Scientist Jobs in Lisle, IL

$42 - $45/hr based on if you choose to opt into medical benefits 1 year initial contract with possible 1 year extension Onsite in North Chicago M-F 8 am to 5 pm with some flexibility for schedule Orion Project Services and a market leading pharmaceutical company are teaming up for an exciting contract opportunity for Scientists in North Chicago, IL!! We are looking for a highly motivated person to support Developability and Formulation Development. The candidate will support early-stage assessment of candidates coming out of the Discovery pipeline, as well as the design and development of stable and robust drug product formulation for biologics used in clinical trials. In this role, the candidate will be part of a global team and will work closely with scientists from multiple functional areas, including Discovery, Analytical, and Process R&D. Job Description: The Biologics Drug Product Development team develops antibody drug conjugates (ADC) and other biologics by state-of-the-art formulation and analytical technologies. We create valuable intellectual property through new formulation compositions, cost effective manufacturing processes and prepare and defend CMC (Chemistry, Manufacturing and Control) regulatory content. Key Responsibilities Include: Support the biologics characterization and stability assessment activities of the assigned biologics, including candidate screening and selection for clinical studies and commercialization of monoclonal antibodies, antibody drug conjugates, bispecifics, and fusion proteins. Execute studies evaluating the stability (chemical & physical) of biologics against solution conditions (pH, ionic strength, temperature, light, etc.) and physical stresses arising from manufacturing process conditions (freeze thaw, mixing, filtration, filling, and lyophilization), and screen excipients (buffers, stabilizers, surfactants, etc.) to develop robust formulations for frozen, refrigerated liquid, and lyophilized dosage forms. Prepare concise and sound scientific presentations of experimental results to the management and assist in authoring detailed scientific technical reports. Stay current with the scientific literature and support new scientific initiatives. Qualifications needed to be successful in this role: BS or MS in a scientific field and typically 4 (BS) or 2 (MS) years of relevant experience. Extensive hands on expertise using analytical methods for chemical and structural characterization of biologics e.g. HPLC, UPLC, capillary electrophoresis, particle analysis, and other biophysical techniques (UV-vis, DLS, DSC, etc.) for protein characterization is a requirement. Scientific understanding of the structure & function of monoclonal antibodies, antibody constructs/conjugates, bispecifics, and fusion proteins and their modes of degradation/stabilization. Strong laboratory skills focused on formulation development for monoclonal antibodies and antibody constructs/conjugates (standard excipient selection, functional excipients, high throughput assays) would be a plus. Solid understanding of the various unit operations of aseptic manufacturing such as bulk freeze thaw, compounding/mixing, filtration, filling, and lyophilization for liquid and lyophilized NBEs. Key Leadership Competencies: Builds strong relationships with peers and cross functionally with partners outside of the team to enable higher performance. Excellent oral communication skills in a scientific setting, as well as sound technical writing and documentation competencies are required. The candidate must be able to work independently, respond to changing priorities and short lead times for multiple tasks; able to identify problems and work toward solutions. Raises the bar and is never satisfied with the status quo. Creates a learning environment, open to suggestions and experimentation for improvement. Embraces the ideas of others, nurtures innovation and manages innovation to reality.

*** This is a regional search in an attempt to draw talent from the city to our company in a more rural location. 100% on site. Great relocation assistance provided. *** Job Title: Senior Scientist - TPO Polymer Formulation Employment Type: Full-Time Experience Level: Senior (10+ years) Job Summary: We are seeking a highly skilled Senior Scientist with over 10 years of specialized experience in the formulation of Thermoplastic Polyolefin (TPO) polymers. The successful candidate will lead cutting-edge research and development efforts to design, optimize, and scale innovative TPO formulations for applications in automotive, roofing, medical, and other industries. This role demands deep technical expertise, strong analytical capabilities, and the ability to collaborate across teams to deliver high-performance, sustainable solutions that align with market and regulatory requirement's Key Responsibilities: Formulation Development: Design and develop advanced TPO formulations, optimizing properties such as impact resistance, flexibility, UV stability, and processability for specific applications (e.g., automotive bumpers, roofing membranes, medical devices). Research & Innovation: Lead R&D projects to explore novel additives, fillers, compatibilizers, and blending techniques to enhance TPO performance, including recyclability and cost-efficiency. Process Optimization: Partner with manufacturing teams to transition formulations from lab-scale to commercial production, ensuring compatibility with processes like injection molding, extrusion, or thermoforming. Testing & Validation: Oversee comprehensive testing of TPO formulations for mechanical, thermal, and environmental performance, using standards like ASTM, ISO, or SAE. Analyze results to refine and troubleshoot formulations. Regulatory Compliance: Ensure formulations comply with industry regulations (e.g., REACH, RoHS, FDA for medical applications) and sustainability goals, such as reducing carbon footprint or incorporating recycled content. Technical Leadership: Mentor junior scientists, provide expertise to cross-functional teams (R&D, engineering, quality assurance), and communicate findings to stakeholders and clients. Project Management: Manage multiple projects concurrently, overseeing timelines, budgets, and deliverables to meet business objectives. Industry Trends: Monitor advancements in TPO technology, competitor products, and market needs to drive innovation and maintain a competitive edge. Qualifications: Education: Ph.D. or Master's degree in Polymer Science, Chemical Engineering, Materials Science, Chemistry, or a related field. Experience: 10+ years of hands-on experience in TPO polymer formulation, with a proven track record of developing commercially successful products. Expertise in TPO compounding, including polyolefin blends, elastomers, fillers, and additives for tailored performance. Strong knowledge of TPO processing techniques (e.g., injection molding, extrusion, blow molding) and scale-up to production. Skills: Advanced proficiency in analytical tools such as DSC, TGA, DMA, FTIR, and mechanical testing for polymer characterization. Familiarity with regulatory requirements for TPO applications in automotive, construction, or medical sectors. Excellent project management and communication skills, with the ability to convey complex technical data to diverse audiences. Collaborative approach with experience mentoring teams and working with cross-functional groups. Preferred Qualifications: Experience with sustainable TPO formulations, such as bio-based or recycled polyolefins. Patents, publications, or presentations in TPO or polyolefin research. Knowledge of related polymer systems (e.g., TPE, PP, or EPDM) is a plus. Why Join Us? Lead transformative projects in a rapidly evolving polymer industry. Collaborate with a global team of experts in a dynamic, innovative environment. Competitive salary, comprehensive benefits, and opportunities for professional growth.

