Associate scientist jobs in Rochester, MN

General Job Description 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 Vyriad is an equal opportunity employer and does not discriminate on the basis of race, color, religion, sex, national origin, age, disability, genetic information, gender identity, sexual orientation, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local laws. This policy applies to all terms and conditions of employment, including, but not limited to, hiring, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.

Job DescriptionDescriptionHelp advance the Well Living Lab's mission: to expand scientific and practical understanding of how indoor environments and human behavior interact to impact health and well-being. Responsibilities: Lead Research Development - Generate research ideas, design and execute protocols, and write proposals for external grant funding. Data Oversight - Direct data collection, management, and analysis using advanced statistical methods; ensure data quality and integrity. Publication & Communication - Prepare manuscripts, presentations, and reports; publish original research in peer-reviewed journals. Collaboration - Work closely with Mayo Clinic scientists, external research organizations, and industry partners. Serve as a scientific lead or co-lead on Well Living Lab (WLL) projects. Integration & Innovation - Align WLL research with broader health and building science platforms; stay current on literature and emerging trends. Team Engagement - Collaborate daily with multidisciplinary researchers, technology and operations staff, and academic/industry partners. You would be a great fit if: PhD in a field related to the built environment or systems. Minimum 5 years of post-doctoral or equivalent experience in human-centered research within the built environment. Expertise in HVAC and environmental controls/engineering and their impact on human health. Strong background in experimental design, simulation, and data analysis (including large datasets and statistical programming). Proven success in grant writing, IRB submissions, and managing research protocols. Track record of peer-reviewed publications and conference presentations. Experience leading research projects and teams, with excellent organizational and project management skills. Exceptional written and verbal communication skills; ability to collaborate across disciplines with flexibility and a positive attitude. Bonus points: Experience managing relationships with academic and industry collaborators. Active involvement in professional organizations (ASHRAE, ASID, AIA, etc.). Knowledge of building science instrumentation (temperature, RH, PM, VOC sensors) and calibration/QA protocols. Familiarity with LabVIEW, MATLAB, or Python for instrument control and data analysis. Ability to interpret and apply building engineering standards (ASHRAE, ASTM, ISO, LEED, WELL). Strong professional network and commitment to staying current on trends in building science, indoor environmental quality, and human-centered design. Note: At this time, we are unable to sponsor employment visas. Applicants must be authorized to work in the United States without the need for current or future sponsorship. Benefits offered include: Medical, Dental & Vision 401(k) Retirement Plan, including employer match (100% vested) Life Insurance (Voluntary Life Insurance and AD&D for employee and dependents) Short-term and long-term disability Health Spending Account (HSA) Commuter Benefits (Pre-Tax) Generous PTO policy Volunteer days off Competitive parental leave policy

