Allogene Therapeutics jobs - 30 jobs

About Allogene: Allogene Therapeutics, with headquarters in South San Francisco, is a clinical-stage biotechnology company pioneering the development of allogeneic chimeric antigen receptor T cell (AlloCAR T™) products for cancer and autoimmune disease. Led by a management team with significant experience in cell therapy, Allogene is developing a pipeline of “off-the-shelf” CAR T cell product candidates with the goal of delivering readily available cell therapy on-demand, more reliably, and at greater scale to more patients. For more information, please visit ***************** and follow @AllogeneTx on X (formerly Twitter) and LinkedIn. About the role: The Clinical Trial Manager (CTM) is responsible for the management of clinical trials from study start-up activities through the clinical study report. The CTM drives completion of all study deliverables, ensuring the highest level of data quality and compliance to quality standards and regulatory guidance; proactively identifies, communicates, and resolves clinical study operational issues; and participates in process improvement initiatives as required. This is a 6-month contract opportunity with the possibility of extension or contract-to-hire. Responsibilities include, but are not limited to: Manage all clinical aspects of study under oversight of Clinical Operations senior management including initial operational feasibility, study timelines, budget and metrics; study document development and review (training documentation, ICF, study specific plans, eCRF Guidelines, lab and radiology manuals, etc.), plans and manages study-specific meetings (e.g., Study Team Meetings, Investigator meetings, etc.). Interface with cross-functional teams as Clinical Operations regional or global study lead (e.g., Medical Monitor, Regulatory Affairs, CMC/Supply Chain, CRO, vendors and Investigators/site staff). Work cross-functionally and with external vendors to proactively manage the execution of the clinical trial. May oversee clinical trial execution in one or more regions within a global clinical trial. Review protocol and amendment development, Informed Consent Forms, clinical trial-related training, and Site Study Tools Ensure clinical trial execution in compliance with the protocol and ICH/GCP guidelines/regulations, including the review of monitoring reports, protocol deviations, and eTMF Partner with Clinical Quality Assurance to follow through on corrective and preventative actions (CAPA) identified during internal and external audits Vendor oversight: effectively communicate expectations to CRO, ensure appropriate site management, hold CRO accountable to timelines, and verify quality metrics Provide study-specific training and leadership to clinical research staff, including CRO, CRAs, sites and other contract personnel. Manage study budget; review and approve clinical invoices against approved scope of work and budget, evaluate and approve vendor change orders, coordinating review of updates or revisions with key cross-functional partners, as necessary. Prepare and present project debriefings to Clinical Operations management. Provide study-related guidance and leadership to internal and external partners, as appropriate. Position Requirements & Experience: Bachelor's degree or equivalent combination of education/experience in science or health-related field with at least 3 years of clinical trial management experience in a Pharmaceutical/Biotech organization. Clinical trial management experience as a contractor or employee of an industry sponsor Vendor management Robust understanding of ICH/GCP, and knowledge of regulatory requirements. Strong clinical study/project management skills. Excellent communication and organizational skills (ability to prioritize a number of tasks of varying complexity), along with problem solving, conflict resolution, leadership and team-building skills. Candidates must be authorized to work in the U.S. Preferred experience: Prior clinical trial experience in oncology therapeutic development with an industry sponsor or Contract Research Organization Multi-regional study management experience advantageous We offer a chance to work with talented people in a collaborative environment. Actual pay will be determined based on experience, qualifications, geographic location, business needs, and other job-related factors permitted by law. As an equal opportunity employer, Allogene is committed to a diverse workforce. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, gender, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job-related characteristics or other prohibited grounds specified in applicable federal, state and local laws. We also embrace differences in experience and background, and welcome diversity of opinions and thought with active recruitment and internships designed to create a stronger and better Allogene that is focused on developing life-changing products for patients. #LI-EL1 #LI-REMOTE

Who We Are Arcellx is a public, clinical-stage biotechnology company reimagining cell therapy by engineering innovative immunotherapies for patients with cancer and other incurable diseases. We believe that cell therapies are one of the forward pillars of medicine and our mission is to destroy cancer and advance humanity by developing cell therapies that are safer, more effective, and more broadly accessible. Our team members are made up of talented innovators and dreamers working from our offices in Rockville, Maryland, and Redwood City, California. At Arcellx, we hire exceptional people and create a fun, diverse, supportive, and informal environment that allows everyone to do their best work. What Matters to Us Living our core values is essential to maintaining a work environment that is high-performing, inclusive, and collaborative. We look for candidates who demonstrate strong values alignment and bring different backgrounds, viewpoints, and abilities to the team. Arcellx Core Values Start with authenticity: We foster an inclusive environment where each person can bring their authentic self to work. Think ‘we' before ‘me': We prioritize collective success, collaborating and supporting one another to achieve our shared goals. Embrace the challenge: We deliver exceptional results by working with shared determination and a commitment to doing what's right. How You'll Make a Difference As a Sr. Cell Therapy Specialist (Manufacturing and MSAT), your mission is to deliver to patients every time! Our potentially life-saving treatments would not exist without the work of our cell therapy team. Your work will have a tremendous impact on our ability to deliver our transformative cell therapy to the patients who need it most. The “Fine Print” - What You'll Do Key Responsibilities Independently execute complex cell therapy manufacturing activities with high proficiency: Operation of manufacturing equipment for batch production Media preparation, reagent handling, buffer preparation Aseptic processing in controlled cleanroom environments Serve as point-of-contact for troubleshooting manufacturing issues in real time Lead and train junior specialists / associates in aseptic techniques and the manufacturing process Provide technical support for T-cell manufacturing process changes, process validation, discrepancy / deviation, and investigation evaluation Document all activities in accordance with Good Documentation Practices (GDPs) Author and review documents including MBRs, protocols, deviation reports, change controls, and SOPs. Participate in risk assessments, gap/facility fit analysis, deviation investigations, change controls, CAPAs, and root-cause analysis. Ensure compliance with internal and regulatory standards Partner closely with MSAT, QA, QC, Supply Chain, and Facilities teams Skills and Experience We Look For Bachelor's degree in in relevant scientific field and 8+ years of industry experience preferably in cell therapy manufacturing Excellent aseptic techniques and experience with cell processing equipment Ability to operate within a clean room environment for