Principal Research Scientist Jobs in Rolling Meadows, IL

Senior Scientist - Neuroinflammation Key Responsibilities: Lead early-stage drug discovery projects focused on neuroinflammatory targets Design and execute experiments to validate novel drug targets Collaborate closely with cross-functional teams in a fast-paced, entrepreneurial environment Stay at the forefront of new technologies and methodologies in the field of neuroinflammation Qualifications: Proven experience in neuroinflammation research Strong background in drug discovery and validation techniques Ability to thrive in a dynamic, fast-paced, and collaborative setting Entrepreneurial mindset and passion for advancing novel therapeutics

Senior Scientist, Drug Metabolism/Pharmacokinetics (DM/PK) Seeking a Senior Scientist to advance our research in Drug Metabolism/Pharmacokinetics (DM/PK). This key position will drive in vivo evaluations of therapeutic candidates, focusing on pharmacokinetics, metabolism, and bioavailability of novel compounds. The role requires a strong DM/PK background, extensive in vivo testing experience, and the ability to design studies and influence drug discovery strategy. Primary Responsibilities Independently design and conduct in vivo pharmacokinetic studies to assess drug candidates' metabolism and bioavailability using various animal models, with an emphasis on mouse models for cancer therapeutics. Develop experimental protocols and oversee the IACUC review/approval process. Collaborate with interdisciplinary teams, including chemists and biologists, to integrate DM/PK data across the drug discovery and development stages. Manage and mentor laboratory technicians, guiding experimental techniques and ensuring smooth lab operations. Qualifications Education: M.S. or Ph.D. in Pharmacokinetics, Drug Metabolism, Pharmacology, or a related field. Experience: M.S. with 10+ years of relevant postdoctoral DM/PK experience or Ph.D. with 5+ years; industry experience is preferred. Extensive experience in in vivo pharmacokinetics, including study design, execution, and data analysis. Skilled in in vivo procedures, such as administering test molecules to mice, tissue collection and processing, and histology techniques, including H&E staining. Proficient in data analysis tools like WinNonlin, Phoenix, or similar PK/PD modeling software. Demonstrated scientific contributions, including peer-reviewed publications. Core Competencies Problem-solving ability with a hands-on approach in a laboratory setting. Strong team collaboration skills within a multidisciplinary research environment. Excellent communication skills, with proficiency in presenting complex data to various stakeholders.

Scientist I Has experience with handling radioactive compounds. Able and willing to continue to work with it. Fast learner and able to adapt to a dynamic environment Able to work together in a team (team player) Cares to get the job done and to do it well. Animal handling skills Job Title: Scientist I - Molecular Imaging Purpose: The primary function of this position is to conduct preclinical in vivo positron emission tomography (PET) imaging studies Responsibilities: Provide experimental support for preclinical imaging studies in rodents and large animals, including formulation and administration of radiotracer/contrast agent/compound, image data acquisition, and blood sampling Operate state of the art imaging systems, including a Mediso LFER 150 PET/CT, a Siemens Inveon PET/CT, and two Bruker MRI systems Function as the study coordinator of several preclinical imaging studies Develop and ensure high quality study protocols Support preclinical PET imaging studies by analyzing blood or tissue samples Perform analysis of imaging data using specialized software Ensure maintenance of imaging equipment, in close collaboration with vendor support team Conduct and interpret literature searches to aid in the understanding and improvement of imaging studies Maintain a clean and safe laboratory environment through diligent handling and use-tracking of radioactive materials Communicate key results to team members and project stakeholders and contribute to study reports Qualifications: BS in pharmacology, biochemistry, cell/molecular biology, or a related field with typically 5 years of experience, or master's degree or equivalent education with typically 3 years of experience Pharmaceutical industry experience preferred The preferred candidate will have diverse experience in animal handling and a well-developed interest in working with advanced imaging techniques Demonstrated skills in molecular imaging or in vivo pharmacology Experience working with radioactivity preferred; willingness and ability to work with radioactivity required

