Senior scientist jobs in Racine, WI - 213 jobs

Your Key Responsibilities: Develop, test, and optimize flavor systems for a wide range of beverages (carbonated drinks, juices, plant-based beverages, RTD cocktails, alcohol, energy drinks, and more) Collaborate with cross-functional teams (sales, marketing, sensory, and flavor creation) to support customer projects and internal initiatives Assist in flavor selection and application based on customer briefs, market trends, and regulatory requirements Prepare samples for customer presentations and innovation showcases. Maintain detailed records of formulations and testing in laboratory information management systems (LIMS) Stay current on industry trends, ingredients, and processing technologies Ensure lab safety, cleanliness, and compliance with regulatory standards Your Qualifications: Bachelor's degree in Food Science, Chemistry, or related field Knowledge of beverage formulation basics, emulsions, acidulants, sweeteners, and functional ingredients Familiarity with analytical tools (pH meters, refractometers, titratable acidity) Sensory acuity and ability to describe flavor performance Strong organizational, mathematical, and communication skills Ability to manage multiple projects and adapt to changing priorities Team-oriented mindset with the ability to work independently

Job Title: Food Safety Scientist Duration: 06 Months potential of extension or conversion Shift: Monday - Friday; 40hours week Pay Rate: $35.51/hr on W2 (all inclusive) Job Summary: This role supports the implementation and execution of key food safety design analytical methods within the US and Canada Zones by managing media preparation, quality control activities, and executing project work to develop microbiological and analytical methods needed to support food safety design and commercialization. The position provides onsite laboratory support and project execution support to Corporate Quality & Food Safety, as well as R&D. Key Components of the role Support project completion through media preparation, quality control activities, and through execution of microbial testing on project by project basis Supports administrative tasks such as managing inventory, ordering supplies, and data entry. Supports the execution of validation studies, to evaluate and approve microbiological test methods (rapid and cultural) for the Laboratory network. Supports proficiency testing program and internal laboratory audit process for internal factories laboratories. This role provides scientific and technical food safety support to US and Canadian business partners to ensure product safety and quality by participating in evaluation of analytical methods. Identify and communicate method related impacts on factory verification programs. Support validation of designed HACCP preventive controls (Cooking, formulation, etc.) and assess validity of data obtained by others. Remain current in scientific and regulatory principles of food safety to ensure most relevant information and emerging issues are identified and incorporated into food safety programs. Supports cross-functional communication of results with internally and externally generated data. Qualifications: Bachelor's degree in Food Science, Microbiology, or related field required. Advanced degree preferred. 0-2 years of experience of relevant food safety or analytical science work Knowledge and experience implementing GLPs(Good Laboratory Practices) Experience with LIMS (Laboratory Management Systems) and data management Experience with microbiology laboratory techniques and rapid test methods analytical chemistry procedures. Awareness of quality systems/processes (ISO, Six Sigma etc.), especially ISO 17025 requirements. Excellent communication skills (presentation, report writing, teaching/training). Work experience in team-oriented functions as well as individual contribution. Action oriented with good project management skills. Travel requirements up to 20% a year.

Bell Flavors & Fragrances is seeking a creative and technically skilled Senior Beverage Applications Scientist to join our Flavors R&D team. In this role, you'll develop, test, and optimize flavor systems for a wide range of beverage applications-including alcoholic and non-alcoholic drinks. You'll collaborate cross-functionally with sales, marketing, sensory, and flavor creation teams to deliver outstanding solutions for our customers and drive internal development initiatives. Your Key Responsibilities: Formulate, bench-test, and optimize beverages (carbonated drinks, juices, plant-based beverages, RTD cocktails, alcohol, energy drinks, etc.) using our internal flavor library Select and apply flavors based on customer briefs, market trends, and regulatory requirements Collaborate with flavorists to match and modify flavors for optimal performance Troubleshoot formulation, processing, and shelf-life challenges Support customer presentations and innovation showcase Maintain accurate records in laboratory information management systems (LIMS) Mentor and coach junior scientists, technicians, and interns Support pilot plant trials and scale-up activities Ensure lab safety, cleanliness, and regulatory compliance Your Qualifications: Bachelor's degree in food science, Chemistry, or related field 7-10+ years of experience in beverage formulation, product development, or flavor applications lab (internships/co-ops count) Experience across multiple beverage types and understanding unique formulation challenges Familiarity with emulsions, acidulants, sweetener systems, protein powders, dairy/nondairy ingredients, and functional ingredients Skilled in analytical tools (pH meters, Brix, titratable acidity, etc.) Sensory acuity and ability to articulate flavor performance Strong presentation, organizational, and communication skills Mathematical skills for calculations, proportions, percentages, weights, and algebra Team-oriented, adaptable, and able to manage multiple projects Preferred Qualifications: Experience with alcoholic beverage formulation or TTB regulations Experience with alcoholic beverage formulation or TTB regulations Proficiency with Genesis R&D, Excel, or LIMS (PV) Pilot plant or manufacturing trial experience Regulatory or labeling knowledge for global beverage markets Knowledge of ISO 9001, cGMP, GLP standards Experience with laboratory safety audits and compliance documentation Why join us: Competitive salary range of $95,000 - $105,000 Full-time benefits package Opportunities for professional growth and development Be part of a supportive and collaborative team Commitment to diversity and inclusion Ready to shape the future of beverage innovation? Apply today and join a team committed to safety, quality, and creativity!

