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Scientist, In Vitro / Ex Vivo Position Summary The Scientist - In Vitro / Ex Vivo supports the design, execution, and analysis of complex in vitro and ex vivo studies, with a primary focus on flow cytometry-based assays. This role requires strong technical expertise, attention to detail, and the ability to collaborate across functional teams and sites to deliver high-quality, reproducible data in support of internal development and client programs. The ideal candidate demonstrates both technical proficiency and sound scientific judgment, including the ability to troubleshoot assays, interpret data, and clearly communicate results in a fast-paced, client-driven environment. This position plays a key role in ensuring data integrity, operational efficiency, and scientific excellence within the In Vitro team. This role is based fully onsite at our Boulder, CO site. Responsibilities and Duties • Design, develop, optimize, and execute flow cytometry-based assays for in vitro and ex vivo studies, • Perform routine and complex laboratory procedures, including:, • Multicolor flow cytometry panel design and optimization, • Sample processing and cell handling (human and/or animal tissues), • Immunophenotyping and functional assays, • Data acquisition, analysis, and interpretation using flow cytometry software (e.g., FlowJo, CytoScribe), • Support the development and refinement of standard operating procedures (SOPs) and assay workflows, • Troubleshoot technical issues and implement corrective actions to ensure reliable data generation, • Maintain accurate and complete experimental records in accordance with company and regulatory requirements, • Collaborate with cross-functional teams (e.g., Operations, Project Management, Scientific Leadership) to meet study timelines and deliverables, • Communicate results clearly through written reports, data summaries, and internal or client-facing discussions, • Ensure compliance with applicable quality standards and internal quality systems, • Participate in the training and mentoring of junior staff, as appropriate Education and Experience • Bachelor's or Master's degree in Immunology, Biology, Cell Biology, or a related life sciences field, • 4+ years of hands-on laboratory experience in flow cytometry and cell-based assays (level may be adjusted based on experience), • Demonstrated experience operating flow cytometry instrumentation and analyzing complex datasets, • Strong understanding of immunology, cell biology, and assay design principles, • Strong organizational skills and attention to detail, • Ability to manage multiple priorities and meet deadlines in a fast-paced environment, • Effective written and verbal communication skills, • PhD in Immunology, Biology, Cell Biology, or a related life sciences field, • Experience working in a contract research organization (CRO) or other client-facing environment, • Experience working with tissues from a variety of species (e.g., human, non-human primate, murine, rat), • Experience contributing to SOP development and/or method validation, • Demonstrated scientific rigor with strong attention to detail and commitment to data quality and integrity, • Strong problem-solving and troubleshooting skills, with the ability to interpret results and identify effective solutions, • Excellent written and verbal communication skills, with the ability to clearly convey technical information, • Ability to work independently and collaboratively within a team environment and interact effectively with scientific staff at all levels, • High level of accountability and reliability, with the ability to manage responsibilities and meet deadlines in a dynamic environment, • Ability to work in a laboratory environment for extended periods, • Ability to lift and move laboratory materials and equipment weighing up to 15 lbs This position operates primarily in a laboratory setting and requires adherence to safety and quality procedures. Work may involve handling biological samples and operating specialized laboratory equipment. Compensation and Benefits This position may be offered at different levels depending on a candidate's combination of education and experience. The annual salary range is $$65,000 to $95,000 and may be adjusted based on the level of the role and the candidate's qualifications. Benefits include health and dental coverage, short- and long-term disability, paid time off, paid parental leave, a 401(k), and more. This position is open until filled. Equal Opportunity Employer Statement Inotiv is an Equal Opportunity Employer. We provide fair and equal employment opportunities to all individuals regardless of age, race, color, religion, sex, gender, gender identity or expression, sexual orientation, genetic information, disability, national origin, veteran status, or any other characteristic protected by law. This policy applies to all aspects of employment, including recruitment, hiring, compensation, discipline, termination, and access to benefits and training. *This position could be offered at different levels for candidates who qualify with a combination of advanced levels of education and/or years of experience. The salary range will adjust along with the level of the role to match the person's relevant experience and/or education level. Inotiv is a growing contemporary drug discovery and development company where we "Play to Win" in an industry rich with opportunity. Together, we face challenges and together we win in the delivery of world-class drug discovery and development solutions that impact the health and well-being of people all over the world. There's an opportunity for everyone at all phases of a career, each individual's unique skill set has an impact on the work we conduct. If you have the talent and desire to impact the quality of people's lives, we have the career opportunities to make it happen. Join us in embracing research and science to impact the health and well-being of people all over the world. Salary will be commensurate with experience and responsibilities. Benefits include health and dental coverage, short- and long-term disability, paid time off, paid parental leave, 401K, and more! Inotiv is an Equal Opportunity Employer. It is our policy to provide a fair and equal employment opportunity to all persons, regardless of age, race, color, religion, sex, gender, gender identity, gender expression, sexual orientation, genetic information, disability, national origin, veteran status, or any other basis prohibited by law. This policy governs all aspects of employment, including selection, job assignment, compensation, discipline, termination and access to benefits and training.