long durations Prior experience mentoring or training team members Strong problem-solving and decision-making capability Strong understanding of cGMP quality principles Excellent organizational and prioritization skills Exceptional collaboration, communication, and interpersonal skills Flexibility to work weekends, holidays, or shift schedules as required Rewards at Arcellx Our people are our greatest asset, and supporting their well-being is an essential part of delivering on our mission and impacting the lives of patients. Putting this belief into practice means offering strong compensation and benefits. The estimated base salary range for this position is $100,000 - $150,000 per year. Where a candidate falls within that range is determined by factors such as years of experience. Our compensation package also includes an annual bonus based on company goals and an equity (RSU) grant. We do offer relocation assistance for roles if required. Our market-leading benefits package includes: 100% coverage for medical, dental and vision for team members and dependents, unlimited vacation, a 3-day weekend every month, fully-paid parental leave for up to 6 months, tuition reimbursement, 401k employer contribution and more. Join us in our quest to reimagine cell therapy and destroy cancer. For more on our technology, culture, and team, go to **************** #LI-Onsite

Who We Are Arcellx is a public, clinical-stage biotechnology company reimagining cell therapy by engineering innovative immunotherapies for patients with cancer and other incurable diseases. We believe that cell therapies are one of the forward pillars of medicine and our mission is to destroy cancer and advance humanity by developing cell therapies that are safer, more effective, and more broadly accessible. Our team members are made up of talented innovators and dreamers working from our offices in Rockville, Maryland, and Redwood City, California. At Arcellx, we hire exceptional people and create a fun, diverse, supportive, and informal environment that allows everyone to do their best work. What Matters to Us Living our core values is essential to maintaining a work environment that is high-performing, inclusive, and collaborative. We look for candidates who demonstrate strong values alignment and bring different backgrounds, viewpoints, and abilities to the team. Arcellx Core Values Start with authenticity: We foster an inclusive environment where each person can bring their authentic self to work. Think ‘we' before ‘me': We prioritize collective success, collaborating and supporting one another to achieve our shared goals. Embrace the challenge: We deliver exceptional results by working with shared determination and a commitment to doing what's right. How You'll Make a Difference As a Director, People & Culture supporting our Commercial organization, you will play a critical role in shaping and executing people strategy during a pivotal time in our company's growth-our build to commercial launch. You will partner closely with Commercial leaders and People teammates to develop and execute strategies that drive a highly engaged team, ensure organization effectiveness, effective talent development, and a high-performance culture. The “Fine Print” - What You'll Do Serve as a strategic advisor to leaders, providing insights and recommendations on talent planning, team design, performance management, and organizational development. Lead workforce planning and support talent acquisition strategies to build a high-performing sales, marketing, and MSL team prepared for successful market entry. Support change management initiatives and culture-building efforts as the organization scales to meet the demands of commercialization. Champion a high-performance, feedback-oriented, and inclusive culture. Develop and implement talent engagement and retention programs tailored to field-based commercial roles in a dynamic, mission-driven cell therapy environment. Use data and analytics to monitor organizational health and recommend targeted interventions. Skills and Experience We Look For Our ideal candidate has demonstrated strong business and people results in high-growth companies, preferably life sciences, and ideally with exposure to commercial launch or new product introduction. They have a good understanding of field-based commercial organizations, including salesforce dynamics, incentive structures, and regional talent strategies. They have demonstrated ability to influence senior leaders and translate business needs into talent strategies, and experience managing organizational change in fast-paced environments. High emotional intelligence and the ability to build meaningful relationships are essential. Rewards at Arcellx Our people are our greatest asset, and supporting their well-being is an essential part of delivering on our mission and impacting the lives of patients. Putting this belief into practice means offering strong compensation and benefits. The estimated base salary range for this position is $180,000-$245,000 per year. Where a candidate falls within that range is determined by factors such as years of experience and location. Our compensation package also includes an annual bonus based on company goals and an equity (RSU) grant. We do offer relocation assistance for roles if required. Our market-leading benefits package includes: 100% coverage for medical, dental and vision for team members and dependents, unlimited vacation, a 3-day weekend every month, fully-paid parental leave for up to 6 months, tuition reimbursement, 401k employer contribution and more. Join us in our quest to reimagine cell therapy and destroy cancer. For more on our technology, culture, and team, go to **************** #LI-Onsite

Fate Therapeutics is seeking a hands-on, service-driven individual to manage general upkeep, cleanliness, and smooth daily operations for our company facilities, focusing on common areas, conference rooms, laboratories and supply management to support a positive and efficient work environment. The successful candidate will have experience managing facility organization and cleanliness for both office and laboratories, including conference room readiness, setting up and breaking down meeting rooms, managing inventory of supplies, biohazardous waste, and reporting maintenance needs to ensure an organized, functional, and safe work environment. This is an entry-level, full-time, non-exempt position located at our corporate headquarters in San Diego, CA. Responsibilities * Support operations across the Company facilities: o keep inventory, order, stage and distribute office supplies to office areas, breakroom supplies to break areas, restroom supplies to restrooms, conference room supplies to conference rooms, and consumables to R&D labs. o set up and breakdown of company meetings and events, including arranging tables, chairs, catering and equipment, restoring and cleanup of space afterward. o maintain daily cleanliness, safety, and professional appearance of the Company facilities including the common areas, supply areas, office areas, conference rooms, break areas, and restrooms. o manage centralized waste including trash, paper, plastics, and other recyclable materials. Support Company's hazardous waste program: o collect, transport, segregate, accumulate, and perform initial disposal of hazardous waste for various labs; determine proper method of accumulation and disposal based on hazard classes and compatibility of chemicals. o package, document, and label waste for shipment to appropriate disposal facilities pursuant to disposal facility, state, and federal requirements. o maintain records such as hazardous and non-hazardous waste manifests and associated documents. o respond to hazardous materials spills and non-hazardous spills and implement clean-up plan. Communicate list of activities to facilities personnel for evening janitorial vendor to complete. Work closely with facilities and HR personnel to support daily facilities requests and maintenance needs. Qualifications * High school/GED with a minimum