Applications Scientist II At Sensient Technologies, we are experts in the science, art and innovation of color and flavor. We are market-savvy and visionary. We are problem solvers. And we will be better with you. We are looking for an Application Scientist II. If you are energized by the idea of developing delicious, real-world food products and enjoy using creativity to solve formulation challenges, this opportunity may be for you. We're looking for a collaborative food scientist who enjoys working hands-on in a lab or pilot plant setting and is ready to make a meaningful impact. This role requires hand-on development in the lab and customer facing presentations for various solutions in applications. This role is based on-site in a collaborative lab environment, where cross-functional teamwork and direct interaction with production teams and commercial partners are part of everyday work. Occasional travel may be required for customer visits and plant support. What you will do Lead hands on bench work and product development activities while managing multiple projects with changing priorities Design and execute experiments using pilot plant and processing equipment while following established procedures and safety standards Identify technical challenges, analyze data, and develop creative solutions that meet customer and business needs Partner cross-functionally with sensory, analytical, quality, regulatory, production, marketing and sales teams to ensure products meet technical and commercial expectations Serve as a technical expert for customers by presenting product concepts, technologies and applications and supporting customer trials and demonstrations Maintain accurate and compliant documentation including formulations, processing instructions, project updates and technical support materials What you will bring Master's degree or BS in Food Science or related technical area required; Master's Degree preferred. 5+ years of experience in the food industry with a strong background in product development for sauces, dips and dressing. Additional experience in soups, broths, seasonings and batters is a plus. Demonstrated understanding of food ingredients, processing and flavor application with expertise in key industry market products and the ability to accurately formulate finished food products. Experience and technical understanding of flavors and flavor enhancers. Excellent organoleptic skills and knowledge of sensory language are required. Strong presentation and communications skills, with the ability to effectively engage customers and internal stakeholders. Ability to travel up to 30% of the time. What you will get The opportunity to work in a hands on laboratory and pilot plant environment where your technical expertise makes a visible impact Regular collaboration with cross functional teams and direct interaction with customers on meaningful development projects Professional growth through mentoring, technical training, customer engagement and industry events A role that blends independent project ownership with team based problem solving Travel opportunities to support customer projects, production trials and industry events, along with an onsite work environment that supports collaboration and innovation About Sensient Sensient Technologies Corporation is a leading global manufacturer and marketer of colors, flavors, and extracts. Sensient employs advanced technologies at facilities around the world to develop specialty food and beverage systems, cosmetic and pharmaceutical systems, specialty colors, and other specialty and fine chemicals. The Company's customers include major international manufacturers representing most of the world's best-known brands. About Sensient Flavors: Sensient Flavors offers innovative, global taste solutions and specialized flavor delivery systems that help bring life to your food and beverage products. Our leading-edge technologies reflect our core philosophies to be dynamic and innovative and to add value to your applications. The salary range for this position is $68,000 - $113,000. Pay within the range is based on several factors, which may include, but are not limited to, education, work experience, specialized training, and labor market conditions. In addition to salary, Sensient is proud to offer a comprehensive and competitive benefits program to support the holistic well-being of our employees and their families. THIRD PARTY AGENCY: Any unsolicited submissions received from recruitment agencies will be considered property of Sensient Technologies, and we will not be liable for any fees or obligations related to those submissions. Sensient is an Equal Opportunity Employer, headquartered in Milwaukee, Wisconsin, USA. #LI-AH1

Sr Scientist Product Development This is a Research and Development (R&D) role leading Product Development initiatives under the Easy Ready Meals team within the Hydration, Desserts, and Meals platform. We're looking for a talented individual to lead product development initiatives working on beloved brands like Ore Ida, Devour and Bagel Bites. The candidate will be leading and driving technical projects to meet business initiatives focused on growth, productivity, and brand maintenance. The Senior Scientist candidate should have a proven record of successfully leading, executing, and commercializing projects ranging in technical complexity with minimal guidance, and getting results in a variety of challenging and complex settings. The candidate should have experience leading business initiatives while exhibiting a collaborative approach and applying innovative solutions. Strong communication and collaboration skills are essential in this role, which operates in a dynamic and cross-functional environment. Key Components · Project Management: Leads development and execution across multiple projects ranging from low to high technical complexity for the Easy Ready Meals Business Unit. · Manage multiple assignments/research projects concurrently and possess the ability to prioritize between a variety of business initiatives · Commercialization: Deep knowledge of commercialization processes and required activities as the technical/R&D lead. Ability to troubleshoot challenges. · Collaboration: Work with cross functional teams acting as the lead product developer to drive execution across multiple projects · Communication: Provide updates to cross-functional teams; Identify hurdles and propose solutions · Translate research findings into meaningful business objectives · Champion an innovation approach and exhibit influence on the cross functional partners · Mentor, coach and collaborate with other colleagues within and outside of your immediate team · Demonstrate the ability to develop relationships with and coordinate commercialization activities across internal and external manufacturing facilities. · Lead and complete product testing, qualification, and commercialization in laboratory and production environments Recipe for Success - apply now if this sounds like you! · Bachelor's Degree (Master's is a Plus) - Food Science, Food Engineering, Chemistry, Chemical Engineering or related fields · 4+ years Product Development and commercialization experience within a CPG or equivalent · Experience with developing and commercializing frozen potato and/or frozen meals & snacks products. · Project management experience, technical expertise, and food science/processing knowledge· Experience with identifying and executing margin improvement projects preferred. · Familiarity with Sensory testing methods and test design. · Excellent communication, influencing, project management and problem solving skills · Highly motivated and able to multi-task varying degrees of complex projects · Willingness to travel up to 30%. Travel could include (but not limited to): to internal plants, co-manufacturers, and suppliers. · Experience delivering consumer centric, innovative solutions. · Demonstrated ability to influence, manage multiple projects concurrently with the ability to prioritize work, and solve problems effectively. · Brings an entrepreneurial spirit and growth mindset · Ability to manage through ambiguity Our Total Rewards philosophy is to provide a meaningful and flexible spectrum of programs that equitably support our diverse workforce and their families and complement Kraft Heinz' strategy and values. New Hire Base Salary Range: $89,800.00 - $112,200.00 Bonus: This position is eligible for a performance-based bonus as provided by the plan terms and governing documents. The compensation offered will take into account internal equity and may vary depending on the candidate's geographic region, job-related knowledge, skills, and experience among other factors Benefits: Coverage for employees (and their eligible dependents) through affordable access to healthcare, protection, and saving for the future, we offer plans tailored to meet you and your family's needs. Coverage for benefits will be in accordance with the terms and conditions of the applicable plans and associated governing plan documents. Wellbeing: We offer events, resources, and learning opportunities that inspire a physical, social, emotional, and financial well-being lifestyle for our employees and their families. You'll be able to participate in a variety of benefits and wellbeing programs that may vary by role, country, region, union status, and other employment status factors, for example: Physical - Medical, Prescription Drug, Dental, Vision, Screenings/Assessments Social - Paid Time Off, Company Holidays, Leave of Absence, Flexible Work Arrangements, Recognition, Training Emotional - Employee Assistance Program , Wellbeing Programs, Family Support Programs Financial - 401k, Life, Accidental Death & Dismemberment, Disability Location(s) Glenview R&D Center Kraft Heinz is an Equal Opportunity Employer - Underrepresented Ethnic Minority Groups/Women/Veterans/Individuals with Disabilities/Sexual Orientation/Gender Identity and other protected classes. In order to ensure reasonable accommodation for protected individuals, applicants that require accommodation in the job application process may contact *********************** for assistance.

