Quality Control Analytical Specialist

Join Umoja Biopharma as a Quality Control Analytical Specialist, where you will play a crucial role in ensuring the quality and safety of our biopharmaceutical products. Your expertise will be essential in performing analytical testing, maintaining laboratory equipment, and ensuring compliance with regulatory standards. This is an exciting opportunity to contribute to innovative therapies that improve patient outcomes.

At Umoja Biopharma, a trailblazing biotech firm with operations in Seattle, WA and Louisville, CO, we strive to revolutionize cancer treatment through our innovative integrated immunotherapy platform. Our mission is to create off-the-shelf therapies that can effectively target any tumor at any time. We are a diverse and dynamic team working in state-of-the-art facilities in both Seattle and Louisville. We welcome passionate and forward-thinking individuals eager to tackle the challenges of cutting-edge drug development. Our commitment to core values and principles shapes our mission, and we strongly encourage applicants who share our vision and are excited to contribute to Umoja's success. Join us in crafting impactful stories for patients and their families.Umoja Biopharma – Your Body. Your Hope. Your Cure.

At Umoja Biopharma, we're at the forefront of biotechnology innovation, with facilities in Seattle, WA and Louisville, CO. Our mission is to revolutionize cancer treatment through a pioneering integrated immunotherapy platform. We envision the creation of off-the-shelf therapies that can address any tumor, at any time. Our diverse and dynamic team operates in state-of-the-art facilities and seeks inventive minds who are passionate about the challenges and rewards of advanced drug development. We invite committed individuals to join us in our journey to enhance patient outcomes and create meaningful narratives that resonate with families and communities.Umoja Biopharma – Your Body. Your Hope. Your Cure.POSITION SUMMARYWe are currently seeking a Senior Analyst in Quality Control Microbiology to oversee testing and monitoring activities essential for the Quality Control Microbiology laboratory and the manufacturing areas at our lentiviral vector production facility.This position reports to the Senior Manager of Quality Control Microbiology and is fully onsite in Louisville, CO.

Eurofins Scientific seeks a Quality Control Lab Technician I for its Louisville facility. This full-time role supports the 1st shift, with a schedule running Tuesday through Saturday. The technician plays a key part in maintaining the quality of lab products and services by following established protocols. Key Responsibilities Carry out routine tests and analyses on laboratory samples Record findings and results with accuracy and clarity Perform maintenance and calibration of laboratory equipment Assist in ensuring compliance with both company and industry standards Work Schedule This position is for the 1st shift and requires availability from Tuesday through Saturday.

Umoja Biopharma stands as a pioneering force in the biotechnology landscape, operating from our advanced facilities in both Seattle, WA, and Louisville, CO. Our mission is to revolutionize cancer treatment through an innovative immunotherapy platform that seeks to offer off-the-shelf therapies capable of targeting any tumor at any time. We take pride in our diverse and dynamic workforce that thrives in a collaborative environment, and we are on the lookout for forward-thinking individuals who are passionate about groundbreaking science and dedicated to tackling the complexities of drug development. We invite enthusiastic candidates to join us in our mission to create impactful stories for patients and their families.Umoja Biopharma – Your Body. Your Hope. Your Cure.POSITION SUMMARY We are currently in search of a Quality Assurance Specialist to enhance our GMP operations at The CLIMB, our state-of-the-art lentiviral vector development and GMP manufacturing facility located in Louisville, CO. This role will entail providing quality oversight of incoming materials, manufacturing processes, and offering general QA support for GMP operations at The CLIMB.This position is fully onsite at our Louisville, CO location.CORE ACCOUNTABILITIESKey responsibilities include:Exemplifying and championing Umoja’s quality cultureEstablishing productive cross-functional collaborationsCollaborating with various departments (Manufacturing, Supply Chain, Quality Control, Facilities, Engineering) to ensure adherence to all relevant procedures and standards.Providing on-site QA support during routine GMP operations and material disposition.Reviewing and approving work instructions, Standard Operating Procedures (SOPs), and material specifications related to GMP operations as necessary.Overseeing the disposition of incoming GMP materials.Initiating Quality Holds as necessary.Providing oversight on new material introductions, including the review and approval of new GMP material onboarding requests.

Oversee the inspection and release process for incoming and returned products, which includes downloading temperature records, communicating results to clients, securing necessary approvals, electronically storing inspection records, managing temperature record disposition, and handling product retains.Assist in generating daily temperature graphs and delegate alarm investigation responsibilities to the appropriate manager.Support calibration and alarm testing to ensure adherence to company SOPs.Facilitate relabeling and kitting operations to meet client needs.Participate in special projects as required.

We are seeking a meticulous and detail-oriented Quality Assurance Tester to join our team. In this role, you will be responsible for validating software applications to ensure they meet the highest quality standards. Your expertise in identifying issues and providing solutions will be crucial in enhancing the user experience.