of one year's experience providing facilities support to a small to mid-size company; biotech or life science preferred. * Experience working in a lab setting preferred. * Mechanical knowledge of equipment and tools, including their design, uses, repair, and maintenance such as biosafety cabinets, refrigerators, freezers, and other general laboratory equipment preferred. * Able to understand general instructions with proficient problem-solving abilities and detail-orientation. * Ability to manage and prioritize end-user facilities requests. * Experience using Microsoft Outlook Word and Excel. * Strong written and verbal communication and customer service skills. * Self-motivated, flexible, able to prioritize, multitask, and work in a professional, fast-paced & dynamic environment. Working Conditions * 100% onsite work at corporate headquarters in San Diego, CA from 7:30am - 4:30pm. * Subject to extended periods of standing and moving with moderate noise levels. * Able to lift up to 35 lbs. on a regular basis. * Will require working with hazardous materials. Compensation * The salary offer will be based on a variety of factors, including level, experience, qualifications, internal equity, and location. * Fate offers a competitive employment package that includes an annual bonus, equity, and a generous benefits package. * The anticipated salary range for this role is $28 - $31 per hour. The preceding job description indicates the general nature and level of work performed by employees within this classification. Additional and incidental duties related to the primary duties may be required from time to time. Equal Employment Opportunity Fate Therapeutics, Inc. is an equal opportunity employer. We value diversity and are committed to creating an inclusive environment for all employees. Privacy Notice To learn about how Fate collects and uses job application information, please visit Fate's online Privacy Notice. About Fate Therapeutics, Inc. Fate Therapeutics is a clinical-stage biopharmaceutical company dedicated to bringing a pipeline of induced pluripotent stem cell (iPSC)-derived cellular immunotherapies to patients. Using its proprietary iPSC product platform, the Company has established a leadership position in creating multiplexed-engineered master iPSC lines and in the manufacture and clinical development of off-the-shelf, iPSC-derived cell products. The Company's pipeline includes iPSC-derived T-cell and natural killer (NK) cell product candidates, which are selectively designed, incorporate novel synthetic controls of cell function, and are intended to deliver multiple therapeutic mechanisms to patients. Fate Therapeutics is headquartered in San Diego, CA. For more information, please visit ************************* ️ Recruitment Fraud Alert Recently, we have been made aware of unauthorized individuals falsely presenting themselves as Fate Therapeutics employees or recruiters as part of online scams or phishing attempts. Impersonators may use the Fate Therapeutics name and logo, as well as employee names and job titles, to gain a job seeker's personal or banking information or to request payment as a condition of being considered for a position at the company. Fate Therapeutics and its employees are not involved in these scams. Here are a few things to be aware of to help identify recruitment fraud: * Our Talent Acquisition team only corresponds from ************************* domain. * At no stage in our hiring process will we require payment or ask you to make deposits in your bank account. * We will only ask for personal information when applying for a position via our Careers page or thereafter. * At no stage during our hiring process will we ask you to click a link to begin a one-way video interview. * We do not use Google Hangouts, WhatsApp, or other third-party messaging platforms to recruit candidates or conduct interviews. Please exercise caution. If something feels off about your interactions, we encourage you to contact us at [email protected] to confirm the authenticity of the message. Your security is important to us, and we appreciate your vigilance. We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

Who We Are Arcellx is a public, clinical-stage biotechnology company reimagining cell therapy by engineering innovative immunotherapies for patients with cancer and other incurable diseases. We believe that cell therapies are one of the forward pillars of medicine and our mission is to destroy cancer and advance humanity by developing cell therapies that are safer, more effective, and more broadly accessible. Our team members are made up of talented innovators and dreamers working from our offices in Rockville, Maryland, and Redwood City, California. At Arcellx, we hire exceptional people and create a fun, diverse, supportive, and informal environment that allows everyone to do their best work. What Matters to Us Living our core values is essential to maintaining a work environment that is high-performing, inclusive, and collaborative. We look for candidates who demonstrate strong values alignment and bring different backgrounds, viewpoints, and abilities to the team. Arcellx Core Values * Start with authenticity: We foster an inclusive environment where each person can bring their authentic self to work. * Think 'we' before 'me': We prioritize collective success, collaborating and supporting one another to achieve our shared goals. * Embrace the challenge: We deliver exceptional results by working with shared determination and a commitment to doing what's right. The "Fine Print" - What You'll Do * Execute GMP-compliant environmental monitoring of cleanrooms by performing non-viable and viable particulate sampling on a routine basis. * Perform growth promotion to qualify media. * Contribute to reviewing SOPs, forms, and logbooks related to environmental monitoring and microbiological methods. * Governing the upkeep, calibration, and preventive maintenance of lab equipment and instruments. * Manage inventory of environmental monitoring samples, lab supplies and materials. * Support tracking and trending of QC data. Skills and Experience We Look For * BS or MS in biological sciences or a related field. * 2+ years of pharmaceutical of biotechnology industry experience, including experience in cell therapy or microbiology. Candidates at the specialist level will require more experience. * Previous experience performing environmental monitoring in a cleanroom. * Excellent written and oral communication skills. Rewards at Arcellx Our people are our greatest asset, and supporting their well-being is an essential part of delivering on our mission and impacting the lives of patients. Putting this belief into practice means offering strong compensation and benefits. The estimated base salary range for this position is $80,000 - $105,000 per year. Where a candidate falls within that range is determined by factors such as years of experience. Our compensation package also includes an annual bonus based on company goals and an equity (RSU) grant. We do offer relocation assistance for roles if required. Our market-leading benefits package includes: 100% coverage for medical, dental and vision for team members and dependents, unlimited vacation, a 3-day weekend every month, fully-paid parental leave for up to 6 months, tuition reimbursement, 401k employer contribution and more. Join us in our quest to reimagine cell therapy and destroy cancer. For more on our technology, culture, and team, go to **************** #LI-Onsite