Job DescriptionUntil is a moonshot company building a “pause button” for biology. Our near-term focus is organ-scale reversible cryopreservation: preserving donated organs at subzero temperatures without ice formation, then rewarming them uniformly for transplant. By solving this grand challenge, we're laying the foundation for whole-body reversible cryopreservation, giving patients a bridge to future cures. To achieve our goal, we are assembling an interdisciplinary team to develop perfusion systems, cryoprotectant formulations, and vitrification and rewarming hardware. We envision a future where no transplantable organ is lost to logistics, and no terminal diagnosis is final because patients can safely wait for future medicine to arrive. About The RoleWe are seeking a Senior Scientist to join as a leader on our whole organ preservation team. You will have large domain of ownership and play a vital role in shaping the company's organ transplant research program. You will apply your expertise in organ perfusion, preservation, viability assessment, and transplant to make successful large organ cryopreservation a reality. You will have the opportunity to collaborate with scientists and engineers across the company on variety of methods inspired by first principles of biology, physics, and chemistry. Creative scientific engagement is a requirement of the role, and new avenues for discovery and optimization are continuously supported.Responsibilities Implement pig organ ex-vivo viability evaluation protocols, including perfusion, histology, omics, etc. Ability to comfortably execute familiar assay protocols as well as identifying and implementing unfamiliar protocols to diagnose damage Propose adjustments to cryopreservation protocol to optimize the health of organs Experience working with ex vivo kidney and / or heart perfusion and viability assessment is a plus Qualifications You've completed a PhD in STEM, ideally in the field of organ preservation or transplant, or otherwise have significant (4+ years) experience working as a scientific leader in an industry context. You have demonstrated a passion for rapid problem solving and exploration of novel topics / protocols, demonstrated success working through hard problems. Desire to work in a laboratory setting to apply your expertise. You demonstrate agency, problem solving, passion for discovery, and a drive to push the boundaries of science through meaningful involvement in an ambitious project. Benefits A unique opportunity to learn new skills, develop impactful technology, and work with an ambitious team Medical and dental insurance coverage Flexible time off and paid holidays Competitive compensation package, including salary and equity Access to a 401(k) retirement savings plan While this represents our expected range based on market data, final compensation will be determined based on your specific qualifications and may be outside this range. Please keep in mind that the equity portion of the offer is not included in this estimate.As an equal opportunity employer, Until is committed to providing employment opportunities to all individuals. All applicants for positions at Until will be treated without regard to race, color, ethnicity, religion, sex, gender, gender identity and expression, sexual orientation, national origin, disability, age, marital status, veteran status, pregnancy, or any other basis prohibited by applicable law. We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

At Richelieu Foods, we are dedicated to a culture of belonging for everyone. Driven by our values of ownership, respect, and growth, we put people, safety, and quality above all else -- delicious pizza, outstanding service, and solid customer relationships are what happens as a result! Richelieu Foods, Inc. is a leading national private label and contract packing food manufacturer focused on frozen pizza. We have two manufacturing facilities located in IL and WI. We provide products to many national retailers, wholesalers, distributors, club and mass stores, as well as industrial accounts including other food manufacturers. JOB SUMMARY: The Bakery Process & Product Scientist serves as the critical technical bridge between R&D, Quality, and high-volume bakery manufacturing operations. This role applies food science, baking chemistry, and manufacturing process principles to diagnose and resolve product and process issues encountered on the production line. The role ensures products developed in R&D can be successfully scaled, stabilized, and consistently produced in a fast-paced automated manufacturing environment while meeting quality, food safety, and cost targets. Reporting to the Sr. Manager, Manufacturing, this position spends significant time on the production floor, partnering directly with line leaders, operators, and quality teams to troubleshoot real-time baking, texture, appearance, and shelf-life challenges. ESSENTIAL FUNCTIONS: Food Science & Quality Assurance * Apply food science principles to improve dough rheology, fermentation, baking processes, and product stability. * Conduct research on new ingredients and technologies to improve product quality, shelf-life, and nutritional value. * Collaborate with R&D teams to support new product development and process validation. * Conduct sensory evaluations and shelf-life studies to maintain product integrity. * Lead product trials and scale-up processes from lab to production, addressing any issues that arise. Quality, Food Safety, & Documentation * Partner with Quality Assurance to ensure compliance with food safety, GMPs, and regulatory standards * Maintain and monitor robust food safety programs * Support root cause analysis for customer complaints or internal quality failures * Contribute to technical documentation including * Process standards * Critical control parameters * Technical troubleshooting guides Manufacturing and Line Support * Serve as the technical expert on bakery line, supporting day-to-day production issues related to: * Dough development and handling * Proofing and fermentation behavior * Oven performance, heat transfer, and bake profiles * Product texture, structure, and moisture * Collaborate with Manufacturing team to diagnose and resolve in-process product defects * Partner with Manufacturing team to optimize line parameters, set points, and changeovers * Ensures that tasks and functions are performed in a safe manner that upholds expectations throughout the production and packaging processes. * Process Optimization & Continuous Improvement * Utilize Lean Manufacturing and Six Sigma methodologies to reduce waste and improve efficiency. * Implement data-driven process controls for temperature, humidity, and ingredient ratios. * Drive automation initiatives and integrate advanced technologies for real-time monitoring. * Support CAPA investigations related to product quality deviations * Compliance & Reporting * In partnership with Divisional Safety, ensure Factory meets OSHA requirements and continually improving safety through TRIR, LTIR, by addressing both physical safety issues as well as unsafe employee behaviors. Maintain and improve housekeeping in all areas. Maintain accurate production records, batch logs, and regulatory documentation. * Prepare KPI reports on yield, efficiency, waste reduction, and quality metrics for senior leadership. * Ensure adherence to environmental and sustainability standards. KNOWLEDGE, SKILLS, & COMPETENCIES: * Highly effective network collaboration skills, able to work and coordinate efficiently across several business functions and key stakeholders * Strong interpersonal skills with the ability to communicate effectively with all levels of skill and experience internally, suppliers and customers * Ability to influence without direct authority, delivering results in partnership with and through people * Strong organizational and planning abilities and excellent analytical, problem solving and decision-making skills * Unwavering integrity and honesty at all times. * Ability to thrive in a fast-paced environment. * Comfortable being hands-on in the plant with demonstrated success in building credibility and respect with manufacturing team for practical, applicable solutions * Ability to translate science into operator-friendly guidance EDUCATION / EXPERIENCE: * Bachelor's in Food Science, Food Technology, Chemical Engineering, or relevant professional experience. * Minimum of seven (7) years food manufacturing experience, at least 4 in commercial or industrial bakery manufacturing * Strong knowledge of ingredient functionality, baking chemistry, and microbiology. * Working knowledge of quality and safety regulatory standards * Demonstrated success supporting live production environments * Working knowledge of and experience using Six Sigma & Lean Manufacturing techniques preferred * Bilingual preferred Universal Pay Verbiage: The following information is provided in accordance with certain state and local laws. Compensation depends on experience, geographic locations, and other factors permitted by law. The expected compensation for this role is between $120,000 and $145,000. This role is also eligible for an annual incentive plan bonus. Benefits for this role include medical, dental, and vision insurance, pre-tax spending accounts, retirement benefits, paid time off, 401K with company match, short-term and long-term disability, and life insurance. Richelieu Foods, Inc. is an Equal Opportunity employer. All qualified applicants will receive consideration for employment 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.