Scientist II - Large molecule chromatography & spectrophotometric enzymatic plate reader Onsite in North Chicago, IL 6 months initial contract Hourly Pay Rate: $40-43/hr (medical benefits available at a cost) Responsibilities: * Independently design and conduct critical experiments that further project goals. * Documentation of experimental activities and results in a GMP compliant fashion using an electronic data acquisition and management systems. * Interpret results and draw conclusions from own multistage experiments, note significant deviations, then suggest, design, and pursue relevant experiments. * Troubleshoot experiments and instrumentation. * Understand relevant scientific literature and apply a theoretical framework to solving problems within scientific discipline in a timely manner * Demonstrate skill in multiple techniques and appropriately modify protocols, as required, to suit the changing needs of research or development sciences. * Place data in proper scientific context by consulting and citing relevant literature. * Demonstrate technical proficiency in his/her field, preferentially in the analytical areas of quantitative and instrumental analysis. * Perform routine and complex tasks competently and independently and generate reliable and consistent results. * Impact projects predominantly through lab and/or pilot plant based activities. * Understand and adhere to corporate standards regarding code of conduct, safety, appropriate handling of materials, controlled drug and radioactive compounds, and GxP compliance, where applicable Preferable Skills: * Familiarity with spectrophotometric enzymatic plate reader methods. * Large and small molecule chromatography experience. * Hands-on dissolution experience in development and testing. * Prior exposure to natural products analytical development. * Exposure to 2D Gel electrophoresis Qualification: * Bachelors Degree/Masters Degree in Chemistry/Analytical focus or equivalent Our role in supporting diversity and inclusion As an international workforce business, we are committed to sourcing personnel that reflects the diversity and values of our client base but also that of Orion Group. We welcome the wide range of experiences and viewpoints that potential workers bring to our business and our clients, including those based on nationality, gender, culture, educational and professional backgrounds, race, ethnicity, sexual orientation, gender identity and expression, disability, and age differences, job classification and religion. In our inclusive workplace, regardless of your employment status as staff or contract, everyone is assured the right of equitable, fair and respectful treatment.

Scientist I Duration: 2 Years The primary responsibility of this position is to conduct preclinical in vivo positron emission tomography (PET) imaging studies. Key Responsibilities: Support preclinical imaging studies in rodents and large animals, including radiotracer/contrast agent formulation, administration, image data acquisition, and blood sampling. Operate state-of-the-art imaging systems (Mediso LFER 150 PET/CT, Siemens Inveon PET/CT, Bruker MRI systems). Function as the study coordinator for multiple imaging studies and ensure high-quality protocols. Perform analysis of imaging data and blood/tissue samples using specialized software. Maintain imaging equipment in collaboration with vendor teams and ensure safety in handling radioactive materials. Communicate results to team members and contribute to study reports. Education & Qualifications: BS in pharmacology, biochemistry, cell/molecular biology, or related field with 5+ years of experience, or MS with 3+ years of experience. Experience with animal handling and molecular imaging or in vivo pharmacology. Pharmaceutical industry experience is a plus. Hands-on experience with radioactivity preferred; willingness and ability to work with radioactive materials required.

The primary function of this position is to conduct preclinical in vivo positron emission tomography (PET) imaging studies Responsibilities Provide experimental support for preclinical imaging studies in rodents and large animals, including formulation and administration of radiotracer/contrast agent/compound, image data acquisition, and blood sampling Operate state of the art imaging systems, including a Mediso LFER 150 PET/CT, a Siemens Inveon PET/CT, and two Bruker MRI systems Function as the study coordinator of several preclinical imaging studies Develop and ensure high quality study protocols Support preclinical PET imaging studies by analyzing blood or tissue samples Perform analysis of imaging data using specialized software Ensure maintenance of imaging equipment, in close collaboration with vendor support team Conduct and interpret literature searches to aid in the understanding and improvement of imaging studies Maintain a clean and safe laboratory environment through diligent handling and use-tracking of radioactive materials Communicate key results to team members and project stakeholders and contribute to study reports Skills/Qualifications Required BS in pharmacology, biochemistry, cell/molecular biology, or a related field with typically 5 years of experience, or Master's degree or equivalent education with typically 3 years of experience Pharmaceutical industry experience preferred The preferred candidate will have diverse experience in animal handling and a well-developed interest in working with advanced imaging techniques Demonstrated skills in molecular imaging or in vivo pharmacology Experience working with radioactivity preferred; willingness and ability to work with radioactivity required 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.

$34 - $37/hour based on experience. Provide experimental support for preclinical imaging studies in rodents and large animals, including formulation and administration of radiotracer/contrast agent/compound, image data acquisition, and blood sampling. Operate state-of-the-art imaging systems, including a Mediso LFER 150 PET/CT, a Siemens Inveon PET/CT, and two Bruker MRI systems. Function as the study coordinator of several preclinical imaging studies. Develop and ensure high-quality study protocols. Support preclinical PET imaging studies by analyzing blood or tissue samples. Perform analysis of imaging data using specialized software. Ensure maintenance of imaging equipment, in close collaboration with vendor support team. Conduct and interpret literature searches to aid in understanding and improving imaging studies. Maintain a clean and safe laboratory environment through diligent handling and use-tracking of radioactive materials. Communicate key results to team members and project stakeholders and contribute to study reports. Qualifications: BS in pharmacology, biochemistry, cell/molecular biology, or a related field with typically 5 years of experience, or master's degree or equivalent education with typically 3 years of experience. Pharmaceutical industry experience preferred The preferred candidate will have diverse experience in animal handling and a well-developed interest in working with advanced imaging techniques. Demonstrated skills in molecular imaging or in vivo pharmacology. Experience working with radioactivity preferred; willingness and ability to work with radioactivity required.