Immediate need for a talented Research Associate Scientific III. This is a 12+months contract opportunity with long-term potential and is located in Round Lake, IL (Onsite). Please review the job description below and contact me ASAP if you are interested. Job ID: 25-67752 Pay Range: $40 - $45/hour. Employee benefits include, but are not limited to, health insurance (medical, dental, vision), 401(k) plan. Key Responsibilities: Conduct nitrosamines and impurities evaluations (routine and non-routine) by performing chemical analysis utilizing LC/MS/MS and associated wet chemistry and sample preparation techniques. Conduct chemical analyses and preparation, including solid-phase extraction (SPE) and liquid-liquid extraction (LLE) in support of nitrosamines studies. Perform experiments specifically for nitrosamines and E&L analysis, within specified timelines. Operate, maintain, and troubleshoot MS instrumentation. Participate in investigations that correspond to atypical or out-of-specification/out-of-trend results. Independently plan and execute method development activities utilizing LC/MS/MS. Generate scientific sound experimental data following written procedures including protocols and standard operating procedures (SOPs). Independently author and contribute to experimental protocols, summaries, and technical reports. Document and review laboratory work using an electronic laboratory notebook per Client's good documentation practices (GDP) and general good laboratory practices (GLP). Follow Client's Quality Manual, SOPs, and Environmental Health, Safety & Sustainability (EHS&S) guidelines in day-to-day activities, to ensure proactive compliance and continuous improvement. Provide support to maintain a compliant, safe, and clean working environment/laboratory. Evaluate analytical results, identify trends, exceptions, and interpretation of results relative to product requirements, definitions, and/or project goals. Competent in interpreting analytical data and presenting in a form that is suitable for a diverse audience. Communicate clearly with management, peers, cross-functional teammates, and non-technical audiences by openly sharing project status and hurdles and seeking input from other team members. Key Requirements and Technology Experience: Key skills; Nitrosamines, LC/MS, GDP Extensive hands-on experience with mass spectrometry analysis; specifically, MS/MS via HPLC or UHPLC tandem with APCI or ESI ionization. Experience with Mass Hunter preferred. Required knowledge and demonstrated experience of analytical chemistry with relevant laboratory skills (hands-on experience with wet chemical techniques and instrumental analysis). Possesses analytical problem-solving mindset, high learning agility, innovative experimental attitude along with good presentation skills. Strong written and verbal communication skills in English. Provide and accept critical feedback from others in a constructive manner. Demonstrates an inclusive attitude and an ability to collaborate with team members and cross-functional team members for project deliverables. Ability to objectively assess, organize, and clearly communicate information. Ability to plan and complete the assigned work to meet project deliverables in a timely manner. Proficient in Microsoft Office applications(Excel, Word, Outlook) Educational and professional qualification: PhD with 0-3 years' experience, or a master's with 3-5 years' experience, or a bachelor's with 5-7 years' experience in a chemistry related field. Analytical or organic chemistry preferred. Our client is a leading Healthcare Industry, and we are currently interviewing to fill this and other similar contract positions. If you are interested in this position, please apply online for immediate consideration. Pyramid Consulting, Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type 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. By applying to our jobs you agree to receive calls, AI-generated calls, text messages, or emails from Pyramid Consulting, Inc. and its affiliates, and contracted partners. Frequency varies for text messages. Message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You can reply STOP to cancel and HELP for help. You can access our privacy policy here.

We are looking for an individual to join a Research and Development team to help develop next generation solar materials and devices. Key Responsibilities: Contribute to research and development initiatives focused on advancing solar and other green energy technologies. Assist the Principal Solar and technology development team in ensuring the successful execution of technology programs within established timelines and budgets. Work collaboratively with team members to facilitate the commercialization of new technologies. Qualifications and Required Skills: Ph.D. in chemistry, materials science, or a related field. At least five years of experience in the development and scaling of next-generation solar technologies. Proficiency in solar device and module fabrication techniques, such as laser scribing for interconnect development, packaging, encapsulation, and barrier layer development. Hands-on experience in fabricating and characterizing materials for current and emerging solar and optoelectronic technologies (experience with perovskite-based materials preferred). Expertise in thin-film vacuum deposition techniques, including sputtering, atomic layer deposition, chemical vapor deposition, and thermal evaporation. Experience in thin-film solution processing techniques, such as blade coating, slot-die coating, and microgravure, is preferred. Familiarity with materials metrology, characterization, and quality assurance/quality control (QA/QC) is a plus. Knowledge of tandem and multi-junction device technologies is advantageous. Proven experience working in cross-functional teams and collaborating with diverse internal and external stakeholders. Strong understanding of intellectual property development and management. Exceptional communication and interpersonal skills, with the ability to mentor junior colleagues and lead through influence. About Teal Energi: TealEnergi is a technical manpower provider with extensive experience supporting the successful execution and operation of major capital project investments. Forged through a desire to provide best-in-class service to clients, candidates, and contractors alike, TealEnergi works through its offices nationwide to provide regional support to a wide range of sectors including both traditional energy and energy transition initiatives (e.g., LNG, hydrogen, wind, solar), as well as manufacturing, mining, and infrastructure. TealEnergi is committed to fostering, cultivating and preserving a culture of diversity, equity and inclusion. All qualified applicants will receive consideration for employment without regard to race, color, age, disability, ethnicity, gender or gender identity, language, national origin, physical or mental ability, political affiliation, religion, sexual orientation, or protected veteran status.