Join our dedicated team at Healthcare Support Staffing as a Quality Improvement Registered Nurse (RN). In this vital role, you will be responsible for assessing and enhancing the quality of patient care. Your expertise will guide initiatives aimed at improving healthcare outcomes and ensuring compliance with regulatory standards.The ideal candidate will possess strong analytical skills and an unwavering commitment to patient safety and quality care. You will collaborate with healthcare professionals to develop strategies that elevate service delivery and foster an environment of continuous improvement.

Umoja Biopharma is a pioneering biotechnology firm with offices in Seattle, WA, and Louisville, CO, dedicated to revolutionizing cancer treatment through an innovative integrated immunotherapy platform. Our mission is to create off-the-shelf therapies capable of addressing any tumor at any time. We pride ourselves on our diverse and expanding team, working in state-of-the-art facilities in downtown Seattle and Louisville. We seek forward-thinking individuals who are passionate about groundbreaking science and technology, and are eager to tackle the challenges that come with cutting-edge drug development. At Umoja, we value the stories we create and invite applicants who are enthusiastic and aligned with our commitment to improving the lives of patients and their families.Umoja Biopharma – Your Body. Your Hope. Your Cure.POSITION SUMMARYThe Vice President of Analytical Development will spearhead technical, operational, and strategic leadership for Umoja’s analytical development division. This role entails oversight of the release, characterization, and lifecycle management of analytical methods that support both clinical and commercial cell and gene therapy products. Reporting directly to the Chief Technical Officer (CTO), the VP will develop and implement the company’s comprehensive analytical strategy in close collaboration with Quality, Manufacturing, Regulatory, and Research departments.This individual will serve as a pivotal leader at the intersection of Research and Discovery, GMP Manufacturing, Quality, and CMC Regulatory, taking charge of analytical method development, qualification, validation, transfer, and specification setting for GMP products. The ideal candidate will possess extensive regulatory expertise—especially in IND and BLA submissions—exemplary leadership skills, and a proven track record in scaling analytical organizations in fast-paced biotech settings.This position is based in Louisville, CO (preferred) or Seattle, WA.

Umoja Biopharma is a pioneering biotechnology firm with cutting-edge facilities in Seattle, WA, and Louisville, CO, dedicated to revolutionizing cancer treatment through an innovative integrated immunotherapy platform. Our mission is to create off-the-shelf therapies that can address any tumor at any moment. We pride ourselves on our diverse and expanding team, and we are seeking inventive minds who are inspired by transformative science and technology and are ready to tackle the complexities of advanced drug development. At Umoja, we value the power of stories, and we invite passionate individuals to join our team to help us craft compelling narratives for ourselves, our colleagues, and, most importantly, for patients and their families.Umoja Biopharma – Your Body. Your Hope. Your Cure.POSITION SUMMARYWe are looking for a motivated Associate Scientist II to join our Analytical Development organization within the Process Analytics department. This role involves delivering routine UPLC analytical methods and transferring or developing separation techniques to quantify residual process reagents in our lentiviral vector (VivoVec) Drug Product and in-process samples. Additionally, you will engage in new method development aimed at enhancing product quality understanding. Early phase validation and the transfer of these methods to Quality Control are essential to facilitate the release testing of GMP lots.The ideal candidate will have a strong background in chromatography systems and various detection methods. You will work independently to meet deadlines, demonstrating a keen attention to detail and ensuring thorough documentation of experimental procedures in an Electronic Laboratory Notebook (ELN). Contributing to report writing is also part of this role, which involves collaboration with other departments to support the development and successful transfer of qualified methods to QC Analytical.This position requires full onsite presence five days a week, primarily lab-based at our Louisville, CO location.

Join our team as a Traffic Control Flagger in Louisville, Kentucky. As a vital member of our operations, you will ensure the safety and smooth flow of traffic at construction sites. This role is ideal for those who are detail-oriented and dedicated to promoting safety in public spaces.

Join our dynamic team at Healthcare Support Staffing as a Quality Improvement / HEDIS Clerk in Louisville, KY. In this vital role, you will play an essential part in enhancing the healthcare quality metrics through meticulous data management and analysis. You will collaborate with healthcare professionals to ensure compliance with Health Effectiveness Data and Information Set (HEDIS) standards, contributing to improved patient outcomes.

