Principal research scientist jobs in Waukesha, WI - 21 jobs

From our home in Janesville, Wisconsin, Impact Confections has been delighting candy lovers with bold flavors and timeless favorites for generations. We're proud to be the makers of WARHEADS , the iconic sour candy that dares taste buds everywhere, and the classic Melster Candies, known for nostalgic treats like Circus Peanuts and seasonal delights that families have cherished for decades. SUMMARY We are seeking a Senior Food Scientist with 5 years of industry experience to contribute to the development, testing, and optimization of innovative confectionery products. This role combines hands-on work with applied research and development (R&D), offering the opportunity to take ownership of projects and drive product innovation from concept to commercialization. The ideal candidate brings a strong technical foundation in food science, practical experience in product development, and a passion for delivering high-quality, market-ready solutions. This opportunity offers a dynamic environment where your expertise directly shapes product innovation. Opportunities to lead projects and influence the future of our product portfolio. Professional growth through exposure to multiple aspects of food R&D with competitive compensation and benefits package. This is a hybrid opportunity the employee must be able to work onsite 3-4 days per week. ESSENTIAL DUTIES AND RESPONSIBILITIES Product Development & Innovation Lead the formulation and development of new food products, from concept through commercialization. Independently conduct ingredient research, prototyping, and iterative product improvements. Apply sensory and consumer insights to refine product performance and quality. Laboratory Testing & Analysis Design and execute experiments to evaluate product stability, shelf life, and sensory attributes. Conduct physical, chemical, and sensory analyses with minimal supervision. Interpret and report test results, providing recommendations for technical improvements. Research & Documentation Stay current with emerging food technologies, ingredients, and regulatory developments. Prepare and maintain accurate technical documentation, reports, and specifications. Present findings to cross-functional teams and provide data-driven recommendations. Collaboration & Project Leadership Partner with Quality, Production, and Marketing to ensure successful scale-up and launch of products. Support pilot plant trials and full-scale manufacturing runs. QUALIFICATIONS Strong knowledge of food safety principles, HACCP, and regulatory compliance. Experience in scaling formulations from lab to production. Excellent organizational, problem-solving, and analytical skills. Strong communication skills, with the ability to collaborate across cross-functional teams. EDUCATION and/or EXPERIENCE Bachelor's degree in food science, Food Technology, Chemistry, or related field. At least 5 years of food industry experience (confectionery experience preferred) demonstrated success in product development and R&D. SUPERVISORY RESPONSIBILITIES There are no supervisory responsibilities with this role. COMPUTER SKILLS Performs basic database updates, queries and searches, and printing of documents/reports. LANGUAGE SKILLS Ability to communicate with co-workers and/or read instructions or written standards in English. MATHEMATICAL SKILLS Ability to perform or learn basic mathematic skills as needed, such as basic accounting terminology. REASONING ABILITY Ability to apply common sense understanding to carry out basic step instructions. Ability to deal with standardized situations with only occasional or limited variables. PHYSICAL DEMANDS The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. WORK ENVIRONMENT The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.

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!

UChicago CASE (Senior) Scientists/Scholars-at-Large will be the default appointment for scientists or scholars without existing ties with a specific unit. A UChicago CASE Scientist/Scholar-at-Large will have the following privileges: Access to UChicago facilities and the library Serve as a PI or co-investigator on grant applications at the University Charge their time to grants at the University without a subcontract Purchase equipment via the University for use on University-administered grants Hire and supervise staff at the University The Office of Research and National Laboratories (RNL) will provide grant administration and HR support for (Senior) Scientists-at-Large, and will oversee the reimbursement process with the home institution, if applicable. --- Application Instructions To be accepted into UChicago CASE, applicants must be approved by the University and the home institution. An application for UChicago CASE membership should include the applicant's rationale for seeking membership, a description of the proposed research or scholarly activities to be undertaken, a University unit where collaborations currently exist or will be established (if applicable), and a list of existing or possible faculty collaborators, a current CV, and a memo of support from the applicant's cognizant supervisor of the home institution. In addition, the applicant must follow any internal process established at the home institution for potential UChicago CASE membership. For more information on that process at Argonne, email ************************. When applying, all required documents MUST be uploaded via the My Experience page, in the section titled Application Documents.