Duration: 12 Months Contract This position will contribute analytical and technical support for nitrosamines and impurities analysis. Conduct nitrosamines and impurities evaluations (routine and non-routine) by performing chemical analysis utilizing LC/MS/MS and associated wet chemistry and sample preparation techniques. Conduct chemical analyses and preparation, including solid-phase extraction (SPE) and liquid-liquid extraction (LLE) in support of nitrosamines studies. Perform experiments specifically for nitrosamines and E&L analysis, within specified timelines. Operate, maintain, and troubleshoot MS instrumentation. Participate in investigations that correspond to atypical or out-of-specification/out-of-trend results. Independently plan and execute method development activities utilizing LC/MS/MS. Generate scientific sound experimental data following written procedures including protocols and standard operating procedures (SOPs). Independently author and contribute to experimental protocols, summaries, and technical reports. Document and review laboratory work using an electronic laboratory notebook per Baxter's good documentation practices (GDP) and general good laboratory practices (GLP). Follow Quality Manual, SOPs, and Environmental Health, Safety & Sustainability (EHS&S) guidelines in day-to-day activities, to ensure proactive compliance and continuous improvement. Provide support to maintain a compliant, safe, and clean working environment/laboratory. Evaluate analytical results, identify trends, exceptions, and interpretation of results relative to product requirements, definitions, and/or project goals. Competent in interpreting analytical data and presenting in a form that is suitable for a diverse audience. Communicate clearly with management, peers, cross-functional teammates, and non-technical audiences by openly sharing project status and hurdles and seeking input from other team members. Qualifications: Extensive hands-on experience with mass spectrometry analysis; specifically, MS/MS via HPLC or UHPLC tandem with APCI or ESI ionization. Experience with MassHunter preferred. Required knowledge and demonstrated experience of analytical chemistry with relevant laboratory skills (hands-on experience with wet chemical techniques and instrumental analysis). Possesses analytical problem-solving mindset, high learning agility, innovative experimental attitude along with good presentation skills. Strong written and verbal communication skills in English. Provide and accept critical feedback from others in a constructive manner. Demonstrates an inclusive attitude and an ability to collaborate with team members and cross-functional team members for project deliverables. Ability to objectively assess, organize, and clearly communicate information. Ability to plan and complete the assigned work to meet project deliverables in a timely manner. Proficient in Microsoft Office applications(Excel, Word, Outlook) Education and/or Experience: PhD with 0-3 years' experience, or a master's with 3-5 years' experience, or a bachelor's with 5-7 years' experience in a chemistry related field. Analytical or organic chemistry preferred. About US Tech Solutions: 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 ************************ US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Recruiter Details: Name: Swati Email: *********************************** Internal Id: 25-36543

Want to grow your career within the manufacturing space? LaSalle Network is partnered with a growing multi-million-dollar manufacturing firm looking to hire a Materials Scientist located in is 100% on-site. The Materials Scientist supports the development and commercialization of a wide variety of composite materials and processes to drive new profitable business growth by working closely with others internally in the Research and Development Center and Business Units as well as externally with vendors, customers, and potential customers. The candidate should have a deep understanding of the chemical and physical properties of materials and how they behave and interact. Materials Scientist Responsibilities: Drive and independently lead projects associated with thermoset composites, including new product development, study of material interactions, and fundamental resin chemistry Work closely with all business units to align with future strategic company goals Lead and support process changes, raw material changes, and quality issues related to existing and new products across multiple manufacturing locations Complete technical reports with analysis and findings Analyze experimental data, summarize key findings, and report at regular team meetings Work with the sales team to leverage technical findings and product properties for strategic share gains Establish relationships with customers to capture VOC and product application insight Stay abreast of state of the art in the composites industry to seek out new materials, ideas, and concepts Utilizing these state-of-the-art ideas develop new to market, innovative prototypes with potential for scale-up commercialization Work on advanced, complex technical projects or business issues requiring state of the art technical or industry knowledge Materials Scientist Requirements: Minimum of 8 years of experience with materials development specifically in composites, resin formulation, or other polymer applications. Significant experience in project leadership BS in Materials Science, Chemistry, Engineering or other suitable technical field required, advanced degree preferred Communicate and work cross-functionally with other disciplines to understand materials requirements and provide feedback based on materials expertise Entrepreneurial in nature Extensive hands-on experience with mechanical testing and physical and chemical properties of material Experience with composites manufacturing preferred, including but not limited to: open molding and close molding, pultrusion, extrusion, injection molding, compression molding Formulation and compounding with a wide variety of materials, including but not limited to: thermoset resins, thermoplastics, fibers, films and coatings, nanocomposites, composites additives, "Green" materials and processes including recycling Experience with commercial continuous manufacturing processes Process development experience, including small scale to large commercial scale Experience with Matlab, Minitab, Python, R, or other programming tools Development of intellectual property Desirable technical skills other than strong polymer chemistry skills include: analytical instrumentation, statistics, including design of experiment, mathematical modeling methods, including finite element analysis. Travel 15-20% Thank you, Linda Daniel Senior Project Manager LaSalle Network LaSalle Network is an Equal Opportunity Employer m/f/d/v. LaSalle Network is the leading provider of direct hire and temporary staffing services. For over two decades, LaSalle has helped organizations hire faster and connect top talent with opportunities, from entry-level positions to the C-suite. With units specializing in Accounting and Finance, Administrative, Marketing, Technology, Supply chain, Healthcare Revenue Cycle, Call Center, Human Resources and Executive Search. LaSalle offers staffing and recruiting solutions to companies of all sizes and across all industries. LaSalle Network is the premier staffing and recruiting firm, earning over 100 culture, revenue and industry-based awards from major publications and having its company experts regularly contribute insights on retention strategies, hiring trends and hiring challenges, and more to national news outlets.

