Postdoctoral scholar jobs in Maplewood, MN - 92 jobs

JOB TITLE: UROP Ignite Scholar PAY RATE: $17.70 per hour HOURS: 20 per week The Undergraduate Research Opportunities Program is now accepting applications for the Ignite Scholars Program. Ignite Scholars are matched to work 200 paid hours to collaborate with a faculty member on research or scholarship in their field for the duration of the summer. The deadline for consideration for this program for Summer 2026 is Monday, February 16, at 9:59 pm. Student applicants may be invited as semi-finalists for open positions. Semi-finalists will be invited to participate in a matching process with the available faculty mentors and submit their ranking of projects during the spring semester. These activities will take place in February and March. Students must participate in matching activities to be eligible for selection. After matching activities are complete, selected students will be designated as Ignite Scholars with matched faculty mentors. Students selected as Ignite Scholars perform the following activities: * Accept a Canvas community site invitation to track your progress in the program * Meet with your faculty mentor prior to the end of spring semester to develop a written collaboration agreement to plan your schedule, activities, and goals for the summer * Participate in a start-of-summer program orientation * Complete 200 hours working in collaboration with the faculty mentor over the course of the summer, planned and scheduled in consultation with your faculty mentor according to your collaboration agreement * Complete all necessary HR paperwork to be hired and get paid as a student employee of the university * Complete the Responsible Conduct in Research and Scholarship Training before beginning the research project * Complete any additional required safety training according to the standards and requirements of your field of work * Perform assigned duties with responsibility and integrity. Maintain good communication with and accountability to your faculty mentor and UROP. * Participate in the Inquiry Poster Session in October 2026 * Complete a final written report or reflection on the program to the Undergraduate Research Opportunities Program by the posted deadline * Complete a program exit survey, which will be received after the poster session To be considered for this award, you must submit this completed job application, a resumé, and a guided personal statement. No additional cover letter is required. QUALIFICATIONS Be enrolled as a degree-seeking associate's or bachelor's program student at the University of St. Thomas during the semester before and the semester after the summer in which you will participate Have completed no more than 4 semesters at St. Thomas towards your current associate's or bachelor's degree as of the beginning of summer 2026 Be available to work 20 paid hours per week on your research project for at least 10 weeks of the summer during regular working hours Additional restrictions apply: * You may not accept a position in this program to conduct research for which you will receive course credit * You may not participate in the Ignite Scholars Program simultaneously with a separate UROP Young Scholars Grant, Community-Based Research Grant, or Sustainability Scholars Grant * You may apply for this program up to twice while a student. If you were selected to participate in Ignite in a previous summer, you are not eligible to reapply. * If you are not in compliance with this or any other Undergraduate Research Opportunities Program (i.e., have not turned in a paper produced with the assistance of an earlier research grant or did not participate in a required Inquiry Poster Session), you are not eligible to receive funding under this program * If selected, you may also be eligible to apply for a UROP Summer Housing Grant Note: International students are eligible to apply. If selected for this program, a student will be employed through an hourly position on campus. International students preparing an application should discuss their employment plans with OISS to ensure that employment as a student researcher will not conflict with any student visa requirements and restrictions. Application Instructions: This program has a 2-part application. To be considered for this program, you must: Complete the application for this St. Thomas student job. * You are required to submit a resumé to apply for any St. Thomas position. For this position, it is recommended that you tailor your resumé to highlight employment, coursework, and volunteer experience that speak to the skills and roles described in the faculty project descriptions. If you are selected as a semi-finalist, your resumé will be shared with your potential faculty mentors as part of the matching process. * No additional cover letter is required. If you include attachments other than a resumé, they will not be reviewed. Submit your personal statement by the stated deadline using this Qualtrics portal. Your statement will not be used to compare you to other candidates. Use this statement as an opportunity to introduce yourself to potential research mentors. * This portal will open by January 28. * The guided personal statement requires you to respond to 3 out of 4 questions provided. Write ~300 words for each question you choose. The 4 questions are: * What motivates you? What makes you curious? * How might collaborating with a faculty member on research and scholarly work relate to your own interests and goals? What do you hope to learn from this experience? * What are some strengths that would make you a good collaborator? What about your learning style, personality, or passions would you like someone to be acquainted with before they start working with you? * Describe a situation where you faced a difficult challenge and explain how you responded. Applications missing a resumé or a personal statement as of the deadline will not advance. ELIGIBILITY To be eligible for student employment, St. Thomas students must be degree seeking at the undergraduate, graduate and doctoral levels. Students must be actively enrolled at least part-time in courses for credit. For further information on eligibility please see the Student Employee Toolkit on One StThomas. The University of St. Thomas is an Equal Opportunity Employer, including disability and protected veteran status.

* Build AI agents using Python, LLMs, LangChain/LangGraph, ReACT/ReWOO, RAG, and A2A protocol. * Explore platforms like Copilot Studio, Azure AI Foundry, and NotebookLM etc for advanced GenAI capabilities. * Prototype workflows and integrations for agentic AI, multimodal experiences, and enterprise copilots. * Assess emerging tools for scalability, security, and alignment with organizational AI strategy. * Document findings and provide recommendations for platform adoption and architecture patterns. * Collaborate with engineering and QE teams to convert prototypes into production-ready solutions. * Experiment with evaluation frameworks and guardrails for research prototypes. * Stay updated on cutting-edge GenAI trends and contribute to internal knowledge sharing. Salary Range: $110,000 $140,000 Year TCS Employee Benefits Summary: Discretionary Annual Incentive. Comprehensive Medical Coverage: Medical & Health, Dental & Vision, Disability Planning & Insurance, Pet Insurance Plans. Family Support: Maternal & Parental Leaves. Insurance Options: Auto & Home Insurance, Identity Theft Protection. Convenience & Professional Growth: Commuter Benefits & Certification & amp; Training Reimbursement. Time Off: Vacation, Time Off, Sick Leave & Holidays. Legal & Financial Assistance: Legal Assistance, 401K Plan, Performance Bonus, College Fund, Student Loan Refinancing. #LI-SP1

