Company Description: Claros Technologies is a venture backed, deep-tech company solving the worldwide challenge of destroying PFAS in the environment. PFAS remediation is rapidly becoming a multi-billion-dollar, global market and is at the center of regulatory action in the US, Europe and Asia that requires the removal of this carcinogen from drinking water, industrial processes and waste sites. Claros has developed a patented, scalable destruction technology proven to fully destroy 99.99% of PFAS in customers' samples. We are a diverse team of scientists, business-builders, and impact leaders committed to solving problems without creating new ones. The company closed a $20M financing round in the beginning of 2024 with leading environment venture capital firms, which provides the credibility and resources required to convert current pilot users into full scale commercial customers as well as to sell easy-to-identify prospects across the globe. If you are a mission driven, highly motivated Research Scientist, join us as we solve one of the greatest environmental challenges of our time. Position Overview: Claros Technologies' Functional Materials team is primarily focused on using sustainable chemistries to enable advanced materials in textiles and selective filtration application areas. We are seeking a collaborative, driven individual to join our team as a Research Scientist. The Research Scientist will be tasked with partnering the technical team to execute application-driven, fundamental research. Reporting to the Director of Functional Materials, this individual will require technical know-how, and will be responsible for day-to-day, hands-on laboratory activities. Essential Job Functions: <ul><li>Designing and executing laboratory experiments</li><li>Collecting and analyzing data</li><li>Reading, understanding, and interpreting scientific publications</li><li>Writing and presenting reports to internal team stakeholders</li><li>Maintaining a clean and safe workspace; Safety first mindset</li><li>General laboratory maintenance and upkeep</li></ul> Competencies & Skills: <ul><li>Strong communication skills, both written and verbal</li><li>Independent thinker; strong problem solving skills; ability to troubleshoot technical issues</li><li>Ability to analyze data and make recommendations </li><li>Inquisitive mindset; curiosity-driven</li><li>Strong organizational skills</li><li>Understanding of basic chemistry principles, preferably exposure to materials science (emphasis on organic chemistry)</li><li>Design of experiments</li><li>Formulation chemistry; basic material characterization techniques such as FTIR, DSC, and TGA</li><li>Comfortable working in a fast past environment in a growing lab</li></ul> Preferred Experience: <ul><li>Bachelor's degree or higher in chemistry related field (preference for materials science or chemistry); Masters degree a plus</li><li>3-5 years experience in a research environment for private, commercial, or governmental work</li></ul> Job Specifications <ul><li>Compensation: $70,000 - $80,000</li><li>Location: In person at the Claros Headquarters in Minneapolis, Minnesota. </li><li>Travel: May be required periodically for purposes such as client site visits; not required on a regular or frequent basis.</li></ul> Claros Technologies offers attractive salary and benefits including health, vision, and dental insurance, PTO as well as 401k plans and options. For more information, please visit www.clarostech.com The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

