Research fellow jobs in Grand Forks, ND

At my client's cutting-edge biotech organization, innovation fuels discovery in the cell, gene, and virus therapy space. This is your chance to join a collaborative team working to transform scientific breakthroughs into life-saving treatments. You'll help define the molecular backbone of tomorrow's medicines-impacting the future of cancer and rare disease therapies. Why You Should Apply Join a mission-driven team accelerating the next generation of cell and gene therapies Hands-on innovation with viral vectors, CRISPR tools, and molecular assay design Work in a collaborative, PhD-led environment that values discovery and scientific integrity Comprehensive benefits including health, dental, vision, life insurance, PTO, and employer-matched IRA What You'll Be Doing Design, develop, and optimize molecular assays to support gene and cell therapy programs Perform advanced PCR (qPCR, dPCR), cloning, and NGS-based analyses Conduct CRISPR-based screening and vector validation projects Interpret data, generate technical reports, and present findings to cross-functional teams Support assay development and QC testing within a dynamic, discovery-focused lab About You Strong expertise in molecular biology, including qPCR/dPCR and NGS workflows Comfortable with CRISPR systems and viral vector design Adept at bioinformatics and data interpretation for molecular assays Thrive in a fast-paced, collaborative environment focused on innovation How To Apply We'd love to see your resume, but we don't need it to have a conversation. Send us an email to ************************* and tell me why you're interested. Or, feel free to email your resume. Please include Job#19593.

Classification $85,000-130,000+ Dependent on Experience, plus annual Administrative Stipend,12-month contract, Exempt 40 hours per week will work onsite at UND Grand Forks, ND campus Purpose of Position The UND College of Engineering & Mines (CEM) is seeking to hire an assistant, associate, or full research professor in Chemical Engineering, with specific research expertise in chemical process engineering and energy systems. This will be a 12-month, non-tenure track position at a rank based on the candidate's documented record of achievement. The successful candidate will also serve as the Director of UND's Center for Process Engineering Research (CPER), one of five research centers managed through the CEM Research Institute. This position will direct CEM's largest research center, CPER, which consists of a multidisciplinary team of faculty, staff, and student researchers performing primarily applied research and technology development in the broad area of process engineering. CPER has established nationally recognized research programs in three primary focus areas: 1) critical minerals and materials, 2) carbon management and advanced fuels, and 3) battery materials and battery technologies. The position includes both administrative leadership and research duties aimed at continuing the success and growth of CPER. Duties & Responsibilities Identify and attract project opportunities and support for research initiatives by actively pursuing state, federal and private sector funding Administrative and strategic leadership of the Center for Process Engineering Research Management and coordination of personnel, facilities, equipment, and financial resources necessary for effective Center operations Execute an externally funded research portfolio as an individual PI or project manager that integrates Center research staff/faculty and graduate student research and graduate student advising, contributing to the academic and research missions of CEM and UND. Required Competencies Broad knowledge of chemical process engineering as a technical field and its application to areas of CPER strengths, including critical minerals and materials, carbon management and advanced fuels, and battery materials and technologies. Deep experience with techno-economic analysis Experience with lifecycle analysis and various process simulation tools, such as AspenPlus. Minimum Requirements PhD in chemical engineering or closely related discipline Documented and proven record of securing external research funding and managing large multidisciplinary research teams ($1+ million projects with external collaborators). Experience in collaborating with industry and small businesses/startups. Experience working with graduate and undergraduate students Successful completion of a Criminal History Background Check In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the US and to complete the required employment eligibility verification form upon hire. This position does not support visa sponsorship for continued employment. Preferred Qualifications Associate or Full Professor candidates must meet the school/college/university standards for appointment to the rank, including significant experience/accomplishments in the candidate's area of expertise. Full Professor candidates must also have national distinction, international recognition, and a substantial scholarly record in the candidate's area of expertise Demonstration of progressive leadership accomplishments in an academic/research organization. Specific experience in being awarded funding from the U.S. Department of Energy Experience with intellectual property development, demonstrated by issued or pending patents or invention disclosures with appropriate entities (e.g., a University technology transfer office). North Dakota energy industry knowledge and experience, and broad industry connections. To Apply To assure full consideration, applications must be received by October 15, 2025 and include the following materials: Cover letter Resume/CV Unofficial transcripts. Please note that the selected candidate will be required to submit official transcripts upon hire. Position is open until filled. Questions can be directed to the Department Chair, Dan Laudal at *********************.

HealthPartners Institute is seeking a Physician Research Investigator - Dementia Research with both clinical and research experience in Alzheimer's disease and related dementias, age-related cognitive decline, or dementia caregiving. Candidates with prior experience in investigator-initiated clinical trials are strongly encouraged to apply. Applicants with expertise in health services research, clinical decision support, or implementation science will also be considered. Research Investigators at HealthPartners Institute may obtain or maintain external academic appointments. Eligible candidates would be encouraged to practice part-time as a neurologist or geriatrician within the HealthPartners Center for Memory & Aging, as part of a multidisciplinary team caring for people with dementia. At HealthPartners Institute, Researcher Investigators are expected to support and develop externally funded research programs, conduct nationally and internationally recognized scholarly clinical or health services research, and collaborate with other investigators, clinicians, and leaders to improve health outcomes and care delivery. Successful candidate(s) will be accountable for conceptualizing and designing research projects, leading, and collaborating on such projects, and disseminating research results through presentations and publication in peer-reviewed journals and conferences. Service on committees and participation in scientific peer-review processes are also expected. HealthPartners Institute Research Investigators are primarily supported through grants and contracts from external sources, including the National Institutes of Health (NIH), Centers for Disease Control and Prevention (CDC), and the Patient-Centered Outcomes Research Institute (PCORI). HealthPartners Institute is focused on improving health and well-being through research, education, and practice. Our Research Investigators are embedded in an integrated health system and our research draws on rich clinical data derived from a comprehensive, fully integrated state-of-the-art electronic medical and dental record and claims data from over a million HealthPartners patients and members. Required Qualifications: MD/DO or equivalent degree and clinical experience in geriatrics, neurology, or related discipline Current Minnesota Medical license or eligible for MN medical license, based on active medical license in another state and in good standing. Prior record leading research projects and independent scholarly publications in the peer-reviewed scientific literature Strong methodologic expertise Strong interpersonal skills Strong oral and written communication skills Preferred Qualifications: Master's degree in public health or similar formal training in research methodology Early to mid-career investigator with demonstrated potential to lead active portfolio of externally funded research. Demonstrated history of successful collaboration in interdisciplinary project teams 3+ years of health care or clinical trial research experience Experience working with electronic health records or other health care data. Experience writing research proposals. For more information on HealthPartners Institute, please visit ******************************************