Who We Are Arcellx is a public, clinical-stage biotechnology company reimagining cell therapy by engineering innovative immunotherapies for patients with cancer and other incurable diseases. We believe that cell therapies are one of the forward pillars of medicine and our mission is to destroy cancer and advance humanity by developing cell therapies that are safer, more effective, and more broadly accessible. Our team members are made up of talented innovators and dreamers working from our offices in Rockville, Maryland, and Redwood City, California. At Arcellx, we hire exceptional people and create a fun, diverse, supportive, and informal environment that allows everyone to do their best work. What Matters to Us Living our core values is essential to maintaining a work environment that is high-performing, inclusive, and collaborative. We look for candidates who demonstrate strong values alignment and bring different backgrounds, viewpoints, and abilities to the team. Arcellx Core Values Start with authenticity: We foster an inclusive environment where each person can bring their authentic self to work. Think ‘we' before ‘me': We prioritize collective success, collaborating and supporting one another to achieve our shared goals. Embrace the challenge: We deliver exceptional results by working with shared determination and a commitment to doing what's right. The “Fine Print” - What You'll Do The Manager, Scoial Media is a creative and thoughtful communications professional who will focus on elevating and amplifying Arcellx's corporate and executive thought leadership story mining through social media channels. This person will develop editorial strategies, including curating content, maintaining a content calendar, managing reviews, scheduling, distribution, and performance measurements across all external platforms and channels, such as graphics, videos, infographics, and long-form articles. This person will manage all external digital platforms, including LinkedIn, X, and Glassdoor, ensuring they are up to date with the latest company developments, research updates, clinical trials, investor relations content, and other corporate information. Collaborate with cross-functional teams to create fresh, engaging content that represents the company's innovations and achievements. The candidate must be an excellent writer and storyteller with the ability to craft thoughtful communications that will engage audiences (internally and externally) and create a unique POV for topics relevant to the executive team, company, and team members. Skills and Experience We Look For Bachelor's degree and at least 3+ years of related experience in journalism, digital media, public relations, in-house, or at an agency. Experience in the biotechnology or pharmaceutical industry is highly preferred. Knowledge of and experience with multiple online channels (YouTube, LinkedIn, X, mobile devices), with a track record of growing and engaging online audiences. Strong attention to detail, project management, copy editing, and a solid understanding of multimedia and visual storytelling are essential. Must be able to take feedback and quickly adapt content in a fast-paced environment. The ability to translate complicated scientific concepts into engaging content is highly preferred. Rewards at Arcellx Our people are our greatest asset, and supporting their well-being is an essential part of delivering on our mission and impacting the lives of patients. Putting this belief into practice means offering strong compensation and benefits. The base salary range for this position is $120,000 - $160,000 per year. Where a candidate falls within that range is determined by factors such as years of experience. Our compensation package also includes an annual bonus based on company goals and an equity (RSU) grant. We do offer relocation assistance for roles if required. Our market-leading benefits package includes: 100% coverage for medical, dental and vision for team members and dependents, unlimited vacation, a 3-day weekend every month, fully-paid parental leave for up to 6 months, tuition reimbursement, 401k employer contribution and more. Join us in our quest to reimagine cell therapy and destroy cancer. For more on our technology, culture, and team, go to **************** #LI-Onsite

Who We Are Arcellx is a public, clinical-stage biotechnology company reimagining cell therapy by engineering innovative immunotherapies for patients with cancer and other incurable diseases. We believe that cell therapies are one of the forward pillars of medicine and our mission is to destroy cancer and advance humanity by developing cell therapies that are safer, more effective, and more broadly accessible. Our team members are made up of talented innovators and dreamers working from our offices in Rockville, Maryland, and Redwood City, California. At Arcellx, we hire exceptional people and create a fun, diverse, supportive, and informal environment that allows everyone to do their best work. What Matters to Us Living our core values is essential to maintaining a work environment that is high-performing, inclusive, and collaborative. We look for candidates who demonstrate strong values alignment and bring different backgrounds, viewpoints, and abilities to the team. Arcellx Core Values Start with authenticity: We foster an inclusive environment where each person can bring their authentic self to work. Think ‘we' before ‘me': We prioritize collective success, collaborating and supporting one another to achieve our shared goals. Embrace the challenge: We deliver exceptional results by working with shared determination and a commitment to doing what's right. The “Fine Print” - What You'll Do Serve as the lead Regulatory representative on the Promotional Review and Medical Review Committees Independently review and approve promotional/non-promotional materials. Ensure regulatory compliance with the current labeling, applicable regulations, guidance documents, and internal policies/best practices Collaborate with Medical, Legal and Commercial to execute and approve key Commercial campaigns. Monitor evolving FDA regulations, enforcement actions, and industry best practices; translate insights into internal training and process improvements. Develop and implement labeling strategies, including creation, review, and maintenance of prescribing information, patient information, and packaging components. Serve as primary liaison with FDA's Office of Prescription Drug Promotion (OPDP) and/or Advertising and Promotional Labeling Branch (APLB) on ad promo submissions, inquiries, and regulatory correspondence. Contribute to broader regulatory strategy and operations as a key leader within a small, agile team preparing for its first product launch. Skills and Experience We Look For Bachelor's degree in life sciences or related field required. 10+ years of regulatory affairs experience in the biopharmaceutical industry, with significant expertise in advertising, promotion, and labeling. In-depth understanding of FDA regulations and guidelines, and other relevant health authority requirements for pharmaceuticals. Ability to apply regulatory knowledge to develop practical solutions and strategies for complex promotional and labeling issues. Proven track record of supporting pre-launch through commercial stages, ideally in oncology or specialty pharmaceuticals. Ability to operate strategically while managing hands-on responsibilities in a small, fast-paced biotech environment. Strong leadership, verbal/written communication, and collaboration skills with the ability to influence internal/external stakeholders. High level of integrity and commitment to regulatory compliance in support of patients and healthcare providers. Rewards at Arcellx Our people are our greatest asset, and supporting their well-being is an essential part of delivering on our mission and impacting the lives of patients. Putting this belief into practice means offering strong compensation and benefits. The estimated base salary range for this position is $220,000 - $255,000 per year. Where a candidate falls within that range is determined by factors such as years of experience. Our compensation package also includes an annual bonus based on company goals and an equity (RSU) grant. We do offer relocation assistance for roles if required. Our market-leading benefits package includes: 100% coverage for medical, dental and vision for team members and dependents, unlimited vacation, a 3-day weekend every month, fully-paid parental leave for up to 6 months, tuition reimbursement, 401k employer contribution and more. Join us in our quest to reimagine cell therapy and destroy cancer. For more on our technology, culture, and team, go to **************** #LI-Onsite