Company Overview ImmunityBio, Inc. (NASDAQ: IBRX) is a commercial-stage biotechnology company developing cell and immunotherapy products that are designed to help strengthen each patient's natural immune system, potentially enabling it to outsmart the disease and eliminate cancerous or infected cells. We envision a day when we no longer fear cancer, but can conquer it, thanks to the biological wonder that is the human immune system. Our scientists are working to develop novel therapies that harness that inherent power by amplifying both branches of the immune system, attacking cancerous or infected cells today while building immunological memory for tomorrow. The goal: to reprogram the patient's immune system and treat the host rather than just the disease. Why ImmunityBio? • ImmunityBio is developing cutting-edge technology with the goal to transform the lives of patients with cancer and develop next-generation therapies and vaccines that complement, harness and amplify the immune system to defeat cancers and infectious diseases., • Opportunity to join a publicly traded biopharmaceutical company with headquarters in Southern California., • Work with a collaborative team with the ability to work across different areas of the company., • Ability to join a growing company with professional development opportunities. Position Summary The Scientist I, Process Sciences - Analytical Development will work alongside Process Sciences and Analytical Development (AD) team members to contribute to our efforts to develop and implement methods across ImmunityBio's platforms, and the advancement of our pipeline by collaborating with internal and external partners. The role is responsible for method development and ensuring timely execution of samples in support of process development activities. The Scientist I, Process Sciences - Analytical Development will assist in data review, method qualification and/or validation, and training of junior team members.. The role will support AD management and Regulatory Affairs personnel with all regulatory filings and will require cross-functional interaction with members of the Manufacturing, Quality Assurance, Quality Control, and Process/Product Development teams. Essential Functions • Perform method development, optimization, and troubleshooting of analytical methods, for various product platforms with minimum supervision., • Ensure the integrity of all data generated., • Perform a variety of techniques to assess product quality and characterize products, including HPLC assays, UV-Vis and analytical chemistry techniques., • Support efforts for method troubleshooting, remediation, change, and optimization efforts in conjunction with Quality Control and Analytical Development., • Author and review analytical methods, SOPs, protocols, and reports., • Support the Process Development teams to characterize process improvements and develop new products., • Support internal and/or external transfers of analytical methods., • Oversee the training and development of junior Analytical Development associates/specialists., • Maintain, calibrate and operate analytical equipment and instruments., • Provide technical expertise to troubleshoot assays. Ensure timely escalation of all assay related issues., • Interface with other departments (e.g., QC, Manufacturing, Engineering, QA and Regulatory) to ensure achievement of ImmunityBio's goals., • Performs ad-hoc and cross-functional duties and/or projects as assigned to support business needs and provide developmental opportunities. Education & Experience • Bachelor's degree in a scientific discipline with 8+ years of relevant experience in a GMP regulated Biologics or Pharmaceutical environment required; or, • Master's degree in scientific discipline with 6+ years of relevant experience in a GMP regulated Biologics or Pharmaceutical environment required., • Experience in method development, method validation, and method transfer is required., • Fundamental knowledge of analytical chemistry and chromatography is required., • Fundamental knowledge of cell and molecular biology, immunology, and/or virology a plus. Knowledge, Skills, & Abilities • Ability to successfully interface with multidisciplinary teams, • Excellent verbal and written skills to communicate cross functionally, • Highly motivated, detail oriented and able to excel in a fast-moving environment., • Expert knowledge and experience with other pharmaceutical test methods to include HPLC analysis, osmolality, pH, conductivity, UV-Vis, and Karl-Fischer, • Knowledge of quality control analytical method development, method validation and method transfer, • Problem solving skills with attention to detail, • Knowledge and understanding of cGMP, 21 CFR 210/211, USP, EP and ICH guidelines, • In-depth knowledge of GMPs and pharmaceutical regulations, • Ability to collaborate with contract testing laboratories, consultants, ensuring compliance with company procedures, • Ability to multi-task and prioritize, • Adept at instrumentation trouble shooting, • Strong statistical analysis skills, • Strong technical writing skills with experience preparing: SOPs, analytical test reports, work instructions, qualification/validation protocols, qualification/validation reports, and summary reports to support FDA and EMA filings. Working Environment / Physical Environment • This position works on site, in Louisville, CO., • Regular work schedule is Monday - Friday, within standard business hours. Flexibility is available with manager approval., • Working environment is within a GMP BSL-2 laboratory with equipment sufficient to complete the tasks described above., • Travel up to 10%., • Occasionally: transporting small equipment, frequent bending, sitting, squatting and lifting up to 40 lbs. This position is eligible for a discretionary bonus and equity award. The annual base pay range for this position is below. The specific rate will depend on the successful candidate's qualifications, prior experience as well as geographic location. $104,000 (entry-level qualifications) to $114,400 (highly experienced) annually The application window is anticipated to close on 60 days from when it is posted or sooner if the position is filled or closed. ImmunityBio employees are as valuable as the people we serve. We have built a resource of robust benefit offerings to best support the total wellbeing of our team members and their families. Our competitive total rewards benefits package, for eligible employees, include: Medical, Dental and Vision Plan Options * Health and Financial Wellness Programs * Employer Assistance Program (EAP) * Company Paid and Voluntary Life/AD&D, Short-Term and Long-Term Disability * Healthcare and Dependent Care Flexible Spending Accounts * 401(k) Retirement Plan with Company Match * 529 Education Savings Program * Voluntary Legal Services, Identity Theft Protection, Pet Insurance and Employee Discounts, Rewards and Perks * Paid Time Off (PTO) includes: 11 Holidays * Exempt Employees are eligible for Unlimited PTO * Non-Exempt Employees are eligible for 10 Vacation Days, 56 Hours of Health Pay, 2 Personal Days and 1 Cultural Day * We are committed to providing you with the tools and resources you need to optimize your Health and Wellness. At ImmunityBio, we are an equal opportunity employer dedicated to diversity in the workplace. Our policy is to provide equal employment opportunities to all qualified persons without regard to race, gender, color, disability, national origin, age, religion, union affiliation, sexual orientation, veteran status, citizenship, gender identity and/or expression, or other status protected by law.