Why Mayo Clinic Mayo Clinic is top-ranked in more specialties than any other care provider according to U.S. News & World Report. As we work together to put the needs of the patient first, we are also dedicated to our employees, investing in competitive compensation and comprehensive benefit plans - to take care of you and your family, now and in the future. And with continuing education and advancement opportunities at every turn, you can build a long, successful career with Mayo Clinic. Benefits Highlights * Medical: Multiple plan options. * Dental: Delta Dental or reimbursement account for flexible coverage. * Vision: Affordable plan with national network. * Pre-Tax Savings: HSA and FSAs for eligible expenses. * Retirement: Competitive retirement package to secure your future. Responsibilities PathAssist is a cutting-edge initiative at Mayo Clinic that uses artificial intelligence to democratize diagnostic expertise in pathology. By leveraging Mayo's vast data ecosystem-including millions of whole slide images, laboratory information system data, and clinical notes-the project aims to develop an AI-driven tool that recommends optimal diagnostic stains and molecular tests using principles of information theory. The Research Associate/Data Science Analyst will play a key role in developing, training, and validating advanced multimodal AI models that integrate digital pathology, clinical text, and population health data. This role involves hands-on data curation, probabilistic and self-supervised model development, statistical performance evaluation, and interdisciplinary collaboration with physicians and scientists in computational pathology and informatics. Ideal candidates combine strong programming and analytical skills with curiosity about medical AI, digital pathology, and the future of diagnostic decision support. A Research Associate in Engineering (ENG) is based on role and responsibilities requiring Engineering skills regardless of Ph.D. background. Main skills used in this track may include setting up mechanical research equipment, developing experimental protocols, biomechanics development in orthopedics, implementing protocols, and/or providing engineering technical expertise and analysis. Responsibilities (depending upon area of research) may also involve use of x-ray computed tomography (CT), radiation dosimetry, x-ray physics, and proficiency in Matlab and/or C++ programs. May work in a special engineering group, process and test algorithms, informatics, data for computer programming, and implement algorithms to apply to concepts, research, and clinical applications and devices. Requires at least three years of postdoctoral research experience at Mayo Clinic or elsewhere. The position is considered non-exempt (hourly), and therefore, all hours worked must be recorded. A Research Associate at Mayo Clinic is a temporary transitional role with the primary purpose to allow qualified individuals to work within an established investigator's program in preparation for an academic and/or independent research career. The ability to perform specialized or complex functions would typically be demonstrated through review of scientific accomplishments, contributions, and peer-reviewed publications averaging at least one per year post doctoral degree. The Research Associate is expected to provide leadership support and training within an established research program. Qualifications Must have a Ph.D., M.D. or equivalent doctoral degree in a field deemed relevant by the program. Requires at least three years of postdoctoral research experience at Mayo Clinic or elsewhere with evidence of publications and other scientific accomplishments. Exemption Status Exempt Compensation Detail $92,242 - $107,910 / year; Education, experience and tenure may be considered along with internal equity when job offers are extended. Benefits Eligible Yes Schedule Full Time Hours/Pay Period 80 International Assignment No Site Description Just as our reputation has spread beyond our Minnesota roots, so have our locations. Today, our employees are located at our three major campuses in Phoenix/Scottsdale, Arizona, Jacksonville, Florida, Rochester, Minnesota, and at Mayo Clinic Health System campuses throughout Midwestern communities, and at our international locations. Each Mayo Clinic location is a special place where our employees thrive in both their work and personal lives. Learn more about what each unique Mayo Clinic campus has to offer, and where your best fit is. Equal Opportunity All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender identity, sexual orientation, national origin, protected veteran status or disability status. Learn more about the 'EOE is the Law'. Mayo Clinic participates in E-Verify and may provide the Social Security Administration and, if necessary, the Department of Homeland Security with information from each new employee's Form I-9 to confirm work authorization. Recruiter Victoria Knight