Who We Are Arcellx is a public, clinical-stage biotechnology company reimagining cell therapy by engineering innovative immunotherapies for patients with cancer and other incurable diseases. We believe that cell therapies are one of the forward pillars of medicine and our mission is to destroy cancer and advance humanity by developing cell therapies that are safer, more effective, and more broadly accessible. Our team members are made up of talented innovators and dreamers working from our offices in Rockville, Maryland, and Redwood City, California. At Arcellx, we hire exceptional people and create a fun, diverse, supportive, and informal environment that allows everyone to do their best work. What Matters to Us Living our core values is essential to maintaining a work environment that is high-performing, inclusive, and collaborative. We look for candidates who demonstrate strong values alignment and bring different backgrounds, viewpoints, and abilities to the team. Arcellx Core Values Start with authenticity: We foster an inclusive environment where each person can bring their authentic self to work. Think ‘we' before ‘me': We prioritize collective success, collaborating and supporting one another to achieve our shared goals. Embrace the challenge: We deliver exceptional results by working with shared determination and a commitment to doing what's right. The “Fine Print” - What You'll Do Act as the lead data manager across one or more clinical studies. Provide expertise and oversight of all clinical database activities from design/start-up to closeout. Reviews protocols for appropriate data capture including electronic (eCRF) design. Support CRF design, review, and validation of clinical database. Provides oversight of database set-up/migrations/upgrades including coordinating and/or performing User Acceptance Testing. Conducts oversight of data management vendors via ongoing review of quality and performance metrics. Generates, resolves, and tracks data queries to ensure the integrity of the clinical data. Facilitates and participates in data cleaning activities. Generates and/or reviews/approves study documents. Responsible for maintaining internal data management timelines and metrics. Maintains study DM related documents/files for inspection readiness. Proactively identifies potential data management issues/risks and communicates it within the study team for further action. Skills and Experience We Look For Minimum BA/BS in scientific or health-related field. Minimum of 7 years of clinical data management experience in the pharmaceutical, biotechnology industry or in a CRO. Oncology trial experience required, hematology/oncology preferred. Possesses a comprehensive understanding of regulatory guidelines and industry standards. Proficient with Medidata RAVE; experience working on Medidata Suite products preferred. Familiarity with various data visualization, analytics, and reporting tools is a plus. Excellent communication skills, strong organizational skills, and ability to work independently and effectively prioritize tasks in a fast-paced setting. Rewards at Arcellx Our people are our greatest asset, and supporting their well-being is an essential part of delivering on our mission and impacting the lives of patients. Putting this belief into practice means offering strong compensation and benefits. The estimated base salary range for this position is $160,000 - $195,000 per year. Where a candidate falls within that range is determined by factors such as years of experience. Our compensation package also includes an annual bonus based on company goals and an equity (RSU) grant. We do offer relocation assistance for roles if required. Our market-leading benefits package includes: 100% coverage for medical, dental and vision for team members and dependents, unlimited vacation, a 3-day weekend every month, fully-paid parental leave for up to 6 months, tuition reimbursement, 401k employer contribution and more. Join us in our quest to reimagine cell therapy and destroy cancer. For more on our technology, culture, and team, go to **************** #LI-Onsite

Arcellx (************************ is a clinical-stage biotech company headquartered in Gaithersburg, MD and Redwood City, CA. Arcellx is focused on the development of novel cell-based cancer therapies. A team of biotechnology professionals with expertise in biologics, discovery and tumor immunology incorporate proprietary technologies into genetically engineered human immune cells therapies. Arcellx's mission is to advance humanity by engineering cell therapies that are safer, more effective, and more broadly accessible. Primary Objective: Arcellx is looking for a Sr. Manager of Quality Management Systems (QMS) reporting to the Sr. Director of Quality Systems. The Sr. Manager of QMS will manage and administer the infrastructure and elements of the QMS department ensuring a QMS quality unit that is compliant, effective, and agile to support a rapidly growing organization. The candidate will provide quality administration for all elements of Arcellx Quality Management System (QMS), which includes: Change Control, Deviation Management, Corrective and Preventive Action, Training, and Document Control for all aspects including identification and escalation of quality system and product issues. Main Accountabilities: Execute day-to-day operations management of an electronic document management system and Electronic Quality Management System (e.g. Complaints, document management, training and change control). Participate in the implementation and enhancements of the various components of the Arcellx QMS function ensuring adherence to established internal standards and in compliance with applicable regulatory requirements. Manage the maintenance of SOPs, training programs, deviations, CAPAs, commercial/investigational product complaints, vendor qualification/auditing, and the documentation of these activities. Provide cross functional day to day support to any QMS related requests or issues. Partner in troubleshooting and investigations to ensure comprehensive and timely closure. Create and provide QMS Key Performance and Key Quality Metrics to senior management and executive management as needed. Maintain records management system including master inventory, secure storage, retrieval, retention and destruction. Provide QMS support and subject matter expertise during Health Authority inspections authority. Participate in inspection readiness efforts. Represent QA on project teams for assigned QMS topics or initiatives. Support continuous improvement planning. Communicate and promote a culture of quality and operational excellence at Arcellx. Requirements and Qualifications: A Bachelor's degree in a scientific or technical discipline is required. A minimum of 7-9 years of experience in GxP and Quality Systems in biotechnology or pharmaceutical environment is required. Experience in implementing and managing electronic Quality Management Systems. Experience in participating in high performing teams. Experience in Inspection Readiness. Knowledge of applicable US and Global compliance regulations and industry practices. Ability to critically evaluate and troubleshoot complex problems and attention to detail. Strong teamwork, collaboration and management skills. Ability to manage multiple priorities and aggressive timelines. Competencies: • Commitment to ethical scientific investigations and rigorous experimental methods. • Ability and desire to multitask and function in a fast-paced entrepreneurial environment. • Sense of urgency in performance of duties. • Interpersonal skills that promote a collaborative and productive lab environment. • Effective and efficient written and oral communication skills. Submit cover letter and resume Without exception, applicants must submit both a cover letter and resume to be considered for these positions and must have experience in one of the fields listed above.

