data integrity and ensure compliance with company SOPs and specifications, FDA, GLP, QSR and cGMP regulations. Participate in functions involving teams, which impact production, increase efficiency, solve problems, generate cost savings, and improve quality. Perform laboratory and manufacturing audits as required. Audit and update, as required, plant SOPs. Perform equipment maintenance and calibrations as required. Document the completion of testing in Notebooks, Controlled documents, Forms and LIMS and maintain accurate and complete quality records. Follow, understand, and comply with Baxter SOP's and policies on cGMP's and safety. Maintain a clean, safe, and organized lab area, and potentially assume responsibility to ensure that others maintain their lab areas. Investigate deviations and write exception/OOL/OOS/OOT documents. Support improvement projects and drive efficiency through utilization of LEAN management principles (i.e., 6S, Kaizen, etc.). Proactively and cooperatively communicate with peers and management to ensure awareness of progress and issues; recommend solutions when issues arise. Maintain and meet the highest standards in quality, customer service and regulatory compliance. What you'll bring Bachelor degree in Chemistry or physical science with 2 or more years' experience. Must have good oral and written communication skills, strong analytical skills and be detail oriented. Knowledge of current Good Manufacturing Practices is preferred. Advanced laboratory skills with basic knowledge of statistical methods. Strong technical problem solving skills. Ability to handle multiple tasks concurrently, and in a timely fashion. Knowledge of Empower Chromatography Data System and LIMS is preferred but not required. Knowledge of GLP, cGMP requirements and familiarity with USP/ICH guidelines is preferred but not required. Must demonstrate effectiveness in ability to train others, empowerment, leadership, results orientation, and task completion. Ability to work independently and as part of a team, self-motivated, demonstrates adaptability, and possesses a positive attitude in a highly dynamic environment. Ability to lift up to 50 pounds when required. Rotating weekend work required Visual acuity 20/25 Near Vision with or without corrective vision required. Must not be color blind. We understand compensation is an important factor as you consider the next step in your career. At Baxter, we are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. The estimated base salary for this position is $64,000 - $88,000 annually. The estimated range is meant to reflect an anticipated salary range for the position. We may pay more or less than of the anticipated range based upon market data and other factors, all of which are subject to change. Individual pay is based on upon location, skills and expertise, experience, and other relevant factors. This position may also be eligible for discretionary bonuses, commission, and/or long-term incentive. For questions about this, our pay philosophy, and available benefits, please speak to the recruiter if you decide to apply and are selected for an interview. Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time. US Benefits at Baxter (except for Puerto Rico) This is where your well-being matters. Baxter offers comprehensive compensation and benefits packages for eligible roles. Our health and well-being benefits include medical and dental coverage that start on day one, as well as insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance. Financial and retirement benefits include the Employee Stock Purchase Plan (ESPP), with the ability to purchase company stock at a discount, and the 401(k) Retirement Savings Plan (RSP), with options for employee contributions and company matching. We also offer Flexible Spending Accounts, educational assistance programs, and time-off benefits such as paid holidays, paid time off ranging from 20 to 35 days based on length of service, family and medical leaves of absence, and paid parental leave. Additional benefits include commuting benefits, the Employee Discount Program, the Employee Assistance Program (EAP), and childcare benefits. Join us and enjoy the competitive compensation and benefits we offer to our employees. For additional information regarding Baxter US Benefits, please speak with your recruiter or visit our Benefits site: Benefits | Baxter Equal Employment Opportunity Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic. Know Your Rights: Workplace Discrimination is Illegal Reasonable Accommodations Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information. Recruitment Fraud Notice Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.