AbbVie (NYSE:ABBV) is a global, research-based biopharmaceutical company formed in 2013 following separation from Abbott Laboratories. The company's mission is to use its expertise, dedicated people and unique approach to innovation to develop and market advanced therapies that address some of the world's most complex and serious diseases. AbbVie employs approximately 28,000 people worldwide and markets medicines in more than 170 countries. Job Description APPLY HERE!!!! mygradjob.com/job/senior-scientist-8/ We are looking for a highly motivated person who drives new technologies and processes. The candidate will develop drug product formulations and scalable manufacturing processes for NBEs used in clinical trials through all phases of development. Working closely with analytical and formulation scientists in an integrated group the candidate will operate via multi-functional, global teams including API manufacturing, Process R&D, Pre-formulation and Pilot Plant Operations. Major Responsibilities The incumbent will participate in the development of parenteral formulation for monoclonal antibodies and antibody drug conjugates, Independently design and execute studies evaluating the stability (chemical & physical) of the monoclonal antibodies and antibody constructs/conjugates against solution conditions (pH, ionic strength, temperature, light e.tc) and physical stresses arising from manufacturing process conditions (freeze thaw, mixing, filtration, filling, filtration and Lyophilization), and screen excipients (buffers, stabilizers, surfactants, tonicity & Tg' modifiers e.t.c) to develop robust formulations for frozen, refrigerated liquid and lyophilized dosage forms Perform upfront manufacturability assessment of the formulation candidates and recommend the best and back up formulation for both FIH and commercialization Make concise scientific presentations of experimental results to the management and author detailed scientific technical reports. Author CMC relevant sections of INDs/CTDs, as well as response questions scientific project lead, generating original technical ideas for formulation and analytical technologies of assigned NBE development projects Establishment and coordination of external development activities including supervision of technical, financial and regulatory requirements Qualifications Basic: BS and typically 10+ years of experience; MS or equivalent education with typically 8+ years of experience; PhD 0+ years of experience in formulation or analytical development of NBEs Scientific understanding of the structure & function of monoclonal antibodies and antibody constructs/conjugates, and their modes of degradation/stabilization An understanding of scientific approach to develop biologic protein formulations Strong lab skills focused on formulation development for monoclonal antibodies and antibody constructs/conjugates (standard excipient selection, functional excipients, high throughput assays) Basic understanding of unit operations of aseptic manufacturing such as bulk freeze thaw, compounding/mixing, filtration, filling and lyophilization for liquid and lyophilized NBEs Hands on expertise of bio analytical test methods for protein pharmaceuticals e.g. mass-spectrometry, HPLC and electrophoretic methods, particle imaging, ELISA, compendial tests Broad expertise around regulatory requirements for NBEs (mAbs, bispecifics, ADCs) and parenteral products is preferred (21 CFR parts 600 & 210, FDA cGMP-, ICH-, EU GMP-guidances). Statistical knowledge and experience is preferred e.g. capability analysis, gauge R&R and design of experiments (DOE) methodologies Additional Information All your information will be kept confidential according to EEO guidelines.

Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracted, assembled and retained key employees who are experts in their fields. This has helped us expand into new sectors and steadily grow. Job Description: Perform analytical testing of biologics products using HPLC and/or CE techniques. Author/review technical documents including eLN, protocols, and reports. Qualifications Education: B. S. Degree required in Analytical Sciences, Biochemistry or related field. Master or Ph. D. preferred Additional Information Feel free to forward my email to your friends/colleagues who might be available. We do offer referral Bonus. Thank you. Kind Regards, Harris Kaushik Clinical Recruiter Integrated Resources , Inc. IT Life Sciences Allied Healthcare CRO DIRECT # - (650)-399-0891 Gold Seal JCAHO Certified ™ for Health Care Staffing “INC 5 0 0 0 's FASTEST GROWING, PRIVATELY HELD COMPANIES” (8th Year in a Row)

Located in Milwaukee, Wisconsin, the Versiti Blood Research Institute (VBRI) is the largest blood-focused research institute in the United States. With over 30 basic, translational, and clinical investigators, the institute is dedicated to advancing scientific knowledge and developing innovative therapies related to blood and blood disorders. The institute's research interests encompass a wide range of topics, including transfusion medicine, cellular therapy, thrombosis/hemostasis, immunology, and hematologic malignancies. As a vital part of Versiti, a non-profit organization with a blood bank at its core, the VBRI strives to improve lives through innovative research and the development of novel diagnostics and treatments. VBRI is part of the Milwaukee Regional Medical Campus, a rapidly growing clinical-translational research hub. VBRI's proximity to the Medical College of Wisconsin, Childrens' Hospital of Wisconsin, and Froedtert Hospital facilitates seamless interdisciplinary collaborations. A range of exemplary core facilities support highly competitive research. In the summer of 2024, construction of a new research building began, doubling existing VBRI research space to enable the recruitment of 10-15 new faculty. With its renowned researchers, strategic expansion plans and location in a highly collaborative environment, the VBRI is poised to maintain and expand its position as one of the leading hematology institutes in the world. Position Summary Develops and elucidates scientific aims, experimental design and execution. A Research Scientist I is equivalent to the Research Assistant Professor position at many universities. The Zhu Lab is primarily focused on unraveling the mechanisms of receptor transmembrane signaling. Specifically, our attention is directed towards cell surface receptors featuring single transmembrane domains, such as integrins, receptor tyrosine kinases, and receptor-like tyrosine phosphatases. Through a multidisciplinary approach encompassing structural biology, protein engineering, biochemistry, and cell biology techniques, we aim to elucidate how these receptors transmit signals across the cell membrane. Our investigations center on understanding the conformational regulation triggered by ligand binding at the extracellular domain or cytoplasmic domain stimulations. Our goal is to illustrate the intricate mechanisms governing receptor-ligand interactions and the conformational changes necessary for transmembrane signaling, spanning the extracellular, transmembrane, and cytoplasmic domains. We are currently engaged in several projects, delving into the conformational requirements for bi-directional transmembrane signaling in integrins, elucidating the structural and functional basis of integrins as pathogen receptors, exploring integrin ligand interactions, and developing antibodies and small molecules that target or stabilize specific integrin conformations. Integrins, crucial cell surface receptors, play a pivotal role in regulating cell-cell and cell-matrix interactions across various biological processes, including development, hemostasis, antigen recognition, homing, and inflammation. Dysregulation of integrin activation is observed in pathological conditions such as autoimmune diseases and thrombosis. Our overarching goal is to uncover the intricate correlation between receptor conformational regulation and signal transduction, aiming to contribute to the design of more efficient and safer therapeutic agents. A new focus of our lab entails unraveling the mechanism behind coronavirus spike protein-mediated cell fusion and viral infection. We aim to apply the gained knowledge to develop inhibitors for antiviral treatment and diverse virus-based applications, including cell-specific gene delivery and oncolysis. Total Rewards Package Benefits Versiti provides a comprehensive benefits package based on your job classification. Full-time regular employes are eligible for Medical, Dental, and Vision Plans, Paid Time Off (PTO) and Holidays, Short- and Long-term disability, life insurance, 7% match dollar for dollar 401(k), voluntary programs, discount programs, others. Responsibilities With direction from PI, assists in designing goal-oriented, hypothesis driven research program(s) Takes advantage of opportunities to apply for local or national grants as applicable to fund relevant research Experimental work and data analyses Maintains an active scientific publication and presentation record based on individual and PI's research. Minimum of one high impact in addition to multiple publications. Provides direction and/or supervise research technologists, pre- and postdoctoral trainees. Actively contributes to the scientific community in the Blood Research Institute Performs other duties as required or assigned which are reasonably within the scope of the duties in this job classification Understands and performs in accordance with all applicable regulatory and compliance requirements Complies with all standard operating policies and procedures Qualifications Education PhD PhD, MD, or equivalent degree in related scientific area required Experience 1-3 years postdoctoral experience required Knowledge, Skills and Abilities Demonstrated ability to independently apply understanding of scientific theory to the structure and execution of research experiments. required Demonstrated ability to interpret and explain the theoretical basis of the work performed. required Ability to perform research procedures independently. required Immediate proficiency in basic and sophisticated tests and procedures required in the scientific field. required Exceptional organizational, communication and problem solving skills. required Strong detail orientation and analytical ability. required Ability to prioritize and execute multiple tasks and meet deadlines. required Ability to supervise, coordinate and plan the work of several individuals involved in a project. required #LI-EH1 #VBRI