Senior Scientific & Regulatory Affairs Program Manager - Ingredients and Packaging The Senior Scientific & Regulatory Affairs (SRA) Program Manager - Ingredients and Packaging North America creates and sustains a competitive advantage for Mars Wrigley by protecting the business against external regulatory headwinds and enabling packaging sustainability and innovation by ensuring food safety. This position leads the regional development and execution of SRA strategy to manage regulatory headwinds on ingredients and contaminants, proactively identifies potential regulatory risks and opportunities, translates to business impact and actions, and leads technical advocacy efforts to shape the external regulatory environment. This position supports the advancement of the Mars sustainability and growth ambition by evaluating new processes and materials against MW safety standards. What are we looking for? Bachelor's degree in a technical area, such as toxicology, food chemistry, nutrition, food science, biology, or chemistry. Master's degree in a technical area preferred. Minimum 8 years of experience in scientific and/or regulatory compliance/affairs and/or a related technical area with food products or related product categories (such as food supplements, cosmetics, and natural health products) with proficiency in food law, ingredient and packaging safety, and regulatory affairs for North America. Demonstrated success working on large-scale regulatory affairs projects that involve working internally with cross-functional teams and externally with trade associations and regulatory bodies; a demonstrated track record of working successfully across functions to achieve shared goals is required. What will be your key responsibilities? Protect the business against external regulatory headwinds on ingredients, packaging, and contaminants in North America. Proactively monitor scientific and regulatory activities in North America in the areas of food ingredients, packaging, and contaminants. Develop and execute the external scientific and regulatory influencing strategy related to food ingredients, packaging, and contaminants legislation in the region. Work with internal partners to understand priorities and impacts of developing legislation, align appropriate external positions, and advocate Mars positions through relevant trade associations. Turn scientific and regulatory insight into foresight and build an appropriate internal and external network (e.g., key experts and allies) to anticipate the impact on the business and shape the regulatory environment. Translate external regulatory developments into business impact to provide visibility to business stakeholders (e.g. Product Development, Packaging Development, Science and Technology, Corporate Affairs), and drive proactive actions to protect our Freedom to Operate. Accountable for leading internal cross-functional communities of practice or technical working groups to provide strategic scientific and regulatory guidance and clear recommendations to relevant internal partners and leadership forums on existing and emerging scientific and regulatory issues on food ingredients, packaging, and contaminants. Ensure safety and compliance of novel ingredients and packaging and their extension of intended use. Enable innovation or renovation projects, review scientific literature on the safety of the new ingredient and packaging in the context of its intended use, collaborate with cross-functional partners, provide safety and compliance evaluation and recommendation, and compile regulatory dossiers and petitions as needed. Conduct toxicological risk assessments of food ingredients, packaging, and contaminants based on available scientific data. What can you expect from Mars? Work with over 140,000 diverse and talented Associates, all guided by the Five Principles. Join a purpose-driven company, where we're striving to build the world we want tomorrow, today. Best-in-class learning and development support from day one, including access to our in-house Mars University. An industry-competitive salary and benefits package, including company bonus. #LI-BM1 Skills: Action Planning, Adaptive Mindset, Compliance Management, Data Collection and Analysis, Negotiation, Organization Design and Development, Planning and Organizing, Reporting, Verbal Communication, Waterfall Model Competencies: Balances Stakeholders, Business Insight, Collaborates, Communicates Effectively, Ensures Accountability, Interpersonal Savvy, Manages Complexity, Organizational Savvy, Persuades, Strategic Mindset The base pay range for this position at commencement of employment is expected to be between the range listed below; however, base pay offered may vary depending on multiple individualized factors, including but not limited to, market location, job-related knowledge, skills, and experience. The total compensation package for this position may also include other elements, if eligible, including variable pay, medical and dental benefits, participation in 401k plan, and paid time off benefits. Eligibility for these additional elements depends on the position offered and the employee's work schedule (i.e., part-time schedule, store associate). Details of participation in these benefit plans will be provided if an applicant receives an offer of employment. USD 133,067.00 - USD 182,958.00 #J-18808-Ljbffr

To create and refine real-time analytic models used to understand conversations and behaviors in order to target users with optimal messaging across different platforms and devices and to Participate in all project phases from concept, requirements, development, test and production support. Responsibilities: Complex Problem Solving - Ability to identify and solve problems by reviewing related information, evaluating options and implementing solutions Critical Thinking - Ability to use logic and reason to identify strengths and weaknesses of alternative solutions, conclusions, or approaches to problems Deductive Reasoning - Ability to apply general rules to specific problems to produce answers that make sense Inductive Reasoning - Ability to combine pieces of information to form general rules or conclusions (includes finding a relationship among seemingly unrelated information or events) Quantitative and Analytical Skills - Ability to apply quantitative and statistical analysis techniques to unstructured problems Strong Communication Skills - Ability to clearly and concisely communicate information and ideas orally and in writing Skills and Experience: Experience with SAS, Python, or R. 3-5 years of experience working in a data analytics capacity Well versed in the application of analytic techniques and predictive modeling Practical ability to visualize data, communicate about the data, and utilize it effectively Innovative instincts and an entrepreneurial spirit

with 2 days a week onsite in Rosemont, IL Our client is seeking a Data Scientist to join their established and growing analytics department. A successful Data Scientist will collaborate on strategic objectives and improve business performance by designing, scaling, and supporting a range of analytical and modeling products. We are looking for someone who is eager to work alongside data scientists, engineers, QA analysts and business leaders to partner in the creation and delivery of end-to-end analytical products. A successful candidate is technically proficient in data science tools and methods, including AI and Cloud technologies, and they ensure their knowledge aids in the development and growth of team members and individuals across the organization. Strong communication, strategic thinking, and problem-solving skills are required to be successful in this role. DUTIES AND RESPONSIBILITIES Balance the complexity of data, usage of multiple coding/visualization platforms, and variety in client needs to develop best in class data products and educate leadership on data driven decision making Collaborate with Data Scientists, Data Engineers and QA Analysts to develop, improve and maintain data pipelines, processes, and Data Science Products Create interactive dashboards and automated reports (using Hex) to maximize the impact of data-driven insights throughout the organization Conduct timely exploratory data analysis using Python notebooks to support the analytics team in handling ad-hoc requests Identify opportunities to expand capabilities and build knowledge of internal data processes, sources, and tools Follow best practices for project/model documentation and version control REQUIRED QUALIFICATIONS Proven ability to handle multiple projects, communicate and collaborate in a team environment and offer suggestions to adjust plans to meet evolving business objectives Strong problem-solving skills, a passion for quality & attention to detail, and the ability to navigate ambiguity and deliver results Intermediate programming skills in Python. Python notebook expertise is strongly preferred with a strong understanding of Pandas and visualizations (Plotly) Highly proficient in SQL with data modeling experience Experience crafting data visualizations, dashboards, and analytical products Experience working with cloud technologies (AWS preferred) and concepts of AI including, but not limited to NLP, ethical usage and governance Experience working with of statistical techniques and concepts including regression, distributions, statistical tests, and others Experience working with of multiple machine learning algorithms, including linear and logarithmic regression, decision trees, and clustering models Strong oral and written communication skills, including presentation skills (MS PowerPoint) BS in Mathematics, Computer Science, Information Management, Statistics, or a Related Technical Field MS in Mathematics, Computer Science, Information Management, Statistics, or a Related Technical Field a plus AWS Cloud Certifications: Cloud Practitioner, Solutions Architect, or a related certifications from another cloud service provider a plus 0-2 years of experience in a project-based role involving data science, data analysis, visualizations, and communication/sharing of findings The anticipated salary range for this position is ($90,000k - $125,000k). Actual salary will be based on a variety of factors including relevant experience, knowledge, skills and other factors permitted by law. A range of medical, dental, vision, retirement, paid time off, and/or other benefits are available.