This is where your work makes a difference. At Baxter, we believe every person-regardless of who they are or where they are from-deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond. Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results. Here, you will find more than just a job-you will find purpose and pride. Your role at Baxter The Quality Lab Associate I encompasses the biological, chemical and physical analyses on pharmaceutical products (biologics and drugs) through all stages of the manufacturing process from incoming raw materials to finished goods, and environmental monitoring programs. *Night shift: 6:00 PM - 6:30 AM on a rotating 2-2-3 schedule (including weekends)* A candidate must not be allergic to Penicillin and Cephalosporin or their related products and /or materials. What you'll be doing Conduct critical chemical and physical analyses on Raw Materials, Initial, In-process and Final products, and samples collected from environmental monitoring programs at Baxter manufacturing facilities. Work under minimum supervision. Use sophisticated laboratory instrumentation (HPLC, FTIR, UV, GC etc) and computer systems to collect and record data. Perform advanced assays requiring precise analytical skills and understanding of biology and chemistry principles. Maintain data integrity and ensure compliance with company SOPs and specifications, FDA, GLP, QSR and cGMP regulations. Participate in functions involving teams, which impact production, increase efficiency, solve problems, generate cost savings and improve quality. Perform laboratory and manufacturing audits as required. Audit and update, as required, plant SOPs. Perform equipment maintenance and calibrations as required. Document the completion of testing in Notebooks, Controlled documents, Forms and LIMS and maintain accurate and complete quality records. Follow, understand and comply with Baxter SOP's and policies on cGMP's and safety. Maintain a clean, safe and organized lab area, and potentially assume responsibility to ensure that others maintain their lab areas. Investigate deviations and write exception/OOL/OOS/OOT documents. Support improvement projects and drive efficiency through utilization of LEAN management principles (i/e/ 6S, Kaizens etc). Proactively and cooperatively communicate with peers and management to ensure awareness of progress and issues; recommend solutions when issues arise. Maintain and meet the highest standards in quality, customer service and regulatory compliance. Other projects as assigned. What you'll bring Bachelor's degree in chemistry or science related degree with 6 months or more of experience. Knowledge of Empower CDS and LIMS is preferred but not required. Knowledge of GLP, cGMP requirements and familiar with USP/ICH guidelines is preferred but not required. Excellent communication (oral and written) and interpersonal skills. Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude in a highly dynamic environment. Ability to lift up to 50 pounds when required. Visual acuity 20/25 Near Vision with or without corrective vision required. Must not be color blind We understand compensation is an important factor as you consider the next step in your career. At Baxter, we are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. The estimated base salary for this position is $64,000 - $88,000 annually. The estimated range is meant to reflect an anticipated salary range for the position. We may pay more or less than of the anticipated range based upon market data and other factors, all of which are subject to change. Individual pay is based on upon location, skills and expertise, experience, and other relevant factors. This position may also be eligible for discretionary bonuses, commission, and/or long-term incentive. For questions about this, our pay philosophy, and available benefits, please speak to the recruiter if you decide to apply and are selected for an interview. Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time. US Benefits at Baxter (except for Puerto Rico) This is where your well-being matters. Baxter offers comprehensive compensation and benefits packages for eligible roles. Our health and well-being benefits include medical and dental coverage that start on day one, as well as insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance. Financial and retirement benefits include the Employee Stock Purchase Plan (ESPP), with the ability to purchase company stock at a discount, and the 401(k) Retirement Savings Plan (RSP), with options for employee contributions and company matching. We also offer Flexible Spending Accounts, educational assistance programs, and time-off benefits such as paid holidays, paid time off ranging from 20 to 35 days based on length of service, family and medical leaves of absence, and paid parental leave. Additional benefits include commuting benefits, the Employee Discount Program, the Employee Assistance Program (EAP), and childcare benefits. Join us and enjoy the competitive compensation and benefits we offer to our employees. For additional information regarding Baxter US Benefits, please speak with your recruiter or visit our Benefits site: Benefits | Baxter Equal Employment Opportunity Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic. Know Your Rights: Workplace Discrimination is Illegal Reasonable Accommodations Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information. Recruitment Fraud Notice Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.