US Tech Solutions is a global staff augmentation firm providing a wide-range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit our website ************************ We are constantly on the lookout for professionals to fulfill the staffing needs of our clients, sets the correct expectation and thus becomes an accelerator in the mutual growth of the individual and the organization as well. Keeping the same intent in mind, we would like you to consider the job opening with US Tech Solutions that fits your expertise and skillset. Job Description · Develop ad qualify highly precise analytical methods for analysis of large molecule products. Support global transfer and trouble shooting of methods. Analyze data, prepare reports and presentations · Essential: Experience in cell culture, immunoassay and bioassay development are required. · Excellent documentation skills. · Preferred: Flow cytometry, Biacore, cell signaling, laboratory automation and DOE experience is preferred · Develop and qualify precise ELISA, CRBA and cell-based potency methods for analysis of large molecule products. Support global transfer, validation and trouble shooting of bioassays. Perform characterization sample testing, statistical data analysis and summarize assay results, prepare e-notebooks and reports. · Experience & Knowledge Essential: · Experience in cell culture, immunoassay and bioassay development are required. Excellent documentation skills. Preferred: Flow cytometry, Biacore, SDS-Page, laboratory automation are preferred. · Develop and qualify precise ELISA, CRBA and cell-based potency methods for analysis of large molecule products . · Support global transfer, validation and trouble shooting of bioassays . · Perform characterization sample testing, statistical data analysis and summarize assay results, prepare e-notebooks and reports . · Experience in cell culture, immunoassay and bioassay development are required. Excellent documentation skills. Preferred: Flow cytometry, Biacore, SDS-Page, laboratory automation are preferred Qualifications · Develop and qualify precise ELISA, CRBA and cell-based potency methods for analysis of large molecule products . · Support global transfer, validation and trouble shooting of bioassays . · Perform characterization sample testing, statistical data analysis and summarize assay results, prepare e-notebooks and reports . · Experience in cell culture, immunoassay and bioassay development are required. Excellent documentation skills. Preferred: Flow cytometry, Biacore, SDS-Page, laboratory automation are preferred Additional Information Regards, Sneha Shrivastava ************

In this role you will be a leading Scientist focused on defining and executing innovative strategies for biocompatibility evaluation and risk analysis of medical devices in the GE HealthCare Imaging/ X-ray/ CT family of businesses. This will include leading strategy for biocompatibility-related standards, acting as GE HealthCare's voice as policies develop, and overseeing programs to ensure successful implementation internally and with external bodies such as standard organizations and regulatory authorities. GE HealthCare is a leading global medical technology and digital solutions innovator. Our mission is to create a world where healthcare has no limits. Unlock your ambition, turn ideas into world-changing realities, and join an organization where every voice makes a difference, and every difference builds a healthier world. **Job Description** **Roles and Responsibilities:** + Design and execute medical device biocompatibility strategies to assure user and patient safety through the application of current biological evaluation and toxicological principles in support of new product development and sustaining activities. + Standardize test methods across multiple material and device types, leveraging common data to derive meaningful conclusions on the potential for biocompatibility concern. + Lead and author Biocompatibility deliverables - e.g., biological evaluation plan & reports, hazard analysis, white paper, technical memo, and other relevant activities in support of global programs. + Implement the use of ISO 10993 series, 21CFR58 GLP for non-clinical studies, and/ or other regulatory guidance documents to qualify GE Healthcare products. + Provide technical and strategic input to meet business objectives at the project team level while assuring compliance with GE Healthcare and external standards. + Interpret raw material, finished device data, and literature to assess overall risk to patient. + Develop justification to address ISO 10993 - 1 endpoints based on study data and literature. + Independently review literature and identify relevant information to support product development and registration. + As needed - engage in standards organization and/ or regulatory committees to ensure emerging regulations are based on well-established science and toxicological principles. + Keep upto date on regulatory requirements and assess the impact of new standards and/or regulations to enable the generation of appropriate strategies for biocompatibility work. **Required Qualifications:** + PhD in physical/organic/biochemistry, toxicology, material science, bioengineering, or an equivalent scientific field. + Expert knowledge in use and application of ISO 10993 series of standards + Experience (10+ years) in design and development of medical devices that are categorized as FDA Class I, II and Class III. + Experience conducting material and chemical characterization of medical devices, physicochemical analyses of polymeric materials, metals, and ceramics. + Excellent verbal and written communication and presentation skills with the ability to speak and write clearly and convincingly in English, tailoring communication methods to customer's requirements. + Advanced experience and proficiency with MS Office word processing, spreadsheet, presentation, and collaboration applications. **Desired Characteristics:** + American Board of Toxicology Diplomate (DABT), or other national equivalent such as ERT. + Experience leading test lab operations that support medical device biocompatibility evaluations. + Experience in mechanical design (15+ years). + Experience as a lead convenor of a Technical Committee (TC) or Working Group (WG) of a Standards Development Organization (SDO) or National Standards Body (NSB) such as ISO, ANSI, or AAMI. + Experience preparing communications for and interacting with multiple regulatory bodies world-wide such as FDA, NMPA, TGA, MHLW, PMDA, CDSCO, BfArM, ANSM, etc. + Experience with high risk, life supporting, and life-sustaining products. + Demonstrated life-long learner; eagerness to obtain new skills and knowledge. + Humility in understanding, but assertive when needed; willing to make decisions and assign clear priorities. + Strong oral and written communication skills. Strong interpersonal and leadership skills. Demonstrated ability to analyze and resolve problems. **Inclusion and Diversity** GE HealthCare is an Equal Opportunity Employer where inclusion matters. 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. We expect all employees to live and breathe our behaviors: to act with humility and build trust; lead with transparency; deliver with focus, and drive ownership - always with unyielding integrity. Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you'd expect from an organization with global strength and scale, and you'll be surrounded by career opportunities in a culture that fosters care, collaboration and support. \#LI-HOU1 **Additional Information** **Relocation Assistance Provided:** Yes