We are seeking an AMO Hardware Scientist in our Brooklyn Park, MN, location. Our team is leading the development, integration, and operation of quantum computing systems at Quantinuum. We are looking for experimental scientists with hands-on experience building and operating devices to manipulate qubits, quantum spin systems, or cold and trapped atomic systems. The perfect candidate will have intimate knowledge of one or more advanced laboratory techniques for controlling quantum systems, which could include precision laser spectroscopy, low noise DC and RF electronics, cryogenic UHV systems, or computer control systems. They will also have excellent communication and collaboration skills as they are working with teams of engineers and other scientists to develop and test new concepts. Our scientists are thought leaders in the field, publishing papers and presenting research to peers. All applicants for placement in safety-sensitive positions will be required to submit to a pre-employment drug test. Key Responsibilities: * You will apply previous experience in experimental laboratory research to design, develop, verify, and deploy quantum computers using trapped ions as qubits. * You will work alongside teams of scientists and engineers to bring new concepts to life. * You will be responsible for working in a research lab environment to collect data on system performance and characterizing device characteristics. * You will generate and implement innovative solutions to improve current and future systems. * You will present scientific results at conferences or in publications. YOU MUST HAVE: * PhD completed prior to starting * Minimum 4+ years' experience (PhD inclusive) involving one or more of the following areas: quantum information, qubits, cold atom or trapped ion physics, vacuum systems, or cryogenics * Due to Contractual requirements, must be a U.S. Person. defined as, U.S. citizen permanent resident or green card holder, workers granted asylum or refugee status * Due to national security requirements imposed by the U.S. Government, candidates for this position must not be a People's Republic of China national or Russian national unless the candidate is also a U.S. citizen. WE VALUE: * PhD Electrical Engineering, applied physics, applied mathematics, computer science, or a related field * A history of excellent experimental practices designing or improving existing advanced systems * Experience programming experimental control systems for data collection, signal processing, and data analysis * Experience performing simulation and modeling to inform experiments * Experience with design or operation of a device for quantum information processing * Experience with laser cooling and trapping of ions or neutral atoms * Excellent written and oral communication skills, with published results within their field of research. * Excellent attention to detail, organization, and a results-oriented mindset * Experience in post-doctoral research positions or other mentorship positions * Demonstrated organizational and leadership skills $124,000 - $170,000 a year Compensation & Benefits: Non-Incentive Eligible The pay range for this role is $124,000 - $170,000 annually. Actual compensation within this range may vary based on the candidate's skills, educational background, professional experience, and unique qualifications for the role. Quantinuum is the world leader in quantum computing. The company's quantum systems deliver the highest performance across all industry benchmarks. Quantinuum's over 650 employees, including 400+ scientists and engineers, across the US, UK, Germany, and Japan, are driving the quantum computing revolution. By uniting best-in-class software with high-fidelity hardware, our integrated full-stack approach is accelerating the path to practical quantum computing and scaling its impact across multiple industries. By joining Quantinuum, you'll be at the forefront of this transformative revolution, shaping the future of quantum computing, pushing the limits of technology, and making the impossible possible. What's in it for you? A competitive salary and innovative, game-changing work Flexible work schedule Employer subsidized health, dental, and vision insurance 401(k) match for student loan repayment benefit Equity, 401k retirement savings plan + 12 Paid holidays and generous vacation + sick time Paid parental leave Employee discounts Quantinuum is an equal opportunity employer. You will be considered without regard to age, race, creed, color, national origin, ancestry, marital status, affectional or sexual orientation, gender identity or expression, disability, nationality, sex, or veteran status. Know Your Rights: Workplace discrimination is illegal We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

Shift: Monday through Friday, 8:00AM - 5:00PM Are you ready to work making the world a safer, healthier place? Join our mission to continuously move science forward; to innovate and advance all aspects of our business to improve the health and safety of our communities and lives. Job Summary The Scientist I will contribute to laboratory operations by performing analytical testing, interpreting data, and maintaining laboratory equipment and documentation in accordance with established protocols and quality standards. Compensation: $70,000.00 - 80,000.00 per year Job Responsibilities * Execute a variety of laboratory analytical tests and experiments following Standard Operating Procedures (SOPs) and client specifications. * Operate, calibrate, and perform routine maintenance on laboratory instrumentation such as HPLC, GC, UV-Vis, Karl Fisher Titrations, Visual Titrations, or other various wet chemistry techniques * Conduct molecular biology techniques such as PCR, ELISA and/or Western Blot * Accurately record, compile, and analyze experimental data, ensuring data integrity and traceability. * Prepare and process samples, reagents, and solutions according to established methods. * Troubleshoot basic instrumentation and assay issues, escalating complex problems to senior staff. * Maintain a clean, organized, and safe laboratory environment, adhering to all safety regulations and good laboratory practices (GLP). * Document all work thoroughly and accurately in laboratory notebooks and electronic systems. * Participate in the review and revision of SOPs and other technical documents as needed. * Communicate effectively with team members, supervisors, and other departments regarding project status and results. * Contribute to continuous improvement initiatives within the laboratory. Job Qualifications * Bachelor's degree in Chemistry, Biochemistry, Analytical Chemistry, or a related scientific discipline. *5-8 years of relevant laboratory experience, preferably in an industrial or contract laboratory setting. * Fundamental understanding of analytical chemistry principles and techniques. * Hands-on experience with common laboratory equipment (e.g., pH meters, balances, centrifuges, pipettes). * Strong attention to detail and ability to follow complex procedures precisely. * Proficiency in data analysis and interpretation, with experience using LIMS or similar data management systems preferred. * Excellent written and verbal communication skills. * Ability to work independently and as part of a team in a fast-paced environment. * Basic computer skills, including Microsoft Office Suite. * Knowledge of GLP/cGMP regulations is a plus. Find Your Place at Pace - We need you - your curiosity, your talents, and your drive - to help us advance this important work. Benefits When you join Pace , you commit to work that makes a positive impact on our communities and our world. We commit to supporting you with benefits and perks that make a positive impact on your life. Full-time roles are eligible for our comprehensive benefits program which includes competitive salaries, medical, dental vision, 401K retirement savings plan (100% vested immediately in the employer match), life, disability and voluntary benefits, paid time off for holiday, sick and vacation days, HSA, wellness program, flexible spending accounts, tuition reimbursement, Employee Assistance program, parental leave, optional legal coverage and ID theft. Equal Opportunity Employer Pace provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, creed, color, religion, genetics, protected veteran status, national origin, sex, age, disability, marital status, sexual orientation, gender identity or expression, citizenship, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.

Shift: Monday through Friday, 8:00 AM - 5:00 PM Are you ready to work making the world a safer, healthier place? Join our mission to continuously move science forward; to innovate and advance all aspects of our business to improve the health and safety of our communities and lives. Job Summary The Scientist I will contribute to laboratory operations by performing analytical testing, interpreting data, and maintaining laboratory equipment and documentation in accordance with established protocols and quality standards. Compensation: $70,000.00 - 80,000.00 per year Job Responsibilities * Execute a variety of laboratory analytical tests and experiments following Standard Operating Procedures (SOPs) and client specifications. * Operate, calibrate, and perform routine maintenance on laboratory instrumentation such as HPLC, GC, UV-Vis, Karl Fisher Titrations, Visual Titrations, or other various wet chemistry techniques * Conduct molecular biology techniques such as PCR, ELISA and/or Western Blot * Accurately record, compile, and analyze experimental data, ensuring data integrity and traceability. * Prepare and process samples, reagents, and solutions according to established methods. * Troubleshoot basic instrumentation and assay issues, escalating complex problems to senior staff. * Maintain a clean, organized, and safe laboratory environment, adhering to all safety regulations and good laboratory practices (GLP). * Document all work thoroughly and accurately in laboratory notebooks and electronic systems. * Participate in the review and revision of SOPs and other technical documents as needed. * Communicate effectively with team members, supervisors, and other departments regarding project status and results. * Contribute to continuous improvement initiatives within the laboratory. Job Qualifications * Bachelor's degree in Chemistry, Biochemistry, Analytical Chemistry, or a related scientific discipline. *5-8 years of relevant laboratory experience, preferably in an industrial or contract laboratory setting. * Fundamental understanding of analytical chemistry principles and techniques. * Hands-on experience with common laboratory equipment (e.g., pH meters, balances, centrifuges, pipettes). * Strong attention to detail and ability to follow complex procedures precisely. * Proficiency in data analysis and interpretation, with experience using LIMS or similar data management systems preferred. * Excellent written and verbal communication skills. * Ability to work independently and as part of a team in a fast-paced environment. * Basic computer skills, including Microsoft Office Suite. * Knowledge of GLP/cGMP regulations is a plus. Find Your Place at Pace - We need you - your curiosity, your talents, and your drive - to help us advance this important work. Benefits When you join Pace , you commit to work that makes a positive impact on our communities and our world. We commit to supporting you with benefits and perks that make a positive impact on your life. Full-time roles are eligible for our comprehensive benefits program which includes competitive salaries, medical, dental vision, 401K retirement savings plan (100% vested immediately in the employer match), life, disability and voluntary benefits, paid time off for holiday, sick and vacation days, HSA, wellness program, flexible spending accounts, tuition reimbursement, Employee Assistance program, parental leave, optional legal coverage and ID theft. Equal Opportunity Employer Pace provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, creed, color, religion, genetics, protected veteran status, national origin, sex, age, disability, marital status, sexual orientation, gender identity or expression, citizenship, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.