Vantive is a vital organ therapy company on a mission to extend lives and expand possibilities for patients and care teams everywhere. For 70 years, our team has driven meaningful innovations in kidney care. As we build on our legacy, we are deepening our commitment to elevating the dialysis experience through digital solutions and advanced services, while looking beyond kidney care and investing in transforming vital organ therapies. Greater flexibility and efficiency in therapy administration for care teams, and longer, fuller lives for patients- that is what Vantive aspires to deliver. 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 is driven to help improve patients' lives worldwide. Join us in advancing our mission to extend lives and expand possibilities. YOUR ROLE The Drug Products and Sciences R&D Stability team supports research and development projects for new and existing products. The Research Associate III, Stability Subject Matter Expert, applies sound chemistry and stability planning expertise to identify and resolve stability indicating characteristics. The effective integration of chemistry and stability enables establishment of shelf life for new or existing products manufactured for rapidly growing markets and allows for the qualification of product changes on a global scale. The Stability Subject Matter Expert develops and designs strategies and makes recommendations that are non-routine to address technical, regulatory, and business requirements. WHAT YOU WILL BE DOING Represent R&D-Stability on project teams as a key member of the project teams' goals and success. Craft and implement stability strategy plans for new product development and sustaining projects. Design GMP stability studies used to establish expiration dating for product development. Contribute to the development of technical justifications for expiration dating for new or modified products and the defense of expiration dating recommendation to key business partners. Provide valuable input to stability assessments and requirements for new products and/or current product changes. Ensure the right methods and specifications are available for stability, compatibility, and release testing. Ensure that the methods are appropriate for the product design over shelf life. Demonstrate the ability to identify risks, issues, and opportunities for improvement of existing methods, technologies, and approaches. Provide sound scientific rationale. Interact with manufacturing facilities to acquire information related to test methods and specifications. Author, review and verify technical data, protocols, and reports. Act as study director for stability projects under guidance of senior Stability team members. Perform stability study administration activities on LIMS including study building and review, identification of product test data requiring modification, and data entry. Develop new and/or optimize existing processes and procedures to enhance stability related practices. Participate in investigations that correspond to atypical or out-of-specification/out-of-trend test results. Review data and author technical evaluations that characterize the stability trending of suspect data. Leverage critical thinking to drive the investigation to conclusions based on sound scientific principles. Optimally plan, coordinate, and oversee the progress of multiple Stability related projects, budgets, and activities working with global teams and CROs as applicable. Contribute to and/or take lead author role for stability sections intended for submission to regulatory authorities. Use computerized systems to retrieve, evaluate, summarize data for reporting. WHAT YOU WILL BRING Bachelor's Degree with 5-7 years, Master's with 3-5 years, or PhD with 0-3 years' experience in a relevant scientific subject area. Ability to organize complex information and demonstrated attention to detail. Apply a logical, methodical approach in independently solving problems, developing solutions, and making sound recommendations. Experience working with sophisticated databases. Possess relevant computer and technical skills including word processing, spreadsheets, table and graph generation, and use of databases and reporting tools. Good technical writing skills. Possess proficiency in analytical chemistry including theoretical knowledge and practical experience. Contribute to efforts beyond own scope of responsibilities to ensure project milestones are met. Functional understanding of FDA, ISO, and Quality systems. Willingness to work in a team environment across multiple time zones and demonstrates an inclusive attitude. Vantive is committed to supporting the need 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 Vantive, 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 $96,000 - $120,000 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 on 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-BT1 US Benefits at Vantive This is where your well-being matters. Vantive offers comprehensive compensation and benefits packages for eligible roles. Our health and well-being benefits include medical, dental and vision coverage that start on day one, as well as insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance. Financial and retirement benefits include the Aon Pooled Employer Plan (“Aon PEP”), Vantive's 401(k) retirement savings plan, to help you prepare for your future. The Aon PEP is designed to help improve retirement outcomes by providing retirement resources more efficiently. The plan offers a robust set of investment options, financial education, and a suite of resources to support your retirement goals. We also offer Flexible Spending Accounts, educational assistance programs, and time-off benefits such as paid holidays, paid time off ranging from 20 to 35 days based on length of service, family and medical leaves of absence, and paid parental leave. Additional benefits include commuting benefits, the Employee Discount Program, the Employee Assistance Program (EAP), and childcare benefits. Join us and enjoy the competitive compensation and benefits we offer to our employees. For additional information regarding Vantive's US Benefits, please speak with your recruiter or visit our Benefits site: Benefits | Vantive Equal Employment Opportunity Vantive is an equal opportunity employer. Vantive 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. Know Your Rights: Workplace Discrimination is Illegal Reasonable Accommodation Vantive 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. Form Link Recruitment Fraud Notice Vantive has discovered incidents of employment scams, where fraudulent parties pose as Vantive 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.

Interested? Give Weatherby a call today and speak with one of our specialty-specific consultants for available dates and details. Schedule details being finalized One year assignment Inpatient hospital setting Metabolic experience highly valued Paid malpractice insurance; pre-paid travel and housing expenses Assignment details and time entry in online portal Competitive compensation 24-hour access to your Weatherby Healthcare consultant Charter member of NALTO From $175.00 to $225.00 hourly Ranges shown should be used as an estimate and are affected by many factors including the critical need of the position, your overall experience and qualifications, and other considerations. Please reach out to your consultant for more information." Since 1995, Weatherby Healthcare has established itself as an expert in locum tenens staffing for physicians, physician assistants, and nurse practitioners. The company employs nearly 600 employees committed to filling locum tenens assignments in large-scale healthcare networks, hospitals, and clinics nationwide. Learn more at ******************************

Clinical Research Investigator DM Clinical Research, the largest privately-owned research management organization in the Houston area and one of the top 50 in the country, is looking for an Investigator for our sites in Minneapolis, MN. This individual will conduct all clinical trials (studies) according to ICH, GCP, local regulations, study protocols, and company processes. Responsibilities Ensures the medical well-being and safety of the participants through the safe performance and execution of the studies. Assists in maintaining clinical oversight and quality on the studies registered on and delivers on study targets, thereby contributing to the commercial success of the site. Reviews enrollment progress, pre-screening and screening success rates, screen failure rates, safety, and retention of participants. Interprets protocols and IB and participates in initiatives to strategize for patient recruitment. Carries out clinical evaluation and assessment of participants to ensure eligible participants are enrolled onto studies. Ensures and protects the welfare and safety of participants through ethical conduct. Fulfills and comply with all medical duties as per protocol, SOP/COP and ICH GCP and local regulations. Exercises meticulous attention to detail in documentation and patient care. Requirements Medical License (MD, DO) At least 2 years of experience as a Clinical Research Investigator. Spanish Bilingual a plus.

Syngenta Seeds is one of the world's largest developers and producers of seed for farmers, commercial growers, retailers and small seed companies. Syngenta seeds improve the quality and yields of crops. High-quality seeds ensure better and more productive crops, which is why farmers invest in them. Advanced seeds help mitigate risks such as disease and drought and allow farmers to grow food using less land, less water and fewer inputs. Syngenta Seeds brings farmers more vigorous, stronger, resistant plants, including innovative hybrid varieties and biotech crops that can thrive even in challenging growing conditions. Syngenta Seeds is headquartered in the United States. Job Description We are seeking a detail-oriented Research Associate to lead complex activities and projects, ensuring the successful execution and management of end-to-end process in seed production across multiple crops. Duties: Functioning as an integral member of a team leading all aspects of small plot seed production activities including packaging, treating, planting, harvesting, inventory, and shipping. Manage and train up to 15 part-time staff. Coordinate weekly labor needs based on current and future workload. Deliver projects on time and within budget. Ensure compliance with safety and stewardship policies. Qualifications PLEASE NOTE -- Candidates must be already located in the United States and not require visa sponsorship Required: B.S. in Agriculture, Logistics, Operations Management, or related field . Experience with seed production quality, quantity, and timelines and knowledge of international shipping logistics for research seed. Demonstrated collaboration and problem solving skills. Ability to lift 70 pounds and work in an outdoor field environment. Ability and willingness to work extended hours and Saturdays' during peak season. Valid driver's license and ability to travel to off-site field locations as required. Excellent communication and team management skills. Bilingual in Spanish and English (a plus). Proficiency in MS Office, especially Excel and Word. Preferred: Familiarity with seed technology industry and plant breeding methodologies. Experience with basic lab equipment (seed counters, scales, scanners). Additional Information What We Offer: A culture that celebrates diversity & inclusion, promotes professional development, and strives for a work-life balance that supports the team members. Offers flexible work options to support your work and personal needs. Full Benefit Package (Medical, Dental & Vision) that starts your first day. 401k plan with company match, Profit Sharing & Retirement Savings Contribution. Paid Vacation, Paid Holidays, Maternity and Paternity Leave, Education Assistance, Wellness Programs, Corporate Discounts, among other benefits. Syngenta has been ranked as a top employer by Science Journal. Learn more about our team and our mission here: ******************************************* Syngenta is an Equal Opportunity Employer and does not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. WL2A #LI-KR1 #LI-ONSITE