Vantive: A New Company Built On Our LegacyBaxter is on a journey to separate our ~$5B Kidney Care segment into a standalone company. Vantive* will build on our nearly 70-year legacy in acute therapies and home and in-center dialysis to provide best-in-class care to the people we serve. We believe Vantive will not only build our leadership in the kidney care space, it will also offer meaningful work to those who join us.At Vantive, you will become part of a community of people who are focused, courageous and don't settle for the mediocre. Each of us are driven to help improve patients' lives worldwide. Join us as we revolutionize kidney care and other vital organ support.* Completion of the proposed separation of Kidney Care from Baxter into a standalone company (to be named Vantive) remains subject to the satisfaction of customary conditions.The Research Scientist II of Preclinical (Toxicology and Biocompatibility) will support a portfolio of drug, drug packaging system, medical device, and/or combination product development and global registration. This individual will apply expertise in toxicology, biocompatibility, and related scientific knowledge, to provide technical leadership for non-clinical safety / efficacy, toxicology risk assessment and/or biocompatibility strategies to assure product (patient) safety and efficacy through the application of innovative pre-clinical science, non-clinical safety assessment, and toxicological principles and methods to enable and support new product development (NPD), sustaining product organization (SPO) and margin improvement projects (MIP) and associated product development lifecycle management (PDLM) processes and initiatives. The role will report to Associate Director of Preclinical Biocompatibility and Toxicology and will be responsible for drugs and devices for Peritoneal dialysis, Hemodialysis, and Acute therapies (~$5B product portfolio with global reach in more than 100 countries).What you will be doing:* Author complicated studies/ toxicology risk assessment reports and review or concur toxicology assessment reports as subject matter expert (SME) in accordance with ICH and ISO10993-17.* Maintain current knowledge of relevant regulatory requirements related to toxicology, product development, design and safety and act as a technical expert in these areas as it pertains to product development and registration.* Perform as preclinical/toxicology representative on project teams.* Design, plan, monitor various GLP toxicity studies, biocompatibility studies, risk/safety assessment (risk assessment and qualification of impurities, leachables, extractables, residual solvents and excipients) for regulatory submissions.* Recommend actions, path forward and decisions aligned with overall project objectives and timelines.* Participate in change control management and impact assessment.* Perform/support audits/inspection (GLP) of studies/sites/facilities (CROs).* Prepare and/or review nonclinical eCTD and PBRER sections* Use Lhasa Derek and Sarah Nexus software to assess toxicological endpoints.Qualifications:* Relevant knowledge of ICH guidelines, ISO 10993-1, ISO 10993-17 and ISO 10993-18 required.* Experience authoring Toxicological Risk Assessments and deriving Tolerable Intake values, Margin of Safety and Analytical Evaluation Thresholds.* Demonstrated technical writing ability and oral presentation to enable clear communication of study results, safety evaluations, and toxicology assessment conclusions.* Demonstrated experience working with regulatory authorities for device and/or drug registrations in US markets (prefer experience with US and European authorities)Education and/or Experience:* MS degree with minimum of 10 years experience OR PhD with 6 years of relevant experience* Experience in conduct and execution of GLP nonclinical safety (toxicology) and toxicological risk assessment on Extractable & Leachable is highly preferred.* Experience with safety and biocompatibility evaluation of medical devices and related regulatory guidance (ICH, USP, ISO 10993, EU MDR, etc).Baxter is committed to supporting the needs for flexibility in the workplace. We do so through our flexible workplace policy which includes a minimum of 3 days a week onsite. This policy provides the benefits of connecting and collaborating in-person in support of our Mission.We understand compensation is an important factor as you consider the next step in your career. At Baxter, we are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. The estimated base salary for this position is $144,000-198,000 annually. The estimated range is meant to reflect an anticipated salary range for the position. We may pay more or less than of the anticipated range based upon market data and other factors, all of which are subject to change. Individual pay is based upon location, skills and expertise, experience, and other relevant factors. This position may also be eligible for discretionary bonuses. For questions about this, our pay philosophy, and available benefits, please speak to the recruiter if you decide to apply and are selected for an interview.#LI-BG1The successful candidate for this job may be required to verify that he or she has been vaccinated against COVID-19, subject to reasonable accommodations for individuals with medical conditions or religious beliefs that prevent vaccination, and in accordance with applicable law.Equal Employment OpportunityBaxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.EEO is the LawEEO is the law - Poster SupplementPay Transparency PolicyReasonable AccommodationsBaxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information.Recruitment Fraud NoticeBaxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.139604