About the Company Vanqua Bio is a biotechnology company located in Chicago, IL focused on developing novel therapies for Parkinson's disease and related neurological disorders. Leveraging a state-of-the-art technology platform and biology insights from the founding team, the company is focused on delivering compelling therapeutics to patients. We offer an excellent compensation package including competitive base salary, company ownership and comprehensive benefits. Vanqua Bio also offers the opportunity to be part of a passionate and driven biotech team in downtown Chicago, IL About the Position We are seeking a highly qualified and motivated scientist with a passion for the discovery of novel therapeutics to join the Vanqua team. This individual should have demonstrated experience in neuroinflammation research and will be responsible for leading early drug discovery efforts to validate novel neuroinflammatory drug targets. This individual should enjoy working with novel technologies and thrive in a small team environment. Beyond the requirements listed below, the ideal candidate will possess the entrepreneurial attitude key to succeeding in a dynamic early-stage biotech. Responsibilities: Independently initiate, design, and execute high-quality experiments with appropriate techniques to advance the project goals and the scientific strategy of the company. Develop new methods, technologies, and standard operating procedures to influence the direction, progression, and rapid advancement of the project. Generate complete data sets to support key Go/No Go decisions on novel drug targets. Critically analyze, organize and communicate results at internal and external meetings. Work effectively with internal and external collaborators to advance ongoing projects. Stay up to date on relevant scientific literature. Contribute to building the external scientific reputation of the company through publications, posters, patents and/or attendance at external scientific meetings. Education, Skills and Experience: Ph.D. in cell/molecular biology, pharmacology, immunology, neuroscience or related field with 2+ years of relevant experience. Demonstrated knowledge of the molecular mechanisms underlying neuroinflammation and its contribution to neurodegenerative disease. Experience working with rodent models of neuroinflammation. Experience with advanced cell culture techniques including culture and differentiation of induced pluripotent stem cells to neurons, microglia, or astrocytes to evaluate mechanisms of neurodegeneration. Proficient with basic laboratory techniques including mammalian cell culture, qPCR, western blotting and ELISAs. Demonstrated ability to learn, understand and master new experimental techniques. Strong organizational skills that enable multitasking and working within aggressive timelines. Demonstrated scientific writing skills and strong verbal communication skills. Strong understanding of scientific literature in the field of neuroinflammation and related areas. Strong team player with the ability to build relationships across and outside the organization. Job title and level will be commensurate with candidates' education and experience. Vanqua is proud to be an equal opportunity employer. All employment offers are contingent upon the applicant successfully completing a background screen. If interested in this position, please submit a cover letter and resume via LinkedIn. For security, resumes will not be accepted directly through email. Please do not send resumes to Vanqua employees or to the company location. Vanqua is not responsible for any fees related to unsolicited resumes.

Salary range is $65-$75k ***ONLY open to BS or MS level candidates*** Associate Scientist/Scientist (similar to Molecular Biologist) Reports to Director, Research Development We are looking for someone who has experience with Ecoli gene knockouts and more molecular and microbiology background. Interested in a candidate with 1-2 years of experience or college grad with internships, but must have Ecoli gene experience with a background in molecular/microbiology. ***ONLY open to BS or MS level candidates*** About the role As an Associate Scientist/Scientist, you will report to the associate director of COUR Protein Labs, playing an essential role in advancing our therapeutic pipeline by applying molecular cloning, gene-editing techniques, and bacterial strain engineering. You will be responsible for designing and performing E. coli modifications, including gene knockouts, and other molecular biology techniques to support our drug discovery and development efforts. Your contributions will support both preclinical research and early-stage manufacturing processes. This role will involve cross-functional collaboration, detailed experimental work, and analysis to ensure successful implementation of genetic modifications for improved strain performance, plasmid design, and expression optimization. What you'll do Perform molecular cloning, plasmid construction, and gene-editing techniques (e.g., CRISPR, homologous recombination) to modify and optimize E. coli strains for expression of target proteins and pathways. Design and execute E. coli knockout experiments and genetic modifications to improve expression systems. Conduct a variety of molecular biology techniques, including PCR, gel electrophoresis, and sequencing, to verify constructs and strain modifications. Perform microbial culturing, maintenance, and preparation of modified bacterial strains for downstream applications. Collaborate with microbiologists, biochemists, and process development scientists to integrate strain engineering with overall production workflows. Analyze experimental data, troubleshoot issues, and report findings to cross-functional teams. Ensure all research complies with applicable regulatory standards and internal quality guidelines. Contribute to scientific reports, presentations, and potential publications based on research findings. ***ONLY open to BS or MS level candidates*** Qualifications B.S or M.S. in Molecular Biology, Microbiology, Genetics, or a related field. Proven experience with molecular cloning, gene editing, and bacterial strain engineering. Strong background in standard molecular biology techniques such as PCR, gel electrophoresis, and sequencing. Experience in bacterial culture, fermentation, and microbial system optimization is a plus. Ability to work in a collaborative, multidisciplinary environment with excellent communication and teamwork skills. Strong analytical and troubleshooting abilities, with a demonstrated ability to overcome technical challenges in molecular biology.