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

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!

Grounded in safety, quality, and ethics, our experts lead their fields and guide our work with rigor, a creative spirit, and vision for growth. We're a place to apply your passion and collaborate with top environmental talents to work on some of the most challenging projects that are critical to our clients. Join a team that has the environment down to a science. Your Opportunity Stantec's thriving Great Lakes Environmental Services and the Brownfield Revitalization team is looking for an entry level Geologist/Environmental Engineer to join us. Our team is growing, and we have a need for a Geologist/Environmental Engineer with 0 to 3 years of relevant experience in the environmental field and a strong interest in environmental assessment/cleanup, community revitalization, and Brownfield redevelopment. This team member will be primarily focused on due diligence and Brownfield revitalization work in Wisconsin but may assist with other out-of-state opportunities within our regional and/or national Environmental Services team. Strong writing and communication skills are critical, as is an understanding of effective field procedures and protocols related to this work. This position will be based in one of our Wisconsin-based offices (Mequon, Green Bay, or Madison). Your Key Responsibilities Develop and implement work plans for soil and groundwater remediation and environmental compliance projects. Support the execution of soil, soil vapor, and groundwater investigation projects under the direction of a senior professional geologist. Oversee drilling contractors conducting soil boring advancement and well installation activities. Complete geological logs and subsequent cross-sections, figure or site plan preparation. Conduct groundwater and surface water sampling, monitoring and testing activities. Assist with onsite construction observation, contractor coordination, and daily reports. Conduct due diligence investigations and reporting Summarize soil and groundwater field and laboratory data and assist with interpretations. Prepare and review technical reports including compilation of historical information and field generated data. Act as liaison between clients, contractors, regulatory officials and third parties on project sites. Exhibit a working understanding of health, safety, security, and environment (HSSE) policies and procedures, including client-specific training (as required). Qualifications - External Your Capabilities and Credentials Ability to engage in creative and critical thought in order to participate and collaborate in a project team setting. Communicate in a professional and positive manner, both in writing and in person, with clients, employees, visitors, and the public at large. Strong technical writing capabilities Recognize when technical problems are developing and collaborate with others to initiate appropriate corrective actions. Manage time to meet project budget and schedule. Ability to check own work for accuracy and completeness. Proficient in Microsoft products (Word, Excel, etc.) and multiple platforms (laptop, tablet, smart phone). Detailed-oriented and reliable notetaker. Ability to work independently or as part of a team in outdoor settings with frequent lifting and carrying. Availability to travel, including overnight travel. Possess a valid driver's license with a good driving record. Ability to pass a drug screen. Education and Experience Required: Bachelor's degree in geology or geosciences. Preferred: Master's degree in geology or geological engineering. One to three years of experience in the environmental consulting field 40-hour HAZWOPER training completed This description is not a comprehensive listing of activities, duties or responsibilities that may be required of the employee and other duties, responsibilities and activities may be assigned or may be changed at any time with or without notice . Stantec is a place where the best and brightest come to build on each other's talents, do exciting work, and make an impact on the world around us. Join our growing global firm of over 30,000 professionals and redefine your personal best.