Passionate about precision medicine and advancing the healthcare industry? Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way. Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time. We are looking for a Clinical Lab Associate who will be responsible for Sample Returns and Sendouts. Duties and Responsibilities: Utilize laboratory software to create and manage batches for organizing specimens designated for return. Use the laboratory asset management system to accurately locate FFPE specimens. Coordinate efficient specimen returns and send-outs to custodian pathology laboratories and Tempus partners. Monitor and prioritize high-urgency requests and audits to support customer retention and satisfaction. Sort, file, and maintain long-term storage of FFPE specimens in accordance with laboratory protocols. Develop a comprehensive understanding of laboratory processes, workflows, and database systems. Ensure all sample return documentation is professional, accurate, and compliant with HIPAA regulations. Report and resolve issues promptly to minimize workflow disruptions. Build and maintain effective working relationships with laboratory colleagues and cross-functional teams. Preferred Qualifications: Bachelor's Degree Highly organized and systematic, superb attention to detail and ability to complete tasks with a high degree of accuracy Show initiative and ability to work as part of a high-level team while working independently on mission-critical tasks Proven ability to learn new skills quickly and adapt to new processes smoothly Computer proficiency with equivalent knowledge of standard software and general familiarity of standard office equipment and technology. Potential Available Shifts: M-F 4pm-12:30am, M-F 12:30pm-9pm, Tu-Sat 9am-5:30pm Note: Candidate will be offered a specific assigned shift. Shift is determined on team and our current needs. Illinois Pay: $20.25 The expected salary range above is applicable if the role is performed from Illinois and may vary for other locations (California, Colorado, New York). Actual salary may vary based on qualifications and experience. Tempus offers a full range of benefits, which may include incentive compensation, restricted stock units, medical and other benefits depending on the position. We are an equal opportunity employer. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

Crete Analytical Laboratory Temporary MERIEUX NUTRISCIENCES As a trusted partner, our Public Health mission is to make food systems safer, healthier and more sustainable. Throughout our global network in 27 countries, we offer to our customers a wide range of testing and innovative solutions dedicated to preventing health risks related to food, environment and consumer goods. External growth has been a key pillar of our history with more than 40 acquisitions completed in the last 10 years. If you want to contribute to an inspiring long-term purpose, to be part of a fast growing company on a high-value market with significant build-up opportunities, and to grow in an entrepreneurial and warm environment, join us! YOUR DAY TO DAY LIFE We are looking for a Microbiologist II (Part Time) in 3600 Eagle Nest Dr, North Building, Crete, IL 60417 USA. Your mission will be to: Purpose (Objective): The incumbent is responsible for the testing of samples using various microbiological analyses. The incumbent provides analytical support for the lab by ensuring that laboratory procedures are being performed within specified quality guidelines. This position serves as a technical resource and provides ongoing technical support related to method and process implementations. This position spends the majority of time or all of their time in diagnostics. Main activities: Act as a technical resource in the laboratory Perform sample analysis. Provide feedback and suggest process improvement changes. Provide instruction on the correct sample process. Educate and train departmental personnel on correct procedures and new analysis methods. Communicate with technical support to provide answers to questions. Complete non-conformance root cause analysis and corrective actions documentation. Maintain knowledge of Laboratory Information Management System (LIMS) that is required to complete job responsibilities Follow appropriate methods and SOPs on all tasks. Maintain quality control documentation Analyze and approve client results. Read, enter, formulate, and evaluate process control samples Assist with managing department inventory and cultures Implement new methods This position has the responsibilities and authority to identify departures from the quality system or test procedures and document such observations in accordance with the prescribed compliant system. Assist other departmental personnel with analysis procedures Maintain accurate quality control documentation of analysis procedures Perform rapid test methods Read, calculate and record analysis data to produce a report for the client. Correct any discrepancies that occur on the worksheet Must keep up-to-date on assigned training Must participate in cleaning schedule and maintain retain samples as required Must be able to perform preventative maintenance and basic troubleshooting of laboratory equipment critical to sample analysis Adhere to all safety policies Responsibility to support laboratory management in the implementation, maintenance, and improvement of the management system. Perform other related tasks as needed Communication: Internal Interlocutors: The incumbent has occasional contact with the personnel outside the immediate working unit. External Interlocutors: N/A YOUR PROFILE Knowledge: The incumbent must have a basic knowledge of microbiology to accurately perform testing procedures and obtain accurate results. Profile: Associates degree required, Bachelors preferred or equivalent work experience. 