Job Description Umoja Biopharma is an industry-leading biotech with locations in Seattle, WA and Louisville, CO, focused on transforming the treatment of cancer with a novel integrated immunotherapy platform. Our vision is to develop off-the-shelf therapies capable of treating any tumor, any time. We are a diverse and growing team working in brand-new facilities in downtown Seattle, Washington and Louisville, Colorado, and we are looking for innovative thinkers who are excited by groundbreaking science and technology, and passionate about squaring up to the challenges inherent to cutting-edge drug development. We are committed to our core values and principles that support our overall mission and strongly invite applications from enthusiastic individuals who share our commitment and help position Umoja to deliver on our goals. We at Umoja believe in the importance of stories; we are looking for great people to join our team to help us create more stories for ourselves, for you, and most importantly for patients and their families. Umoja Biopharma – Your Body. Your Hope. Your Cure. POSITION SUMMARY Umoja's Analytical Development organization is seeking a driven Senior Research Associate within the Process Analytics sub team to support in-process and drug substance and product testing of Lentiviral Vector (LVV) . This role will play a key part in routine sample testing, new method development, and method lifecycle management. In addition, they will advance assay execution, data quality, and turnaround time through increased automation by incorporating tools such as AI and Ganymede to support efficient data capture, analysis and decision making. The successful candidate will have experience performing a variety of molecular, cellular, biophysical, and biochemical protocols. This position works cross-functionally with other departments to test LVV samples as well. This position plays a critical role in advancing Umoja's pipeline and Analytical Development capabilities. This is a full-time onsite lab-based position 5 days/week at our Louisville, CO location. CORE ACCOUNTABILITIES Specific responsibilities include: • Assist with method development, execution, analysis, and data review to support the development of gene therapy product, • Perform routine testing (e.g., ELISA, qPCR, ddPCR, flow cytometry) to support process development and stability studies., • Ability to perform analysis and calculations manually using software such as Excel, JMP, flowjo, prism and R/Python., • Strong understanding of the automation workflows including analysis platforms (such as Ganymede)and an ability to integrate this tool into multiple analytical methods., • Maintain clear records of experimental work using an electronic notebook system that adheres to company guidelines., • Manage sample submissions in Benchling (ELN) for assigned methods and turn around data in timely manner., • Supports process mapping and identify sources of waste in a workflow and identifies automation opportunities to increase efficiency., • Exemplifies the company core values and adheres to company policies to ensure safety and quality of gene therapy products, our people, and our facility., • Bachelors Degree in Biology, Biochemistry, or related discipline with at least 2 years of experience or an Associate's Degree and 4 years of hands-on laboratory experience. Equivalent combinations of education and experience will be considered., • Hands-on experience with ddPCR, qPCR, ELISA, and/or flow cytometry., • Excellent communication skills with the proven ability to build open and collaborative relationships and work effectively as a member of a multidisciplinary team, • Proficient in basic data analysis, and experience developing more complex analyses., • Self-motivated, organized, and clear documentation., • 100% compliance with personal protective equipment (PPE) requirements in laboratory environments, including gloves, protective clothing, and eye safety glasses., • Perform physical tasks required for the role, including standing, walking, bending, kneeling, sitting, working your hands in a biosafety cabinet, and occasionally moving materials up to 50 pounds.

Job Description Umoja Biopharma is an industry-leading biotech with locations in Seattle, WA and Louisville, CO, focused on transforming the treatment of cancer with a novel integrated immunotherapy platform. Our vision is to develop off-the-shelf therapies capable of treating any tumor, any time. We are a diverse and growing team working in brand-new facilities in downtown Seattle, Washington and Louisville, Colorado, and we are looking for innovative thinkers who are excited by groundbreaking science and technology, and passionate about squaring up to the challenges inherent to cutting-edge drug development. We are committed to our core values and principles that support our overall mission and strongly invite applications from enthusiastic individuals who share our commitment and help position Umoja to deliver on our goals. We at Umoja believe in the importance of stories; we are looking for great people to join our team to help us create more stories for ourselves, for you, and most importantly for patients and their families. Umoja Biopharma – Your Body. Your Hope. Your Cure. CORE ACCOUNTABILITIES Specific responsibilities include: • Model Umoja values by setting clear expectations, coaching performance, and building an inclusive, high-accountability culture within QC Analytical., • Own day-to-day QC Analytical lab operations (planning, staffing, scheduling, and execution) across analytical testing, stability programs, and sample management to ensure compliant, on-time delivery of testing results in support of corporate goals and program milestones., • Lead a matrixed team of full time employees and contractors, including recruiting, performance management, and talent development, • Oversee use and continuous improvement of QC Analytical programs, processes, and systems to ensure consistent cGMP execution and scalability., • Drive implementation and adoption of lab digital and automation tools (e.g., LIMS, reagent management, electronic lab notebook) to improve throughput, right-first-time performance, and compliance., • As QC Analytical management, collaborate with Analytical Development to ensure method readiness for QC (transfer, qualification/validation, training, and routine execution) in support of analytical method lifecycle