Intermediate level position in the Research Department which we are seeking someone with some basic agriculture and field research knowledge. The main responsibility for this job will be conducting mini-strip and replicated testing as well as participating in other facets of Beck's Research Department. As a member of the Beck's Family of employees, all full-time employees are eligible for a generous benefits package: Health benefits including two medical plan options and company HSA contributions, dental, vision, employer paid life/AD&D for you and your dependents, disability insurance, and access to an onsite Nurse Practitioner 401k plan match & company sponsored pension plan and access to a Financial Advisor to help you manage your retirement savings Paid time off, Paid Holidays, Wellness Programs, & Corporate Discounts Company Christmas Party, Free Lunch, Two-Hundred Dollar Merchandise Allowance, & Much More Responsibilities Coordinate plot locations and logistics with plot cooperators Measuring and setting flags Working with cooperators to ensure proper seedbed preparation, fertility program and weed control Seed Preparation Prepare seed for mini-strip and replicated testing Planting of mini-strip and replicated plots Transporting planting equipment to outlying locations Ensuring plots are planted as directed by the Testing Site Lead Data Collection Stand counts, early vigor, and plot ratings Flowering data Physical characteristics (Plant and ear heights, etc) Disease evaluation and agronomic notes Plot Maintenance Work with cooperators to ensure plots are maintained to Beck's Hybrids' standards Apply fertilizer, herbicide, and insecticide as needed Plot Harvest Transport harvest equipment to outlying locations Collect fall agronomic notes (stability, plant integrity, etc) Conduct harvest of mini-strip and replicated plots Research Equipment Maintenance Ensure machinery is maintained to Beck's Hybrids' standards to minimize downtime Diagnose and make repairs as needed Data Reporting Some duties may include reporting notes, harvest data, and preparation of yield reports for Beck's Product Development Staff Warehousing/distribution Inventory incoming shipments Organize and stage outgoing shipments Load/unload trucks as needed Perform seed deliveries as needed Aid in isolated corn block, nursery, and winter nursery work Supervise full time employees, part time employees, and interns that report to the Research Associates as needed Work in other areas of Beck's Hybrids' operations as directed by the Testing Site Lead to ensure efficient site operations. Job Requirements Education and training: Minimum of high school diploma or GED equivalent, advanced degree preferred Class A CDL required Pesticide applicator license or the ability to obtain Must possess and maintain valid driver's license and insurable driving record as determined by Beck's automobile insurance policy Technical knowledge: Excellent verbal and written communication skills Possess strong agronomic and mechanical skills Possess positive attitude Ability to establish priorities, work independently, work as a team member, and proceed with objectives without supervision. Skill to use personal computer and various software packages 3. Physical demands: Ability to pass DOT physical examination and obtain Medical Examiner's Certificate is required Overnight travel is required Must be able to lift up to 70 pounds unassisted Experience: Field Research and/or Agriculture experience preferred Previous experience with replicated test plots preferred Previous experience with operating combine harvesters preferred ** In an effort to provide a safer, drug-free workplace for employees, all full-time applicants to whom offers of employment are made must submit to a drug test and background check, subject to applicable local, state, or federal laws or regulations. Employment at Beck's is contingent upon passing these pre-employment screenings.

Acceligen is a global leader in precision gene-editing of animal cells create safer, healthier more humanely-raised food animals. The company is engaged in the development, production and worldwide sale of large animal models for agricultural interests. Acceligen serves its customers/industry partners using innovative research strategies and patented technology to address needs in the agricultural markets through precision breeding. We are currently seeking a motivated Research Associate to join our collaborative team in New Brighton, MN. As a Research Associate, you will be self-motivated and apply your technical skills and knowledge in the life science field to support Acceligen' research and developmental programs. You will have a solid understanding of molecular biology, cell biology, biochemistry, and protein analytical techniques is required and be willing to perform in vitro work in the laboratory as well as in vivo work at our large animal facilities, if needed. Proficiencies critical to successful employment include: Molecular biology techniques including PCR and cloning DNA/RNA/protein isolation and quantification DNA sequencing Mammalian cell culture Tissue harvesting Immunohistochemistry Cell sorting Solution making Required Qualifications: BS/BA in a life science-related field plus one year of related laboratory experience. A combination of education and work experience to equal 4+ years is acceptable. Practical experience in a molecular biology/ cell culture laboratory is highly preferred. Exceptional documentation skills (electronic notebook), attention to detail, well-organized and detail-oriented Solid time management skills, excellent interpersonal skills and ability to take direction. Ability to work a standard Monday-Friday work week with additional rotating weekend lab responsibility schedule Ability to follow established procedures and protocols. This position requires prolonged standing, lifting of up to 40 pounds, repetitive hand/wrist activities, and use of a personal computer.