Title: Senior Food Scientist Direct Hire Pay Range: 110-125k depending on experience Bonus: 10% annual bonus Primary Purpose The position of Senior Food Scientist assumes primary responsibility for undertaking and executing product development projects of major importance, complexity, or scope pertaining to all business areas. Major Responsibilities To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Leads product development initiatives for various confectionary products across Innovation, Renovation, Brand Maintenance, and Quality. Leads and executes work on several technical platforms including but not limited to depositing, panning, tableting, taffy, and extrusion. Partners with cross functional team such as Marketing, Supply Chain, Quality, Regulatory, Engineering and Manufacturing in project execution, scale-up, technology transfer, and problem solving. Lead innovation projects from early concept development through scale up and commercialization. Demonstrate proactive ideation and prototype development to contribute to the Innovation Pipeline. Observes, records, and evaluates experimental data. Prepares project reports. Works with other technical and professional personnel within R&D to progress projects. Interacts with Quality and Regulatory Compliance and plant QA on quality issues. Provides leadership and instruction to support junior product developers on the team. Interacts with vendors, suppliers, and contract manufacturers Travels, both domestically and internationally (Travel often in Chicago area to pilot plants, but there could be some additional international travel based on project needs Ensures adherence to all company policies and procedures. Understands and demonstrates the Company's core values. Performs other duties as assigned. Competencies/Skills/Knowledge Required The requirements listed below are representative of the knowledge, skill, and/or ability required. Fundamental knowledge of at least one branch of the sciences. Ability to apply scientific knowledge to technology (including mogul depositing technology). Comfortable operating laboratory, pilot plant, and plant equipment Problem Solving Original Thinking Drive for Results (Can be counted on to exceed goals successfully) Deals with Ambiguity (Can effectively and comfortably cope with change and shifting of gears) Attention to Detail Works well with others and individually Time management (Uses his/her time effectively and efficiently) Education and Experience BS, Master's, or Ph.D. in Food Science, or related field, required. 5-10 years' experience in food industry or related field. Excellent written and verbal communication skills (bilingual if possible: Spanish preferred)

Monopar is a growing biotech company seeking a bright, motivated, and collaborative Clinical Research Data Scientist to support the company's late-stage rare disease and Phase 1 radiopharmaceutical pipeline. You will join a growing, talented team and will be a member of the core cross-functional team that is leading an FDA New Drug Application for Monopar's Wilson disease candidate with significant opportunities for impact and growth. What you'll do... The Clinical Research Data Scientist applies advanced data analysis and statistical methodologies to clinical trial data, synthesizes findings into clear and concise summaries for internal and external communication, and supports future commercial operations. This role will work cross-functionally with scientists, clinicians, statisticians, and management to generate actionable insights that support the company's regulatory filings and scientific publications. The main activities include analysis and reporting of clinical trial data, creation of documentation for regulatory filings, and supporting the development of program regulatory and market initiatives. Contribute to advancement and filing of a New Drug Application (NDA) for Monopar's late-stage rare disease program Review and analyze data objectively to lead Monopar's rare disease team toward recommendations that highlight opportunities, address potential risks, and proactively provide appropriate mitigations Support statistical analysis and exploratory data analysis (EDA) to uncover insights from complex biomedical and real-world datasets Develop and apply quantitative models to analyze clinical trial data, patient outcomes, and real-world evidence (RWE) Analyze and interpret clinical outcomes, safety, and other program data into clear and concise summaries, diagrams and presentations Create clear and effective visualizations to communicate insights to technical and non-technical audiences Ensure data quality, integrity, and compliance with regulatory standards. Work in a team-oriented setting across scientific disciplines to support overall program goals and regulatory submissions Effectively communicate project-related information including the planning, creation and maintenance of key metrics (e.g., timelines, deliverables, budgets) Work in an office (Wilmette, IL north of Chicago) with a dynamic, talented team What skills & experience you'll bring to us… Required Qualifications Bachelor's degree in a scientific discipline (e.g., Biology, Chemistry, Pharmaceutical Sciences, Chemical Engineering, or related field) A minimum of 5 years of experience in data management and/or research with a focus within the biotechnology industry Knowledge of FDA and ICH guidance documents and regulations Proactive attitude with a demonstrated ability to adapt to new challenges and evolving project needs Strong organizational abilities with ability to manage multiple tasks simultaneously and prioritize effectively Excellent communication (oral and/or written) and analytical skills to facilitate clear and effective communication with internal teams and external partners Multitasker, self-starter, proactive, problem solver; ability to work effectively both independently and collaboratively in a team environment Possess a sense of curiosity and interest in science Preferred Qualifications Advanced degree in a scientific discipline (e.g., Master's or PhD) Experience supporting a successful New Drug Application Experience in development of investigational products with Fast Track designation, or other expedited regulatory development pathways; experience with Orphan Drug development (desirable) Experience in analyzing large datasets to support drug development decisions Knowledge of pharmaceutical regulatory guidelines and GxP compliance Monopar Therapeutics (NASDAQ:MNPR) is a clinical-stage biotechnology company developing a new treatment for Wilson Disease, a rare genetic disorder, and novel radiopharmaceuticals for oncology. Its pipeline includes late-stage ALXN1840, a treatment for Wilson Disease, and radiopharmaceuticals to image and treat advanced solid tumors, including Phase 1 MNPR-101-Zr for imaging as well as Phase 1 MNPR-101-Lu and late-preclinical MNPR-101-Ac for therapy.