About This Role Veranex has an exciting opportunity to join the Research & Strategy team. You will be part of a team working to improve lives globally through healthcare innovation. You will play a key role in planning, supporting and synthesizing a range of qualitative research projects for world-leading MedTech organizations. This role reports to the Director of Research and Strategy and collaborates with Research, Design and Development teams globally. As a Design Researcher (Level 2), you will be part of a cross-functional team that conducts global research (both virtually and in-person) to identify, capture and understand user needs, pain points and current workflow/journeys to ensure these are captured and communicated in an actionable format, and to help inform subsequent strategic decisions and product development. The ideal candidate should be an innovative, creative, and well-organized self-starter who is excited by global travel, conducting primary research (including clinical site visits) and immersing themselves in the healthcare ecosystem. What You'll Do Help to plan, conduct, and synthesize qualitative research under the guidance of a project lead and functional manager. In this role you will have a strong understanding and experience with exploratory qualitative research and be able to support conducting primary and secondary fieldwork. Support participant moderation and observations using methodologies including ethnography, contextual inquiry, formative and validation studies. Ability to draft research protocol materials including recruitment screeners, discussion guide materials, presentations and notetaking/debriefing templates. Assist with research analysis, synthesis and user need documentation, including personas, customer journey/workflow maps and storytelling methods. Support research project activities and present research updates/outputs to clients Ability to support the project team's goals. Ability to develop client presentations, capturing the design research process. Ability to work through tight deadlines by planning activities, setting expectations and pacing yourself to deliver within timeline and budget on projects. Support the adoption, development and implementation of Research and Strategy best practice approaches. Interest in staying up to date with best practices and emerging trends in human-centered design methodologies. Apply to follow and implement company and industry policies and procedures to ensure the safe and ethical delivery of design research. Support the engagement and growth of our clinical observation sites to expand our network globally. Work with Project Managers to help support clinician site observation recruitment. Assist with managing the relationships with stakeholders across our clinical sites. Support the creation and maintenance of clinical site engagement materials. Required Qualifications BFA, BS, BA or BSID in Industrial Design, Anthropology, Psychology, Human Factors Engineering, or related field. 2-4 years of experience in exploratory research. Working knowledge of design research, qualitative research and/or human centered design methodologies. Working knowledge in Microsoft Office, Adobe Creative Suite, and white boarding apps like Miro Excellent written and verbal communication skills. Excellent attention to detail Multi-tasking and time management skills with the ability to prioritize tasks. Preferred Qualifications Experience working in or with the healthcare industry, preferably medical device markets and/or have a clinical background Good visual design skills Good problem-solving skills Experience working as a consultant

I work as our Leading Scientific Hiring Recruiter for the state of Minnesota and Western Wisconsin. I hire for the following job positions: + Lab Technician + Lab Assistant + Microbiologist + Biologist + Associate Scientist + Clinical Lab Technician + Biochemist + Chemist - Formulations or Analytical + Data Analyst + Bioinformatics + Medical Sales + Animal Scientist + Lab Managers + Study Coordinators + Study Directors + Etc I hire for candidates who are entry level or who have extensive industry experience. Please apply to this positing if you are looking for any positions in this field and I would be happy discuss all of our current openings with you. You can also email me at *****************************, directly, if you prefer. Job Type & Location This is a Contract to Hire position based out of Minneapolis, MN. Pay and Benefits The pay range for this position is $30.00 - $50.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: - Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Minneapolis,MN. Application Deadline This position is anticipated to close on Feb 2, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.

**What Real World Evidence and Clinical Research contributes to Cardinal Health** The **Scientist, Real World Evidence (Clinical Research)** , will have responsibility to support the design and implementation of innovative Real-World Evidence (RWE)/Health Economics & Outcomes Research (HEOR) strategies and activities to produce scientific evidence and publications for our pharmaceutical clients, with guidance from Lead/Senior Scientists. Ideally, this individual will have experience conducting observational research studies from various data sources including administrative claims, electronic health records (EHR), or through primary data collection. This Scientist will collaborate with cross-functional teams in developing study proposals, research protocols, interpreting data, and reporting results. A majority of the work this team is involved with is focused in oncology. **_Responsibilities_** + Support the generation of high-quality real-world research studies using administrative claims, EHR, and primary data collection. + Conduct background product/disease area literature reviews. + Draft portions of research proposals, research protocols, table shells, statistical analysis plans, and study reports. + Proactively address research design and analytical issues. + Will work in a fast-paced environment engaging on multiple projects with multiple manufacturers at the same time. + Support the development of research study concepts, protocol, and reports. + Utilize appropriate research methods and data sources to deliver high-value and quality real-world research to pharmaceutical manufacturers. + Prepare proposal requests for RWE/HEOR work projects and manages selection process. + Prepare technical presentations and actively engage with the external environment in improving the state of the discipline. + Prepare HEOR data as background materials for discussion with pharmaceutical customers. + Communicate effectively and professionally with pharmaceutical HEOR customers. + Ability to provide excellent customer service when delivering work on projects. + Develop expertise in RWE/HEOR through publications and presentations of scientific research. + Collaborate with HEOR team, as required, to compile evidence required to execute projects for pharmaceutical clients. + Generate communication materials, publications, and reports. + Interact with HEOR personnel to assist with background materials for reports and publications. + Interact with HEOR staff to identify research activities and/or evidence to advance health care efficiencies for pharmaceutical clients. **_Qualifications_** + Experience with research protocol development and conducting observational research, highly preferred. + Experience (in education or through work experience) in a clinical setting, a plus. + Experience in Statistics or an individual with a degree in Public Health or Epidemiology, a plus. + Experience in Oncology, a plus but not required. + Problem-solving capability with well-developed conceptual and integrative thinking required. + Demonstrated success implementing projects, including engagement with key stakeholders, with high degree of autonomy, preferred + Excellent written and verbal communication skills, required. **_What is expected of you and others at this level_** + Applies comprehensive knowledge and a thorough understanding of concepts, principles, and technical capabilities to perform varied tasks and projects + May contribute to the development of policies and procedures + Works on complex projects of large scope + Develops technical solutions to a wide range of difficult problems. Solutions are innovative and consistent with organization objectives + Completes work independently; receives general guidance on new projects + Work reviewed for purpose of meeting objectives + May act as a mentor to less experienced colleagues **Anticipated Pay Range:** $94,900 - $122,000 **Bonus Eligible:** No **Benefits** : Cardinal Health offers a wide variety of benefits and programs to support health and well-being. + Medical, dental and vision coverage + Paid time off plan + Health savings account (HSA) + 401k savings plan + Access to wages before pay day with my FlexPay + Flexible spending accounts (FSAs) + Short- and long-term disability coverage + Work-Life resources + Paid parental leave + Healthy lifestyle programs **Application window anticipated to close** : 2/13/2025 * if interested in opportunity, please submit application as soon as possible. _** The salary range listed is an estimate. Pay at Cardinal Health is determined by multiple factors including, but not limited to, a candidate's geographical location, relevant education, experience and skills and an evaluation of internal pay equity._ _Candidates who are back-to-work, people with disabilities, without a college degree, and Veterans are encouraged to apply._ _Cardinal Health supports an inclusive workplace that values diversity of thought, experience and background. We celebrate the power of our differences to create better solutions for our customers by ensuring employees can be their authentic selves each day. Cardinal Health is an Equal_ _Opportunity/Affirmative_ _Action employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, ancestry, age, physical or mental disability, sex, sexual orientation, gender identity/expression, pregnancy, veteran status, marital status, creed, status with regard to public assistance, genetic status or any other status protected by federal, state or local law._ _To read and review this privacy notice click_ here (***************************************************************************************************************************