Job Title: New Product Development Scientist Location: Owatonna, MN Summary This position will be based out of Owatonna, MN manufacturing plant reporting to the Technical Director. NPD Scientist is responsible for overseeing and executing product development activities and providing technical support to internal and external stakeholders related to the Duraco Specialty Tapes & Liners business. This includes recommending, planning, prioritizing, and conducting experimental lab work, product prototyping and optimization, product testing, literature research, as well as data gathering, processing, and reporting. NPD Scientist will also be responsible for maintaining relationships with key suppliers, new raw material qualifications, supporting secondary raw material qualifications, cost savings efforts, and working closely with other functional teams on NPD trial, scale-up, and new product commercialization activities. Responsibilities Oversee and execute development and technical support for Duraco Specialty Tapes & Liners New Product Development (NPD) pipeline, with ability to deliver minimum 5 product launches per year Conduct required laboratory experimentation and testing, provide leadership in Silicone release coating formulation development, new release liner prototyping, materials design, process optimization, and product testing that aligns with Duraco Specialty Tapes & Liners site capabilities and strategic initiatives Provide technical assistance in related regulatory compliance matters related to Silicone release coatings and liner products Engage and collaborate with customers as well as Marketing and Sales Teams to identify key development opportunities and appropriately prioritize projects and initiatives Strong collaboration with Production, Quality, and other functional teams to ensure efficient product development, scale-up, performance optimization, consistent quality, and successful commercialization Establishing and cultivating relationships with suppliers of key raw materials Provide technical leadership in support of cost-savings initiatives including, but not limited to, alternate raw material identification, insource/outsource decisions, and Silicone release coating formulation enhancements for increased throughput and efficiencies Provide timely data processing, organizing, and reporting to superiors and functional teams, including generating and sharing ideas for NPD projects and opportunities Proactively identify and implement best safety practices in both laboratory and manufacturing settings Enhance NPD and Project Management processes and establishing improved IP protection practices Other duties as assigned Personal Attributes: Results driven and able to focus on, prioritize, and execute individual activities Curious and eager to learn - enjoys leveraging new knowledge to enhance current Silicone release coating chemistries, release liner constructions, and products Excellent written and verbal communication skills Excellent laboratory and analytical skills including FTIR, XRF, and basic Release Liner testing Comfortable working in a high-pace manufacturing and laboratory environments, and navigating changing priorities Effective in engaging and collaborating with cross-functional teams, including production floor supervisors, operators and QC technicians Outstanding personal integrity and ethics Understands and easily connects products, technologies, and capabilities across a diverse portfolio of customers and markets Demonstrated ability to work across different systems and adapt to new processes Strong planning and organizational skills and high degree of comfort working in and around production / manufacturing settings Qualifications: Required Skills, Education, and Experience BS or MS in a Technical field; preferably Chemistry, Polymer Science, Chemical Engineering, Material Science, or Plastics Engineering with excellent hands-on lab experience 3-5 Years of proven track record of developing new Silicone release coating formulations and paper and film release liner products Understanding and experience with PSAs and PSTC testing methods is desired to help complement release liner and Silicone coating formulation development Experience with development methodologies including project management, stage-gate, ideation, Design of Experiments (DOE), IP management, and literature and patent research Good knowledge of additives, formulation processing, applications, and analytical test methods as they relate to the development of Si release coating formulations Experience in Silicone release coating and web handling processes is highly desirable Knowledge of Microsoft Office products with advanced experience in Excel and analytics programs (e.g., Minitab, JMP, etc.) Travel Must be able to travel within the US 10-15% Domestic Travel The job description is not an exhaustive listing of all responsibilities and may be revised at any time.

**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** The Department of Clinical Genomics at Mayo Clinic is seeking a Physician with a research program to combine clinical and research careers at Mayo Clinic. This is a position intended to grow the departmental research program leading to important discoveries and clinical applications that will impact currently unmet needs of patients with rare and common genetic disorders. We are seeking a **board-certified MD or MD/PhD** candidate highly skilled in functional, translational, therapeutic, computational, and/or clinical trial research with a broad understanding of genetics and genomics and expertise in integrating novel technologies into clinical practice. Candidates must possess research experience as well as proficiency in directing and designing program projects, facilitating and promoting early feasibility and first-in-human clinical trials, securing extramural funding, and a strong publication record. A proven record of collaborative science endeavors also is desired to work with researchers on initiatives and priorities in AI, immunology, cancer, exposome, discovery science, and entrepreneurship at the Mayo campus. Mayo Clinic's values of teamwork and collaboration are essential to providing integrated research and medical and surgical care to patients with complex conditions. The faculty member will have an academic appointment in The Mayo Clinic College of Medicine and Science commensurate with prior background. The Department of Clinical Genomics in Rochester, MN is part of the Enterprise Clinical Genomics Department across all Mayo Clinic sites. The department is committed to transforming clinical practice by developing, analyzing, and rapidly diffusing innovative solutions to deliver high value care to our patients. Clinical Genomics research has a well-developed infrastructure that supports conducting early feasibility and multi-center basic and translational research and clinical trials that includes staff with expertise in study development, assessment, start-up, and conduct. The Clinical Genomics research portfolio at Mayo Clinic is supported by NIH grants, foundation awards, and philanthropic gifts. The Department of Clinical Genomics partners with several departments and centers within Mayo Clinic, including the Department of Biochemistry and Molecular Biology, Department of Quantitative Health Sciences, Center for Regenerative Medicine, Center for Individualized Medicine, Center for Clinical and Translational Science, and Center for the Science of Health Care Delivery. Bold.Forward.Unbound. (****************************************************************************************************************************************************************************************************** Bold. Forward. Unbound. is a six-year strategic initiative to the Rochester, MN campus that advances Mayo Clinic's overarching mission to Cure, Connect, and Transform healthcare for the benefit of patients everywhere. This $5 billion transformation reimagines the downtown Rochester campus through a combination of innovative care concepts, digital technologies, and state-of-the-art facilities. For physicians, this means practicing in a groundbreaking environment where inpatient, outpatient, and virtual care are seamlessly integrated - empowering you to deliver exceptional outcomes with the support of advanced tools, interdisciplinary collaboration, and a culture rooted in Mayo Clinic's patient-first values. Joining Mayo Clinic during this pivotal moment offers a rare opportunity to shape the future of medicine while advancing your own academic and clinical career. **Qualifications** + Board-certified MD or MD/PhD + Highly skilled in functional, translational, therapeutic, computational, and/or clinical trial research with a broad understanding of genetics and genomics and expertise in integrating novel technologies into clinical practice. **Exemption Status** Exempt **Compensation Detail** The minimum starting salary for Medical specialties may range from $202,000 to $663,037. This range reflects full-time total base compensation prior to consideration of additional experience or duties. Pay for the selected candidate will vary based on specialty, experience, FTE, internal equity, or external market data. **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** Kate Coleman **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.