Join Our Team as an R&D Chemist and Help Shape the Future of Personal Care & Cosmetics! We're looking for an innovative R&D Chemist to join our dynamic team and work with some of the biggest names in the personal care and cosmetic industries. Stay ahead of the latest trends, ingredients, and innovations to drive exciting new products. If you're ready to make a real impact in the personal care industry, we want you on our team! Schedule: M-F 1st shift (flexibility with start time) Salary: 60K-75K Location: Countryside, IL Key Responsibilities: Research and develop skin, body, and other personal care products using cosmetic science. Help improve and scale manufacturing processes for products. Keep detailed and accurate records of experiments and formulations. Stay updated on new trends, ingredients, and innovations in the market. Strong understanding of cosmetic science. Ability to create, test, and improve product formulas. Skilled at solving formulation problems creatively. Ability to analyze data and make decisions to improve products. Good communication skills and experience writing reports. Qualifications: B.S. degree in Chemistry or a related field. 1-3 years of experience within personal care industry working with products like lotions, shampoos, conditioners, etc Cosmetic experience is a plus! ***This job description is a complete list of all desired skills but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!***

The Materials Scientist supports the development and commercialization of a wide variety of composite materials and processes to drive profitable business growth working closely with others in the Research and Development Center and Business Segment as well as externally with suppliers and customers. The candidate should have a deep understanding of the chemical and physical properties of materials and how they behave and interact. Responsibilities And Duties Drive and independently lead projects associated with thermoset composites, including new product development, study of material interactions, and fundamental resin chemistry. Work closely with each market segment to ensure alignment with strategic goals. Lead and support process changes, raw material changes, and quality issues related to existing and new products across multiple manufacturing locations. Complete technical reports with analysis and findings. Analyze experimental data, summarize key findings, and report out in team settings. Work with the sales team to leverage technical findings and product properties for share gains. Establish relationships with customers to capture VOC and product application insight Stay current in latest technology in the composites industry and seek out new materials, ideas, and concepts to develop differentiated, innovative prototypes with potential for scale-up. Work on advanced, complex technical projects or business issues requiring state-of-the-art technical or industry knowledge. Qualifications And Competencies Minimum of 8 years of experience with materials development specifically in composites, resin formulation, or other polymer applications.Significant experience in project leadership. BS in Materials Science, Chemistry, Engineering or other suitable technical field required, advanced degree preferred. Communicate and work cross-functionally to understand materials requirements and provide feedback based on materials expertise. Entrepreneurial in nature. Extensive hands-on experience with mechanical testing and physical and chemical properties of materials Experience with composites manufacturing preferred, including but not limited to: open molding and close molding, pultrusion, extrusion, injection molding, compression molding Formulation and compounding with a wide variety of materials, including but not limited to: thermoset resins, thermoplastics, fibers, films and coatings, nanocomposites, composites additives, “Green” materials and processes including recycling Experience with commercial continuous manufacturing processes. Process development experience, including small scale to large commercial scale. Experience with Matlab, Minitab, Python, R, or other programming tools Development of intellectual property Desirable technical skills other than strong polymer chemistry skills include: analytical instrumentation, statistics, design of experiment, mathematical modeling methods, finite element analysis Company Summary Crane Composites Inc. is the world's leading provider of fiber-reinforced composite materials. We manufacture fiberglass-reinforced plastic (FRP) panels and coils used primarily in the manufacturing of recreational vehicles, truck bodies and truck trailers, and commercial and industrial buildings. Since 1954, Crane Composites has pioneered numerous patented technologies for industrial and commercial product applications. We have built a proven reputation for industry leadership by partnering with customers and suppliers to deliver advanced, industry-leading solutions. We are an equal opportunity employer and value diversity. Our goal is to have a diverse workforce representative of the communities where we are located. All employment decisions are based on qualifications, merit, and business needs.

EPS Environmental Services, Inc., an established Chicago based environmental consulting firm is seeking an Environmental Scientist for a full time position completing Phase I Environmental Assessments. Under the direction and supervision or guidance of experienced field personnel and/or direct supervision of the project manager or senior staff, represent EPS Environmental and interact in a professional manner with clients/representatives, ensure administrative policies and procedures are followed, and understand and apply safety requirements. Responsibilities include conducting Phase I Environmental and similar Assessments per ASTM standards, traveling to field assignments and technical writing. Qualifications and Skills 3-5 years of prior related work experience; experience in due diligence consulting including Phase I Environmental Assessment report writing and similar environmental assessments; understanding of standards and regulations which apply to ASTM 1527; conduct file reviews to assist in the compilation of data and information for the property investigations; report preparation including reviewing laboratory data, previous environmental reports/investigations; ability to work effectively as a team as well as independently; Bachelor's Degree in Environmental Science or related field required. Experience with desktop and industry-specific software (e.g., MSOffice, AutoCAD). Must have sound written and verbal communication skills with strong attention to detail and ability to communicate clearly with on-site contacts, supervisor or project manager regarding work assignments; strong sense of responsibility and work ethic and demonstrate efficiency in writing with the ability to manage time and multiple projects; other related duties and responsibilities may also be assigned. Must possess a valid driver's license and be insurable with a clean driving record.