VectorBuilder is a rapidly growing biotechnology company specializing in advanced genetic engineering solutions for research and medicine. In particular, VectorBuilder has established itself as a global leader in a range of products and services related to gene delivery, including vector design and optimization, vector cloning, virus packaging, library construction and screening, stable cell line generation, and GMP manufacturing of clinical-grade plasmids, mRNAs, proteins and viruses. One highlight of VectorBuilder's innovative solutions is a revolutionary online platform for designing and ordering custom vectors. This award-winning platform has become highly popular with researchers around the world and has grown into an industry standard for its rich functionalities, extensive experimental validations, and easy-to-use graphical user interface. By leveraging the popularity of this platform, VectorBuilder has built a comprehensive portfolio of offerings covering virtually all gene delivery needs from bench to bedside. We are currently seeking an Application Scientist to join our team! Responsibilities: Provide technical advice to customers on the use of VectorBuilder. Coordinate project management with our scientists, production, and customer support in China. Write and update product literature including web content. Provide technical support on logistics. Related duties as needed. Qualifications: Bilingual in Mandarin and English. PhD in genetics/molecular biology or closely-related field required. Hands-on vector cloning experience required. Hands-on mammalian cell culture and virus packaging experience strongly preferred. Compensation is based on background and experience.

Principal Research Scientist - Product Sustainability We are looking for a highly skilled and motivated technical leader to guide our research and standards team focused on product sustainability. In the role of Principal Research Scientist, you will be pivotal in conducting research and analysis to support the development and implementation of sustainability standards and services. Working closely with cross-functional teams, you will provide technical expertise, drive innovation, and contribute to advancing sustainable practices across industries. Responsibilities Conduct Research and Analysis: Lead research projects to assess and enhance sustainability practices across various industries. Analyze industry trends, evaluate the environmental and social impacts of different processes, and identify opportunities for improvement. Develop Sustainability Standards and Frameworks: Collaborate with both internal teams and external stakeholders to develop and refine sustainability standards. This includes reviewing literature, analyzing best practices, and contributing to the creation of guidelines and criteria for sustainable practices. Stay Current on Sustainability Trends and Regulations: Keep up-to-date with emerging regulations, industry standards, and best practices in sustainability. Apply this knowledge to inform the development of services and standards. Provide Technical Expertise: Support the creation and implementation of sustainability services, including assessments, certifications, and reporting. Offer technical guidance to both internal teams and clients on sustainability-related issues and opportunities. Collaborate with Cross-Functional Teams: Work alongside consultants, project managers, and other stakeholders to deliver high-quality sustainability services. Share knowledge and contribute to the overall success of sustainability projects. Communicate Research Findings: Prepare and present research results to internal teams, management, and external stakeholders. Effectively communicate the environmental and social impacts of various practices and propose strategies for improvement. Foster Partnerships and Collaborations: Build and maintain relationships with external partners, research institutions, and industry organizations. Collaborate on joint research initiatives to stay at the forefront of sustainability practices and innovations. Qualifications Ph.D. or Master's degree in sustainability, environmental science, engineering, or a related field. A strong background in sustainability research and standards development is preferred. Proven experience in conducting research and analysis related to sustainability, including industry assessments, benchmarking, and best practice analysis. In-depth understanding of sustainability principles, frameworks, and relevant regulations and standards. Proficiency in sustainability assessment tools, data analysis software, and other relevant software applications. Strong analytical and problem-solving skills, with the ability to interpret complex data and draw meaningful conclusions. Excellent communication and presentation skills, with the ability to effectively convey technical information to both technical and non-technical audiences. Ability to work both independently and collaboratively in a fast-paced, multidisciplinary environment. Strong project management skills, with the ability to prioritize and manage multiple projects simultaneously. Proficiency in Microsoft Office Suite and other relevant software applications. This role offers a unique opportunity to make a significant impact on sustainability practices while collaborating with a dynamic team of experts. If you're passionate about driving innovation and advancing sustainability, we encourage you to apply. #J-18808-Ljbffr