2-5 years relevant work experience. The incumbent must have a general knowledge of microbiology to accurately perform testing procedures and obtain the correct results. Basic chemistry knowledge is needed to prepare the media to the specification of the sample. A basic knowledge of food science is necessary to analyze the microbiological content of samples. Required skills: Analytical skills are essential to complete analysis procedures and determine the concentration of the microorganism. A general knowledge of the Laboratory Information Management System is required to process client data. Physical dexterity is required for manipulating samples. A basic knowledge of laboratory safety procedures and practices is required to ensure a safe working environment. Interpersonal skills are required to effectively work within teams. Management (Size and characteristics of the team(s)): None Work Environment: The incumbent works in a laboratory setting with proper lighting and temperature control. Occasional exposure to laboratory fumes, chemicals, and materials will occur when in the laboratory. Safety equipment of gloves, laboratory coat and eyeglasses may need to be worn depending on the testing process. The incumbent may use the autoclave daily to complete the analysis process. Continuous lifting of analysis materials weighing up to 50 pounds are necessary to transport media materials. The incumbent can expect extended time spent in a standing position. The incumbent should be able to detect slight variation in shades of colors. Pay Range: $23 - $25 WHY JOIN US? * Because you would contribute to an inspiring Public Health purpose, supported by long-term and visionary shareholders. * Because you would have an impact on our strategic pillars that build on 50 years of experience and expertise. * Because you would be part of a community of an enthusiastic and skilled group of people who love co-building together and serving a purpose bigger than them. * Because you would be welcome as you are, in a diverse and open-minded environment that is rich in our singularities and differences. * Because you would grow in an international group of more than 8200 fantastic team members, with plenty of opportunities to learn and share. Ready for the journey? To apply please click on 'Apply now' button

Crete Science Center Regular MERIEUX NUTRISCIENCES As a trusted partner, our Public Health mission is to make food systems safer, healthier and more sustainable. Throughout our global network in 27 countries, we offer to our customers a wide range of testing and innovative solutions dedicated to preventing health risks related to food, environment and consumer goods. External growth has been a key pillar of our history with more than 40 acquisitions completed in the last 10 years. If you want to contribute to an inspiring long-term purpose, to be part of a fast growing company on a high-value market with significant build-up opportunities, and to grow in an entrepreneurial and warm environment, join us! YOUR DAY TO DAY LIFE We are looking for a Molecular Microbiologist in 3600 Eagle Nest Dr, Crete, IL 60417 USA. Your mission will be to: Purpose (Objective): The incumbent prepares isolates, RNA and DNA, maintains process documentation to facilitate microbiological and molecular biology analysis procedures and may interpret results for final release. Main activities: ●Performs microbiological tests including gene sequencing, DNA subtyping analysis, MALDI-TOF for identification and real-time PCR methods including non-commercial PCR methods (e.g., open source PCR). ●Perform literature and nucleic acid sequence searches as necessary to investigate and understand results. ●Verifies results before release to the clients. Read and record analysis data to produce a report for the client. Correct any discrepancies that occur. Proactive in contacting industry technical support to troubleshoot results or equipment issues. ●Troubleshooting of data, methods and equipment as required. ●Performs sub-culturing using proper aseptic technique and determines growth conditions for a variety of groups of microorganisms. ●Perform necessary housekeeping duties in a timely manner, keeping the work areas and equipment clean and sanitized. Perform standard maintenance for key pieces of equipment. Perform cleaning protocols for GMP and ISO 17025 laboratory work space. Maintain accurate quality control documentation of analysis