As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. Discover Impactful Work The Senior Process Development (Sr. PD) Scientist is responsible for developing, optimizing, and technology transfer of processes to the production area, while meeting specific quality, schedule, and cost requirements. The Sr. PD Scientist designs and carries out multiple, complex steps of chemical reactions and purifications of products independently and in accordance with established procedure. The Sr. PD Scientist also provides a high level of technical expertise and leadership across the company and must exercise judgment within broadly defined practices and policies. A Day in the life Follow established methods and standard operating procedures Work independently or lead a team to troubleshoot problems, recommend and execute improvements in laboratory operations and equipment use Analyze and simulate existing/new processes; design and execute experiments for characterization, isolation and purification of new product/processes using various techniques in process development/manufacturing Discover, develop and optimize reliable, robust and cost-efficient processes that are amenable to scale change. Evaluate processes for safety and reproducibility during development and scale up Write technical reports, critical experiment plan, item qualification and operating procedures for product manufacturing and equipment Provide product costing analysis. Evaluate equipment need, and provide selection and safety recommendation Provide technical leadership, coaching, and training to Manufacturing and Process Development staff on process optimization and scale up. Provide technical presentation to staff and Management team When needed, act as the project manager when working individually or with cross-functional teams to prepare for new product launches or other operational projects Participate/lead PPI projects The individual must understand and comply with RCRA Standards The position is also responsible for any other duties apparent or assigned. Keys to Success Education Ph.D. required, or an equivalent combination of degree and experience in nucleic acids or peptide chemistry. Experience 8+ years of demonstrated industrial experience in multistep organic synthesis, purification, process development/validation, scale up of heterocyclic compounds (Nucleic Acids/Peptide preferred), product analysis and instrumentation (HPLC, LC/MS, NMR) Demonstrated experience in process development techniques and application (process optimization, experimental design, and data analysis) Must possess expert analytical, troubleshooting, mathematical/data analysis, and technical writing skills, along with the ability to present information effectively to audiences of varying technical understanding Strong understanding of analytical data, troubleshooting, and method development Knowledge, Skills and Abilities Must be available to work overtime, including weekends as project schedule warrants Ability to regularly handle chemicals, solvents, and potentially hazardous substances Be mechanically adept and able to apply mechanical fundamentals to properly operate, the equipment within their area of responsibility Specific vision abilities required: close vision, distant vision, depth perception, ability to adjust focus, and differentiate colors The employee is occasionally required to walk, sit, stoop, bend, kneel, crouch, and crawl and frequently lift and/or move 50 pounds and occasionally lift and/or move more than 50 pounds with assistance Benefits We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!

SGS is the global leader and innovator in inspection, verification, testing and certification services. Founded in 1878, SGS is recognized as the global benchmark in quality and integrity. With over 97,000 employees in 130 countries and operating a network of more than 2,400 offices and laboratories, we provide services to almost every industry by assuring quality and safety of products and services. Trusted all over the world, SGS is a market leader because we put 100% passion, pride and innovation into everything we do. We encourage new ideas. We welcome people who challenge the way we do things. And we will be 100% committed to helping you reach your full potential. Execute and perform testing as per methods, following the company's Standard Operating Procedures, Deviations and Change Control programs and cGMP guidelines as required by client submissions. Duties here include preparation for testing by using good time management skills for each assigned task, such as confirming availability of resources (standards, equipment, etc.) and adequacy of testing documentation, proper application of test procedures, proper technique for data capture and recording, and preparation of the final report of analysis. Ability to execute method verifications, validations, transfers based on signed protocols with supervision. Perform routine and more complex analysis/testing of pharmaceutical and biopharmaceutical finished products and raw materials. Strictly follows the latest approved version of methods, SOPs, QA manuals unless authorized by Department Manager and/or Group/Scientific Leader in writing. Record findings in standardized format, keeping all records and analyst note book in good order. Ensure that all reasonable client requests pertaining to the conduct of a given test are met in a timely and ultimately efficient manner. Ensure that all client requests for information pertaining to analytical testing (or any of SGS other services) are passed on to appropriate company personnel in a timely and effective manner. Ensure that routine testing submitted by clients is completed within established parameters governing turnaround time and quality-of-work expectations. Participation in departmental and/or company-wide projects designed to improve the nature of SGS client services. Work as a team with other scientists and communicate effectively with peers and superiors. Prioritize, schedule and plan daily work in order to maintain efficient work flow to assure completion of scheduled tasks and to meet established due dates. Report and Assist in the failure investigations as instructed. Ensure that equipment are maintained in good order; perform calibrations and qualifications as required. With supervision, prepare study protocols, study reports, forms and SOP's. Constantly look for ways to improve analytical techniques, documentation and daily work duties. Conduct trouble shooting where testing/analytical failures occur in liaison with Group/Scientific Leader and designate. Inform the Department Manager and/or Group/Scientific Leader, as far in advance as possible, if the assigned work order cannot be satisfactorily completed within established scheduled time and quality of work expectations. Qualifications Bachelors, Masters/MBA or Doctorate degree in Biochemistry, Chemistry, Biology, or equivalent. Minimum 5-10 years of experience respectively with demonstrated ability to complete more complex role/duties OR equivalent combination of education and experience Must have experience working with MS, LC-MS, LC-MS/MS, MALDI-TOF, N-term sequencing and other Mass Spec related projects. Knowledgeable in all regulatory guides impacting their specialized field, such as ICH, FDA, TPP, pharmacopeias Must possess very strong communication skills allowing them to navigate sensitive and often complex matters with both clients and SGS staff Additional Information SGS is an Equal Opportunity Employer, and as such we recruit, hire, train, and promote persons in all job classifications without regard to race, color, religion, sex, national origin, disability, age, marital status, sexual orientation, gender identity or expression, genetics, status as a protected veteran, or any other characteristics protected by law. To perform this job successfully, an individual must be able to perform each essential duty satisfactorily with or without reasonable accommodations. The requirements listed above are representative of the knowledge, skills, and/or abilities required. This job description should not be construed as an exhaustive statement of duties, responsibilities or requirements, but a general description of the job. Nothing contained herein restricts the company's rights to assign or reassign duties and responsibilities to this job at any time. If you are applying for a position within the United States and you have difficulty completing the on-line employment application because of a disability, please call ************ for assistance and leave a message. You will receive a callback. Please note, this phone number is not for general employment information but is only for individuals who are experiencing difficulty applying for a position due to a disability.