Who We Are Arcellx is a public, clinical-stage biotechnology company reimagining cell therapy by engineering innovative immunotherapies for patients with cancer and other incurable diseases. We believe that cell therapies are one of the forward pillars of medicine and our mission is to destroy cancer and advance humanity by developing cell therapies that are safer, more effective, and more broadly accessible. Our team members are made up of talented innovators and dreamers working from our offices in Rockville, Maryland, and Redwood City, California. At Arcellx, we hire exceptional people and create a fun, diverse, supportive, and informal environment that allows everyone to do their best work. What Matters to Us Living our core values is essential to maintaining a work environment that is high-performing, inclusive, and collaborative. We look for candidates who demonstrate strong values alignment and bring different backgrounds, viewpoints, and abilities to the team. Arcellx Core Values Start with authenticity: We foster an inclusive environment where each person can bring their authentic self to work. Think ‘we' before ‘me': We prioritize collective success, collaborating and supporting one another to achieve our shared goals. Embrace the challenge: We deliver exceptional results by working with shared determination and a commitment to doing what's right. How You'll Make a Difference The Senior Director, Statistical Programming, is a key leadership role responsible for overseeing the design, development and delivery of statistical programming solutions across all clinical trials conducted by Arcellx. Your work will have a direct impact on our ability to successfully navigate our trials and get our transformative therapy to patients. The “Fine Print” - What You'll Do Provide oversight development of datasets (SDTMs/ADaMs) in CDISC compliant format by CROs. Review of SDTM mapping specifications, annotated CRFs, ADaM specifications, define XML documents and reviewers' guides per CDISC and FDA specifications and guidelines. Provide technical leadership, problem solving of moderate to high complexity and within project timelines while providing high quality deliverables. Demonstrate expertise in SAS language, procedures, and options commonly used in clinical trial reporting including the Macro language, BASE SAS, SAS/STAT & SAS/GRAPH. Oversee and manage work of other programmers. Develop and/or validate standard macros to automate output production. Assist with infrastructure development of the department. Skills and Experience We Look For BS/BA degree in related discipline. 13+ years of experience in statistical programming with clinical data and SAS. Experience in oncology therapeutic area preferred. Strong SAS programming skills required with proficiency in SAS/Base, SAS/Stat and SAS/Macros. CDISC expertise required. Uses broad expertise or unique knowledge and skills to contribute to development of company objectives and principles, and to achieve goals in creative and effective ways. Excellent interpersonal communication skills. Rewards at Arcellx Our people are our greatest asset, and supporting their well-being is an essential part of delivering on our mission and impacting the lives of patients. Putting this belief into practice means offering strong compensation and benefits. The estimated base salary range for this position is $265,000 - $289,000 per year. Where a candidate falls within that range is determined by factors such as years of experience. Our compensation package also includes an annual bonus based on company goals and an equity (RSU) grant. We do offer relocation assistance for roles if required. Our market-leading benefits package includes: 100% coverage for medical, dental and vision for team members and dependents, unlimited vacation, a 3-day weekend every month, fully-paid parental leave for up to 6 months, tuition reimbursement, 401k employer contribution and more. Join us in our quest to reimagine cell therapy and destroy cancer. For more on our technology, culture, and team, go to **************** #LI-Onsite

Who We Are Arcellx is a public, clinical-stage biotechnology company reimagining cell therapy by engineering innovative immunotherapies for patients with cancer and other incurable diseases. We believe that cell therapies are one of the forward pillars of medicine and our mission is to destroy cancer and advance humanity by developing cell therapies that are safer, more effective, and more broadly accessible. Our team members are made up of talented innovators and dreamers working from our offices in Rockville, Maryland, and Redwood City, California. At Arcellx, we hire exceptional people and create a fun, diverse, supportive, and informal environment that allows everyone to do their best work. What Matters to Us Living our core values is essential to maintaining a work environment that is high-performing, inclusive, and collaborative. We look for candidates who demonstrate strong values alignment and bring different backgrounds, viewpoints, and abilities to the team. Arcellx Core Values * Start with authenticity: We foster an inclusive environment where each person can bring their authentic self to work. * Think 'we' before 'me': We prioritize collective success, collaborating and supporting one another to achieve our shared goals. * Embrace the challenge: We deliver exceptional results by working with shared determination and a commitment to doing what's right. How You'll Make a Difference As a Sr. Cell Therapy Specialist (Manufacturing and MSAT), your mission is to deliver to patients every time! Our potentially life-saving treatments would not exist without the work of our cell therapy team. Your work will have a tremendous impact on our ability to deliver our transformative cell therapy to the patients who need it most. The "Fine Print" - What You'll Do * Key Responsibilities * Independently execute complex cell therapy manufacturing activities with high proficiency: * Operation of manufacturing equipment for batch production * Media preparation, reagent handling, buffer preparation * Aseptic processing in controlled cleanroom environments * Serve as point-of-contact for troubleshooting manufacturing issues in real time * Lead and train junior specialists / associates in aseptic techniques and the manufacturing process * Provide technical support for T-cell manufacturing process changes, process validation, discrepancy / deviation, and investigation evaluation * Document all activities in accordance with Good Documentation Practices (GDPs) * Author and review documents including MBRs, protocols, deviation reports, change controls, and SOPs. * Participate in risk assessments, gap/facility fit analysis, deviation investigations, change controls, CAPAs, and root-cause analysis. * Ensure compliance with internal and regulatory standards * Partner closely with MSAT, QA, QC, Supply Chain, and Facilities teams Skills and Experience We Look For * Bachelor's degree in in relevant scientific field and 8+ years of industry experience preferably in cell therapy manufacturing * Excellent aseptic techniques and experience with cell processing equipment * Ability to operate within a clean room environment for long durations * Prior experience mentoring or training team members * Strong problem-solving and decision-making capability * Strong understanding of cGMP quality principles * Excellent organizational and prioritization skills * Exceptional collaboration, communication, and interpersonal skills * Flexibility to work weekends, holidays, or shift schedules as required Rewards at Arcellx Our people are our greatest asset, and supporting their well-being is an essential part of delivering on our mission and impacting the lives of patients. Putting this belief into practice means offering strong compensation and benefits. The estimated base salary range for this position is $100,000 - $150,000 per year. Where a candidate falls within that range is determined by factors such as years of experience. Our compensation package also includes an annual bonus based on company goals and an equity (RSU) grant. We do offer relocation assistance for roles if required. Our market-leading benefits package includes: 100% coverage for medical, dental and vision for team members and dependents, unlimited vacation, a 3-day weekend every month, fully-paid parental leave for up to 6 months, tuition reimbursement, 401k employer contribution and more. Join us in our quest to reimagine cell therapy and destroy cancer. For more on our technology, culture, and team, go to **************** #LI-Onsite