procedures.Perform necessary tasks related to quality control parameters for the function being preformed. ●Preparation of reagents, chemical solutions and media as required ●Interact with other department personnel to maintain smooth flow of work. ●Maintain knowledge of Laboratory Information Management System (LIMS) that is required to complete job responsibilities. ●Support corporate quality and continuous improvement process.Responsibility to support laboratory management in the implementation, maintenance, and improvement of the management system. ●This position has the responsibilities and authority to identify departures from the management system or test procedures and document such observations accordance with the prescribed non-conforming system and notifies the supervisor. ●Adhere to all safety policies. ●Perform other related tasks as needed. YOUR PROFILE Profile: ●Good knowledge of molecular biology and microbiology to accurately perform testing procedures and obtain the correct results. ●Knowledge of growth conditions of a variety of microorganisms is required. ●A basic knowledge of food science is necessary to interpret results. ●A broad knowledge of laboratory safety procedures and policies is necessary to ensure a safe working environment. ●Basic chemistry knowledge is needed to prepare the media to the specification of the sample. ●Maintain knowledge of Laboratory Information Management System (LIMS) that is required to complete job responsibilities. Required skills: ●Analytical skills are helpful to complete analysis procedures and determine the concentration of the microorganism. ●Physical dexterity with pipetting is required for pipetting. ●Laboratory skills obtained as a laboratory technician or similar position are essential to perform the necessary analyses. ●Oral and written communication skills are necessary to supervise departmental personnel. ●Organizational and planning skills are useful to schedule testing to ensure that analysis is completed within the specified time period. The incumbent encounters routine difficulties frequently that require the analysis of each situation to determine the cause. Problems can result from incorrect growth conditions and improper technique. Testing procedures require precise measurement and knowledge of microorganisms to be made to avoid problems. The microorganisms do not follow the same pattern continuously and may require testing to be modified by assessment of previous results. The source of the problem will determine the method of solution. Standard procedures and established guidelines provide the needed information to solve testing problems. Coordination of departmental activities with those of other departments is necessary to accomplish accurate analysis of sample. The incumbent recommends action to the supervisor to solve problems using previous knowledge of the position and Standard Operating Procedures. Unique or unusual problems can require the input of the supervisor to determine the optimal solution. Modifications may be unfamiliar to the incumbent and require further research before recommending action. Research can be conducted using written company policies and procedures as well as position precedents. The recommendations will impact the progress of the analysis procedures within the immediate work unit and operating expenses of the procedure. The incumbent receives general supervision. The incumbent works toward specific goals and targets established with the supervisor to provide prompt and accurate service to the client. Results and progress are reviewed on a daily basis. The testing procedure must be completed within an established timeframe to avoid delay in client receiving the results. Repeating the analysis or inaccurate results can strain client relations and increase the cost of the procedure. Compensation: $23/hr Full Time Eligible Benefits Overview: Comprehensive medical, dental, and vision insurance plans. Generous paid time off (PTO) package to support work-life balance following state and local ordinances. Optional 401(k) plan with employer matching contributions. The information above provides a general overview and may vary based on specific job responsibilities, location, or other factors. Details will be clarified during the hiring process. WHY JOIN US? * Because you would contribute to an inspiring Public Health purpose, supported by long-term and visionary shareholders. * Because you would have an impact on our strategic pillars that build on 50 years of experience and expertise. * Because you would be part of a community of an enthusiastic and skilled group of people who love co-building together and serving a purpose bigger than them. * Because you would be welcome as you are, in a diverse and open-minded environment that is rich in our singularities and differences. * Because you would grow in an international group of more than 8200 fantastic team members, with plenty of opportunities to learn and share. Ready for the journey? To apply please click on 'Apply now' button