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

Senior Scientist - Research & Development PS Seasoning, our craft is flavor. A third-generation strong company, we believe that the best recipes are passed down from one generation to the next. From the award-winning food products we make to the customers we serve, our commitment to excellence is the foundation of everything we do. Just like the recipes we create, our team is only successful with a foundation of key ingredients: Customer Focus, Development, Family, Integrity, Teamwork, and Excellence. Since our inception in 1986, we've cultivated a culture of support, togetherness, respect, loyalty, and family values. When you join the PS team, you're part of a family and part of our recipe for success. Position Summary: As part of PS Seasonings' mission to build a world-class R&D organization, the Senior Scientist is a technical leader who will drive innovation in seasonings, sauces, and blends. This role combines hands-on formulation expertise with strategic influence, helping shape the future of flavor at PS. The Senior Scientist will lead complex projects from concept to commercialization, mentor Food Scientists, and partner cross-functionally to bring new ideas to life that delight customers, strengthen partnerships, and fuel business growth. What You'll Do: Lead development of new seasonings, sauces, and blends, including clean-label, functional, and encapsulated technologies. Translate culinary trends and customer requests into differentiated, scalable products. Manage high-complexity projects from concept through commercialization using the Stage Gate process. Conduct pilot trials, scale-ups, and plant validations while solving technical challenges. Partner with suppliers to identify innovative ingredients, technologies, and processes. Collaborate with Sales, Marketing, Operations, Supply Chain, and Quality to align on project goals. Ensure compliance with FDA/USDA regulations, HACCP, GFSI standards, and PS quality systems. Represent PS expertise during customer presentations, tastings, and innovation sessions. Mentor Food Scientists and Technicians, providing coaching and technical guidance. Drive cost-savings initiatives through ingredient optimization, yield improvement, and process efficiency. Maintain product specifications, nutritional documentation, and labeling accuracy. Stay current on food science trends, regulations, and emerging technologies. Other duties as assigned by manager. What We're Looking For: MS/PhD in Food Science, Food Chemistry, or related field; BS with extensive experience considered. 7-10+ years of product development experience, preferably in seasonings, sauces, condiments, or blends. Expertise in flavor systems, ingredient functionality, sensory science, and scale-up. Experience with encapsulation, clean-label strategies, or advanced flavor delivery preferred. Strong knowledge of FDA/USDA labeling, nutrition, and food safety requirements. Proven leadership in managing projects and cross-functional collaboration. Excellent communication skills with both technical and non-technical stakeholders. Hands-on problem-solving ability in plant environments. Highly organized, proactive, and growth-oriented mindset. Benefits of Working at PS Seasoning: When you join the PS family, you'll receive: Competitive Pay • Health, Dental, Vision & Life Insurance • 401K with Company Match • Paid Holidays & Vacation • 50% Off Employee Discount • Employee Appreciation Events • Outdoor Courtyard with Putting Green • Delicious Smells PS Seasoning is an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or disability status. PS Seasoning participates in E-Verify and will verify employment eligibility for all new hires.