At LifeStance Health, we believe in a truly healthy society where mental and physical healthcare are unified to make lives better. Our mission is to help people lead healthier, more fulfilling lives by improving access to trusted, affordable, and personalized mental healthcare. Everywhere. Every day. It's a lofty goal; we know. But we make it happen with the best team in behavioral health. Thank you for taking the time to explore a career with us. As the fastest growing behavioral health practice group in the country, now is the perfect time to join our clinical team! We are actively looking to hire talented Clinical Psychologists in the area for LifeStance Health Edgewood Clinical Services, who are passionate about patient care and committed to clinical excellence. We offer Psychologists: Description: LifeStance Health candidates for Post-Doctoral Fellowship positions. We accept post-docs on a rolling admission. LifeStance Health is a national group that has locations across the state of Illinois. Currently, we have opening for post-doctoral fellows in the following cities: Bloomington, Champaign, Darien, South Naperville, Bourbonnais, and Chicago, IL. LifeStance Health offers a wide range of psychotherapy services (e.g. individual therapy, group therapy, couples therapy, and family therapy) in addition to psychological/neuropsychological/pre-surgical evaluations and psychiatry services. Our post-doctoral fellows would provide a combination of psychological/neuropsychological testing and counseling. Our nation-wide presence gives us the ability to partner our fellows with clinicians across the state, and provide continuing education from experts across the nation, for high quality training opportunities. LifeStance believes in a truly healthy society where mental and physical healthcare are unified to make lives better. Our mission is to help people lead healthier, more fulfilling lives by improving access to trusted, affordable, and personalized mental healthcare. WE'RE EXCITED TO OFFER TO YOU: Full-Time position (40 hours) Competitive financial compensation Comprehensive Medical, Dental, and Vision benefits Ancillary Benefits including Life, Long-Term, and Short-Term Disability Insurance Voluntary Benefits including Critical Illness and Accident insurance Malpractice insurance 401K with employer match Opportunity for employment upon completion of fellowship Free, Bi-Weekly CE's presented by our national team and access to unlimited CE's through CE4Less Training in-house to administer, score, and interpret the ADOS-2 (*gold standard for Autism Evaluations) Opportunity to develop, explore, and expand upon your area of interest Agency training opportunities including continuing education, case conference, psychology department meetings Access to a robust in-house administrative team that supports all clinical programming including intake, verification of benefits, billing, coding, collections, and credentialing QUALIFICATIONS: Completion of all doctoral degree requirements for a PhD or PsyD in Clinical Psychology. Strong assessment skills (particularly child psychological and neuropsychological testing) are highly recommended Child and adolescent experience preferred WE'RE LOOKING FOR APPLICANTS WHO: Can work 40 hours weekly Have an interest in collaborating with other staff members and working as a team, sharing knowledge and resources with others, developing leadership skills, and finding creative solutions to meeting the needs of our community Are able to carry a full caseload of psychotherapy and psychological testing clients for a diverse population Are able to handle a rigorous schedule with a wide variety of experiences Are looking to take the EPPP licensure exam prior to or immediately following the one-year mark of post-doctoral fellowship LifeStance provides the compensation range and benefits that it in good faith believes it might pay and/or offer for this position. LifeStance reserves the right to ultimately pay more or less than the posted range and offer additional benefits and other compensation, depending on circumstances not related to an applicant's sex or other status protected by local, state, or federal law.To apply for this position please submit a curriculum vitae and writing sample (psychological evaluation) to Scott Whitlow ****************************. Applications are accepted on a rolling basis. About LifeStance Health LifeStance is a national provider of mental healthcare services focused on evidenced-based, medically driven treatment services for children, adolescents and adults suffering from a variety of mental health issues in an outpatient care setting, both in-person at its clinics nationwide and through its digital health telemedicine offering. The company employs psychiatrists, psychologists, psychiatric nurse practitioners, and licensed therapists throughout the US. LifeStance Health is an equal opportunity employer. We celebrate diversity and are fully committed to creating an inclusive work environment for all our employees. Our values:Belonging: We cultivate a space where everyone can show up as their authentic self.Empathy: We seek out diverse perspectives and listen to learn without judgment.Courage: We are all accountable for doing the right thing - even when it's hard - because we know it's worth it.One Team: We realize our full potential when we work together towards our shared purpose.

R&D lab Technician - Food Industry Duration: 7+ Months Job Type: Contract Work Type: Onsite Payrate: $ 28.00 - 30.00/hr. TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients world-wide Our client is an American food company formed by the merger of client Food and the third-largest food and beverage company in North America Job Description: This job will primarily focus on performing quality analysis of a variety of frozen potato products by grading on market product following standardized grading procedures. The candidate will be responsible for procuring samples from the store or through the client's sample request system, executing required testing, collecting data and presenting findings. In addition to this, the candidate may also be asked to assist with a variety of tasks within the lab including weighing ingredients, preparing samples and executing basic laboratory procedures. The ideal candidate will be organized, have the ability to keep on task and self-manage, and be able to clearly communicate the results of their work. 3 Must Haves: Organized: Ability to maintain order and structure in their work. Self-managing: Capability to stay on task and manage their own workload effectively. Clear communication: Proficiency in clearly conveying the results of their work. TekWissen Group is an equal opportunity employer supporting workforce diversity.

Quantitative, Translational & ADME Sciences Department has an open position for a Scientist II position. The successful candidate will be responsible for non-regulated quantitative LC-MS/MS bioanalysis of small molecules from in vivo and in vitro samples, including extraction, data analysis and interpretation. Responsibilities: • Perform high throughput quantitative in vivo and in vitro LC-MS/MS analysis, troubleshooting and problem solving of small molecule compounds from various bio-matrices. • Operate, perform routine maintenance, and hands-on troubleshooting of AB Sciex LC-MS/MS systems. • Train and mentor junior scientists. • Maintain excellent documentation of all work including LIMS, electronic notebooks, test methods, and protocols. • Work closely with multiple teams across Discovery and QTAS to support bioanalysis. • Write or contribute to study reports for regulatory submissions. Skills: • Proven method development experience using various extraction, chromatographic and analytical methodologies. • Proven experience with quantitative bioanalysis of small molecules. • Proven experience operating and troubleshooting Agilent HPLCs, Leap/CTC PAL autosamplers and AB Sciex Mass Spectrometers. • Detail oriented and committed to generating high-quality results within tight deadlines and across different projects. • Proven ability to work independently or under minimal supervision in a high-throughput environment to design and conduct experiments, interpret, document, and communicate results, as well as in a team environment to collaborate successfully across other groups within R&D. • Communication, interpersonal, and presentation skills. • Work experience in regulated bioanalysis and/or CRO Facility settings is a plus. Education and experience: • M.S. (2+ years preferred), or B.S. (3-6+ years preferred) in analytical chemistry or related field with relevant academic/pharmaceutical industry experience. Leadership Competencies: • Builds strong relationships with peers and cross functionally with partners outside of team to enable higher performance. • Learns fast, grasps the "essence" and can change course quickly where indicated. • Raises the bar and is never satisfied with the status quo. • Creates a learning environment, open to suggestions and experimentation for improvement. • Embraces the ideas of others, nurtures innovation and manages innovation to reality. About US Tech Solutions: 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 ************************ US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Recruiter Details: Name: Shivangi Email: ********************************* Internal Id: 25-35903