Site: Mass General Brigham Incorporated Mass General Brigham relies on a wide range of professionals, including doctors, nurses, business people, tech experts, researchers, and systems analysts to advance our mission. As a not-for-profit, we support patient care, research, teaching, and community service, striving to provide exceptional care. We believe that high-performing teams drive groundbreaking medical discoveries and invite all applicants to join us and experience what it means to be part of Mass General Brigham. This role is hybrid with 4 days onsite and 1 day remote. The salary range for this position is $80,000 to $110,000 annually. At Mass General Brigham, we believe in recognizing and rewarding the unique value each team member brings to our organization. Our approach to determining base pay is comprehensive, and any offer extended will take into account your skills, relevant experience, if applicable, education, certifications, and other essential factors. The base pay information provided offers an estimate based on the minimum job qualifications; however, it does not encompass all elements contributing to your total compensation package. In addition to competitive base pay, we offer comprehensive benefits, career advancement opportunities, differentials, premiums, and bonuses as applicable, and recognition programs designed to celebrate your contributions and support your professional growth. We invite you to apply, and our Talent Acquisition team will provide an overview of your potential compensation and benefits package. Job Summary The Gene and Cell Therapy Institute (GCTI) is a newly created system-wide Institute under Mass General Brigham. The Institute will foster a world-class gene and cell therapy program that will leverage ongoing, groundbreaking scientific research efforts across the MGB system. The mission of GCTI is to bring together the community of MGB investigators which can utilize gene and cell therapy platforms to achieve their scientific and clinical goals and improve the health of patients. The Institute will differentiate itself by harnessing the exceptional strengths of clinician scientists, the large and unique patient population, and major discoveries throughout the hospital system to propel MGB as the leader in Gene & Cell therapies. The Abudayyeh-Gootenberg Gene Editing lab at the Mass General Brigham Gene and Cell Therapy Institute is seeking a talented AI Scientist and Engineer to join the Mass General Brigham Gene and Cell Therapy Institute. This role will work across multiple groups within the institute, including the Abudayyeh-Gootenberg lab, gene editing core, and RNA core. The successful candidate will contribute to developing AI solutions for gene and cell therapy, support general computational efforts, and help shape strategic directions for the institute. This is a unique opportunity to work at the intersection of cutting-edge technology development and groundbreaking biomedical research. You will be part of a dynamic team focused on advancing gene therapy, cell therapy, stem cell biology, regenerative medicine, and biomanufacturing, through the application of advanced machine learning approaches. Your work will directly contribute to our understanding of large-scale data across different fields and the development of novel technologies and therapeutics. As an AI Scientist and Engineer in our institute, you will play a crucial role in developing models to understand and model large amounts of biological data, including single-cell, genomics, and transcriptomic data. This work will ultimately yield predictive and generative models that can program biology and enable new technologies and therapeutics. Your position will also be highly collaborative, involving close interaction with experimental scientists, computational biologists, and other researchers across the institute and labs. We actively encourage creativity and leadership from our computational experts, and you will have the opportunity to lead multiple projects within the institute. This role offers the exciting prospect of being at the forefront of AI applications in gene and cell therapy, with the potential to make significant contributions to the field. What We Offer: * Opportunity to work at the forefront of AI applications in gene and cell therapy * Collaboration with world-class researchers and cutting-edge technologies * Access to state-of-the-art facilities and resources * Potential to contribute to groundbreaking discoveries in regenerative medicine * Supportive and innovative work environment that encourages creativity and leadership Qualifications Qualifications: * Ph.D. in Computer Science, Computational Biology, Bioinformatics, or a related field required * Previous Research experience 5-7 years required Skills/Abilities/Competencies: * Strong programming skills and experience with machine learning frameworks * Expertise in processing and analyzing single cell data * Familiarity with deep learning models and their applications in biological data * Experience with large-scale data management and computing clusters * Knowledge of molecular biology, stem cell biology, gene therapy, and/or cell therapy is highly desirable * Excellent communication skills and ability to collaborate with multidisciplinary teams * Strong organizational and project management abilities * Ability to manage small teams towards high-level goals and priorities * Demonstrated ability to work in a fast-paced, dynamic research environment Essential Functions * Trains/mentors study staff. * Mentor a team of data analysts in statistical analysis, study design, and coding. * Overseeing progress across multiple research and evaluation projects. * Identifies, assimilates, and synthesizes data needed for computer models and manages databases relating to statistical and related software. * Work closely with cross-functional teams (analytical chemistry, sensory, applications & flavor creation) to achieve desired results. * Lead internal encapsulation science research program as well as external research collaborations. * Design, execute and interpret research experiments * Analyze and present data at internal and external meetings. * Performs other duties as assigned * Complies with all policies and standards Additional Job Details (if applicable) Remote Type Hybrid Work Location 65 Landsdowne Street Scheduled Weekly Hours 40 Employee Type Regular Work Shift Day (United States of America) EEO Statement: 0100 Mass General Brigham Incorporated is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religious creed, national origin, sex, age, gender identity, disability, sexual orientation, military service, genetic information, and/or other status protected under law. We will ensure that all individuals with a disability are provided a reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. To ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Veteran's Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact Human Resources at **************. Mass General Brigham Competency Framework At Mass General Brigham, our competency framework defines what effective leadership "looks like" by specifying which behaviors are most critical for successful performance at each job level. The framework is comprised of ten competencies (half People-Focused, half Performance-Focused) and are defined by observable and measurable skills and behaviors that contribute to workplace effectiveness and career success. These competencies are used to evaluate performance, make hiring decisions, identify development needs, mobilize employees across our system, and establish a strong talent pipeline.