Fate Therapeutics is seeking a hands-on, service-driven individual to manage general upkeep, cleanliness, and smooth daily operations for our company facilities, focusing on common areas, conference rooms, laboratories and supply management to support a positive and efficient work environment. The successful candidate will have experience managing facility organization and cleanliness for both office and laboratories, including conference room readiness, setting up and breaking down meeting rooms, managing inventory of supplies, biohazardous waste, and reporting maintenance needs to ensure an organized, functional, and safe work environment. This is an entry-level, full-time, non-exempt position located at our corporate headquarters in San Diego, CA.Responsibilities Support operations across the Company facilities: o keep inventory, order, stage and distribute office supplies to office areas, breakroom supplies to break areas, restroom supplies to restrooms, conference room supplies to conference rooms, and consumables to R&D labs.o set up and breakdown of company meetings and events, including arranging tables, chairs, catering and equipment, restoring and cleanup of space afterward.o maintain daily cleanliness, safety, and professional appearance of the Company facilities including the common areas, supply areas, office areas, conference rooms, break areas, and restrooms.o manage centralized waste including trash, paper, plastics, and other recyclable materials. Support Company's hazardous waste program: o collect, transport, segregate, accumulate, and perform initial disposal of hazardous waste for various labs; determine proper method of accumulation and disposal based on hazard classes and compatibility of chemicals. o package, document, and label waste for shipment to appropriate disposal facilities pursuant to disposal facility, state, and federal requirements. o maintain records such as hazardous and non-hazardous waste manifests and associated documents. o respond to hazardous materials spills and non-hazardous spills and implement clean-up plan. Communicate list of activities to facilities personnel for evening janitorial vendor to complete. Work closely with facilities and HR personnel to support daily facilities requests and maintenance needs. Qualifications High school/GED with a minimum of one year's experience providing facilities support to a small to mid-size company; biotech or life science preferred. Experience working in a lab setting preferred. Mechanical knowledge of equipment and tools, including their design, uses, repair, and maintenance such as biosafety cabinets, refrigerators, freezers, and other general laboratory equipment preferred. Able to understand general instructions with proficient problem-solving abilities and detail-orientation. Ability to manage and prioritize end-user facilities requests. Experience using Microsoft Outlook Word and Excel. Strong written and verbal communication and customer service skills. Self-motivated, flexible, able to prioritize, multitask, and work in a professional, fast-paced & dynamic environment. Working Conditions 100% onsite work at corporate headquarters in San Diego, CA from 7:30am - 4:30pm. Subject to extended periods of standing and moving with moderate noise levels. Able to lift up to 35 lbs. on a regular basis. Will require working with hazardous materials. Compensation The salary offer will be based on a variety of factors, including level, experience, qualifications, internal equity, and location. Fate offers a competitive employment package that includes an annual bonus, equity, and a generous benefits package. The anticipated salary range for this role is $28 - $31 per hour. The preceding job description indicates the general nature and level of work performed by employees within this classification. Additional and incidental duties related to the primary duties may be required from time to time. Equal Employment OpportunityFate Therapeutics, Inc. is an equal opportunity employer. We value diversity and are committed to creating an inclusive environment for all employees. Privacy NoticeTo learn about how Fate collects and uses job application information, please visit Fate's online Privacy Notice. About Fate Therapeutics, Inc.Fate Therapeutics is a clinical-stage biopharmaceutical company dedicated to bringing a pipeline of induced pluripotent stem cell (iPSC)-derived cellular immunotherapies to patients. Using its proprietary iPSC product platform, the Company has established a leadership position in creating multiplexed-engineered master iPSC lines and in the manufacture and clinical development of off-the-shelf, iPSC-derived cell products. The Company's pipeline includes iPSC-derived T-cell and natural killer (NK) cell product candidates, which are selectively designed, incorporate novel synthetic controls of cell function, and are intended to deliver multiple therapeutic mechanisms to patients. Fate Therapeutics is headquartered in San Diego, CA. For more information, please visit ************************* ⚠️ Recruitment Fraud Alert Recently, we have been made aware of unauthorized individuals falsely presenting themselves as Fate Therapeutics employees or recruiters as part of online scams or phishing attempts. Impersonators may use the Fate Therapeutics name and logo, as well as employee names and job titles, to gain a job seeker's personal or banking information or to request payment as a condition of being considered for a position at the company. Fate Therapeutics and its employees are not involved in these scams. Here are a few things to be aware of to help identify recruitment fraud:- Our Talent Acquisition team only corresponds from our @fatetherapeutics.com domain.- At no stage in our hiring process will we require payment or ask you to make deposits in your bank account.- We will only ask for personal information when applying for a position via our Careers page or thereafter.- At no stage during our hiring process will we ask you to click a link to begin a one-way video interview.- We do not use Google Hangouts, WhatsApp, or other third-party messaging platforms to recruit candidates or conduct interviews. Please exercise caution. If something feels off about your interactions, we encourage you to contact us at **************************** to confirm the authenticity of the message. Your security is important to us, and we appreciate your vigilance.