Job DescriptionSenior Scientist - Research & Development PS Seasoning, our craft is flavor. A third-generation strong company, we believe that the best recipes are passed down from one generation to the next. From the award-winning food products we make to the customers we serve, our commitment to excellence is the foundation of everything we do. Just like the recipes we create, our team is only successful with a foundation of key ingredients: Customer Focus, Development, Family, Integrity, Teamwork, and Excellence. Since our inception in 1986, we've cultivated a culture of support, togetherness, respect, loyalty, and family values. When you join the PS team, you're part of a family and part of our recipe for success. Position Summary: As part of PS Seasonings' mission to build a world-class R&D organization, the Senior Scientist is a technical leader who will drive innovation in seasonings, sauces, and blends. This role combines hands-on formulation expertise with strategic influence, helping shape the future of flavor at PS. The Senior Scientist will lead complex projects from concept to commercialization, mentor Food Scientists, and partner cross-functionally to bring new ideas to life that delight customers, strengthen partnerships, and fuel business growth. What You'll Do: Lead development of new seasonings, sauces, and blends, including clean-label, functional, and encapsulated technologies. Translate culinary trends and customer requests into differentiated, scalable products. Manage high-complexity projects from concept through commercialization using the Stage Gate process. Conduct pilot trials, scale-ups, and plant validations while solving technical challenges. Partner with suppliers to identify innovative ingredients, technologies, and processes. Collaborate with Sales, Marketing, Operations, Supply Chain, and Quality to align on project goals. Ensure compliance with FDA/USDA regulations, HACCP, GFSI standards, and PS quality systems. Represent PS expertise during customer presentations, tastings, and innovation sessions. Mentor Food Scientists and Technicians, providing coaching and technical guidance. Drive cost-savings initiatives through ingredient optimization, yield improvement, and process efficiency. Maintain product specifications, nutritional documentation, and labeling accuracy. Stay current on food science trends, regulations, and emerging technologies. Other duties as assigned by manager. What We're Looking For: MS/PhD in Food Science, Food Chemistry, or related field; BS with extensive experience considered. 7-10+ years of product development experience, preferably in seasonings, sauces, condiments, or blends. Expertise in flavor systems, ingredient functionality, sensory science, and scale-up. Experience with encapsulation, clean-label strategies, or advanced flavor delivery preferred. Strong knowledge of FDA/USDA labeling, nutrition, and food safety requirements. Proven leadership in managing projects and cross-functional collaboration. Excellent communication skills with both technical and non-technical stakeholders. Hands-on problem-solving ability in plant environments. Highly organized, proactive, and growth-oriented mindset. Benefits of Working at PS Seasoning: When you join the PS family, you'll receive: Competitive Pay • Health, Dental, Vision & Life Insurance • 401K with Company Match • Paid Holidays & Vacation • 50% Off Employee Discount • Employee Appreciation Events • Outdoor Courtyard with Putting Green • Delicious Smells PS Seasoning is an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or disability status. PS Seasoning participates in E-Verify and will verify employment eligibility for all new hires.

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.

New Berlin, WI, USA Full-time ** **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.**