By joining Bio-Techne, you'll join a company with a powerful and positive purpose of enabling cutting-edge research in Life Sciences and Clinical Diagnostics. Bio-Techne, and all of its brands, provides tools for researchers to further treat and prevent disease worldwide. Pay Range: $40,300.00 - $66,250.00 Position Summary: As a Research Associate in the Conjugation lab, you will be responsible for preparing conjugated proteins, antibodies, enzymes, oligonucleotides, and microparticles for both manufacturing and research purposes. In addition, you may help prepare and test other chemistry related reagents for manufacturing and QC teams. Key Responsibilities: Prepare conjugated proteins, antibodies, enzymes and microparticles for both manufacturing and research according to written SOPs. Occasionally develop new procedures for new products. Perform in-process testing of conjugates stocks used in Bio-Techne assay platforms. Complete post-manufacturing processing, sterile filtering, vialing, and labelling of conjugated products. Troubleshoot problematic conjugates with guidance. Consider opportunities to improve department efficiency and cost-savings. Manage information and data in batch records, spreadsheets, computer databases, paper documentation, etc. Follow guidelines for company safety, quality, training procedures, and regulation policies. Perform additional duties as assigned. Education and Experience: Bachelor's degree in chemistry, biological sciences, or equivalent (chemistry or biochemistry preferred) required with 0 to 2 years of conjugation, protein purification, and/or immunoassay experience. Knowledge, Skills, and Abilities: Basic knowledge of purification, conjugation, and structure of proteins and antibodies. Knowledge of general and sterile lab techniques, pipetting, equipment, and inventory. Ability to handle repetitive complex tasks. Proficiency with Microsoft Office with emphasis on Excel. Aptitude to plan, organize, and multi-task to complete assignments in an efficient manner. Capability to work in a fast-faced environment with shifting priorities and deadlines. Ability to pay attention to detail and perform at a high level of accuracy. Skills in problem solving, including the ability to identify and appropriately evaluate a course of action. Knowledge of safety and company procedures and practices. Proficiency in professional communication, both orally and in writing. Capacity to work independently on routine assignments or projects and work with a team. Ability to work hours that conform to standard business operations (typically 8:00 A.M. to 5:00 P.M.). Why Join Bio-Techne: We offer competitive insurance benefits starting on day one: medical, dental, vision, life, short-term disability, long-term disability, pet, and legal and ID shield. We invest in our employees' financial futures through 401k plans, an employee stock purchase plan (ESPP), Health Saving Account (HSA), Flexible Spending Account (FSA), and Dependent Care FSA. We empower our employees develop their careers through mentorship, promotional opportunities, training and development, tuition reimbursement, internship programs, and more. We offer employee resource groups, volunteer paid time off, employee events, and charity drives to build a culture of caring and belonging. We offer an accrued leave policy with paid holidays, paid time off, and paid parental leave. We foster a culture of empowerment and innovation, where employees feel valued and encouraged to bring their new ideas to the table. Bio-Techne is an E-Verify Employer in the United States. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. To protect the interests of all, Bio-Techne will not accept unsolicited resumes from any source other than a candidate application. Any unsolicited resumes sent to Bio-Techne will be considered Bio-Techne property.

Join a pioneering team and contribute to the development of a groundbreaking product that aims to transform the lives of individuals with autoimmune diseases. Responsibilities * Perform animal technician duties, including animal health checks and maintenance. * Assist with operating room and necropsy procedures. * Maintain strict documentation control functions in compliance with GLP/GMP regulations. * Follow SOPs and FDA Good Manufacturing Practices. * Ensure adherence to AAALAC, USDA/AWA regulations. Essential Skills * At least 6 months of documentation experience in a regulated environment, ideally in the pharmaceutical or medical device industry. * Proficiency in quality assurance practices. * Familiarity with FDA, SOP, GLP, and GMP regulations. * Experience in animal husbandry and handling. * Strong communication skills, both written and verbal. * Ability to manage multiple tasks in a work setting. * Comfortable working with pigs and boars, and being on feet for extended periods. * Strong computer skills, including proficiency in Microsoft Teams, 365, etc. * Willingness to comply with health and safety requirements of the facility. Additional Skills & Qualifications * Bachelor's degree is a plus. * Swine husbandry experience. * Experience working with large animals. * Previous experience in an FDA-regulated environment. * Veterinary technician or veterinary assistant certification. Job Type & Location This is a Contract to Hire position based out of Stillwater, MN. Pay and Benefits The pay range for this position is $21.00 - $26.00/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 Stillwater,MN. Application Deadline This position is anticipated to close on Dec 19, 2025. 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.

HealthPartners Institute is seeking a full-time Physician Research Investigator (0.8 FTE - 1.0 FTE) with both clinical and research experience relevant to the study of chronic disease in adult populations. Areas of focus may include diabetes, cardiovascular disease, and other chronic diseases prevalent in adults. Eligible candidates may bring expertise in a range of study designs including observational or interventional studies. Candidates with prior experience in health services research, clinical decision support, or implementation science are encouraged to apply. Research Investigators at HealthPartners Institute may obtain or maintain external academic appointments. Eligible candidates are encouraged to practice part-time within the HealthPartners Medical group depending on practice interest and availability (up to 40% of Total FTE could be clinical work). At HealthPartners Institute, Researcher Investigators are expected to support and develop externally funded research programs, conduct nationally and internationally recognized scholarly clinical or health services research, and collaborate with other investigators, clinicians, and leaders to improve health outcomes and care delivery. Successful candidate(s) will be accountable for conceptualizing and designing research projects, leading, and collaborating on such projects, and disseminating research results through presentations and publications in peer-reviewed journals and conferences. Service on committees and participation in scientific peer-review processes are also expected. HealthPartners Institute Research Investigators are primarily supported through grants and contracts from external sources, including the National Institutes of Health (NIH), Centers for Disease Control and Prevention (CDC), and the Patient-Centered Outcomes Research Institute (PCORI). HealthPartners Institute is focused on improving health and well-being through research, education, and practice. Our Research Investigators are embedded in an integrated health system and our research draws on rich clinical data derived from comprehensive, fully integrated state-of-the-art electronic medical and dental record and claims data from over a million HealthPartners patients and members. In addition, HealthPartners Institute is a member of numerous research networks, including the Health Care Systems Research Network (HCSRN) and the Minnesota EHR Consortium, providing opportunities to conduct multisite and population-based studies. We offer a supportive, collegial work environment and mentoring for early and mid-career investigators. HealthPartners fosters an environment that is inclusive, encourages creative thinking, and celebrates diversity. We're committed to living our values of excellence, compassion, integrity, and partnership. If you feel your skills are a match for this role, we would love to hear from you and provide additional information about how we support our researchers. Required Qualifications: MD/DO or equivalent degree and clinical experience in internal medicine, family medicine, hospital medicine, preventive medicine, or a related discipline Early to mid-career investigator with demonstrated leadership skills and potential to lead active portfolio of externally funded research. Prior history as first author of scholarly peer-reviewed publications Experience authoring research proposals. Methodologic expertise in qualitative or quantitative approaches Strong people skills Strong oral and written communication skills Current Minnesota or Wisconsin Medical license or eligible for MN or WI medical license, based on active medical license in another state and in good standing. Preferred Qualifications: PhD or master's degree in public health or similar formal training in research methodology Demonstrated history of successful collaboration in interdisciplinary project teams 3+ years of health care research experience Experience working with electronic health records or other health care data. For more information on HealthPartners Institute, go to ******************************************