Shift: Monday through Friday, 8:30 AM - 5:00 PMAre you ready to work making the world a safer, healthier place? Join our mission to continuously move science forward; to innovate and advance all aspects of our business to improve the health and safety of our communities and lives. *SUMMARY* Responsible for providing or overseeing the analysis, administration and oversight of standard chemistry/biochemistry policies, programs and practices; feedback and guidance regarding the analysis of samples using fundamental professional and technical knowledge of chemistry/biochemistry or related instrumentation, wet chemistry testing, and procedures. Compensation: $23.00 per hour *ESSENTIAL FUNCTIONS* * Provides fundamental analysis in support of standard testing materials, products and/or devices utilizing standard analytical instrumentation; follows Standard Operating Procedures and methods to perform testing. * Provides fundamental review, analysis, interpretation, and documentation of testing results. * Overseeing or reviewing, completing, and processing various types of standard chemistry/biochemistry forms, documents, databases, and related materials and information. * Provides fundamental analysis and interpretation and counsel to staff, management, and functional leaders regarding chemistry/biochemistry policies, programs, and practices; involves standard operations. * Provides standard research, feedback, and decisions to resolve management and employee questions and requirements; assists with receiving customer feedback and coordinating resources and responses as required. * Analyzes and reviews process, results, feedback, and related chemistry/biochemistry information on an ongoing to as needed basis to determine trends, draw conclusions, interpret findings, and presents results, proposals, and recommendations to management. * Ensures the accuracy of more fundamental tests, equipment, actions, procedures and operational databases, reports, and related details through audits, queries, and operational reviews; works with teams to resolve discrepancies; resolves discrepancies or escalates discrepancies to ensure quality assurance in testing process/results. * Assists with developing or participating in chemistry/biochemistry or cross functional project or program objectives, which includes proposed budgets, timelines, materials, personnel, and other project requirements, receives direction, and presents information to management. * Cleans, maintains, prepares, and calibrates equipment, samples, and related areas. * Interprets and applies department policies and procedures and assists with applicable laws, rules, and regulations; receives guidance within these areas as needed. * Contributes to the efficiency and effectiveness of the department's service to its customers by offering suggestions and directing or participating as an active member of a work team. * Promotes and supports the overall mission of Pace Analytical by demonstrating courteous and cooperative behavior when interacting with customers and staff; acts in a manner that promotes a harmonious and effective workplace environment. *QUALIFICATIONS* *Education and Experience* Bachelor's degree in chemistry/biochemistry, or a closely related field; OR an equivalent combination of education, training, and experience. *Required Knowledge and Skills* *Required Knowledge* * Fundamental principles, practices, and techniques of chemistry/biochemistry. * Standard understanding of the administration and oversight of chemistry/biochemistry programs, policies, and procedures. * Fundamental methods to resolve chemistry/biochemistry problems, questions, and concerns. * Standard understanding of applicable chemistry/biochemistry laws, codes, and regulations. * Understanding of standard testing tools, instruments, and calibration. * Computer applications and systems related to the work. * Principles and practices to serving as an effective project team member. * Methods to communicate with staff, coworkers, and customers to ensure safe, effective, and appropriate operations. * Correct business English, including spelling, grammar, and punctuation. *Required Skills* * Performing fundamental professional-level chemistry/biochemistry duties in a variety of assigned areas. * Overseeing and administering standard chemistry/biochemistry functions. * Training others in policies and procedures related to the work. * Serving as a team member and the development and management of projects. * Operating in a both a team and individual contributor environment. * Interpreting, applying, and explaining applicable laws, codes, and regulations. * Preparing fundamental functionals reports, correspondence, and other written materials. * Using initiative and independent judgment within established department guidelines. * Using tact, discretion, and prudence in working with those contacted in the course of the work. * Performing effective oral presentations to large and small groups across functional peers and the department. * Contributing effectively to the accomplishment of team or work unit goals, objectives and activities. * Establishing and maintaining effective working relationships with a variety of individuals contacted in the course of the work. Find Your Place at Pace - We need you - your curiosity, your talents, and your drive - to help us advance this important work. Benefits When you join Pace , you commit to work that makes a positive impact on our communities and our world. We commit to supporting you with benefits and perks that make a positive impact on your life. Full-time roles are eligible for our comprehensive benefits program which includes competitive salaries, medical, dental vision, 401K retirement savings plan (100% vested immediately in the employer match), life, disability and voluntary benefits, paid time off for holiday, sick and vacation days, HSA, wellness program, flexible spending accounts, tuition reimbursement, Employee Assistance program, parental leave, optional legal coverage and ID theft. *Equal Opportunity Employer* Pace provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, creed, color, religion, genetics, protected veteran status, national origin, sex, age, disability, marital status, sexual orientation, gender identity or expression, citizenship, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. The Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 50 countries. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. Job Description The SST Associate Scientist I shall assist other SST Laboratory personnel in general lab duties. The SST Associate Scientist I shall be responsible for ensuring quality and accurate data in a timely fashion. Responsibilities and Duties General: Communicate effectively internally and externally. Work cooperatively. Propose and communicate process improvements for technical area. Participate in general laboratory maintenance. Ensure quality and accurate data in a timely fashion in all processes in a given area. Follow work instructions and direct sample flow for efficiency. Perform sample analysis and document results. Participate in lab and equipment maintenance. Communicate inventory needs to appropriate staff. Communicate sample/test issues to appropriate responsible manager. Identify and report any opportunities to improve efficiency, customer satisfaction, and quality. Perform their assigned tasks according to company procedures and work instructions in the most cost-effective way. May be required to sit for 8 hours; May be required to stand for 8 hours. Specific: Ensure ALL goals are met for the day and encourage others to meet their goals as well. Will perform evaluation tests according to work instructions and follow AOSA, Canada, or ISTA rules depending on testing requested. Performs tasks as defined by lab manager. Be able to drive the process and motivate individuals to get the work done. Ensure the consistent and repeatability of results in a timely fashion. Propose and communicate process improvements for planting and/or evaluation. Be able to evaluate TZ Tests (both Post Germ and straight TZ Tests). Maintain appropriate inventory and organizing supplies. Based on years of experience, be able to guide or assist newer staff with questions. Direct newer staff in the right direction if the answer of the question is unknown. Ensure accurate and efficient execution of work instructions. Minimize the number of mistakes made throughout the workday/week. Reliable work schedule. During the months of October through March, may be requested to work (but not required) at least 45 hours per week to assist the lab manager in maintaining the SST lab. Qualifications Education/Experience: HS degree recommended with an aptitude for science. Certificates/Licenses: Certification by the Society of Commercial Seed Technologists is recommended. Supervisory Responsibilities: None required. Skills: Attention to detail, ability to maintain focus, mental addition and subtraction, computer operation including email and LIMS. Be able to work under pressure to meet deadlines for test completion, be self- motivated, understand priorities, willingness to learn new things, gets along with team members, takes the initiative, and be flexible. Other Factors: None required. Additional Information Schedule: Monday-Friday 8:00am-4:30pm What we offer: Excellent full time benefits including comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays Eurofins USA Genomic Services is a Disabled and Veteran Equal Employment Opportunity employer.

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. The Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 50 countries. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. Job Description The SST Associate Scientist I shall assist other SST Laboratory personnel in general lab duties. The SST Associate Scientist I shall be responsible for ensuring quality and accurate data in a timely fashion. Responsibilities and Duties General: Communicate effectively internally and externally. Work cooperatively. Propose and communicate process improvements for technical area. Participate in general laboratory maintenance. Ensure quality and accurate data in a timely fashion in all processes in a given area. Follow work instructions and direct sample flow for efficiency. Perform sample analysis and document results. Participate in lab and equipment maintenance. Communicate inventory needs to appropriate staff. Communicate sample/test issues to appropriate responsible manager. Identify and report any opportunities to improve efficiency, customer satisfaction, and quality. Perform their assigned tasks according to company procedures and work instructions in the most cost-effective way. May be required to sit for 8 hours; May be required to stand for 8 hours. Specific: Ensure ALL goals are met for the day and encourage others to meet their goals as well. Will perform evaluation tests according to work instructions and follow AOSA, Canada, or ISTA rules depending on testing requested. Performs tasks as defined by lab manager. Be able to drive the process and motivate individuals to get the work done. Ensure the consistent and repeatability of results in a timely fashion. Propose and communicate process improvements for planting and/or evaluation. Be able to evaluate TZ Tests (both Post Germ and straight TZ Tests). Maintain appropriate inventory and organizing supplies. Based on years of experience, be able to guide or assist newer staff with questions. Direct newer staff in the right direction if the answer of the question is unknown. Ensure accurate and efficient execution of work instructions. Minimize the number of mistakes made throughout the workday/week. Reliable work schedule. During the months of October through March, may be requested to work (but not required) at least 45 hours per week to assist the lab manager in maintaining the SST lab. Qualifications Education/Experience: HS degree recommended with an aptitude for science. Certificates/Licenses: Certification by the Society of Commercial Seed Technologists is recommended. Supervisory Responsibilities: None required. Skills: Attention to detail, ability to maintain focus, mental addition and subtraction, computer operation including email and LIMS. Be able to work under pressure to meet deadlines for test completion, be self- motivated, understand priorities, willingness to learn new things, gets along with team members, takes the initiative, and be flexible. Other Factors: None required. Additional Information Schedule: Monday-Friday 8:00am-4:30pm What we offer: Excellent full time benefits including comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays Eurofins USA Genomic Services is a Disabled and Veteran Equal Employment Opportunity employer.