Current Employees: If you are currently employed at any of the Universities of Wisconsin, log in to Workday to apply through the internal application process. The Scientist will become an integral team member at the UW Institute for Research on Poverty (IRP) for the evaluation of the SeniorCare Pharmaceutical Benefit for Low-Income Seniors program. The SeniorCare program and its evaluation is funded by the Wisconsin Department of Health Services (DHS), Division of Medicaid Services. The purpose of the SeniorCare program is to provide discounted drug coverage to older adults not currently receiving full Medicaid benefits to help delay or prevent 1) future enrollment into Medicaid, and 2) more serious and expensive health services. The Scientist will evaluate the SeniorCare programs' drug utilization including indicators of medication adherence and high-risk medication use. Drug expenditure data will be used to measure financial hardship for members as well as cost savings to the Medicaid program. Avoidable health outcomes will be measured including nursing home and other long-term care use. The Scientist will assist with cleaning and preparing Medicaid and Medicare claims data; consult on research methodologies based on analytic plans from the investigators; prepare analytic code for dissemination; prepare output tables; prepare analytic findings; and assist investigators with writing evaluation reports to the Wisconsin DHS and for scholarly publications. In this role, the Scientist will: Analyze large complex research data sets including Medicaid and Medicare health care claims. Analyze data using causal inference analytic techniques to determine differences in pharmaceutical drug utilization and health outcomes between treatment and comparison groups. Document analysis code and results according to established policies and procedures for research transparency, standardization, and replication. Conduct literature reviews to support and enhance analysis plans and report preparation. Execute and provide consultation on analysis plans to measure changes in pharmaceutical drug utilization and expenditures. Prepare analysis findings for presentation in reports and publications. Assist investigators with the writing of evaluation reports and scholarly publications in support of continued professional development and the dissemination of research information. Key Job Responsibilities: Collects and analyzes research data, conducts experiments and interviews, and documents results according to established policies and procedures under general supervision and limited responsibility Assists with the identification of research problems and the development of research methodologies and procedures Writes or assists in developing grant applications and proposals to secure research funding Conducts literature reviews, prepares reports and materials, and disseminates information to appropriate entities Attends and assists with the facilitation of scholarly events and presentations in support of continued professional development and the dissemination of research information Serves as a main point of contact and liaison with internal and external stakeholders providing information and representing the interests of a specialized research area Department: College of Letters & Science | Institute for Research on Poverty (IRP) Compensation: The typical starting salary for this position is $70,000 - $100,000 depending on qualifications and experience. Employees in this position can expect to receive benefits such as generous vacation, holidays and paid time off; competitive insurance and saving accounts; and retirement benefits. Required Qualifications: Quantitative statistical analysis skills in economics or related field utilizing statistical analysis packages (such as SPSS, SAS, R, Python or STATA) measuring longitudinal trend changes relative to comparison groups Minimum two years of experience with data management and statistical data analysis Experience utilizing and managing large databases and especially experience with tools for working with large data sets Familiarity with causal inference methods for observational studies, such as difference-in-differences, regression discontinuity, and instrumental variables Preferred Qualifications: Experience with Medicaid and/or Medicare claims data Previous research experience focusing on pharmaceutical use Education: Ph.D. required in health services research, economics, pharmacy, or a related field How to Apply: Click the "Apply" button to start the application process. You will be prompted to upload the following documents: -Resume -Letter of Qualifications/Cover Letter Applicants should attach a letter of qualifications/cover letter and resume detailing their training and experience relating to the required and preferred qualifications referenced above. The application reviewers will be relying on written application materials to determine which qualified applicants will advance in the recruitment process. Please note, there is only one attachment field. You must upload all of your documents in the attachment field. Once finalists are identified, they will be asked to provide names and contact information for at least three professional references, including a current/former supervisor. References will not be contacted without advanced notice. Please note that successful applicants are responsible for ensuring their eligibility to work in the United States (i.e. a citizen or national of the United States, a lawful permanent resident, a foreign national authorized to work in the United States without need of employer sponsorship) on or before the effective date of appointment. Contact Information: Tim Connor, ***************** Relay Access (WTRS): 7-1-1. See RELAY_SERVICE for further information. Institutional Statement on Diversity: Diversity is a source of strength, creativity, and innovation for UW-Madison. We value the contributions of each person and respect the profound ways their identity, culture, background, experience, status, abilities, and opinion enrich the university community. We commit ourselves to the pursuit of excellence in teaching, research, outreach, and diversity as inextricably linked goals. The University of Wisconsin-Madison fulfills its public mission by creating a welcoming and inclusive community for people from every background - people who as students, faculty, and staff serve Wisconsin and the world. The University of Wisconsin-Madison is an Equal Opportunity Employer. Qualified applicants will receive consideration for employment without regard to, including but not limited to, race, color, religion, sex, sexual orientation, national origin, age, pregnancy, disability, or status as a protected veteran and other bases as defined by federal regulations and UW System policies. We promote excellence by acknowledging skills and expertise from all backgrounds and encourage all qualified individuals to apply. For more information regarding applicant and employee rights and to view federal and state required postings, visit the Human Resources Workplace Poster website. To request a disability or pregnancy-related accommodation for any step in the hiring process (e.g., application, interview, pre-employment testing, etc.), please contact the Divisional Disability Representative (DDR) in the division you are applying to. Please make your request as soon as possible to help the university respond most effectively to you. Employment may require a criminal background check. It may also require your references to answer questions regarding misconduct, including sexual violence and sexual harassment. The University of Wisconsin System will not reveal the identities of applicants who request confidentiality in writing, except that the identity of the successful candidate will be released. See Wis. Stat. sec. 19.36(7). The Annual Security and Fire Safety Report contains current campus safety and disciplinary policies, crime statistics for the previous 3 calendar years, and on-campus student housing fire safety policies and fire statistics for the previous 3 calendar years. UW-Madison will provide a paper copy upon request; please contact the University of Wisconsin Police Department.