Classification * $16.00 hourly, Non-Exempt (Eligible for overtime) * 10-20 hours per week * 100% Remote Work Availability: No * Hybrid Work Availability (requires some time on campus): No This is a part-time, non-benefited position. Only UND students are eligible to be hired in this position. Duties & Responsibilities * Duties will entail in-lab physical, chemical, and biological (including DNA extraction) analysis of soil and plant samples collected from field sites and natural areas across the Great Plains and Pacific Northwest. Minimum Requirements * Must be enrolled in an undergraduate degree program and majoring OR minoring in a degree program in the College of Arts & Sciences, College of Engineering, or College of Education * Successful completion of a Criminal History Background Check In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the US and to complete the required employment eligibility verification form upon hire. This position does not support visa sponsorship for continued employment. To Apply For full consideration, applications must be received by the closing date and include the following materials: * Cover letter Please include in the application if you are currently or have in the past 12 months been employed with the University of North Dakota, the North Dakota University System or any other North Dakota State agency. If so, include which agency/department, as well as how many hours you work a week. Career Services is here to help students looking for student employment positions at UND by offering individual sessions that include resume, cover letter reviews, and interview preparation. Please schedule an appointment through Hawk Central or email us at **************************.

**Why Mayo Clinic** Mayo Clinic is top-ranked in more specialties than any other care provider according to U.S. News & World Report. As we work together to put the needs of the patient first, we are also dedicated to our employees, investing in competitive compensation and comprehensive benefit plans (************************************** - to take care of you and your family, now and in the future. And with continuing education and advancement opportunities at every turn, you can build a long, successful career with Mayo Clinic. **Benefits Highlights** + Medical: Multiple plan options. + Dental: Delta Dental or reimbursement account for flexible coverage. + Vision: Affordable plan with national network. + Pre-Tax Savings: HSA and FSAs for eligible expenses. + Retirement: Competitive retirement package to secure your future. **Responsibilities** PathAssist is a cutting-edge initiative at Mayo Clinic that uses artificial intelligence to democratize diagnostic expertise in pathology. By leveraging Mayo's vast data ecosystem-including millions of whole slide images, laboratory information system data, and clinical notes-the project aims to develop an AI-driven tool that recommends optimal diagnostic stains and molecular tests using principles of information theory. The Research Associate/Data Science Analyst will play a key role in developing, training, and validating advanced multimodal AI models that integrate digital pathology, clinical text, and population health data. This role involves hands-on data curation, probabilistic and self-supervised model development, statistical performance evaluation, and interdisciplinary collaboration with physicians and scientists in computational pathology and informatics. Ideal candidates combine strong programming and analytical skills with curiosity about medical AI, digital pathology, and the future of diagnostic decision support. A Research Associate in Engineering (ENG) is based on role and responsibilities requiring Engineering skills regardless of Ph.D. background. Main skills used in this track may include setting up mechanical research equipment, developing experimental protocols, biomechanics development in orthopedics, implementing protocols, and/or providing engineering technical expertise and analysis. Responsibilities (depending upon area of research) may also involve use of x-ray computed tomography (CT), radiation dosimetry, x-ray physics, and proficiency in Matlab and/or C++ programs. May work in a special engineering group, process and test algorithms, informatics, data for computer programming, and implement algorithms to apply to concepts, research, and clinical applications and devices. Requires at least three years of postdoctoral research experience at Mayo Clinic or elsewhere. The position is considered non-exempt (hourly), and therefore, all hours worked must be recorded. A Research Associate at Mayo Clinic is a temporary transitional role with the primary purpose to allow qualified individuals to work within an established investigator's program in preparation for an academic and/or independent research career. The ability to perform specialized or complex functions would typically be demonstrated through review of scientific accomplishments, contributions, and peer-reviewed publications averaging at least one per year post doctoral degree. The Research Associate is expected to provide leadership support and training within an established research program. **Qualifications** Must have a Ph.D., M.D. or equivalent doctoral degree in a field deemed relevant by the program. Requires at least three years of postdoctoral research experience at Mayo Clinic or elsewhere with evidence of publications and other scientific accomplishments. **Exemption Status** Exempt **Compensation Detail** $92,242 - $107,910 / year; Education, experience and tenure may be considered along with internal equity when job offers are extended. **Benefits Eligible** Yes **Schedule** Full Time **Hours/Pay Period** 80 **International Assignment** No **Site Description** Just as our reputation has spread beyond our Minnesota roots, so have our locations. Today, our employees are located at our three major campuses in Phoenix/Scottsdale, Arizona, Jacksonville, Florida, Rochester, Minnesota, and at Mayo Clinic Health System campuses throughout Midwestern communities, and at our international locations. Each Mayo Clinic location is a special place where our employees thrive in both their work and personal lives. Learn more about what each unique Mayo Clinic campus has to offer, and where your best fit is. (***************************************** **Equal Opportunity** All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender identity, sexual orientation, national origin, protected veteran status or disability status. Learn more about the "EOE is the Law" (**************************** . Mayo Clinic participates in E-Verify (******************************************************************************************** and may provide the Social Security Administration and, if necessary, the Department of Homeland Security with information from each new employee's Form I-9 to confirm work authorization. **Recruiter** Victoria Knight **Equal opportunity** As an Affirmative Action and Equal Opportunity Employer Mayo Clinic is committed to creating an inclusive environment that values the diversity of its employees and does not discriminate against any employee or candidate. Women, minorities, veterans, people from the LGBTQ communities and people with disabilities are strongly encouraged to apply to join our teams. Reasonable accommodations to access job openings or to apply for a job are available.