Our client, a leading organization in the healthcare and diagnostics industry, is seeking an Associate Scientist I to join their team. As an Associate Scientist I, you will be part of the Laboratory Support Department supporting Verification and Data Analysis Teams. The ideal candidate will have problem-solving skills, strong data analytics capabilities, and excellent communication skills, which will align successfully in the organization. **Job Title:** Associate Scientist I **Location:** Abbott Park, IL **Pay Range:** **What's the Job?** + Write and execute system-related verification and characterization protocols for hardware, software, and assays. + Support data package summaries in accordance with governing procedures. + Operate instruments at a basic level and perform repairs as needed. + Assist in troubleshooting hardware, software, and assay performance issues across multiple system functions. + Apply quantitative methods to analyze data, evaluate results, draw conclusions, and suggest improvements. **What's Needed?** + Problem solving and technical troubleshooting skills. + Proficiency in data analytics and laboratory procedures. + Basic PC skills including Word, Excel, and PowerPoint. + Good written and verbal communication skills in English. + Experience with ARCHITECT and Alinity I platforms, and knowledge of regulations affecting IVDs and Biologics. **What's in it for me?** + Opportunity to work in a collaborative, goal-driven environment. + Hands-on experience with advanced diagnostic systems. + Professional growth and development in a reputable organization. + Engagement in meaningful work that impacts patient health and safety. + Supportive team environment with a focus on innovation and excellence. **Upon completion of waiting period consultants are eligible for:** + Medical and Prescription Drug Plans + Dental Plan + Vision Plan + Health Savings Account + Health Flexible Spending Account + Dependent Care Flexible Spending Account + Supplemental Life Insurance + Short Term and Long Term Disability Insurance + Business Travel Insurance + 401(k), Plus Match + Weekly Pay 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.

Job Title: Scientist 1, Sample Management and Sample ProcessingJob Description Join an innovative Genomic Technologies lab team at the forefront of genomic research and discovery. We seek an experienced and highly organized Sample Management and Processing Scientist to support impactful reverse translation projects. The role focuses on gDNA isolation from clinical samples across various therapeutic areas, executing manual and automated workflows for high-quality nucleic acid extraction, and maintaining detailed documentation in LIMS. Effective cross-functional communication with researchers is essential to ensure the integrity of isolated gDNA for downstream analyses. Responsibilities + Adhere to department and company standard operating procedures for communication, lab operations, project reporting, and lab safety. + Perform nucleic acid extraction, quality control, and data interpretation with minimal supervision, aligned to project timelines. + Achieve operational proficiency for required daily functions within training schedules. + Independently and collaboratively troubleshoot wet lab tasks. + Maintain clear and accurate documentation of all processes. + Communicate project progress, completion, and data through reports, meetings, and presentations. + Record and document wet lab processes and progress in LIMS and project management applications according to policies and procedures. + Support the development and testing of LIMS workflows. + Maintain instrumentation as outlined by laboratory standards and manuals. Essential Skills + Bachelor's degree in Genetics/Genomics or related field with 4+ years relevant experience, or Master's degree with 2+ years relevant experience. + Experience in performing routine and complex nucleic acid workflows from various source materials. + Proficiency in performing nucleic acid quality control and data analysis, including fluorescence quantification and integrity analysis. + Experience with sample processing from source materials to nucleic acids within a laboratory management system. + Skilled in micropipetting and wet lab automation for genomic laboratory techniques. + Ability to strictly adhere to SOPs and lab guidelines and report deviations promptly. + Proficient computer skills, especially in Microsoft Office Suite. + Self-directed in delivering timely results independently and collaboratively in a fast-paced environment. + Strategic project planning and critical thinking to resolve routine and complex problems. Additional Skills & Qualifications + Experience with low and high throughput sample tracking and data management (LIMS). + Experience with automation platforms and maintaining workflows. + Experience in a CLIA-certified or other regulated laboratory environments. + Experience in clinical writing and editing documents/manuals. + Ability to work well in a multidisciplinary team environment. + Capacity to learn new methodologies and drive innovation to improve workflows. + Demonstrates effective and efficient communication. Work Environment The work environment involves working in an advanced Genomic Technologies lab, utilizing cutting-edge technologies and equipment. The role requires adherence to lab safety standards and SOPs. The team fosters a collaborative and innovative atmosphere, encouraging strategic project planning and problem-solving. Job Type & Location This is a Contract position based out of North Chicago, IL. Pay and Benefits The pay range for this position is $40.00 - $42.00/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 North Chicago,IL. Application Deadline This position is anticipated to close on Jan 26, 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.

Salary: $65,000 - $70,000 annually, commensurate with experience The Center for Cancer Cell Biology, Immunology, and Infection (Department of Microbiology & Immunology) in the Chicago Medical School at Rosalind Franklin University of Medicine & Science is inviting applications for two Research Scientists positions. They will be involved in studying molecular virology, host-pathogen interaction, and substance use/abuse comorbidity. Who We Are Rosalind Franklin University of Medicine and Science (RFU) is a graduate health sciences university committed to serving the population through the interprofessional education of health and biomedical professionals and the discovery of knowledge dedicated to improving wellness. The university embodies the spirit of inquiry and excellence modeled by its namesake Dr. Rosalind Franklin, whose Photo 51 was crucial to solving the structure of DNA. RFU is nationally recognized for its research in areas including neuroscience, brain-related diseases, inherited disorders, proteomics, cancer cell biology and immunology, cardiac resuscitation, and gait and balance. Essential Duties & Responsibilities The individuals will be expected to perform the following duties and responsibilities: (1) Design and conduct experiments; (2) Maintain detailed laboratory records; (3) Collect, analyze, and present data; (4) Work independently and as a team; (4) Prepare manuscripts. Conditions of Employment Must achieve satisfactory results from a background check Required Education & Experience PhD in biology, biomedical science, and related fields Required Knowledge, Skills, & Abilities A minimum of 3 years of wet laboratory research experience and skills broad biomedical knowledge and understanding well versed in main cell biology, biochemistry, and molecular biology techniques exceptional organization skills and adept with Microsoft Office tools, GraphPad Prism (or other data analysis software) Preferred Qualifications training or work experience in virology work experience with mice Typical Physical Demands & Working Conditions Selected candidates must have the mental and physical capabilities to perform the essential functions of the position with or without reasonable accommodations. EOE, Including Disability / Vets