Our award-winning client is seeking a Senior Food Scientist to join their team.As a Senior Food Scientist / Culinologist, you will play a crucial role in developing and innovating new food products. You will be responsible for conducting research, formulating new products, and optimizing existing formulations. Your expertise in food science and culinary arts will be essential to driving product development and meeting customer needs. Responsibilities: Develop and formulate new food products, including dairy-based products, to meet customer requirements. Create and evaluate flavors to enhance the taste and aroma of food products. Conduct sensory and analytical testing to assess product quality and performance. Optimize production processes to improve efficiency and reduce costs. Provide technical support to customers and sales teams. Ensure compliance with food safety and regulatory standards. Maintain accurate and detailed documentation of research, development, and testing activities. Required Qualifications: Master's degree in Food Science or related field, or Bachelor's degree with 3-10 years of relevant experience. Strong understanding of food science principles, including chemistry, microbiology, and sensory evaluation. Experience in dairy science and fermentation chemistry is a plus. Excellent problem-solving and analytical skills. Strong communication and interpersonal skills. Ability to work independently and as part of a team. Experience with laboratory equipment and techniques. Knowledge of food safety and regulatory requirements. Benefits: Competitive salary and bonus potential. Comprehensive benefits package including health, dental, and vision insurance. 401(k) with company match. Generous PTO and paid holidays. Relocation assistance.

Job DescriptionDescription: At Curion, We Connect Brands to People. Our expertise and passionate pursuit of insights enable our clients to make informed decisions that drive meaningful impact. Our vision? Advancing the way brands connect to people to build a better future. Our core values: Integrity, Resiliency, Accountability, Curiosity, and Collaboration. Position Summary: As a member of the onsite team and under the supervision of the Account Manager, the Sensory Panel Leader has responsibility for supporting the sensory research programs and clients by coordinating Descriptive Analysis (DA), and other research as needed including test set-up, execution, and data analysis. Curion is looking for someone with a strong potential for growth into a leadership position. The ideal candidate would have a solid technical background in sensory testing methodology and the ability to effectively communicate with clients. Key Responsibilities: · Panel leadership and management, including but not limited to leading training and testing, communicating with panelists, managing panel dynamics, engagement, etc. · Support and execute panel performance measurement plan including but not limited to implementing calibration/validation exercises and providing panelists performance feedback. · Create and/or program ballots and questionnaires to support studies as needed. · Manage high quality, timely research in response to the client needs. · Interact with clients to ensure a clear understanding of project objectives, progress, product tracking, timelines, and deliverables. Receive project requests and communicate with client to schedule testing. Attend project meetings as needed. · Support study reporting with data entry, graphing, photographing samples, and editing presentations as needed. · Support special projects including, but not limited to, coordinating department meetings, setting up new procedures, and documenting protocols. · Actively participate on technical team offering suggestions, making recommendations, and assuming responsibility as needed. · Develop and enhance skills in sensory evaluation, consumer research, and data analysis. · Identify, develop, and execute new, novel approaches to research individually or as part of a team. · Perform other duties to ensure lab functions at high level such as procurement, sample preparation, etc. as needed. Physical Requirements: Reasonable Accommodations Statement To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Reasonable Accommodations may be made to enable qualified individuals with disabilities to perform the essential functions. · Standing, bending, walking, lifting/carrying, and reaching required to perform essential job functions in a laboratory environment including but not limited to preparation and storage of chemical dilutions, lab cleanup, test area setup and breakdown, etc. · Be able and willing to smell various fragrances and malodors and participate in odor evaluation training as needed · Be able and willing to apply and evaluate products on the skin. Qualifications: Education and Experience · Undergraduate degree in science or related major. · 1 or more years of experience in a research environment; experience with sensory testing or product research strongly preferred. Essential Skills · Ability to communicate effectively with others, both orally and in writing. · Assertiveness - Ability to act in a self-confident manner to facilitate completion of a work assignment or to defend a position or idea · Excellent organizational, planning and prioritization skills to meet challenging deadlines · Ability to effectively present information publicly · Ability to adapt to change in the workplace · Ability to accept responsibility and account for their actions. · Strong analytical skills · Excellent interpersonal skills - Ability to get along well with a variety of personalities and individuals, and to actively listen, and be approachable. · Motivation - Ability to inspire oneself and others to reach a goal and/or perform to the best of their ability. · Reliability - The trait of being dependable and trustworthy. · Ability to solve problems and manage conflict within a group setting. Computer Skills · Proficient in Office 365 including Microsoft Word, Excel, PowerPoint, Outlook, OneNote, and MS Project. · Sensory Data collections software experience preferred (e.g., RedJade, Compusense, FIZZ, EyeQuestion, etc.) For Curion's Associate Sensory Scientist position, we offer a starting hourly rate between $20.00-$23.00 per hour based on the qualifications and experience of each individual. Curion offers a benefits package for this position which includes: 401(k) retirement account with company match Health, dental, vision, basic life, short and long-term disability, accident insurance, critical insurance, pet insurance, flexible spending account (FSA), and more. Paid time off (PTO) Company paid holidays Curion is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. About Curion: Curion specializes in delivering impactful insights to the world's top CPG companies, helping them develop winning, repeatedly purchased products. Curion's deep data-driven product insights, sensory expertise, and state-of-the-art consumer centers enable them to uncover responses to critical client objectives. With over five decades of experience in the product testing industry, Curion is dedicated to guiding clients with their proprietary XP Xperience Performance platform, connecting brands to consumers at every step. An innovator in the industry, Curion recently developed a groundbreaking benchmarking product testing method, the Curion Score™, which has become a trusted and sought after tool within the industry. As one of the largest product and consumer insights companies in the U.S., Curion has built a reputation for excellence and trust among the world's leading consumer brands. Curion's commitment to innovation and expertise, coupled with a passion for delivering actionable insights, makes Curion a valuable partner for companies looking to develop and launch successful products. Requirements:

Job Description PSG/CIP is a multi-service community-based social services organization that fulfills its mission of helping individuals and families achieve their greatest potential through dynamic and innovative programming responsive to the needs of diverse communities. The Post-Doctoral Fellow is responsible for providing a variety of clinical services including mental health therapy and psychological evaluations to consumers, both in an in-home/community setting and in the clinic/outpatient setting in several of PSG's clinical locations including Milwaukee, Kenosha, Washington, Jefferson, or Rock county. ESSENTIAL FUNCTIONS: Interview and evaluate individuals and/or families to complete the intake process. Provide assessments for therapeutic needs. Provide individual, family, and group counseling as needed. Provide psychological and/or neuropsychological evaluations. Exercise judgment to intervene as an advocate for clients in emergency and crisis situations. Understand and respond to all client treatment needs. Regularly attend clinical supervision with one of PSG's licensed psychologists Attend all needed staffing meetings and make appropriate recommendations as requested. Respond to all Division of Milwaukee Child Protective Services, Kenosha Division of Child and Family Services, or other county entity requests. Attend court hearings and present client treatment progress or evaluation results. Advocate for any additional services as needed. Complete documentation on a timely basis. WHY WORK WITH PSG/CIP: Be part of a passionate team dedicated to making a difference in the community! Flexible hours and great work-life balance Mileage Reimbursement Work culture that values not only the health and well-being of the clients we serve, but also our staff Opportunities for advancement and professional development Competitive benefits package, including: paid time off and company holidays; health, vision, dental, and life insurance; short-term disability; 401k and profit sharing; and Employee Assistance Program (EAP) One of our health insurance plans is now offered with no monthly premium! SALARY: $45,000 annually REQUIREMENTS: Must possess either a Ph.D. or Psy.D. and be eligible for future licensure as a Psychologist in the State of Wisconsin. Previous experience providing individual, family and group therapy as well as experience providing psychological/neuropsychological evaluation is required. Must have reliable transportation on a daily basis, a valid driver's license and automobile insurance. Possession of an LPC or related training license is preferred. Equal Employment Opportunity/M/F/disability/protected veteran status Job Posted by ApplicantPro