activities., • Forecast demand and build capacity plans (headcount, training, equipment, and coverage) aligned to manufacturing timelines and program needs., • Bachelor's degree in Biochemistry, Molecular and Cellular Biology, Immunology, Biology, or related life science, plus 8+ years of experience in cGMP Quality Control. Equivalent combinations of advanced education and experience will be considered. Extensive knowledge of analytical method qualification, validation, and transfer., • 4+ years of demonstrated people leadership experience in a cGMP environment—hiring, coaching, developing, and retaining talent while setting clear priorities and driving accountability., • Deep hands-on and applied knowledge of molecular biology analytical techniques (e.g., PCR, ELISA, flow cytometry, cell-based assays), • Working knowledge of applicable regulations and compendial/industry guidance (e.g., ICH, USP) with the ability to translate requirements into practical, inspection-ready QC practices., • Experience leading teams with direct reports, including performance management, talent development, and building a culture of quality, collaboration, and continuous improvement., • Proven Operational Excellence/Continuous Improvement capability, applying Lean principles and data-driven problem solving to improve quality, throughput, and right-first-time performance., • Strong judgment and risk-based decision-making—able to propose solutions, communicate risks, and anticipate downstream impact in a fast-paced, evolving environment., • Track record of raising team performance through clear expectations, effective communication, strong follow-through, and consistent accountability., • Experience building and scaling an early phase QC laboratory, including quality systems and analytical method lifecycle ownership (transfer, qualification, validation, and method performance)., • Cell and gene therapy experience in a cGMP setting, specifically QC testing in support of lot release/stability and successful cross-functional partnerships with Technical Operations, Analytical Development and Quality., • Experience leading through audits/inspections (internal, client, or regulatory) and driving inspection readiness., • Experience implementing and optimizing LIMS/data integrity controls and digital transformation at scale., • Ability to work onsite 5 days/week at our Louisville, CO location, • Ability to work evenings and/or weekends as needed, • Ability to gown aseptically and work in a Clean Room environment, • Ability to wear personal protective equipment including gloves, protective clothing, and eye safety glasses., • Ability to work while gowned for extended periods of time

Job Description Principal Investigator - Pharmacology-Gastrointestinal Job Summary: This is a high-touch leadership role that helps the team focus on customer service and scientific rigor while helping to move the science forward with their expertise leading from the bench. The Principal Investigator - Pharmacology-Gastrointestinal directly reports to the Senior Director of Pharmacology and is responsible for executing, planning, and managing assigned studies. The successful candidate will have direct knowledge of the time and costs associated with a given amount of scientific work, can communicate their scientific expertise to other scientists, directors, VPs, and CEOs of client companies, and can execute multiple, concurrent studies within a guaranteed time frame. Primary Responsibilities: • Manage a team of technical staff (5 direct and 20 indirect) and assist with all aspects of the study design, • Generate clear study guidelines and protocols with all clients and customers, • Aid with disease induction and study modeling, • Assess and report on projects to all stakeholders, • Coordinate study activities with all participants, including animal technicians and principal investigators, • Communicate significant knowledge of conducting animal disease models and related activities, • Follow and support company policies (Handbook, OHS, SOPs, QPBR, Program for Care and Use of Animals, IACUC), • Review and enter data into study management systems Secondary Responsibilities: • Collect blood and dosing (as needed), • Conducts necropsies (as needed), • Compound formulation (test articles, disease induction, and positive controls), • Process and store study samples Qualifications/Education: • Master of Science Degree in Biology, Ph.D. Preferred, • Experience working with Intestinal Disease Models, • Previous management of technicians is a plus Employees are offered a fun, fast-paced work environment with competitive pay, benefits package including medical, dental, and vision insurance, 401k with company match, stock options, and much more!

Job Description Overview The Job in a Nutshell: This role requires an outgoing personality and passion for sharing nutrition knowledge and inspiring people to act and achieve their health goals. You’ll wear many hats while working in a fast-paced retail setting conducting classes, private coaching sessions, community outreach, and retail operations (e.g., customer service, stocking shelves, cleaning, etc.). As the store’s nutrition professional, you will act as an educational resource providing science-based nutrition education/training to the store Crew, our customers, and the community. This position is a front-line contributor to the Natural Grocers mission and plays an integral role helping Natural Grocers improve the health and wellbeing of our communities. Through providing free nutrition education and helping people understand why their food choices matter, you will play an important role in Natural Grocers commitment creating a sustainable, Just, regenerative food system where humans, animals, and the earth can thrive. Applications are accepted by the date below, which may be updated if the hiring timeline is extended. 