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

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. 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.

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

Salary range: $78,000 - $102,000 Full-time, exempt The Protein Purification Scientist supports the development and optimization of protein purification processes. This role will involve working closely with cross-functional teams to purify and characterize proteins for therapeutic and research applications. Duties and responsibilities * Develop, optimize, and scale-up protein purification processes for recombinant proteins - predominantly expressed in mammalian cells. * Operate and maintain AKTA FPLC systems and other purification equipment. Perform chromatography techniques, including affinity, ion exchange, size exclusion, and hydrophobic interaction chromatography. * Analyze protein purity and quality by SDS-PAGE, Western blot, UV/Vis spectroscopy, and other analytical methods. * Characterize proteins using biophysical and biochemical methods, such as binding kinetics (BLI), thermal stability (DSF/SLS), and secondary structure (CD). * Troubleshoot and resolve technical challenges in protein purification workflows. * Manage a catalog of protein reagents, defining and maintaining quality control and release criteria, as well as generating Certificates of Analysis. Document experimental procedures, results, and findings in detailed reports and presentations. * Collaborate with upstream and downstream teams to ensure seamless process integration, to align project objectives, timelines, and design needs with downstream applications * Oversee quality control and release criteria, generate Certificates of Analysis, and manage the shipment of protein materials to internal and external partners * Stay current with advancements in protein purification technologies and methodologies. - Ensure compliance with safety protocols and maintain a clean and organized laboratory environment. * Additional duties as assigned. Education and experience requirements * Bachelor's, Master's, or Ph.D. in Biochemistry, Chemical / Protein Engineering, or a related field; with hands-on experience with protein expression and purification (Mammalian & E. Coli). * Good understanding of molecular and cellular biology preferred. * 3+ years of relevant experience and hands-on experience in protein purification (industry experience preferred), including Protein A, Protein G, Protein L, Ni-NTA, StrepTactin, C-tag. * Proficiency in chromatography techniques and AKTA systems. * Strong analytical skills and experience with protein characterization methods. Proficiency in biophysical and analytical methods: SPR/BLI, CD, SEC-MALS, DSF, SDS-PAGE, and Western blotting. * Strong understanding of the biophysics of protein structure/function relationships and confidence with structure modeling and visualization tools (e.g., PyMOL, ChimeraX, AlphaFold) preferred. * Experience with scale-up and tech transfer of purification processes preferred. * Familiarity with automation and high-throughput purification systems preferred. Required skills and/or qualifications * Excellent problem-solving abilities and attention to detail. * Ability to work independently and collaboratively in a fast-paced environment. * Strong communication and organizational skills. * Comfortable working in a fast-paced, interdisciplinary team * Strong communication skills and ability to present data and proposals to a range of audiences 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

A Research Associate position in Life Sciences (LS) will require an advanced knowledge of either clinical-based research or laboratory-based research. 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. 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.

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.

