Senior Manager, Manufacturing

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 We are seeking a Senior Manager of Manufacturing who has strong leadership capabilities and extensive manufacturing experience to lead our Drug substance fill and Drug product Manufacturing team. This is a newly created position reporting into the head of Manufacturing at our Louisville, Colorado GMP cell/gene Manufacturing facility. This person will play a critical role helping lead the manufacturing team through a period of growth and change as we advance our clinical pipeline to later phases of development. Primary job responsibilities include, but are not limited to, commercial launch readiness planning and project leadership, DS/DP fill process and material improvements identification and implementation management, ensuring staff is fully trained and qualified to execute aseptic fills and DP visual inspection, ensuring high aseptic technique standards, and assisting with tech transfers both internally and externally. They will also be expected to lead continuous improvement initiatives and provide strategic planning to ensure a high operational success rate. Success is measured by successful outcomes of drug substance film and drug product manufacturing operations. This role will interact with internal process engineers, Process sciences, facilities, warehouse/supply chain, EHS, Quality Assurance, and Quality Control on a regular basis. Strong communication and risk-based strategic leadership skills are essential to effectively work in this matrix environment. This is an opportunity to be part of an excellent team working in an exciting environment, focused on realizing the challenge of targeting solid tumors successfully with novel cell/gene therapies. This role will be fully onsite at our Louisville, CO facility. This person will need to be able to work weekends, holidays, or evenings when needed. CORE ACCOUNTABILITIES: Lead successful completion of the drug product fill process, the final step in ensuring product safety and efficacy for patients. Strategizes and coordinates the execution and continuous improvement of compliant and technically sound programs and systems in support of Drug substance fill and Drug product GMP manufacturing operations (e.g., aseptic process simulations, drug product process continuous improvement and validation) Authors and reviews-controlled documents and standard operating procedures on behalf of Manufacturing Operations Partners with Process Science to co-lead both internal and external technology transfer of drug product manufacturing processes at various scales. Supports manufacturing process execution through on the floor escalation troubleshooting and risk-based, patient focused decision making Supports deviation investigations in the drug substance fill, drug product process area to correct root cause and appropriate corrective actions. Ensures adherence to Standard Operating Procedures, good manuf…

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