04/31/2026 Responsibilities Main Ingredients: • Acts as the nutrition education resource for the customers, Crew, and community., • Provides private individual one-on-one health coaching sessions, • Seeks outreach opportunities (to provide nutrition education and build brand awareness), • Assists management with coordinating, organizing, and executing companywide events, • Responsible for printing materials used in classes, outreach, and coaching sessions, • Responsible for placing orders for nutrition education supplies, • Provides training to Crew on promoting the NHC services, instore events, and promotions, • Attends monthly meetings (NHC webinar, Regional and Sales Building calls) Qualifications Recipe for Success: • Microsoft Office skills (i.e., Excel, Outlook, etc.), • Excellent public speaking skills, • Ability to engage customers and start conversations to promote events, services, and sales, • Excellent interpersonal skills, • Excellent organizational skills and priority management, • Self-directed and able to maximize time management, • Able to work well with a team and accept constructive feedback, • Motivated to grow and develop knowledge and skills, • Inspired to provide nutrition education to employee Crew, customer’s and the community This job description is not an employment contract. It does not guarantee a job or that the above listed duties are the limit of responsibilities. The job and job description are subject to change with and without notice. Employees are required to accomplish any and all tasks assigned to him/her by their Manager and/or other Store Support Center manager that might not be listed in this job description. Here’s an overview of the benefits we offer our good4u Crew to help ensure the health and wellbeing of you and your family, now and well into the future: All Crew Members • Birthday Bonus Pay, • Vitamin Bucks (up to $2,080 earned as store credit annually), • Holiday Pay for 5 Holidays – Stores Closed, • Paid Time Off (sick days and vacation) that Increases with Tenure, • Paid Nutrition Education, • good4u Crew Member Discount, • {N}power Program (customer appreciation and rewards program), • Regular, Scheduled Pay Increases, • Advancement Opportunities and Career Development, • Health and Wellness Program, • Employee Assistance Program (EAP), • Employee Referral Program Full-Time Crew Members (30+ hours/week) • Medical, Dental and Vision Insurance, • Paid Parental Leave, • Paid Medical Leave (through company paid short-term disability insurance), • Company Paid Short-Term Disability Insurance, • Company Paid Life Insurance, • Voluntary Benefits Including Hospital Indemnity, Accident Insurance, Long-Term Disability Insurance, Term Life Insurance, • Retirement Savings Plan (401k) with discretionary Company Match, • Healthcare and Dependent Care Flexible Spending Account (FSA) At the heart of Natural Grocers' commitment to our community and crew is this belief: All people should be empowered to experience health and wellbeing! We cannot be true to this conviction without honoring diversity and cultivating inclusion throughout every aspect of our organization. At Natural Grocers, we honor our differences, embrace diversity, and cultivate inclusion because both individual and societal health are rooted in these principles. Our Crew is diverse not only in gender, race, ethnicity, sexual orientation, religion, abilities, and age but also in cultural backgrounds, thoughts, and ideas. Celebrating our diversity refreshes, expands, and shapes our perspective, energizing our mission of equitable access to health and wellness for all. We welcome everyone who would like to join us in this mission, with gratitude for the unique life experience each person brings to the table. We’re committed to nurturing an ecosystem of diversity and inclusion in which our Crew can continue to thrive. Physical Capabilities and Environmental Demands: N = Never O = Occasional; 1-33% of time F = Frequent; 34-66% of time C = Constant; 67-100% of time Physical Requirements: • Must have the ability to constantly lift or carry up to 10 lbs., frequently lift or carry 11-20 lbs., and occasionally lift or carry 21-50 lbs. Must also have the ability to occasionally lift or carry 51-100 lbs. with a team lift., • Must have the ability to frequently push or pull up to 15 lbs. and occasionally push or pull 16-100 lbs., • Must be able to occasionally use the computer for data entry and use of mouse., • Must be able to constantly walk, stand, use fine motor manipulations, grip, bend, twist, turn, and reach outward for the duration of the work shift., • Must be able to frequently to reach above chest., • Must be able to occasionally sit, squat, kneel, and climb as needed. Environmental Requirements: • Must be able to frequently work with sharp tools and equipment, dust, fumes, and congested worksite., • Must be able to occasionally work with noise, cold, heat, wet, humid, outside, heights, and contact stress.

Job Description Principal Investigator - Inflammatory Pharmacology Job Summary: This high-touch leadership role helps the team focus on customer service and scientific rigor while helping to move the science forward with their expertise leading from the bench. The Principal Investigator – Inflammatory Pharmacology directly reports to the Senior Director of Pharmacology and is responsible for the execution, planning, and management of assigned studies. The successful candidate will have direct knowledge of the time and costs associated with a given amount of scientific work, can communicate their scientific expertise to other scientists, directors, VPs, and CEOs of client companies, and can execute multiple, concurrent studies within a guaranteed time frame. Primary Responsibilities: • Manage a team of technical staff and assist with all aspects of the study design, • Generate clear study guidelines and protocols with all clients and customers, • Aid with disease induction and study modeling, • Assess and report on projects to all stakeholders, • Coordinate study activities with all participants, including animal technicians and principal investigators, • Communicate significant knowledge of conducting animal disease models and related activities, • Follow and support company policies (Handbook, OHS, SOPs, QPBR, Program for Care and Use of Animals, IACUC), • Review and enter data into study management systems Secondary Responsibilities: • Collect blood and dosing (as needed), • Conducts necropsies (as needed), • Compound formulation (test articles, disease induction, and positive controls), • Process and store study samples Qualifications/Education: • Master of Science Degree in Biology, Ph.D. Preferred, • Experience working with Inflammatory Disease Models, • Previous management of technicians is a plus Employees are offered a fun, fast-paced work environment with competitive pay, benefits package including medical, dental, and vision insurance, 401k with company match, stock options, and much more!