The Principal Scientist, Functional Ingredients & Bioactives provides scientific and regulatory expertise to enable the development and execution of Mars Snacking mid to long-term growth strategy achieved through breakthrough innovation for competitive advantage. This role involves identifying and navigating regulatory pathways and frameworks to substantiate claims for novel functional ingredients and bioactives in Mars Wrigley products. What are we looking for? Masters in Nutrition Sciences, Biochemistry or related human or pet health science. PhD preferred. Minimum 5 years' experience in scientific & regulatory affairs with food products and/or related product categories (such as food supplements, cosmetics) with proficiency in food law and novel ingredient/claims approvals. A solid working knowledge of regulatory and human health issues; demonstrated track record of working successfully across functions to achieve shared goals; and proven ability to interact cross-functionally at all levels within a large organization are required. Demonstrated experience and success partnering with trade associations and government agencies to clarify and resolve regulatory matters is required. What will be your key responsibilities? Develops and communicates science-based information, regulatory positions and guidance to key internal stakeholders (Health & Wellness CoE, Science & Technology, Product Development, Corporate Affairs, Legal, Senior Leadership) on functional claims and emerging scientific and regulatory issues of interest to Mars Snacking. Manages regulatory programs related to functional ingredients and bioactives and their use in finished products by collaborating with internal cross-functional stakeholders, in addition to consultants and external industry/scientific groups. Monitors external scientific and regulatory landscape in topic area of expertise to proactively guide business toward right fit solutions to satisfy emerging consumer demand spaces and Mars growth ambition. Provides global guidance across the R&D function in the area of functional ingredients & claims and actively participates in the development of new innovation concepts, claims, standards, and relevant policies. Guides Mars' claims review and approval activities and provides strong partnership with Science & Technology business partners for the advancement of innovation platforms through Mars ‘Technical Readiness Level' process. Drives regulatory-enabled development of consumer demand spaces by identifying opportunities for value creation. Evaluates finished product and claims readiness with a multi-dimensional approach (risk level/external landscape/required time and investment), while providing best pathway for scientific substantiation to ensure compliancy upon commercialization. What can you expect from Mars? Work with diverse and talented Associates, all guided by the Five Principles. Join a purpose driven company, where we're striving to build the world we want tomorrow, today. Best-in-class learning and development support from day one, including access to our in-house Mars University. An industry competitive salary and benefits package, including company bonus. Skills: Action Planning, Adaptive Mindset, Compliance Management, Data Collection and Analysis, Negotiation, Organization Design and Development, Planning and Organizing, Reporting, Verbal Communication, Waterfall Model Competencies: Balances Stakeholders, Business Insight, Collaborates, Communicates Effectively, Ensures Accountability, Interpersonal Savvy, Manages Complexity, Organizational Savvy, Persuades, Strategic Mindset #J-18808-Ljbffr

At LifeStance Health, we believe in a truly healthy society where mental and physical healthcare are unified to make lives better. Our mission is to help people lead healthier, more fulfilling lives by improving access to trusted, affordable, and personalized mental healthcare. Everywhere. Every day. It's a lofty goal; we know. But we make it happen with the best team in behavioral health. Thank you for taking the time to explore a career with us. As the fastest growing behavioral health practice group in the country, now is the perfect time to join our clinical team! We are actively looking to hire talented Clinical Psychologists in the area for LifeStance Health Edgewood Clinical Services, who are passionate about patient care and committed to clinical excellence. We offer Psychologists: Description: LifeStance Health candidates for Post-Doctoral Fellowship positions. We accept post-docs on a rolling admission. LifeStance Health is a national group that has locations across the state of Illinois. Currently, we have opening for post-doctoral fellows in the following cities: Bloomington, Champaign, Darien, South Naperville, Bourbonnais, and Chicago, IL. LifeStance Health offers a wide range of psychotherapy services (e.g. individual therapy, group therapy, couples therapy, and family therapy) in addition to psychological/neuropsychological/pre-surgical evaluations and psychiatry services. Our post-doctoral fellows would provide a combination of psychological/neuropsychological testing and counseling. Our nation-wide presence gives us the ability to partner our fellows with clinicians across the state, and provide continuing education from experts across the nation, for high quality training opportunities. LifeStance believes in a truly healthy society where mental and physical healthcare are unified to make lives better. Our mission is to help people lead healthier, more fulfilling lives by improving access to trusted, affordable, and personalized mental healthcare. WE'RE EXCITED TO OFFER TO YOU: Full-Time position (40 hours) Competitive financial compensation Comprehensive Medical, Dental, and Vision benefits Ancillary Benefits including Life, Long-Term, and Short-Term Disability Insurance Voluntary Benefits including Critical Illness and Accident insurance Malpractice insurance 401K with employer match Opportunity for employment upon completion of fellowship Free, Bi-Weekly CE's presented by our national team and access to unlimited CE's through CE4Less Training in-house to administer, score, and interpret the ADOS-2 (*gold standard for Autism Evaluations) Opportunity to develop, explore, and expand upon your area of interest Agency training opportunities including continuing education, case conference, psychology department meetings Access to a robust in-house administrative team that supports all clinical programming including intake, verification of benefits, billing, coding, collections, and credentialing QUALIFICATIONS: Completion of all doctoral degree requirements for a PhD or PsyD in Clinical Psychology. Strong assessment skills (particularly child psychological and neuropsychological testing) are highly recommended Child and adolescent experience preferred WE'RE LOOKING FOR APPLICANTS WHO: Can work 40 hours weekly Have an interest in collaborating with other staff members and working as a team, sharing knowledge and resources with others, developing leadership skills, and finding creative solutions to meeting the needs of our community Are able to carry a full caseload of psychotherapy and psychological testing clients for a diverse population Are able to handle a rigorous schedule with a wide variety of experiences Are looking to take the EPPP licensure exam prior to or immediately following the one-year mark of post-doctoral fellowship LifeStance provides the compensation range and benefits that it in good faith believes it might pay and/or offer for this position. LifeStance reserves the right to ultimately pay more or less than the posted range and offer additional benefits and other compensation, depending on circumstances not related to an applicant's sex or other status protected by local, state, or federal law.To apply for this position please submit a curriculum vitae and writing sample (psychological evaluation) to Scott Whitlow ****************************. Applications are accepted on a rolling basis. About LifeStance Health LifeStance is a national provider of mental healthcare services focused on evidenced-based, medically driven treatment services for children, adolescents and adults suffering from a variety of mental health issues in an outpatient care setting, both in-person at its clinics nationwide and through its digital health telemedicine offering. The company employs psychiatrists, psychologists, psychiatric nurse practitioners, and licensed therapists throughout the US. LifeStance Health is an equal opportunity employer. We celebrate diversity and are fully committed to creating an inclusive work environment for all our employees. Our values:Belonging: We cultivate a space where everyone can show up as their authentic self.Empathy: We seek out diverse perspectives and listen to learn without judgment.Courage: We are all accountable for doing the right thing - even when it's hard - because we know it's worth it.One Team: We realize our full potential when we work together towards our shared purpose.