Job 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 has just closed a $20M financing round 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, positively aggressive scienist, join us as we solve one of the greatest environmental challenges of our time. Position Overview: The Associate Scientist will work closely with the technological development team focused on industrial PFAS wastewater treatment on the lab scale. The duty of this position includes the evaluation of our destruction system performance on customer-specific wastewater and the fundamental exploration of reaction chemistry. The Associate Scientist will also assist in processing data, preparing customer reports, and patent e. The selected candidate will receive thorough training in experimental procedures and data presentation techniques. Essential Job Functions: Become the expert on the operation of Claros PFAS destruction technology Evaluate and execute adjustments as necessary to Claros solutions to ensure the technology meets customer specifications Complete experiments in aid of customer proposals, implementations, and continued operation of Claros PFAS destruction technology Partner with internal stakeholders to ensure the successful implementation and operation of Claros solutions Perform experiments independently with occasional guidance from senior team members Keep a clean and safe workplace both inside and outside of the laboratory Competencies & Skills: Adequate knowledge of water/wastewater treatment processes Strong background in water chemistry An eagerness to learn new skills and acquire new knowledge in the field of water treatment Strong writing skills Excellent teamwork skills, with a collaborative spirit and the ability to work effectively in a diverse team environment Management of multiple projects timelines/tasks Preferred Experience: Bachelor's or master's degree in environmental engineering/chemical engineering/chemistry/atomic physics or a related field 1-2 years experience working with wastewater treatments, preferably with PFAS (inclusive of academic experience) Attention to detail Job Specifications Compensation: $62,000 - $72,000 Location: In person at the Claros Headquarters in Minneapolis, Minnesota. Travel: none 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 ****************** 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.

I work as our Leading Scientific Hiring Recruiter for the state of Minnesota and Western Wisconsin. I hire for the following job positions: * Lab Technician * Lab Assistant * Microbiologist * Biologist * Associate Scientist * Clinical Lab Technician * Biochemist * Chemist - Formulations or Analytical * Data Analyst * Bioinformatics * Medical Sales * Animal Scientist * Lab Managers * Study Coordinators * Study Directors * Etc I hire for candidates who are entry level or who have extensive industry experience. Please apply to this positing if you are looking for any positions in this field and I would be happy discuss all of our current openings with you. You can also email me at *****************************, directly, if you prefer. Job Type & Location This is a Contract to Hire position based out of Minneapolis, MN. Pay and Benefits The pay range for this position is $30.00 - $50.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Minneapolis,MN. Application Deadline This position is anticipated to close on Feb 2, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

The University of St. Thomas invites qualified candidates to apply for a Postdoctoral Scholar position at the Center for Microgrid Research. The position will support the Center's research on reliability, security, and resilience of microgrid systems. This includes advanced control system design, modeling and analysis, control architecture design and communication-based control and optimization, system integration and testing. The successful candidate will be required to conduct independent research, develop new ideas and contribute to research proposals, engage with faculty, staff, and students, prepare manuscripts for publication, and present their work at conferences. JOB SUMMARY The St. Thomas Center for Microgrid Research (CMR) is seeking candidates for a postdoctoral scholar position in the area of microgrid control. The scholar will be part of a rapidly growing team of engineers and researchers and will have a unique opportunity to work simultaneously on a real-world industry-grade microgrid and state-of-the-art Hardware-in-the-loop HIL testbeds. Essential functions: Develop innovative solutions and technical approaches to design, modeling, and implementation of advanced control systems in microgrid applications. Create a digital twin of the current and planned microgrid and test control systems on the digital twin and real-world microgrid Serve as lead author on project reports, journal articles, conference papers, and presentations. Develop experimental test plans to collect data to validate modeling and analysis work. Leads and supports technical proposals for developing new projects Meet grant goals and deliverables by completing assigned research tasks and reports. Supervise and lead student researchers (undergraduate and graduate). Work closely with the Center's director and the CMR team. Contributes to the overall success of the Center by performing other essential duties and responsibilities as assigned. JOIN OUR COMMUNITY The University of St. Thomas offers a competitive and comprehensive benefits program, which includes: Tuition Remission for employees, spouses, and dependents Generous Retirement Contributions to support your future Comprehensive Health Coverage including medical, dental, and vision Fully Paid Insurance: disability, life, and AD&D Paid Parental Leave to support growing families This position is grant-funded. We anticipate this to be a one year, benefits-eligible term appointment, dependent on the needs of the department. The position duration is renewable to up to 3 years depending on performance, department needs, and availability of funds. Salary Range: $54,830 to $57,576 The University of St. Thomas has provided a salary range that represents its good faith estimate of what the University may pay for the position at the time of posting. The specific salary offered will be determined based on factors such as the qualifications of the selected candidate, departmental budget, internal salary equity considerations, and available market information. ABOUT US: The University of St Thomas School of Engineering: The University of St Thomas School of Engineering (SOE) is a primarily undergraduate teaching institution focusing on engineering education within the context of a liberal arts framework. As part of the largest private university in Minnesota, the School of Engineering comprises nearly 15% of the campus population. The UST School of Engineering offers undergraduate and masters level programs in the areas of Electrical Engineering, Data Science, Software Engineering, Mechanical Engineering, Civil engineering, and Manufacturing Engineering. The Center for Microgrid Research: The Center for Microgrid Research is in the midst of an exciting growth phase with more than $25 Million grants from the National Science Foundation (NSF), Department of Defense (DOD), and Minnesota Department of Commerce. In the next year, it is anticipated that the CMR team will grow to more than 10 full-time staff and 15 student researchers. Through the awards, the Center's infrastructure is expanding in capability and size. The microgrid's on-site generation capacity is increasing to more than 1.5 MW to feed power to 5 buildings on campus, covering more than 400,000 sq. ft. of space. The expanded microgrid will be made up of 2 smaller microgrids and have 4 points of connection with the local utility resulting in a unique networked-microgrids layout. The research and development infrastructure is growing to include state-of-the-art Hardware-in-the-loop (HIL) testbeds for controller-HIL, power-HIL, and power-system-HIL. Research findings developed and prototyped on the HIL testbeds will be immediately applied to the real-world microgrid for real-world case studies and experiments. Moreover, the CMR's industry partnership network is rapidly broadening. As an example, the CMR is a founding member of the Minnesota Cleantech Consortium which includes 3M, Cummins, Xcel Energy, Connexus, Great Plains Institute, and many others. The University of St. Thomas embraces belonging and equal opportunity for all. Our convictions of dignity, diversity and personal attention call us to embody and champion an inclusive environment. The University is an Equal Employment Opportunity Employer (EEO). All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, status as a protected veteran, or other protected characteristic. This commitment to inclusion and equal opportunity is consistent with our mission: Inspired by Catholic intellectual tradition, the University of St. Thomas educates students to be morally responsible leaders who think critically, act wisely, and work skillfully to advance the common good. A successful candidate will possess a commitment to the ideals of this mission. QUALIFICATIONS Minimum Qualifications Completed a PhD degree (U.S. or foreign equivalent), in Electrical Engineering, Energy Engineering, or a closely related. Proven expertise in microgrid modeling and controls in Matlab/Simulink or similar Demonstrated publication record Proven communication, time management, and teamwork skills This project is funded by the Department of Defense. Export control laws define US person as US citizen, permanent resident (green card), or refugee/asylee. DoD restrictions on project personnel exist for some, but not all, non-US persons such as citizens from China, Iran, and Russia Preferred Qualifications Experience with modeling high power systems such as advanced inverters (grid-forming techniques), generators, flywheels, motors, Electric vehicles chargers, or nonlinear loads Experience in hardware-in-the-loop testbeds and digital twin creation Experience with SEL RTAC 3555 or similar Experience in advanced microgrid controls such as nonlinear methods and data-driven techniques. HOW TO APPLY Apply online at ******************************* After creating and submitting an applicant profile, you will be taken to the job-specific application. Here you will be asked to copy/paste a cover letter, detailing your interest in the position. Additionally, upload the following materials to your profile: Curriculum vitae with a list of publications Complete the reference section of the application by providing contact information for 3 professional references. No references will be contacted without first getting the permission of the candidate. In light of its commitment to create and maintain a safe learning and working environment, employment with the University of St. Thomas requires consent and successful completion of a background screening. The University of St. Thomas, Minnesota Human Resources Department advertises the official job listing on its website at ********************** The University of St. Thomas is an Equal Opportunity Employer