Umoja Biopharma develops integrated immunotherapy solutions targeting cancer, with teams based in Louisville, Colorado and Seattle, Washington. The company focuses on creating off-the-shelf therapies for a broad range of tumors, emphasizing collaboration, scientific rigor, and a dedication to improving patient outcomes. Role overview This Senior Research Associate position sits within the Analytical Development team, specifically the Process Analytics sub-team. The role is full-time and requires on-site laboratory work in Louisville, Colorado, five days a week. What you will do Support in-process testing for Lentiviral Vector (LVV) drug substances and products. Carry out routine sample testing and assist in developing new analytical methods. Oversee the lifecycle management of current analytical methods. Improve assay execution, data quality, and turnaround time by implementing automation, including AI and Ganymede for data capture and analysis. Use a variety of molecular, cellular, biophysical, and biochemical protocols. Work with other departments to test LVV samples and contribute to Umoja’s pipeline. Requirements Hands-on experience with molecular, cellular, biophysical, and biochemical assay protocols. Ability to work on-site in Louisville, CO, five days per week. Proficiency in assay execution, data analysis, and method development. Familiarity with automation tools and data management platforms, including AI and Ganymede. Strong collaboration skills for cross-functional teamwork. Location Louisville, Colorado, United States (on-site, full-time)

Join our dedicated team as a Quality Improvement Registered Nurse (RN) where your expertise will directly enhance patient care and outcomes. In this pivotal role, you will work closely with healthcare professionals to assess and improve the quality of services provided to our patients.Your responsibilities will include conducting quality audits, analyzing data for trends, and implementing improvement initiatives. You will play a crucial role in ensuring compliance with healthcare standards and regulations, while fostering a culture of continuous improvement.

Join our dynamic team at sosi1 as a SCA Analytic Linguist specializing in Spanish. This part-time role offers an exciting opportunity to apply your linguistic expertise in analyzing and interpreting complex data. You will work with a dedicated team to ensure high-quality output that meets the needs of our clients.

Umoja Biopharma develops integrated immunotherapy platforms aimed at advancing new cancer treatments. The Louisville, Colorado site supports a growing team focused on drug development, working alongside colleagues in Seattle, WA. Umoja emphasizes diversity, collaboration, and scientific progress in its approach. Role overview The Senior Manager, Quality Assurance Operations leads GMP operations at The CLIMB, Umoja’s lentiviral vector development and manufacturing facility in Louisville. This leadership role manages the QA Operations team and is responsible for ensuring compliance across all GxP areas, including Manufacturing, Supply Chain, Facilities, and Engineering. The position plays a key part in upholding quality standards and supporting best practices throughout the site. Location and schedule Onsite role in Louisville, Colorado Full-time, five days per week May require work on weekends or holidays as needed

Join our dynamic team as a Product/Event Specialist, where you'll play a pivotal role in executing successful product promotions and events. You'll collaborate with various stakeholders to ensure exceptional presentation and engagement during product showcases. This position is perfect for individuals who are passionate about delivering memorable customer experiences and driving brand loyalty.

We are seeking a dedicated and detail-oriented Grievance and Appeals Specialist to join our dynamic team in Louisville, Kentucky. In this role, you will be responsible for managing and resolving grievances and appeals from clients, ensuring compliance with regulatory requirements and company policies.The ideal candidate will have strong analytical skills, excellent communication abilities, and a passion for customer service. You will work closely with various departments to gather information, investigate issues, and provide timely responses to inquiries.

AMP Sortation is at the forefront of transforming the global recycling industry through the innovative application of AI-powered sortation technologies. By modernizing waste management systems, we empower recycling leaders to significantly cut labor expenses, enhance resource recovery, and ensure consistent operational reliability. With a robust presence across North America, Asia, and Europe, our technology fundamentally reshapes the economics of recycling and waste management.Based in Louisville, Colorado, AMP Sortation has been recognized as one of the top workplaces in the state by the Denver Post and BuiltIn Colorado. We're expanding our reach with opportunities in areas such as Atlanta, Cleveland, Portsmouth, Virginia, and Europe. Our goal is to cultivate a dynamic environment where passionate individuals can thrive and make a meaningful impact. We welcome unconventional thinkers ready to join our mission of creating a waste-free world. At AMP, your contributions are valued and can drive real change. Supported by prominent investors and awarded North American Cleantech Company of the Year, we continuously seek innovative methods to enhance our operations and collaboration. Discover more at AMPSortation.com.AMP is on the lookout for a Marketing and Communications Specialist who will play a crucial role in the development and execution of strategic marketing and communication initiatives aimed at boosting brand visibility and enhancing audience engagement. This position involves content creation and editing, campaign coordination, social media management, and keeping marketing materials up-to-date. Collaborating closely with senior team members, the specialist ensures alignment of messaging with brand standards and project objectives. The ideal candidate will possess 2-3 years of relevant experience, exceptional writing and organizational capabilities, and a proactive approach to learning and adapting in a fast-paced work environment.

Join our dynamic team at AECOM as an Insurance Specialist. In this role, you will be responsible for managing client accounts, providing expert advice on insurance products, and ensuring compliance with industry regulations. Your keen analytical skills will help assess client needs and develop tailored insurance solutions. We are looking for a proactive individual who thrives in a fast-paced environment and is committed to delivering exceptional customer service.