Job Description Umoja Biopharma is an industry-leading biotech with locations in Seattle, WA and Louisville, CO, focused on transforming the treatment of cancer with a novel integrated immunotherapy platform. Our vision is to develop off-the-shelf therapies capable of treating any tumor, any time. We are a diverse and growing team working in brand-new facilities in downtown Seattle, Washington and Louisville, Colorado, and we are looking for innovative thinkers who are excited by groundbreaking science and technology, and passionate about squaring up to the challenges inherent to cutting-edge drug development. We are committed to our core values and principles that support our overall mission and strongly invite applications from enthusiastic individuals who share our commitment and help position Umoja to deliver on our goals. We at Umoja believe in the importance of stories; we are looking for great people to join our team to help us create more stories for ourselves, for you, and most importantly for patients and their families. Umoja Biopharma – Your Body. Your Hope. Your Cure. POSITION SUMMARY Umoja Biopharma is seeking a Senior Manager, Quality Assurance (QA) Operations to support GMP operations at Umoja's state-of-the-art lentiviral vector development and manufacturing facility, The CLIMB, in Louisville, CO. This position delivers leadership and management oversight of the QA Operations team, which provides QA partnership and oversight of all GxP functions (e.g., Manufacturing, Supply Chain, Facilities, Engineering, etc.) at The CLIMB. This role is fully onsite at our Louisville, CO location 5 days/week. This role may require weekend, evening, or holiday work when necessary. CORE ACCOUNTABILITIES Specific responsibilities include: • Exemplifying, role modeling, and maturing Umoja's quality culture, • Managing, building, and maturing a high-performing, solution-oriented function that nurtures strong cross-functional working relationships, • Leading, managing, and supporting QA Operations to provide QA partnership and oversight (e.g., controlled documents, change controls, deviations, CAPAs, work orders, etc.) of GxP functions (e.g., Manufacturing, Supply Chain, Facilities, Engineering, etc.) at The CLIMB, • Supports QA Operations teams collaborative interactions with cross-functional partners in translating applicable laws, regulations, and guidance (e.g., FDA, ICH, EMA, etc.) into compliant & efficient internal procedures and ways of working in accordance with phase-appropriate cGMPs and effective quality risk management principles, • Engaging with key stakeholders and utilizing Operational Excellence principles and tools to drive continual improvement of the Umoja Quality Management System, • Championing Umoja QA's "purposeful presence" initiative, ensuring productive and intentional QA partnership with cross-functional teams, • Overseeing disposition of product and incoming materials, • Advancing Umoja's Quality Risk Management (QRM) program and associated processes, • Partnering with senior Quality management to develop a QA Operations functional strategy to achieve short-term and long-term organizational and company goals & objectives, • Translating functional area strategy into an efficient tactical execution plan that prioritizes functional workload, • Establishing, monitoring, and maturing key business performance metrics to facilitate continual improvement opportunity identification and execution., • Developing and maintaining capacity and resource modeling tools for the QA Operations functions, • Development of QA Operations team through engaging, purposeful development planning and routine follow-up, • Representing QA Operations on cross-functional leadership and project teams, • Supporting the preparation of documents and sections for regulatory dossiers (e.g., briefing books, IND sections, BLA sections, etc.), • Providing support for audits and inspections, where needed, • Bachelor's degree in Biochemistry, Molecular and Cellular Biology, Immunology, Biology, or other life science with minimum of 10+ years of work experience in an FDA regulated industry., • Minimum of 4+ years of successful people management experience with demonstrated ability to build, develop, and lead a high-performing team., • Advanced knowledge and understanding of regulatory governing bodies, requirements, and guidance documents, and how to practically apply these in a cGMP biopharmaceutical environment across different phases of product development, • Strong understanding of foundational Quality systems (e.g., audits/inspections, documentation, NC/CAPA, Quality Risk Management, etc.), • Previous experience releasing product for clinical and/or commercial use, • Independent and risk-based decision-making capability with clear understanding of decision-making impact in dynamic GMP environment, • Ability to think and lead conceptually, strategically, and tactically, arriving at practical and pragmatic conclusions, • Ability to translate complex processes and competing priorities into a clear, actionable plan for execution, • Previous experience with audits and health authority inspections, • Ability to gown aseptically and work in a Clean Room environment, • Ability to work while gowned for extended periods of time, • Ability to stand for extended periods of time to fulfill on-the-floor Quality duties, • Use of laboratory equipment includes handling chemicals and biological materials, • Must have the ability to work around laboratories, manufacturing areas and equipment, and regularly lift 10-20 lbs. and periodically lift up to 50 lbs.

Job Description Umoja Biopharma is an industry-leading biotech with locations in Seattle, WA and Louisville, CO, focused on transforming the treatment of cancer with a novel integrated immunotherapy platform. Our vision is to develop off-the-shelf therapies capable of treating any tumor, any time. We are a diverse and growing team working in brand-new facilities in downtown Seattle, Washington and Louisville, Colorado, and we are looking for innovative thinkers who are excited by groundbreaking science and technology, and passionate about squaring up to the challenges inherent to cutting-edge drug development. We are committed to our core values and principles that support our overall mission and strongly invite applications from enthusiastic individuals who share our commitment and help position Umoja to deliver on our goals. We at Umoja believe in the importance of stories; we are looking for great people to join our team to help us create more stories for ourselves, for you, and most importantly for patients and their families. Umoja Biopharma – Your Body. Your Hope. Your Cure. POSITION SUMMARY Umoja Biopharma is looking for a Senior Analyst, Quality Control Microbiology to perform testing and monitoring activities in support of the QC Microbiology laboratory and manufacturing areas at Umoja's lentiviral vector manufacturing facility. This role reports to the Senior Manager, Quality Control Microbiology and will be based fully onsite in Louisville, CO. REQUIREMENTS Specific responsibilities include: • Performs and reviews routine Quality Control laboratory work, including environmental monitoring, clean utility sampling and testing, microbiological material qualification and maintenance, microbial identification, raw material sampling and inspection, bioburden testing, endotoxin testing, compendial testing, and container closure integrity testing, • Generates and revises Quality Control documents according to established document management processes, • Assists in the development of training materials and independently delivers training to staff for QC programs, systems, and processes, • With management oversight, executes qualification/validation activities for QC laboratory equipment, instruments, and systems, • With management oversight, executes internal and external method establishment (e.g., qualify, validate, verify, transfer) protocols to ensure QC readiness for production activities, • Initiates and supports microbial excursion investigations related to facility and personnel monitoring programs (e.g., environmental monitoring, aseptic gowning, utility monitoring, etc.) through collaboration with other functions (Engineering, Manufacturing, MSAT, etc.), • Applies and advances Operational Excellence/LEAN philosophy within the QC laboratories to ensure continuous improvement across all programs, processes, and systems, • Prepares, ships, and tracks samples to outside testing laboratories, • Demonstrates the Umoja values as part of a high-performing, people-focused, inclusive, and collaborative organization, • Bachelor's degree in Biochemistry, Molecular and Cellular Biology, Immunology, Biology, or other life science with 3-5 years of experience working in a cGMP regulated QC environment. Equivalent combinations of education and experience will be considered., • A passion for teamwork and unwavering commitment to purpose, team success, and contribution to an outstanding workplace culture, • Quality Control experience in an FDA-regulated industry supporting cGMP manufacturing areas, • Previous experience working in a clean room environment, • Previous experience working in cGMP cell and gene therapy manufacturing and/or testing facility, • Ability to work on-site 5 days/week at Umoja's manufacturing facility in Louisville, CO, • Ability to aseptically gown and work while standing for extended periods of time Specialist, Quality Control Microbiology Salary Range: $92,900- $97,545 Benefits Offerings Umoja Biopharma offers its employees competitive Medical, Dental, and Vision plans. Additionally, we offer Umojians access to a 401k plan through Fidelity, with a 100% match up to their first 4% deferral. Umoja also provides a generous Paid Time Off policy, employee commuter benefits, and cell phone stipend. For a full breakdown of our benefits offerings, please see the Benefits section of our website.