Shift: Monday through Friday, 8:30 AM - 5:00 PM Are you ready to work making the world a safer, healthier place? Join our mission to continuously move science forward; to innovate and advance all aspects of our business to improve the health and safety of our communities and lives. SUMMARY Responsible for providing or overseeing the analysis, administration and oversight of comprehensive chemistry/biochemistry policies, programs and practices; may provide feedback and guidance to clients regarding the analysis of materials, products and/or devices utilizing complex to specialized professional and technical knowledge of chemistry/biochemistry/formulation development or related equipment, testing, and procedures. May design and develop robust and scalable formulations for small molecules and biologics for early-stage clinical trials. May develop and optimize manufacturing processes for drug products. May interpret analytical data to guide formulation and process development decisions. Compensation: $23.00 per hour ESSENTIAL FUNCTIONS Serves as a lead to staff to include providing work direction, guidance, and training. Overseeing or reviewing, completing, and processing comprehensive types of forms, documents, databases, and related materials and information. Provides complex to specialized analysis in support of various testing materials, products and/or devices utilizing various analytical instrumentation; follows Standard Operating Procedures and methods to perform testing. Provides complex to specialized review, analysis, interpretation, and documentation of testing results. Analyzes and reviews complex to specialized operations, results, feedback, and related chemistry/biochemistry/formulation information on an as needed basis to determine trends, draw conclusions, interpret findings, and presents results, proposals, and recommendations to management and/or clients. Provides training and guidance on analytical tests, methods, and instrumentation, as required. Provides complex to specialized analysis, interpretation and counsel to clients, staff, management, and functional leaders regarding chemistry/biochemistry policies, programs, and practices; involves broad operations and leading implementation and change. Analyzes and reviews complex to specialized operations, results, feedback, and related chemistry/biochemistry/formulation information on an ongoing to as needed basis to determine trends, draw conclusions, interpret findings, and presents results, proposals, and recommendations to management and/or clients. Assists with developing or participating in chemistry/biochemistry/formulation or cross functional project or program objectives, which includes proposed budgets, timelines, materials, personnel, and other project requirements, receives direction, and presents information to management and/or clients. Develop validate and transfer analytical methods. Provide routine and non-routine analysis using instruments such as HPLC, GC, LC-MS, and FTIR, among others. Design and develop robust and scalable formulations for small molecules and biologics for early-stage clinical trials. May develop and optimize manufacturing processes for drug products. Ensure all activities adhere to SOP's, regulatory guidelines, GLP and GMP standards. Contributes to the efficiency and effectiveness of the department's service to its customers by offering suggestions and directing or participating as an active member of a work team. Promotes and supports the overall mission of Pace Analytical by demonstrating courteous and cooperative behavior when interacting with customers and staff; acts in a manner that promotes a harmonious and effective workplace environment. QUALIFICATIONSEducation and Experience Bachelor's degree in chemistry/biochemistry, or a closely related field Required Knowledge and SkillsRequired Knowledge Complex to specialized principles, practices, and techniques of chemistry/biochemistry and formulation development. Broad understanding of the administration and oversight of chemistry/biochemistry programs, policies, and procedures. Complex to specialized methods to resolve chemistry/biochemistry problems, questions, and concerns. Broad understanding of applicable chemistry/biochemistry laws, codes, and regulations. Understanding of broad testing tools, equipment, and calibration. Computer applications and systems related to the work. Principles and practices to serving as an effective project team member. Methods to communicate with staff, coworkers, and customers to ensure safe, effective, and appropriate operations. Correct business English, including spelling, grammar, and punctuation. Required Skills Performing complex to specialized professional-level chemistry/biochemistry duties in a variety of assigned areas. Overseeing and administering broad and varied chemistry/biochemistry/formulation functions. Ability to operate and train others in analytical instruments and manufacturing equipment. Training others in policies and procedures related to the work. Serving as a team member and the development and management of projects. Operating in a both a team and individual contributor environment. Interpreting, applying, and explaining applicable laws, codes, and regulations. Preparing advanced to expert functionals reports, correspondence, and other written materials. Using initiative and independent judgment within established department guidelines. Using tact, discretion, and prudence in working with those contacted during the work. Performing effective oral presentations to large and small groups across functional peers and the department. Contributing effectively to the accomplishment of team or work unit goals, objectives and activities. Establishing and maintaining effective working relationships with various individuals contacted in the work. Find Your Place at Pace - We need you - your curiosity, your talents, and your drive - to help us advance this important work. Benefits When you join Pace , you commit to work that makes a positive impact on our communities and our world. We commit to supporting you with benefits and perks that make a positive impact on your life. Full-time roles are eligible for our comprehensive benefits program which includes competitive salaries, medical, dental vision, 401K retirement savings plan (100% vested immediately in the employer match), life, disability and voluntary benefits, paid time off for holiday, sick and vacation days, HSA, wellness program, flexible spending accounts, tuition reimbursement, Employee Assistance program, parental leave, optional legal coverage and ID theft. Equal Opportunity Employer Pace provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, creed, color, religion, genetics, protected veteran status, national origin, sex, age, disability, marital status, sexual orientation, gender identity or expression, citizenship, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.