Grounded in scientific and technical excellence, teamwork, collaboration, and high ethical standards, Stantec ChemRisk staff are leaders in their fields and guide our work with rigor, a creative spirit, and a vision for growth and opportunity. Our team uses state-of-the-art techniques and methodologies to provide sustainable, science-based solutions to complex challenges. We draw from traditional public health disciplines and are committed to fostering an inclusive community of diverse talents, backgrounds, and expertise. Stantec ChemRisk is a place to apply your passion and collaborate with top environmental talents on work that is critical to our clients and the communities we support. Join a nationwide team that has solutions down to a science. Your Opportunity Stantec ChemRisk has an immediate need for a Principal, Senior Principal, or Managing Principal Health Scientist, focused on leveraging your own and our staff's extensive technical expertise, expanding your and the firm's client base, building revenue production and drawing power, and serving as a strategic leader for the firm. You will have the opportunity to work with highly skilled support staff, collaborate with other exceptional experts, and develop and lead publications and internally funded research projects. Stantec ChemRisk is respected worldwide for its risk assessment experience, technical capabilities, industry leadership, and pioneering spirit. We specialize in helping clients characterize the health and environmental risks associated with complex exposures involving chemical and physical hazards in a variety of media and environments. It is an exciting time to join us as we continue our success and create more opportunities for our staff's growth and development. Your Key Responsibilities Works under minimal supervision with broad guidelines to assign, review, and evaluate the performance of new project orders, directing interdisciplinary project teams as needed to ensure project needs are met. Manages and directs several technically complex and diverse projects comprised of relatively large teams of diverse disciplines. Serves as a senior reviewer and/or Principal-In-Charge of projects, research efforts, and manuscripts. Generates revenue; broadens client relationships with new services. Presents the consulting business and risk assessment process in client meetings and for business development leads with no oversight. Works independently and directs business development staff to strategize around and win project work from new or existing clients. Develops and expands the client network which leads to building revenue and independent draw power. Serves as a strategic leader to develop, expand, and leverage new technical areas to broaden the technical and revenue diversity of the firm. Attracts and manages 5 - 10 projects totaling at least $1,000,000, including budgeting and tracking project financials, scoping project strategic plans, managing project team member tasks, and maintaining excellent client relationships. Identifies when deliverables are not up to Stantec ChemRisk standards and works with project staff to ensure final deliverables are high quality. Expands technical expertise in specific areas of risk assessment, toxicology, epidemiology, and exposure assessment by participating as a primary writer and technical contributor to one manuscript or 2-3 diverse technical projects annually. Stays abreast of relevant scientific literature and regulations. Participates in the scientific community and is recognized as a leader and expert in multiple areas of technical expertise. Guides, teaches, and mentors 5 - 10 staff members daily, including being responsible for their workload and career development. Works with staff to broaden their skill sets and has inspired them to an expanded vision for their careers. Follows the ethical guidelines and standard methodologies for their field. Qualifications Your Capabilities and Credentials Highly proficient in critical thinking, problem-solving, writing, teaching, and public speaking. Possesses business development skills necessary to maintain and grow excellent client relationships. Comprehensive understanding of the consulting business and risk assessment process. Recognized as an independent expert which results in attracting clients. Demonstrated project management skills, including but not limited to: scoping work establishing schedules project plan development routine tracking/reporting throughout project implementation. Possesses high attention to detail with proven time management and organizational skills. Ability to professionally and positively communicate in writing and verbally across a variety of stakeholders with varying technical understanding. Capable of presenting to a variety of audience sizes on a wide range of projects. Ability to work both independently and collaboratively. Education and Experience Bachelor of Science (minimum) in public health, biology, chemistry, or other closely related degree required. Master's or Ph.D. preferred. Professional certification (DABT, CIH, etc.) is ideal. A minimum of 10-15 years of proven experience in a similar role required. 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 ChemRisk 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 us and redefine your personal best. Salary Range(s): $141,400 - $219,100 Min/Max Pay Range(s) for postings located in NYC/NY. $123,400 - $191,300 Min/Max Pay Range for postings located in CO and HI. $132,400 - $219,100 Min/Max Pay Range for postings located in CA (SF Area includes SF, SJS & WLC). The final agreed upon compensation is based on individual education, qualifications, experience, and work location. At Stantec certain roles are bonus eligible. Benefits Summary: Regular full-time and part-time employees have access to medical, dental, and vision plans, a wellness program, health saving accounts, flexible spending accounts, 401(k) plan, employee stock purchase program, life and accidental death & dismemberment (AD&D) insurance, short-term/long-term disability plans, emergency travel benefits, tuition reimbursement, professional membership fee coverage and paid family leave. Regular full-time and part-time employees will receive ten paid holidays in each calendar year. In addition, employees will be eligible to accrue vacation between 10 and 20 days per year and eligible for paid sick leave (and if more generous, in accordance with state and local law). Temporary/casual employees have access to 401(k) plans, employee stock purchase program, and paid leave, in accordance with state and local law. The benefits information listed above may not apply to union positions because benefits for such positions are governed by applicable collective bargaining agreements. Primary Location : United States-New York-Brooklyn Other Locations : United States-Illinois-Chicago, United States-Colorado-Denver, United States-California-Irvine, United States-Ohio-Blue Ash Organization : BC-2389 EnvSvcs-US Advisory Employee Status : Regular Job Level : Individual Contributor Travel : No Schedule : Full-time Job Posting : Feb 8, 2024, 2:10:54 PM Req ID: 240000J6 #additional Stantec provides equal employment opportunities to all qualified employees and applicants for future and current employment and prohibit discrimination on the grounds of race, color, religion, sex, national origin, age, marital status, genetic information, disability, protected veteran status, sexual orientation, gender identity or gender expression. We prohibit discrimination in decisions concerning recruitment, hiring, referral, promotion, compensation, fringe benefits, job training, terminations or any other condition of employment. Stantec is in compliance with local, state and federal laws and regulations and ensures equitable opportunities in all aspects of employment. EEO including Disability/Protected Veterans #J-18808-Ljbffr