<h3>Job Description</h3><div>Job Description<div><div></div>ABOUT INSPIRE MEDICAL SYSTEMSInspire is the first of its kind medical device designed to make a difference in the lives of those living with Obstructive Sleep Apnea (OSA). We are revolutionizing the sleep industry with our FDA-approved medical device, designed to reduce OSA severity for those who cannot tolerate or get consistent benefit from CPAP. Our focus on patient outcomes is at the core of everything we do, and our “think I can” attitude drives us to make a difference in the lives of those seeking alternative sleep apnea treatments. WHY JOIN OUR FAST-GROWING TEAMAt Inspire, we value people – your diverse experiences, backgrounds, and thoughts. We elevate voices and encourage learning opportunities to build a professional network that grows into community. We embrace a people-first culture by offering hybrid work schedules, excellent benefits, 401k matching, ESPP, flexible time off (FTO), and tuition reimbursement. If you’re passionate about making a difference in people’s lives and want to work with innovative technology, come be a part of our great team! ABOUT THIS POSITION This position will provide technical leadership for new therapy and technology development of medical device solutions for treating obstructive sleep apnea and other unmet clinical needs.OPPORTUNITIES YOU WILL HAVE IN THIS ROLE <ul><li>Lead technology and therapy development efforts to optimize therapy response to upper airway stimulation for treatment of obstructive sleep apnea</li><li>Identify clinical needs to improve outcomes & treatment efficiency for obstructive sleep apnea treatment including patient selection, operative techniques and post-implant care</li><li>Develop therapy and technology solutions by conducting pre-clinical and clinical feasibility studies</li><li>Generate peer-reviewed publications and conference presentations to support therapy adoption</li><li>Protect intellectual properties by filing patent applications</li><li>Support clinical study procedures at investigation sites, including device implant and therapy titration procedures</li><li>Participate in next generation product development efforts in partnership with new product planning, development, and regulatory teams</li><li>Support training of new employees and new customers</li></ul>WHAT YOU CAN BRING TO OUR GREAT TEAM Required:<ul><li> B.S. degree with 10+ related experience; OR M.S. degree with 7+ years of experience; OR PhD with 5+ years of related experience</li><li>10+ years of experience with implanted neuromodulation therapy research</li></ul>Preferred:<ul><li>Minimum of 5 years of related experience in the medical device industry or sleep apnea research field</li></ul>Inspire Medical Systems provides equal employment opportunity (EEO) to all employees and applicants without regard to race, color, religion, creed, sex, national origin, age, disability, marital status, familial status, sexual orientation, status regarding public assistance, membership or activity in a local commission, military or veteran status, genetic information, or any other status protected by applicable federal, state, and local laws. This policy applies to all aspects of the employment relationship, including recruitment, hiring, compensation, promotion, transfer, disciplinary action, layoff, return from layoff, training, and social and recreational programs. Inspire Medical Systems complies with applicable laws governing non-discrimination in employment in every location in which Inspire Medical Systems has facilities. All such employment decisions will be made without unlawfully discriminating on any prohibited basis. Inspire Medical Systems is an equal opportunity employer with recruitment efforts focused on ensuring a diverse workforce. Applicants with a disability that need accommodation to complete the Inspire Medical Systems application process should contact Human Resources at 844-672-4357 or email careers@inspiresleep(dot)com Inspire Medical Systems participates in E-Verify.<div><div><div><div> </div></div></div></div></div></div>