Site: The General Hospital Corporation Mass General Brigham relies on a wide range of professionals, including doctors, nurses, business people, tech experts, researchers, and systems analysts to advance our mission. As a not-for-profit, we support patient care, research, teaching, and community service, striving to provide exceptional care. We believe that high-performing teams drive groundbreaking medical discoveries and invite all applicants to join us and experience what it means to be part of Mass General Brigham. Job Summary Responsible for maintaining laboratory equipment, organizing and preparing samples, conducting experiments, and recording and analyzing data. Candidates who are in the process of completing their bachelor's degree have a grace period of six months from their hire date (up to 1 year if starting per diem) to provide degree equivalency verification. Does this position require Patient Care? No Essential Functions * Perform laboratory experiments following established protocols and procedures. * Prepare and handle samples, reagents, and solutions, ensuring accuracy and adherence to safety guidelines. * Operate and maintain laboratory equipment and instruments, conducting routine calibration and troubleshooting as needed. * Record experimental data accurately and maintain organized records of procedures, protocols, and results. * Compile and analyze data using appropriate statistical and analytical methods. * Assist in data interpretation and presentation, contributing to research findings and reports. Qualifications Education Bachelor's Degree Related Field of Study required Can this role accept experience in lieu of a degree? Yes Licenses and Credentials Experience Prior laboratory experience, either through academic coursework, internships, or employment 1-2 years preferred Knowledge, Skills and Abilities * Strong theoretical and practical knowledge of laboratory techniques and procedures. * Familiarity with common laboratory equipment and instruments used in research experiments. * Proficiency in data collection, analysis, and scientific software tools. * Excellent attention to detail, organizational skills, and the ability to multitask and prioritize tasks effectively. * Strong problem-solving skills and the ability to troubleshoot technical issues. * Excellent written and verbal communication skills to effectively convey experimental procedures, results, and challenges. Additional Job Details (if applicable) Remote Type Onsite Work Location 600 Main Street Scheduled Weekly Hours 40 Employee Type Regular Work Shift Day (United States of America) Pay Range $19.76 - $28.44/Hourly Grade 5 At Mass General Brigham, we believe in recognizing and rewarding the unique value each team member brings to our organization. Our approach to determining base pay is comprehensive, and any offer extended will take into account your skills, relevant experience if applicable, education, certifications and other essential factors. The base pay information provided offers an estimate based on the minimum job qualifications; however, it does not encompass all elements contributing to your total compensation package. In addition to competitive base pay, we offer comprehensive benefits, career advancement opportunities, differentials, premiums and bonuses as applicable and recognition programs designed to celebrate your contributions and support your professional growth. We invite you to apply, and our Talent Acquisition team will provide an overview of your potential compensation and benefits package. EEO Statement: 1200 The General Hospital Corporation is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religious creed, national origin, sex, age, gender identity, disability, sexual orientation, military service, genetic information, and/or other status protected under law. We will ensure that all individuals with a disability are provided a reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. To ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Veteran's Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact Human Resources at **************. Mass General Brigham Competency Framework At Mass General Brigham, our competency framework defines what effective leadership "looks like" by specifying which behaviors are most critical for successful performance at each job level. The framework is comprised of ten competencies (half People-Focused, half Performance-Focused) and are defined by observable and measurable skills and behaviors that contribute to workplace effectiveness and career success. These competencies are used to evaluate performance, make hiring decisions, identify development needs, mobilize employees across our system, and establish a strong talent pipeline.

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. The Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 50 countries. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. Job Description The GTS Department is dedicated to supporting ELISA/HB planting, harvesting, extraction, and testing; DNA QA grinding, plating, and testing; MBGT planting, plating and testing; Electrophoresis planting, plating, extraction and testing. The GTS Department includes genetic purity testing using Isozyme Electrophoresis, trait purity testing using ELISA/Herbicide Bioassay testing, and adventitious presence and zygosity testing using in DNA QA using PCR. The DNA Associate Scientist is responsible for helping in all activities, as directed, for the GTS/MBGT work streams, with primary focus in DNA extraction, testing, and data analysis. Responsibilities and Duties General: Communicate effectively internally and externally Work cooperatively Participate in general laboratory maintenance Effectively communicate sample/internal issues to Manager and/or Group Lead as appropriate Effectively communicate personnel issues to Manager and/ or Group Lead Specific: Assist with the creation of plate maps for DNA QA Assist in DNA QA extraction, testing, data analysis, and reporting Become proficient in all areas of GTS planting/sample prep/evaluating/harvesting/extraction/testing Help, support and maintain EBDI Safety program Help, support and maintain EBDI ISO quality system Ensure accurate and efficient execution of written protocols Technical training on equipment/processes in different labs as needed Other duties as needed Qualifications Education/Experience: High school and science aptitude Certificates/Licenses: NA Supervisory Responsibilities: None required Skills: Attention to detail Flexible Good communication skills Other Factors: Eager to learn Additional Information Schedule: Monday-Friday 8:00am-4:30pm What we offer: Excellent full time benefits including comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays Eurofins USA Genomic Services is a Disabled and Veteran Equal Employment Opportunity employer.

Shift: Monday through Friday, 8:00 AM - 5:00 PM Are you ready to work making the world a safer, healthier place? Join our mission to continuously move science forward; to innovate and advance all aspects of our business to improve the health and safety of our communities and lives. This is a full-time, onsite, Scientist 1 position located in Minneapolis, MN, Monday through Friday, 8:00 a.m. - 5:00 p.m. Compensation: $22.00 per hour Make an impact. Build a career. At Pace , everything we do is built upon an unwavering commitment to making the world a safer, healthier place. We continually work to develop innovative practices that drive sustainability and empower our partners with accurate, quality data at every critical moment and milestone. That's why we need you -- your curiosity, your talents, and your drive -- to help us advance this important work, and your career. Find your place at Pace Join us as a Scientist I, where you'll put your love of science to work performing and overseeing projects within the wet chemistry department of our environmental testing laboratory. What you'll do Facilitate and support the analysis, administration, and oversight of air, water, and soil samples using standard chemistry/ biochemistry policies, programs, and practices Clean, maintain, and calibrate instruments Maintain detailed and organized documentation on all laboratory work What you'll bring Bachelor's degree in Chemistry/ Biochemistry or a closely related field, or an equivalent combination of education, training and experience Ability to perform work in a lab or office setting, remain standing for long periods while conducting tests, work around strong smells, and wear personal protective equipment while handling samples (e.g., lab coat, safety glasses, and gloves; all PPE provided by Pace ). What we promise Comprehensive benefit program, including medical, vision, and dental insurance, 401(k) matching, and tuition reimbursement Opportunities to build a rewarding career An inclusive culture that stands for integrity, innovation, and growth PHYSICAL/MENTAL REQUIREMENTS: The physical demands described herein are representative of those that must be met by an employee to successfully perform the essential functions of the job. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. Mobility to work in a lab and office setting, use standard office and lab equipment and stamina to sit for extended periods of time; exerting up to 20 pounds of force occasionally and/or up to 10 pounds of force frequently to lift, carry, push, pull or move objects; vision to read printed materials and computer screens; and hearing and speech to communicate in person or over the telephone. WORKING ENVIRONMENT: Work is performed in a lab and office setting. Work is subject to chemicals, fumes, gases, noxious odors, and related items in a lab and sample setting. Find Your Place at Pace - We need you - your curiosity, your talents, and your drive - to help us advance this important work. Benefits When you join Pace , you commit to work that makes a positive impact on our communities and our world. We commit to supporting you with benefits and perks that make a positive impact on your life. Full-time roles are eligible for our comprehensive benefits program which includes competitive salaries, medical, dental vision, 401K retirement savings plan (100% vested immediately in the employer match), life, disability and voluntary benefits, paid time off for holiday, sick and vacation days, HSA, wellness program, flexible spending accounts, tuition reimbursement, Employee Assistance program, parental leave, optional legal coverage and ID theft. Equal Opportunity Employer Pace provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, creed, color, religion, genetics, protected veteran status, national origin, sex, age, disability, marital status, sexual orientation, gender identity or expression, citizenship, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.