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! Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

A UChicago CASE (Senior) Scientist/Scholar Affiliated with a Unit will have the following privileges: Access to UChicago facilities and the library Serve as a PI or co-investigator on grant applications at the University Charge their time to grants at the University without a subcontract Purchase equipment via the University for use on University-administered grants Hire and supervise staff at the University Co-supervise and co-mentor students and postdocs Authority to approve membership Affiliated with a Unit will be delegated by the Provost to the Division/School in which the unit resides. The Division/School within which the academic unit is situated will be responsible for setting the criteria and approval process required for affiliated membership. The criteria and process for affiliation may differ for different Divisions and Schools. The details of these processes will be communicated by the Division/School to the RNL so that the Steering Committee understands the criteria at time of renewal. To prevent undue burden on the administrative unit, the transition process from at-Large to Affiliated membership after approval by the Division/School has been granted will be administered by the RNL. The Division/School will be responsible for providing grant administration and human resources support for the affiliated scientists/scholars. RNL will oversee the reimbursement process and/or the effort reconciliation process with the participating institutions to provide expertise and ensure proper execution. --- Application Instructions To be accepted into UChicago CASE, applicants must be approved by the University and the home institution. An application for UChicago CASE membership should include the applicant's rationale for seeking membership, a description of the proposed research or scholarly activities to be undertaken, the University unit where collaborations currently exist or will be established, and a list of existing or possible faculty collaborators, a current CV, and a memo of support from the applicant's cognizant supervisor of the home institution. In addition, the applicant must follow any internal process established at the home institution for potential UChicago CASE membership. For more information on that process at Argonne, email ************************. When applying, all required documents MUST be uploaded via the My Experience page, in the section titled Application Documents.

Sensory Scientist Application works under the guidance of the Applications Manager and collaborates cross-functionally with Sales, R&D, and Management. This role combines benchwork and sensory science responsibilities to support the development and presentation of innovative ingredient solutions. This position operates within FDA, FSMA, and Global Food Safety Initiative (GFSI) requirements defining food safety standards for the safe production of food in the plant and offices, within the standards of defined risk levels by area. ESSENTIAL FUNCTIONS Reasonable Accommodations Statement To perform this job successfully, an individual must be able to satisfactorily perform each essential function. Reasonable Accommodations may be made to enable qualified individuals with disabilities to perform the essential functions. Essential Functions Statement(s) Apply deep knowledge of Butter Buds' products to develop innovative applications and demos. Conduct benchwork and maintain accurate records of formulas, batch sheets, and results. Design, execute, and improve sensory testing (e.g., triangle, preference), ensuring reliable data. Develop and maintain a standardized sensory lexicon for internal and customer-facing use. Present sensory and application data to Sales, R&D, and leadership to support decision-making. Coordinate and lead internal tastings and sensory panels. Support training efforts and provide technical guidance to Applications, Sales, and Marketing. Stay current with food and sensory science trends to drive innovation. Prepare samples and technical presentations for trade shows and customer visits. Maintain a safe, clean, and organized lab workspace. Collaborate cross-functionally on sensory initiatives. POSITION QUALIFICATIONS Competency Statement(s) Communication, Oral - Ability to communicate effectively with others using the spoken word. Problem Solving - Ability to find a solution for or to deal proactively with work-related problems. Communication, Written - Ability to communicate in writing clearly and concisely. Accountability - Ability to accept responsibility and account for his/her actions. Commitment Ability to work within companys policies of customer satisfaction and teamwork within a collaborative environment. SKILLS & ABILITIES Education: Advanced degree in sensory, food science or related field of study. Experience: 4-8 years technical experience in a food laboratory. Working knowledge of food chemistry: protein, carbohydrates, fats and their interactions. Computer Skills: Proficient with Microsoft Word and Excel.