Vantive is a vital organ therapy company on a mission to extend lives and expand possibilities for patients and care teams everywhere. For 70 years, our team has driven meaningful innovations in kidney care. As we build on our legacy, we are deepening our commitment to elevating the dialysis experience through digital solutions and advanced services, while looking beyond kidney care and investing in transforming vital organ therapies. Greater flexibility and efficiency in therapy administration for care teams, and longer, fuller lives for patients- that is what Vantive aspires to deliver. 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 is driven to help improve patients' lives worldwide. Join us in advancing our mission to extend lives and expand possibilities. Your Role The Kidney Care R&D - Analytical Chemistry team currently has an opening for an experienced versatile Analytical Chemist who can be an analytical lead, direct and execute lab experiments in the Renal Care Solutions R&D chemistry lab. The successful candidate will effectively contribute solid technical knowledge to a variety of projects within the relevant discipline with minimal assistance and display basic technical understanding of related disciplines including: Support strategies and research projects, which are routine and non-routine within areas of expertise to address specific technical requirements of a project. Display a solid understanding of theories/practices utilized in the primary area of expertise. Support research or design strategies to achieve the technical vision for a new or improved product/process/method or to prove a new theory, applying a solid understanding of theories/practices including those from other disciplines outside the primary area of expertise. Provides assistance and interpretation of project results to team members and other key personnel. Direct or train other analytical chemists in the interpretation of results or new analytical techniques. What you'll be doing Effectively contribute solid technical knowledge to a variety of projects within the relevant discipline. Independently or with the assistance of Senior Analytical Leads, support the design and execution of the analytical plan for exploratory, new product development, and sustaining projects. Conduct analytical problem-solving efforts to meet business needs. Collaborates with other functions such as project management, regulatory, formulation, manufacturing, and quality control in project teams. Perform SOP assessments, analytical method developments and validations, author protocols and reports, and may act as a study director. Transfers analytical methods to manufacturing plants, CRO and other R&D centers. Contributes to technical feasibility analysis of complex research and design concepts. Some knowledge of relevant regulatory requirements and Quality System Regulations related to R&D (product development, design and safety) to ensure compliance in all research, data collection and reporting activities. Supports internal initiatives that enhance operational excellence. Reach conclusions based on research analysis and incorporate recommendations into larger projects. Share research outcomes, methodology and cycle-time reduction methods with team members and other divisional personnel. What you'll bring Knowledge of analytical method development, validation and transfer. A good understanding of ICH, USP guidelines and cGxP practice. Some experience with a combination of the following instruments: ICP-MS, ICP-OES, IC, AA, UPLC/HPLC, GC, UV, Polarimeter, (NMR a plus) and other analytical instruments and software (Open Lab, ELN, Empower). Ability to learn quickly and to solve problems in a timely manner using analytical chemistry skills. Possess technical writing and computer skills (MS Word, Excel and etc.). Ability to organize, assess and communicate complex information that engages the project team. Ability to make decisions when provided with limited information and to make routine decisions independently. Ability to suggest experiments and draw meaningful conclusions from lab data in addition to critically review peers' work. Ability to work in a team environment. Understand data management and data migration. Demonstrates flexibility and can shift gears comfortably. Interpret laboratory data and make recommendations to resolve technical challenges. Education and/or Experience: Bachelor's or Master's Degree in a scientific discipline (preferred Chemistry) with 3+ years of experience. Wet Chemistry & Analytical lab experience, cGxP experience, cross-functional teamwork, and independent experimentation in method development and validation. Vantive 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 Vantive, 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 $80,000 - $120,000 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 on upon location, skills and expertise, experience, and other relevant factors. This position may also be eligible for discretionary bonuses, commission, and/or long-term incentive. 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 US Benefits at Vantive This is where your well-being matters. Vantive offers comprehensive compensation and benefits packages for eligible roles. Our health and well-being benefits include medical, dental and vision coverage that start on day one, as well as insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance. Financial and retirement benefits include the Aon Pooled Employer Plan (“Aon PEP”), Vantive's 401(k) retirement savings plan, to help you prepare for your future. The Aon PEP is designed to help improve retirement outcomes by providing retirement resources more efficiently. The plan offers a robust set of investment options, financial education, and a suite of resources to support your retirement goals. We also offer Flexible Spending Accounts, educational assistance programs, and time-off benefits such as paid holidays, paid time off ranging from 20 to 35 days based on length of service, family and medical leaves of absence, and paid parental leave. Additional benefits include commuting benefits, the Employee Discount Program, the Employee Assistance Program (EAP), and childcare benefits. Join us and enjoy the competitive compensation and benefits we offer to our employees. For additional information regarding Vantive's US Benefits, please speak with your recruiter or visit our Benefits site: Benefits | Vantive Equal Employment Opportunity Vantive is an equal opportunity employer. Vantive 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. Know Your Rights: Workplace Discrimination is Illegal Reasonable Accommodation Vantive 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. Form Link Recruitment Fraud Notice Vantive has discovered incidents of employment scams, where fraudulent parties pose as Vantive 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.