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. The Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 50 countries. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2020, Eurofins generated total revenues of EUR € 5.4 billion, and has been among the best performing stocks in Europe over the past 20 years. Job Description Position Summary The Scientist I performs testing activities as directed by Senior Scientist, Monograph Supervisor, or Specialty Supervisor in accordance with all applicable company and regulatory guidelines and designs experiments, operates instruments, assists other chemists, collects and interprets data, writes but also peer reviews data and/or reports especially for challenging, non-routine investigations, custom method development, method validation, unknown/material identification, failure analysis, simple de-formulations and select product testing/development work. Legal and Insurance work will typically be performed under the guidance of the Scientist II. Essential Duties and Responsibilities Perform testing activities as directed by Senior Scientist, Monograph Supervisor, or Specialty Supervisor in accordance with all applicable company and regulatory guidelines. Wet chemistry techniques utilized will include but are not limited to gravimetry, titrimetry, colorimetry and others as needed including sample preparation, isolations, filtrations, extractions. Instrumentation utilized will include a wide array including not limited to FTIR, HPLC, LCMS, GCFID/ECD, GCMS, ICP-OES, ICP-MS, AA, IC, FIA, LECO N2, Calorimetry, Physical and Thermal Analysis (includes DSC, TGA, DMA - outsourced) NMR interpretation and other instruments and techniques as needed to meet customer expectations (includes outsourcing selective testing when appropriate). Perform and document method transfers, development work, validations/verifications. Maintain neat and accurate records. Interact with clients to assist in selection of test methods and interpretation of test data. Assist Sales and Business Team members on quote review if requested. Design custom projects or studies, and offer interpretation, custom reports or consultation on test data. Enter testing data into LIMS and monitor for QC failures. Assist lab staff in determining corrective actions for QC failures. Review and approve laboratory analytical data including peer review Review and issue reports to clients. Issue quotations for standard testing services where existing tests/methods are utilized. Maintain chemical/reagent traceability. Support the maintenance of controlled documents related to laboratory operations/testing through editing of documents and/or reviewing revisions. Support quality system improvements through completion of Corrective and Preventive Action forms, documenting Non-Conformances and Client Complaints, and assisting with internal audit findings as assigned by Quality Manager. Support the completion of unknown and failure investigations through testing performance and/or imparting chemical knowledge. Maintain regular attendance and punctuality Conducts all activities in a safe and efficient manner Performs other duties as assigned Assist with case studies, white papers if requested by Sr. Management for marketing purposes. Attend industry-appropriate symposia, training, webinars, journals to remain current on analytical techniques, new developments. Qualifications Education/Experience MS or PhD in Chemistry or related field or BS and 2+ years experience in a commercial laboratory. Experience as Expert Witness on Legal and Insurance Cases is highly desirable. Ability/Skills: Proficiency at GC, GCMS, HPLC, LCMS and knowledge of all other major analytical instrument capabilities is imperative. Additional Information What we offer: Excellent full time benefits including comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays Eurofins USA Food Testing is a Disabled and Veteran Equal Employment Opportunity employer.

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. The Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 50 countries. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2020, Eurofins generated total revenues of EUR € 5.4 billion, and has been among the best performing stocks in Europe over the past 20 years. Job Description Position Summary The Scientist I performs testing activities as directed by Senior Scientist, Monograph Supervisor, or Specialty Supervisor in accordance with all applicable company and regulatory guidelines and designs experiments, operates instruments, assists other chemists, collects and interprets data, writes but also peer reviews data and/or reports especially for challenging, non-routine investigations, custom method development, method validation, unknown/material identification, failure analysis, simple de-formulations and select product testing/development work. Legal and Insurance work will typically be performed under the guidance of the Scientist II. Essential Duties and Responsibilities Perform testing activities as directed by Senior Scientist, Monograph Supervisor, or Specialty Supervisor in accordance with all applicable company and regulatory guidelines. Wet chemistry techniques utilized will include but are not limited to gravimetry, titrimetry, colorimetry and others as needed including sample preparation, isolations, filtrations, extractions. Instrumentation utilized will include a wide array including not limited to FTIR, HPLC, LCMS, GCFID/ECD, GCMS, ICP-OES, ICP-MS, AA, IC, FIA, LECO N2, Calorimetry, Physical and Thermal Analysis (includes DSC, TGA, DMA - outsourced) NMR interpretation and other instruments and techniques as needed to meet customer expectations (includes outsourcing selective testing when appropriate). Perform and document method transfers, development work, validations/verifications. Maintain neat and accurate records. Interact with clients to assist in selection of test methods and interpretation of test data. Assist Sales and Business Team members on quote review if requested. Design custom projects or studies, and offer interpretation, custom reports or consultation on test data. Enter testing data into LIMS and monitor for QC failures. Assist lab staff in determining corrective actions for QC failures. Review and approve laboratory analytical data including peer review Review and issue reports to clients. Issue quotations for standard testing services where existing tests/methods are utilized. Maintain chemical/reagent traceability. Support the maintenance of controlled documents related to laboratory operations/testing through editing of documents and/or reviewing revisions. Support quality system improvements through completion of Corrective and Preventive Action forms, documenting Non-Conformances and Client Complaints, and assisting with internal audit findings as assigned by Quality Manager. Support the completion of unknown and failure investigations through testing performance and/or imparting chemical knowledge. Maintain regular attendance and punctuality Conducts all activities in a safe and efficient manner Performs other duties as assigned Assist with case studies, white papers if requested by Sr. Management for marketing purposes. Attend industry-appropriate symposia, training, webinars, journals to remain current on analytical techniques, new developments. Qualifications Education/Experience MS or PhD in Chemistry or related field or BS and 2+ years experience in a commercial laboratory. Experience as Expert Witness on Legal and Insurance Cases is highly desirable. Ability/Skills: Proficiency at GC, GCMS, HPLC, LCMS and knowledge of all other major analytical instrument capabilities is imperative. Additional Information What we offer: Excellent full time benefits including comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays Eurofins USA Food Testing is a Disabled and Veteran Equal Employment Opportunity employer.