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

The PET Radiochemist is responsible for the daily production and quality control of routine PET drugs. The PET RC assists in the synthesis of PET radiopharmaceuticals for clinical and research studies. The PET Radiochemist will also be responsible for completing and maintaining the appropriate documentation required by federal and state agencies associated with the production and distribution of the PET drug product/radioisotopes. The PET Radiochemist will help in set up and maintain automated chemistry modules and other laboratory equipment and the development of synthesis procedures in the production of PET radiopharmaceuticals/radioisotopes and will provide instruction and training to other radiochemistry staff as needed. PET Radiochemist - quality control: • Responsible for daily quality control of routine PET drug products • Responsible for setup and use of analytical chemistry equipment • Responsible for assessing suitability of incoming materials • Responsible for determining acceptability of productions for release • Responsible for retrospective testing on productions post-release • Responsible for quality control method validation and post repair instrument verification. PET Radiochemist - quality assurance: • Responsible for qualification and monitoring of all vendors and suppliers. • Responsible for the accuracy and upkeep of documentation used in all aspects of the facility • Responsible for ensuring adequate training of all PET Radiochemists • Responsible for conducting regular internal audits and self-inspections • Involved in deviation/OOS and CAPA investigations • Reviews and approves change control events and processes. This vacancy is not eligible for sponsorship/we will not sponsor or transfer visas for this position. Also, Mayo Clinic DOES NOT participate in the F-1 STEM OPT extension program. Bachelor's degree in chemistry or nuclear medicine technology certification, or pharmacy certification. Must have a strong background in analytical chemistry, preferably organic chemistry. Experience working with radioactivity such as in a PET radiochemistry laboratory, nuclear medicine environment, or commercial nuclear pharmacy specializing in PET drug production. Strong word processing and database skills specifically with Microsoft Word and Excel. Additional Qualifications: Two years' experience in production, manufacturing and handling PET drug products is preferred. Experience assisting in the development of PET drug synthesis procedures is preferred. Prior experience teaching, training, group interaction and presentations.

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. 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.

Salary range: $78,000-$102,000 Full time, Exempt The Quality Control Scientist provides technical expertise to research and develop new, or improve existing analytical processes to evaluate oncolytic viral and viral vector based therapeutics, pipeline assets, and to improve overall efficiency in QC processes towards commercialization. Key responsibilities include performing and supporting analytical testing, method development and validation, and quality control (QC) release activities in compliance with cGMP and regulatory standards. The QC Scientist will work closely with internal teams to ensure the timely release of materials, intermediates, and final products used in various phases of drug pipeline. Supervisory Responsibilities None Duties and Responsibilities Method Development and Product Testing * Perform GMP testing of various sample types, which may include raw materials, in-process samples, cell banks, viruses/viral vectors, and final drug products using molecular, biochemical, and/or cell-based analytical methods. * Execute assays including qPCR/dPCR, flow cytometry, ELISA, infectivity/titer assays, vector genome copy number determination, potency assays, and detection of production contaminants * Support method development, qualification, validation, and transfer for novel analytical methods specific to various biologic/cell and gene therapy platforms. * Participate in stability studies, and trending of analytical data to ensure product consistency and compliance. * Review and interpret analytical data, ensuring data integrity and alignment with specifications, SOPs, and regulatory requirements. * Support investigations of deviations, OOS/OOT results, and implementation of CAPAs. * Author, review, and revise controlled documents, including test methods, protocols, reports, and SOPs. * Collaborate with QA, Manufacturing, Process Development, and Regulatory teams to support product release and regulatory filings (e.g., IND, BLA, IMPD). * Maintain laboratory equipment and ensure calibration, qualification, and preventive maintenance activities are completed as required. * Uphold GMP compliance, data integrity, and safety practices in a dynamic, fast-paced environment. * Additional duties as assigned Education and Experience * Advanced degree (Ph.D. and/or relevant degree highly desirable) and 2+ years of related work experience, or a Bachelor's degree with 5+ years of related work experience * Minimum of 1 year working in biologics drug product role with a good understanding of working with a defined QMS and assay qualification. * Experience with setting up, supporting, and troubleshooting multiple pieces of drug product analytical equipment. * Experience with advanced QC techniques, including qPCR/dPCR, flow cytometry, potency assays, and/or ELISA. * Experience conducting process characterization, analysis and development with minimal supervision. * Knowledge of ICH Q2(R2), FDA/EMA regulations for ATMPs, and cGMP testing principles. * Excellent analytical, documentation, and communication skills. 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

A Research Associate position in Life Sciences (LS) will require an advanced knowledge of either clinical-based research or laboratory-based research. 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. 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.