Center 1 (19052), United States of America, McLean, Virginia Principal Associate, Data Scientist - US Card (Bureau Data Team) At Capital One, data is at the center of everything we do. When we launched as a startup we disrupted the credit card industry by individually personalizing every credit card offer using statistical modeling and the relational database, cutting edge technology in 1988! Fast-forward a few years, and this little innovation and our passion for data has skyrocketed us to a Fortune 200 company and a leader in the world of data-driven decision-making. As a Data Scientist at Capital One you will leverage analytic and technical skills to innovate, build, and maintain well-managed data solutions and capabilities to tackle business problems. Role Description: Credit bureau data is at the heart of underwriting decisions at US Card. This role is with the Bureau Data Strategy team, and supports a broad customer base in Card Data. The team is responsible for generating insights and extracting value from Bureau Data. This role exposes you to tech, modeling, product, and the US Card business teams and it involves: developing credit bureau data SME; creating insightful features from bureau data; developing and maintaining strategic partnerships with stakeholders; performing deep dive analysis on credit bureau data and presenting to senior LT members; and improving key production infrastructure. Our ideal candidate: Customer first. You love the process of analyzing and creating, but also share our passion to do the right thing. You know at the end of the day it's about making the right decision for our customers. A leader. You challenge conventional thinking and work with stakeholders to identify and improve the status quo. You're passionate about talent development for your own team and beyond. Technical. You're comfortable with open-source languages and are passionate about developing further. You have hands-on experience developing data science solutions using open-source tools and cloud computing platforms. Statistically-minded. You've built models, validated them, and backtested them. You know how to interpret a confusion matrix or a ROC curve. You have experience with clustering, classification, sentiment analysis, time series, and deep learning. A data guru. “Big data” doesn't faze you. You have the skills to retrieve, combine, and analyze data from a variety of sources and structures. You know understanding the data is often the key to great data science. Basic Qualifications: Currently has, or is in the process of obtaining a Bachelor's Degree plus 5 years of experience in data analytics, or currently has, or is in the process of obtaining a Master's Degree plus 3 years in data analytics, or currently has, or is in the process of obtaining PhD, with an expectation that required degree will be obtained on or before the scheduled start date. At least 1 year of experience in open source programming languages for large scale data analysis. At least 1 year of experience with machine learning. At least 1 year of experience with relational databases. Preferred Qualifications: Master's Degree in “STEM” field (Science, Technology, Engineering, or Mathematics) plus 3 years of experience in data analytics, or PhD in “STEM” field (Science, Technology, Engineering, or Mathematics). At least 3 years of experience with machine learning. At least 3 years of experience with Spark. At least 3 years of experience with SQL. At least 1 year of experience with AWS. At least 3 years of experience with Python, including Object Oriented Programming, unit testing, and design patterns. At least 3 years of experience with data storytelling and presenting to senior leadership. The minimum and maximum full-time annual salaries for this role are listed below, by location. Please note that this salary information is solely for candidates hired to perform work within one of these locations, and refers to the amount Capital One is willing to pay at the time of this posting. Salaries for part-time roles will be prorated based upon the agreed upon number of hours to be regularly worked. New York City (Hybrid On-Site): $165,100 - $188,500 for Princ Associate, Data Science. Candidates hired to work in other locations will be subject to the pay range associated with that location, and the actual annualized salary amount offered to any candidate at the time of hire will be reflected solely in the candidate's offer letter. This role is also eligible to earn performance based incentive compensation, which may include cash bonus(es) and/or long term incentives (LTI). Incentives could be discretionary or non discretionary depending on the plan. Capital One will consider sponsoring a new qualified applicant for employment authorization for this position. Capital One offers a comprehensive, competitive, and inclusive set of health, financial and other benefits that support your total well-being. Learn more at the Capital One Careers website. Eligibility varies based on full or part-time status, exempt or non-exempt status, and management level. This role is expected to accept applications for a minimum of 5 business days. No agencies please. Capital One is an equal opportunity employer committed to diversity and inclusion in the workplace. All qualified applicants will receive consideration for employment without regard to sex (including pregnancy, childbirth or related medical conditions), race, color, age, national origin, religion, disability, genetic information, marital status, sexual orientation, gender identity, gender reassignment, citizenship, immigration status, protected veteran status, or any other basis prohibited under applicable federal, state or local law. #J-18808-Ljbffr