Crete Analytical Laboratory Regular MERIEUX NUTRISCIENCES As a trusted partner, our Public Health mission is to make food systems safer, healthier and more sustainable. Throughout our global network in 27 countries, we offer to our customers a wide range of testing and innovative solutions dedicated to preventing health risks related to food, environment and consumer goods. External growth has been a key pillar of our history with more than 40 acquisitions completed in the last 10 years. If you want to contribute to an inspiring long-term purpose, to be part of a fast growing company on a high-value market with significant build-up opportunities, and to grow in an entrepreneurial and warm environment, join us! YOUR DAY TO DAY LIFE We are looking for a Microbiology Technician - Pipeline in 3600 Eagle Nest Dr, North Building, Crete, IL 60417 USA. Your mission will be to: Purpose (Objective): The incumbent prepares samples for processing and maintains documentation of process to facilitate testing procedures. Main Activities: ● Prepare sample for analysis by recording, weighing, and blending ● Write identification onto plates so that client and sample number can be tracked ● Pipette sample solution into tubes or plates according to the analysis process being performed ● Pour the agar into plates or tubes to begin the growth process ● Collect plates and place them in the incubator for the specified amount of time and temperature ● Prepare media and broth for use in pathogen testing as required ● Ensure that media and materials are prepared for the next testing sequence ● Maintain knowledge of Laboratory Information Management System (LIMS) that is required to complete job responsibilities ● Set up equipment and materials needed for analysis ● Read plates and tubes, as required, to determine the number of organisms in the sample ● Support corporate quality and continuous improvement process ● Perform necessary housekeeping duties in a timely manner, keeping the work areas and equipment clean and sanitized ● Must participate in cleaning schedule and maintain retain samples as required ● Adhere to all safety policies ● Responsibility to support laboratory management in the implementation maintenance, and improvement of the management system ● Perform other related tasks as needed YOUR PROFILE Must be able to work evenings and weekends Profile (required education/qualification and professional background): HS Diploma and 1+ year relevant work,. The incumbent must have a basic knowledge of science to accurately perform testing procedures and obtain accurate results. A basic knowledge of personal computers is useful to accurately enter testing data and results. A basic knowledge of laboratory safety procedures and policies is necessary to ensure a safe working environment. Planning skills are useful to maintain supplies of analysis materials and ensure analysis is completed within specified time. Required skills: Time management skills, ability to prioritize samples and tasks in a fast paced environment. Attention to detail. Analytical skills are essential to complete analysis procedures and determine the concentration of the microorganism. A general knowledge of the Laboratory Information Management System is required to process client data. Physical dexterity is required for manipulating samples. Work Environment: The incumbent works in a laboratory setting with proper lighting and temperature control. Occasional exposure to laboratory fumes, chemicals, and materials will occur when in the laboratory. Safety equipment of gloves, laboratory coat and eyeglasses may need to be worn depending on the testing process. The incumbent may use the autoclave daily to complete the analysis process. Continuous lifting of analysis materials weighing up to 50 pounds are necessary to transport media materials. The incumbent can expect extended time spent in a standing position. The incumbent should be able to detect slight variation in shades of colors. Compensation Package Overview: Compensation Range $18 - $20/ hourly USD Full Time Eligible Benefits Overview: Comprehensive medical, dental, and vision insurance plans. Generous paid time off (PTO) package to support work-life balance following state and local ordinances. Optional 401(k) plan with employer matching contributions. The information above provides a general overview and may vary based on specific job responsibilities, location, or other factors. Details will be clarified during the hiring process. #LI-DNP WHY JOIN US? * Because you would contribute to an inspiring Public Health purpose, supported by long-term and visionary shareholders. * Because you would have an impact on our strategic pillars that build on 50 years of experience and expertise. * Because you would be part of a community of an enthusiastic and skilled group of people who love co-building together and serving a purpose bigger than them. * Because you would be welcome as you are, in a diverse and open-minded environment that is rich in our singularities and differences. * Because you would grow in an international group of more than 8200 fantastic team members, with plenty of opportunities to learn and share. Ready for the journey? To apply please click on 'Apply now' button