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 A Research Associate position in Life Sciences (LS) will require an advanced knowledge of either clinical-based research or laboratory-based research. 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 $77,961 - $91,204 / 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 Schedule Details Hours between 7am and 5pm, evenings as needed Weekend Schedule as needed 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 Kara Schott

**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** Independently sets up and performs experiments and procedures in support of lab goals and grant commitments (e.g. assays, cell/tissue culture, animal studies, etc.). Contributes to the planning, design and modification of studies and experiments in the research lab setting. Monitors results, reports unusual outcomes and suggests modifications. Collects, enters, summarizes, and analyzes data. May oversee and assist with the training of residents, fellows and temporary lab personnel in lab techniques. Works with minimal supervision and performs assignments independently as discussed and approved by Principal Investigator. **Qualifications** Requires bachelor's degree in biology, chemistry, or other relevant science with 4 years of research laboratory experience. Master's degree in biology, chemistry, or other relevant science preferred. **Exemption Status** Exempt **Compensation Detail** Education, experience and tenure may be considered along with internal equity when job offers are extended.; $66,123 - 99236 annually. **Benefits Eligible** Yes **Schedule** Full Time **Hours/Pay Period** 80 **Schedule Details** M-F 8-5 Schedule could vary depending on lab needs This is a limited tenure position that has been approved for 1 year and may have the possibility of extending one additional year. **Weekend Schedule** Occasionally depending on lab needs. **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** Jill Squier **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.

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 Independently sets up and performs experiments and procedures in support of lab goals and grant commitments (e.g. assays, cell/tissue culture, animal studies, etc.). Contributes to the planning, design and modification of studies and experiments in the research lab setting. Monitors results, reports unusual outcomes and suggests modifications. Collects, enters, summarizes, and analyzes data. May oversee and assist with the training of residents, fellows and temporary lab personnel in lab techniques. Works with minimal supervision and performs assignments independently as discussed and approved by Principal Investigator. Qualifications Requires bachelor's degree in biology, chemistry, or other relevant science with 4 years of research laboratory experience. Master's degree in biology, chemistry, or other relevant science preferred. Exemption Status Exempt Compensation Detail Education, experience and tenure may be considered along with internal equity when job offers are extended.; $66,123 - 99236 annually. Benefits Eligible Yes Schedule Full Time Hours/Pay Period 80 Schedule Details M-F 8-5 Schedule could vary depending on lab needs This is a limited tenure position that has been approved for 1 year and may have the possibility of extending one additional year. Weekend Schedule Occasionally depending on lab needs. 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 Jill Squier

**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** The PET Radiochemist is responsible for the daily production and quality control of routine PET drugs. The PET RC assists in the synthesis of PET radiopharmaceuticals for clinical and research studies. The PET Radiochemist will also be responsible for completing and maintaining the appropriate documentation required by federal and state agencies associated with the production and distribution of the PET drug product/radioisotopes. The PET Radiochemist will help in set up and maintain automated chemistry modules and other laboratory equipment and the development of synthesis procedures in the production of PET radiopharmaceuticals/radioisotopes and will provide instruction and training to other radiochemistry staff as needed. PET Radiochemist - quality control: - Responsible for daily quality control of routine PET drug products - Responsible for setup and use of analytical chemistry equipment - Responsible for assessing suitability of incoming materials - Responsible for determining acceptability of productions for release - Responsible for retrospective testing on productions post-release - Responsible for quality control method validation and post repair instrument verification. PET Radiochemist - quality assurance: - Responsible for qualification and monitoring of all vendors and suppliers. - Responsible for the accuracy and upkeep of documentation used in all aspects of the facility - Responsible for ensuring adequate training of all PET Radiochemists - Responsible for conducting regular internal audits and self-inspections - Involved in deviation/OOS and CAPA investigations - Reviews and approves change control events and processes. **This vacancy is not eligible for sponsorship/we will not sponsor or transfer visas for this position. Also, Mayo Clinic DOES NOT participate in the F-1 STEM OPT extension program.** **Qualifications** + Bachelor's degree in chemistry or nuclear medicine technology certification, or pharmacy certification. + Must have a strong background in analytical chemistry, preferably organic chemistry. + Experience working with radioactivity such as in a PET radiochemistry laboratory, nuclear medicine environment, or commercial nuclear pharmacy specializing in PET drug production. + Strong word processing and database skills specifically with Microsoft Word and Excel. **Additional Qualifications:** + Two years' experience in production, manufacturing and handling PET drug products is preferred. + Experience assisting in the development of PET drug synthesis procedures is preferred. + Prior experience teaching, training, group interaction and presentations. **Exemption Status** Nonexempt **Compensation Detail** $41.48 - $62.25 / hour **Benefits Eligible** Yes **Schedule** Full Time **Hours/Pay Period** 80 **Schedule Details** Monday to Friday shift. Details TBD. **Weekend Schedule** No. **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** Stephanie Brackey **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.