Title: Formulations Scientist Salary: $70-80,000 + Benefits Shift: 8:30am-5:00pm | Mon-Fri DUTIES AND RESPONSIBILITIES Formulating and executing product development from bench to production scale for new products and/or product improvements across various product lines/programs, while adhering to project timeline and cost parameters. Perform new product development that require knowledge and experience in both processing technologies and product formulation. Optimize existing formulas to achieve cost savings. Create and maintain formulations, specifications, processes, and testing procedures. Coordinate bench samples for prototyping and Sales/Marketing presentations. Collaborate with Operations, Quality Control, Supply Chain, Packaging and Business Development to conduct trials, complete projects and meet production timing. Work with contract customers as needed. Adhere to all GMP and SQF procedures. Work with vendors to identify ingredient improvements, innovative ingredient applications and process improvements. EDUCATION and/or EXPERIENCE Must have a minimum of 3 years of experience in product development formulating nutritional and food products. Ability to work with others in a high-paced environment. Organizational skills to manage multiple projects, timelines and communication to appropriate team members. Sensory evaluation skills, be able to set up, conduct and analyze results. General knowledge of manufacturing procedures, capabilities, and departments i.e. powder blending and filling, liquid processing and filling, etc. Bachelor s degree in food science, chemistry or biology required, Masters in Food Science a plus. Dietary supplement formulation experience a plus. Experience with Genesis Nutrition Software a plus. KNOWLEDGE, SKILLS, and ABILITIES Must have excellent communication skills, written and verbal. Must have strong analytical skills. Passion for the creation of new and exciting products Self-starter that is naturally curious and enjoys working in a fast-paced innovation centric environment Project management, attention to detail and organizational skills BENEFITS Medical/Dental/Vision Insurance 401 K ROTH Plan with Company Match Life Insurance Supplemental Insurance Paid Time Off + Paid Holidays Employee Assistance Program with a comprehensive of emotional, financial, physical, and social well-being programs. Continuous learning opportunities through various platforms and resources

**Sr Quantitative Researcher (options)** Chicago, IL Our client helps the world price and manage risk. Their culture is highly collaborative across traders, quants, technologists and development teams who work together to solve the toughest problems markets have to offer. They strive to make a positive impact on the industry, the lives of their employees, and the communities to which they belong. THE ROLE: Quantitative research is a key driver of innovation and one of the pillars upon which the firm is built. Our client is seeking an experienced Senior Quantitative Researcher to strategically partner with Trading and Technology to strengthen, scale, and evolve the firm's trading capabilities within their core Options Market Making (OMM) business. As a Senior Quantitative Researcher, you will be central to a trading desk, working close to the “tip of the spear” in a dynamic environment. This includes partnership with trading through quantitative problem solving, trading strategy generation, back-testing, statistical analysis, and system design. WHAT YOU WILL DO: * Partner directly with trading to turn market observation and intuition into working hypotheses * Collaborate with trading and technology to build world class options pricing models that help us describe the ever-changing world around us * Use intuition, data, and first principles to own the reliability of both current models and new candidate models * Drive a rapid innovation cycle that produces demonstrable wins through the feedback loop of quantitative research, trading, post-trade analysis, and iterative workflows * Autonomously conduct research and experiments to improve existing strategies and deploy new strategies that monetize opportunities in a constantly evolving market environment. * Build data-based tools and workflows to further systematize our approach to trading and risk management. * Learn from an experienced team with a diverse knowledge base across trading, quant, and technology * Lead, mentor, and develop other quants * Share in the responsibility of driving strategy level and portfolio level Net Trading Profits WHAT WE'RE LOOKING FOR * Advanced quantitative research capabilities with a demonstrated track record in the derivatives industry * History of success working in a team first environment - we hold the success of the team above personal recognition * Ability to learn from mistakes and continuously improve * Excellent communication skills - ability to effectively deconstruct complex systems and ideas into simpler concepts that are explainable to all levels of experience, both written and verbally * Track record of mentoring, developing and leading quants or research teams * Demonstrated ability to take your own ideas or those of others and elevate them into tangible actions and results. * Expertise in C++ or Python required * PhD is not required, but will be thoughtfully considered in the application process ***Thank you for illuminating hiring with Quanta Search!*** ****************************

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: NO TESTING Position available at this time. 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 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 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 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.