The pay range is $93,800.00 - $168,800.00 Pay is based on several factors which vary based on position. These include labor markets and in some instances may include education, work experience and certifications. In addition to your pay, Target cares about and invests in you as a team member, so that you can take care of yourself and your family. Target offers eligible team members and their dependents comprehensive health benefits and programs, which may include medical, vision, dental, life insurance and more, to help you and your family take care of your whole selves. Other benefits for eligible team members include 401(k), employee discount, short term disability, long term disability, paid sick leave, paid national holidays, and paid vacation. Find competitive benefits from financial and education to well-being and beyond at . JOIN US AS A SR OPERATION RESEARCH SCIENTIST - LAST MILE About Us: As a Fortune 50 company with more than 350,000 team members worldwide, Target is an iconic brand and one of America's leading retailers. Working at Target means helping all families discover the joy of everyday life. We bring that vision to life through our values and culture. Learn more about Target here (. We prioritize relationships, develop talent by creating growth opportunities and succeed as one Target team. At our core, our purpose is ingrained in who we are, what we value and how we work. It's how we care, grow, and win together. Every time a guest enters a Target store or browses , they experience the impact of Target's investments in technology and innovation. We're the technologists behind one of the most loved retail brands, delivering joy to millions of our guests, team members, and communities. About this opportunity: Do you want to shape the future Supply Chain and Logistics strategy for a fortune 50 company and one of America's leading Retailer? Do you want to optimize Target's Global Supply Chain end to end, from sourcing to delivery of packages to guest? Are you excited at the prospect of analyzing large data sets and developing complex algorithms, simulation and optimization models to solve real world problems? A role in Operations Research team means opportunity to contribute to the team that is at the forefront of defining future Omni channel operating model for Target's Global Supply Chain across first mile, middle mile and last mile. You will develop cutting edge data pipelines, optimization and simulation models to design and operate Target's Global Supply Chain in fast and efficient manner and work with stake holders across the company in Finance, Merchandising, Stores and GSCL teams to enable supply chain transformation. Target's supply chain is an evolving at a fast pace global team. We are constantly reimagining how we get the right product to the right guest faster and more efficiently. Enterprise Network Strategy (ENS) team is at the forefront of defining future road map for growth and profitability for Target. ENS team work directly with business leaders and product owners to build industry leading network topology to support inventory flow and last mile capabilities. As a Senior Operations Research Scientist you will: Know your business and understand Supply chain operational metrics and cost of end to end operations of supply chain. Analyze large amounts of supply chain data at the most granular level & develop key metrics to evaluate the performance and optimization opportunities for Supply Chain across sales, transportation, operations and inventory. Perform root cause analysis to understand key drivers related to operational performance and variance in the projected outcomes. Utilize operations research methodologies (e.g., linear programming, stochastic processes, simulation) to solve complex business problems. Collaborate with cross-functional teams including engineers, data scientists, and business stakeholders to gather inputs assumptions and understand business process along the way. Interpret results from the models and provide insights to the leadership team. Develop a clear and concise inference with data to influence decision making with senior leadership teams. Core responsibilities of this job are described within this job description. Job duties may change at any time due to business needs. About You: 4-year degree in quantitative disciplines (Science, Technology, Engineering, Mathematics) or equivalent experience PhD or MS in Operations Research, Industrial Engineering, Computer Science, Data Science, Applied Mathematics or equivalent work experience 3+ years of experience in retail supply chain or equivalent domain experience Demonstrated industry experience in probability statistics, optimization and simulation Strong demonstrated experience in SQL and programming in Python or R Extensive knowledge of supply chain concepts such as forecasting, inventory planning, optimization and logistics Knowledge of statistics and data mining techniques/tools to analyze and derive insights from historical sales data and simulation or experiment results Deep passion for problem solving, empirical research and continuous improvement Ability to communicate complex concepts in easy to understand terminology with multiple audiences This position may be considered for a Remote or Hybrid (known internally at Target as 'Flex for Your Day') work arrangement based on Target's needs. A Remote work arrangement means the team member works full-time from home or an alternate location that's not a Target location, does not have a desk at a Target location and may travel to HQ up to 4 times a year. A Hybrid/Flex for Your Day work arrangement means the team member's core role may be performed either remote or onsite at a Target location depending upon what your role, team and tasks require for that day. Work duties cannot be performed outside of the country of the primary work location, unless otherwise prescribed by Target. Americans with Disabilities Act (ADA) In compliance with state and federal laws, Target will make reasonable accommodations for applicants with disabilities. If a reasonable accommodation is needed to participate in the job application or interview process, please reach out to . Application deadline is : 09/29/2024

Research Scientist Jobs in Minneapolis, MN

Research Scientist Functional Materials
November 18, 2024

Research Scientist Ii Of Preclinical Toxicology And Biocompatibility
November 11, 2024

Principal Research Scientist
October 28, 2024

Sr Operations Research Scientist Last Mile Fulfillmentremote Or Hybrid
October 25, 2024

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Research Scientist Jobs in Minneapolis, MN

Research Scientist Functional MaterialsNovember 18, 2024

Research Scientist Ii Of Preclinical Toxicology And BiocompatibilityNovember 11, 2024

Principal Research ScientistOctober 28, 2024