Salary range: $52,000-$67,000 Full-time, exempt Vyriad is a clinical stage biotechnology company based in Rochester MN. We are developing the next generation of targeted genetic medicines for cancer therapy. As a Research Associate, you will be an integral part of a dynamic team focused on advancing scientific knowledge and developing innovative solutions in the Process Development and Manufacturing department. Your role will involve learning various analytical assays, conducting experiments, analyzing data, and presentation of the results. You will collaborate with scientists, technologists and other team members to achieve team goals and support the development of new manufacturing processes. Supervisory Responsibilities None Duties and responsibilities * Perform routine testing and review testing data and results to ensure compliance to appropriate test methods, specifications, and protocols. * Performs lab support functions e.g. ordering, inventory checks, stocking, reagent prep, equipment cleaning * Clearly documents data and experiments in laboratory records * Authors protocols, technical reports and other associated documentation. * Participate in group meetings, present results of work, interpret data, and draw conclusions regarding presented material and nature of work. * Work in collaboration with more senior scientists to design experiments and advance state-of-the-art techniques * Serves as a departmental liaison by providing data project updates. * Apply statistical and other software for analysis of process data. * Issue knowledge base reports summarizing conclusion of data reviews. * Collaborate and operate effectively in a fast-paced environment. * Any other duties required as needed Education and experience requirements * Life sciences degree (Bachelors) in Scientific, Engineering or Healthcare subject area. * Research or analytical experience with cGMP production highly desirable. * Viral vector and aseptic mammalian cell culture experience is highly desirable. * Prior laboratory experience in research and/or analytical technique preferred. * Experience with upstream and/or downstream manufacture and testing of biologics under cGMP compliance is preferred. Required skills and/or qualifications * The successful candidate will possess an understanding of analytical method development, strong critical thinking skills, and excellent communication skills. * Ability to apply scientific principles utilized to solve operational, as well as routine production tasks. * Excellent documentation skills including comprehension, review and establishing Batch Production Records, SOPs, deviations and summary reports. Physical Requirements * Prolonged periods of standing at laboratory benches. * Prolonged periods of sitting at a desk and working on a computer. * Must be able to lift up to 15 pounds at times. Benefits * Group Healthcare Plan, including company paid dental and vision. * Short- and long-term disability, life and AD&G insurance. * Simple IRA with employer match * Educational assistance program * Holiday and PTO

By joining Bio-Techne, you'll join a company with a powerful and positive purpose of enabling cutting-edge research in Life Sciences and Clinical Diagnostics. Bio-Techne, and all of its brands, provides tools for researchers to further treat and prevent disease worldwide. Pay Range: $40,300.00 - $66,250.00 We are seeking a Research Associate for Bio-Techne's Protein Purification department in Minneapolis. Our group supports 5000 different protein products used in academic research, pharmaceutical research, and all facets of biological science including: neurodegenerative diseases, stem cell research, glycobiology, developmental biology, etc. This individual will collaborate with many different departments to support the manufacturing processes of our products and contribute to the ongoing development of our growing and evolving portfolio. This position provides a potential for growth and career advancements within the company. This is a fantastic opportunity for an individual to gain problem solving and troubleshooting experience in a collaborative lab environment. This position also provides continuous learning and development, flexible working hours, and the ability to learn and apply a variety of lab techniques every day. Key Responsibilities: Purify proteins and enzymes for restock and modify existing protocols. Perform chromatography and SDS-PAGE. Revise protocols after making modifications for process methods. Follow standard operating procedures. Maintain lab equipment (concentrators, pH meter, columns, etc.). Maintain lab order and cleanliness. Filter and aliquot product for bulk storage. Prepare common buffers and reagents. Improve operation efficiency and contribute to reducing costs. Work with supervisor and manager to facilitate scheduling of projects. Maintain compliance with quality training and documentation. Follow company policies and practices as outline in the Handbook and follow guidelines regarding safety as outline in the AWAIR, Chemical Hygiene and Exposure Control manuals in accordance to the job. Perform additional duties as assigned. Minimum Qualifications: Must be able to work in a fast paced environment where multitasking is required. Must have good verbal and written communication skills. Must have strong organizational skills and attention to detail. Must work well both independently and in a team environment. Working knowledge of Microsoft Word and Excel is required. Preferred Qualifications: Experience with AKTA systems and Unicorn software or other FPLC system is a plus. Corporate work experience in a lab setting, preferably in a problem-solving role. Experience in protein purification either in a corporate or academic setting or as part of a school research project. Working knowledge of SDS-PAGE, protein concentration determination (Bradford and/or A280), protein concentration (Amicon and/or tangential flow filtration), dialysis, protein expression ( E. coli , mammalian, insect cell) and protein structure and function. Education and Experience: This position requires a minimum of a Bachelors or Masters degree in Biochemistry or equivalent degree with experience in protein purification or chromatography. Why Join Bio-Techne: We offer competitive insurance benefits starting on day one: medical, dental, vision, life, short-term disability, long-term disability, pet, and legal and ID shield. We invest in our employees' financial futures through 401k plans, an employee stock purchase plan (ESPP), Health Saving Account (HSA), Flexible Spending Account (FSA), and Dependent Care FSA. We empower our employees develop their careers through mentorship, promotional opportunities, training and development, tuition reimbursement, internship programs, and more. We offer employee resource groups, volunteer paid time off, employee events, and charity drives to build a culture of caring and belonging. We offer an accrued leave policy with paid holidays, paid time off, and paid parental leave. We foster a culture of empowerment and innovation, where employees feel valued and encouraged to bring their new ideas to the table. Bio-Techne is an E-Verify Employer in the United States. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. To protect the interests of all, Bio-Techne will not accept unsolicited resumes from any source other than a candidate application. Any unsolicited resumes sent to Bio-Techne will be considered Bio-Techne property.

Join a pioneering team and contribute to the development of a groundbreaking product that aims to transform the lives of individuals with autoimmune diseases. Responsibilities + Perform animal technician duties, including animal health checks and maintenance. + Assist with operating room and necropsy procedures. + Maintain strict documentation control functions in compliance with GLP/GMP regulations. + Follow SOPs and FDA Good Manufacturing Practices. + Ensure adherence to AAALAC, USDA/AWA regulations. Essential Skills + At least 6 months of documentation experience in a regulated environment, ideally in the pharmaceutical or medical device industry. + Proficiency in quality assurance practices. + Familiarity with FDA, SOP, GLP, and GMP regulations. + Experience in animal husbandry and handling. + Strong communication skills, both written and verbal. + Ability to manage multiple tasks in a work setting. + Comfortable working with pigs and boars, and being on feet for extended periods. + Strong computer skills, including proficiency in Microsoft Teams, 365, etc. + Willingness to comply with health and safety requirements of the facility. Additional Skills & Qualifications + Bachelor's degree is a plus. + Swine husbandry experience. + Experience working with large animals. + Previous experience in an FDA-regulated environment. + Veterinary technician or veterinary assistant certification. Job Type & Location This is a Contract to Hire position based out of Stillwater, MN. Pay and Benefits The pay range for this position is $21.00 - $26.00/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 Stillwater,MN. Application Deadline This position is anticipated to close on Dec 19, 2025. 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.