Skills Needed Chromatography and enzyme assay needed. Plate reader, large molecules separation skills. Familiarity with spectrophotometric enzymatic plate reader methods Dissolution work along with downstream work. BS Degree -Chemistry with some industry work. R&D lab. Job Description Responsibilities Independently design and conduct critical experiments that further project goals. Documentation of experimental activities and results in a GMP compliant fashion using an electronic data acquisition and management systems. Interpret results and draw conclusions from own multistage experiments, note significant deviations, then suggest, design, and pursue relevant experiments. Troubleshoot experiments and instrumentation. Understand relevant scientific literature and apply a theoretical framework to solving problems within scientific discipline in a timely manner Demonstrate skill in multiple techniques and appropriately modify protocols, as required, to suit the changing needs of research or development sciences. Place data in proper scientific context by consulting and citing relevant literature. Demonstrate technical proficiency in his/her field, preferentially in the analytical areas of quantitative and instrumental analysis. Perform routine and complex tasks competently and independently and generate reliable and consistent results. Impact projects predominantly through lab and/or pilot plant based activities. Understand and adhere to corporate standards regarding code of conduct, safety, appropriate handling of materials, controlled drug and radioactive compounds, and GxP compliance, where applicable Qualification/Skills Required Bachelors Degree/Masters Degree in Chemistry/Analytical focus or equivalent Familiarity with spectrophotometric enzymatic plate reader methods. Large and small molecule chromatography experience. Hands-on dissolution experience in development and testing. Prior exposure to natural products analytical development. Exposure to 2D Gel electrophoresis 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.

We are seeking a highly skilled and motivated Scientist with a strong background in synthetic chemistry, peptide chemistry and solid-phase peptide synthesis. This role is primarily lab-based, focused on design, synthesis and biochemical characterization of preclinical compounds for oncology applications. If you are a skilled and enthusiastic chemist, eager to contribute to the discovery of novel therapeutics, we encourage you to apply and become a part of our team. Key Responsibilities: Design, synthesize, purify, and characterize peptide starting materials that will serve as building blocks for our proprietary Precision-Linked Proteomimetics. Characterize compounds using analytical methods including HPLC, LC-MS, NMR and other relevant analytical methods. Conduct biochemical assays to determine target-binding potency of starting-point peptides and PLP compounds. Execute experimental plans, troubleshoot synthetic challenges, and optimize peptide characteristics (physicochemical properties, target binding, etc.). Required Skills and Experience: Ph.D. with 2+ years of industry/postdoctoral experience or MS with 3+ year of industrial experience in a relevant scientific field (Chemistry, Biochemistry, Medicinal Chemistry, etc.) with a strong academic track record. High degree of proficiency in synthetic organic chemistry with experience in peptide chemistry and solid-phase peptide synthesis. Experienced with compound purification and characterization methods such as HPLC, LC-MS, NMR, and MALDI. Experience with peptide design, including SAR studies and optimization. Expertise in in vitro biochemical assay design and execution (SPR, BLI, TR-FRET, MST, etc.). Experience applying computational methods to designing compounds is a plus. Knowledge of automation and validation of assays for HTS is a plus. Strong commitment to a lab-based role, with a high level of comfort working in a hands-on capacity in a synthetic chemistry environment Strong organizational skills and attention to detail, with the ability to manage multiple tasks and maintain accurate records of experimental work Excellent teamwork and communication skills, with the ability to work effectively with senior scientists and contribute to a collaborative research environment

· Independently design and conduct critical experiments that further project goals. · Documentation of experimental activities and results in a GMP compliant fashion using an electronic data acquisition and management systems. · Interpret results and draw conclusions from own multistage experiments, note significant deviations, then suggest, design, and pursue relevant experiments. · Troubleshoot experiments and instrumentation. Responsibilities: · Independently design and conduct critical experiments that further project goals. · Documentation of experimental activities and results in a GMP compliant fashion using an electronic data acquisition and management systems. · Interpret results and draw conclusions from own multistage experiments, note significant deviations, then suggest, design, and pursue relevant experiments. · Troubleshoot experiments and instrumentation. · Understand relevant scientific literature and apply a theoretical framework to solving problems within scientific discipline in a timely manner · Demonstrate skill in multiple techniques and appropriately modify protocols, as required, to suit the changing needs of research or development sciences. · Place data in proper scientific context by consulting and citing relevant literature. · Demonstrate technical proficiency in his/her field, preferentially in the analytical areas of quantitative and instrumental analysis. · Perform routine and complex tasks competently and independently and generate reliable and consistent results. · Impact projects predominantly through lab and/or pilot plant based activities. · Understand and adhere to corporate standards regarding code of conduct, safety, appropriate handling of materials, controlled drug and radioactive compounds, and GxP compliance, where applicable Experience: · MUST have 2 years industry experience with below desired skills · Chromatography and enzyme assay needed. · Plate reader, large molecules separation skills. · Familiarity with spectrophotometric enzymatic plate reader methods · Dissolution work along with downstream work. Skills: · Familiarity with spectrophotometric enzymatic plate reader methods. · Large and small molecule chromatography experience. · Hands-on dissolution experience in development and testing. · Prior exposure to natural products analytical development. · Exposure to 2D Gel electrophoresis Education: · Bachelors Degree/Masters Degree in Chemistry/Analytical focus or equivalent 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: Deepak Email: ****************************** Internal Id: 24-25590