Job Description Umoja Biopharma is an industry-leading biotech with locations in Seattle, WA and Louisville, CO, focused on transforming the treatment of cancer with a novel integrated immunotherapy platform. Our vision is to develop off-the-shelf therapies capable of treating any tumor, any time. We are a diverse and growing team working in brand-new facilities in downtown Seattle, Washington and Louisville, Colorado, and we are looking for innovative thinkers who are excited by groundbreaking science and technology, and passionate about squaring up to the challenges inherent to cutting-edge drug development. We are committed to our core values and principles that support our overall mission and strongly invite applications from enthusiastic individuals who share our commitment and help position Umoja to deliver on our goals. We at Umoja believe in the importance of stories; we are looking for great people to join our team to help us create more stories for ourselves, for you, and most importantly for patients and their families. Umoja Biopharma – Your Body. Your Hope. Your Cure. POSITION SUMMARY The Vice President of Analytical Development will provide technical, operational, and strategic leadership for Umoja's analytical development organization, with responsibility for release, characterization, and lifecycle management of analytical methods supporting clinical and commercial cell and gene therapy products. Reporting to the Chief Technical Officer (CTO), this role will define and execute the company's end-to-end analytical strategy in close partnership with Quality, Manufacturing, Regulatory, and Research. This individual will be a critical leader at the interface of Research and Discovery, GMP Manufacturing, Quality, and CMC Regulatory, with accountability for analytical method development, qualification, validation, transfer, and specification setting for GMP products. The ideal candidate brings deep regulatory experience—particularly IND and BLA submissions—strong people leadership, and a proven ability to scale analytical organizations in fast-paced biotech environments. This position is based in Louisville, CO (preferred) or Seattle, WA. CORE ACCOUNTABILITIES Specific requirements include: Strategic Leadership & Execution • Provide strategic leadership and operational oversight for the Analytical Development and Process Analytics teams, including routine testing to support process and product development., • Define and own Umoja's overarching analytical strategy across development stages, from early clinical programs through BLA and commercialization., • Lead the design, implementation, and continuous improvement of laboratory systems and workflows, including development of high-throughput and automated testing strategies., • Lead analytical method development, process analytics, and lifecycle management for intermediates, drug substance, and drug product testing., • Establish analytical strategies for specification setting, comparability, and assay robustness consistent with regulatory expectations., • Provide subject matter expertise to support CMC strategy, regulatory interactions, and responses to agency questions., • Build and maintain strong cross-functional partnerships to ensure effective handoffs of technologies, methods, and data across Research, Manufacturing, Quality, and Regulatory., • Lead strategic planning, annual goal setting, talent development, succession planning, and organizational design for the function., • Own OPEX and CAPEX planning and execution in collaboration with Finance and HR., • Ensure the organization meets budgeted financial goals and operates within approved timelines., • Select, manage, and oversee external contract laboratories and vendors. Setting Strategy • Articulates a clear, compelling vision for the Analytical Development organization aligned with Umoja's mission and long-term goals., • Demonstrates creativity and entrepreneurial thinking to push scientific and operational boundaries., • Sets ambitious goals and holds self and others accountable for delivery., • Thrives in ambiguous, rapidly evolving environments and leads effectively through change., • Builds trust, inspires collaboration, and develops talent across functions and geographies., • Models resilience, perseverance, and a commitment to excellence., • Builds strong, authentic relationships through emotional intelligence and clear communication., • Influences through credibility, passion, and purpose rather than authority alone., • Advanced degree in Biology, Biochemistry, Chemistry, or a related life sciences discipline (MS or PhD preferred)., • Minimum of 15 years of experience in biopharmaceutical development, with significant leadership experience in analytical development., • Minimum of 5 years' experience building, leading, and developing high-performing teams., • Deep expertise in analytical techniques relevant to cell and gene therapies, including flow cytometry, ELISA, qPCR, ddPCR, and cell-based assays., • Strong working knowledge of analytical development, CMC regulatory strategy, and Quality systems in the cell and gene therapy space., • Demonstrated success scaling organizations and infrastructure in growth-stage biotech companies., • Strong understanding of ICH guidelines, pharmacopeial standards, and global regulations governing GMP release testing., • Excellent strategic, operational, financial, and business acumen., • Ability to manage complexity, prioritize across multiple programs, and influence across a diverse stakeholder landscape., • Ability to travel up to 20%

Job DescriptionBenefits: • Complimentary Workouts for 1 family member, • Complimentary Workouts, • Bonus based on performance, • Training & development, • Competitive salary, • Free uniforms "If you have enthusiasm, a positive attitude and good communication, I have a fun and fulfilling Personal Training Position just for YOU!" We understand that everyone knows they should exercise, and everyone wants to be fit and healthy. But, that is easier said than done given busy schedules, and in some cases somewhat beat-up bodies. Thousands of people every day enjoy the best possible workout for them at our 200 nationwide studios. The Exercise Coach brand was built upon the belief that staying strong and healthy shouldnt feel like a hassle! Members of our team enjoy benefits like: • Access to state-of-the-art, iso-kinetic fitness technology, • One rate of pay for all scheduled hours (not just for training clients), • Complimentary memberships - improve your own strength and health as well as for a loved one!, • Company-paid certifications and uniforms, • Lead individual and small-group exercise sessions, • Track fitness results for clients and lead client education, • Grow the business through selling memberships - no cold calling!, • Conduct initial consultations and body composition measurementsNo fitness experience is necessary, but candidates with experience in personal training or small-group fitness instruction will receive priority consideration. All employees will receive full training in The Exercise Coach methods and technologies and must be able and willing to participate both in our exercise and nutrition methodology. This role is great for you if you have: • Passion for Health & Fitness: This is where it all begins!, • Good Communication Skills: You must be comfortable conversing in person and on the phone and know how to conduct yourself professionally, and deliver clear instructions to the clients., • People skills and personality: You must LOVE working with people! As mentioned above you must be very comfortable working with people. This is an exciting studio and you must be able to show your clients energy and excitement while working with them., • Health and Fitness Education: A college degree in a health-related field is nice, but not required. However, fundamental knowledge of exercise science and human biology is essential. You do not need a great deal of personal training experience, but you should have a working knowledge of the human body and the various components of good health and fitness.If you would like to inspire and empower people to enjoy the strength, wed love for you to consider joining our team! Certification: • Successful completion of The Exercise Coach Certification Course (provided on-line and in studio), • Valid CPR/AED certificate from a nationally-recognized provider., • Must be eligible to work in the USA.Preferred Skills & Experience:, • Sales - no cold calls here, we source and track social media leads & referrals through the sales process, • Experience with various strength training applications, • Experience working with adults and their various conditions, • Basic nutrition knowledge

Job Description Umoja Biopharma is an industry-leading biotech with locations in Seattle, WA and Louisville, CO, focused on transforming the treatment of cancer with a novel integrated immunotherapy platform. Our vision is to develop off-the-shelf therapies capable of treating any tumor, any time. We are a diverse and growing team working in brand-new facilities in downtown Seattle, Washington and Louisville, Colorado, and we are looking for innovative thinkers who are excited by groundbreaking science and technology, and passionate about squaring up to the challenges inherent to cutting-edge drug development. We are committed to our core values and principles that support our overall mission and strongly invite applications from enthusiastic individuals who share our commitment and help position Umoja to deliver on our goals. We at Umoja believe in the importance of stories; we are looking for great people to join our team to help us create more stories for ourselves, for you, and most importantly for patients and their families. Umoja Biopharma – Your Body. Your Hope. Your Cure. POSITION SUMMARY Umoja Biopharma is seeking a Quality Assurance Specialist to support GMP operations at Umoja's state-of-the-art lentiviral vector development and GMP manufacturing and testing facility, The CLIMB, in Louisville, CO. This position will provide quality oversight of incoming materials, manufacturing, and general QA support of GMP operations at The CLIMB. This role is fully onsite based out of our Louisville, CO location. CORE ACCOUNTABILITIES Specific responsibilities include: • Exemplify and role model Umoja's quality culture, • Build strong, effective, and productive cross-functional working relationships, • Interfaces with other departments (e.g., Manufacturing, Supply Chain, Quality Control, Facilities, Engineering) to ensure compliance with all applicable procedures, policies, regulations, and standards., • Provides QA "on the floor" support to Manufacturing during routine GMP operations at the site and Warehouse for material support and disposition., • Reviews and approves work instructions, Standard Operating Procedures (SOPs), Material specifications, and other controlled documents related to GMP operations and other cGMP activities as needed, • Performs disposition of incoming GMP materials, • Initiates Quality Holds as required, • Provides oversite on new material introductions including review and approval of new GMP material onboarding requests, • Partners with Manufacturing to review and post-approve GMP executed batch records and protocols, • Reviews and approves Master Batch Records, process SOPs, and supporting forms for products, • Supports line clearance/product changeover activities including the review and approval of associated documentation, • Approves work orders within Blue Mountain Regulatory Asset Manager (BMRAM), as needed, • Review and approves QC documentation (e.g., stability protocols), • Provides Quality support to approve, review and close quality records (e.g., Change Controls, Deviations, and CAPAs, etc.) as necessary, • Identify, propose, and actively participate in opportunities for continuous improvement, • Bachelor's degree in Engineering, Biochemistry, Molecular and Cellular Biology, Immunology, Biology, or other life science with minimum of 5 years of work experience in an FDA regulated industry, • Previous experience in a Quality organization supporting cGMP biopharmaceutical internal manufacturing facility operations, • Knowledge and understanding of regulatory governing bodies, requirements, and guidance documents, and how to practically apply these in a cGMP biopharmaceutical environment, • An understanding of foundational Quality systems (e.g., Good Documentation Practices, data integrity, audits/inspections, Change Control, Deviation/CAPA, etc.), • Risk-based and practical decision-making capability, with an understanding on when decision making escalation is required, • Ability to work onsite 5 days/week at our Louisville, CO location, • Ability to lift up to 20 lbs. on occasion, • Ability to stand for extended periods of time, • Adherence to proper personal protective equipment (PPE) when necessary, such as but not limited to high-visibility safety vest, cold gloves, lab coat, safety glasses, gowning for manufacturing (scrubs, coveralls, hair net, beard net, etc), etc.