Who We Are Arcellx is a public, clinical-stage biotechnology company reimagining cell therapy by engineering innovative immunotherapies for patients with cancer and other incurable diseases. We believe that cell therapies are one of the forward pillars of medicine and our mission is to destroy cancer and advance humanity by developing cell therapies that are safer, more effective, and more broadly accessible. Our team members are made up of talented innovators and dreamers working from our offices in Rockville, Maryland, and Redwood City, California. At Arcellx, we hire exceptional people and create a fun, diverse, supportive, and informal environment that allows everyone to do their best work. What Matters to Us Living our core values is essential to maintaining a work environment that is high-performing, inclusive, and collaborative. We look for candidates who demonstrate strong values alignment and bring different backgrounds, viewpoints, and abilities to the team. Arcellx Core Values Start with authenticity: We foster an inclusive environment where each person can bring their authentic self to work. Think ‘we' before ‘me': We prioritize collective success, collaborating and supporting one another to achieve our shared goals. Embrace the challenge: We deliver exceptional results by working with shared determination and a commitment to doing what's right. The “Fine Print” - What You'll Do Execute GMP-compliant environmental monitoring of cleanrooms by performing non-viable and viable particulate sampling on a routine basis. Perform growth promotion to qualify media. Contribute to reviewing SOPs, forms, and logbooks related to environmental monitoring and microbiological methods. Governing the upkeep, calibration, and preventive maintenance of lab equipment and instruments. Manage inventory of environmental monitoring samples, lab supplies and materials. Support tracking and trending of QC data. Skills and Experience We Look For BS or MS in biological sciences or a related field. 2+ years of pharmaceutical of biotechnology industry experience, including experience in cell therapy or microbiology. Candidates at the specialist level will require more experience. Previous experience performing environmental monitoring in a cleanroom. Excellent written and oral communication skills. Rewards at Arcellx Our people are our greatest asset, and supporting their well-being is an essential part of delivering on our mission and impacting the lives of patients. Putting this belief into practice means offering strong compensation and benefits. The estimated base salary range for this position is $80,000 - $105,000 per year. Where a candidate falls within that range is determined by factors such as years of experience. Our compensation package also includes an annual bonus based on company goals and an equity (RSU) grant. We do offer relocation assistance for roles if required. Our market-leading benefits package includes: 100% coverage for medical, dental and vision for team members and dependents, unlimited vacation, a 3-day weekend every month, fully-paid parental leave for up to 6 months, tuition reimbursement, 401k employer contribution and more. Join us in our quest to reimagine cell therapy and destroy cancer. For more on our technology, culture, and team, go to **************** #LI-Onsite

Who We Are Arcellx is a public, clinical-stage biotechnology company reimagining cell therapy by engineering innovative immunotherapies for patients with cancer and other incurable diseases. We believe that cell therapies are one of the forward pillars of medicine and our mission is to destroy cancer and advance humanity by developing cell therapies that are safer, more effective, and more broadly accessible. Our team members are made up of talented innovators and dreamers working from our offices in Rockville, Maryland, and Redwood City, California. At Arcellx, we hire exceptional people and create a fun, diverse, supportive, and informal environment that allows everyone to do their best work. What Matters to Us Living our core values is essential to maintaining a work environment that is high-performing, inclusive, and collaborative. We look for candidates who demonstrate strong values alignment and bring different backgrounds, viewpoints, and abilities to the team. Arcellx Core Values * Start with authenticity: We foster an inclusive environment where each person can bring their authentic self to work. * Think 'we' before 'me': We prioritize collective success, collaborating and supporting one another to achieve our shared goals. * Embrace the challenge: We deliver exceptional results by working with shared determination and a commitment to doing what's right. The "Fine Print" - What You'll Do * Independently provide effective phase-appropriate strategic guidance/input related to current regulatory requirements and expectations for clinical trial applications and marketing applications for development projects. * Plan, prepare, and manage submissions to HAs. * Lead regulatory interactions with HAs. * Represent the regulatory function on cross-functional product development teams, providing innovative strategic and tactical advice to achieve timely and efficient development of programs while ensuring compliance. * Effectively communicate the regulatory strategy, risks, mitigations and overall plans to Regulatory Affairs, program teams, senior management, and external stakeholders (as relevant). * Deliver clear and engaging presentations to internal teams and senior management. * Remain current on Regulatory Intelligence, new guidance documents, and competitive information to provide comprehensive information to program teams * Support or lead non-project activities, as needed such as SOP/standards development. Skills and Experience We Look For * Bachelor's degree in life sciences or related field required. * 10+ years of experience in regulatory affairs with a focus on regulatory documentation and lifecycle management within the pharmaceutical or biotechnology industry is a must, including experience in leadership roles. * Experience with oncology products. * Knowledge of regulatory requirements across development stages and post-approval is essential. Experience with regulations for: * Biologics and/or small molecules required * Cell/gene therapy desired * Combination products desired. * Expert working knowledge of full drug development process and knowledge of FDA and ICH regulatory requirements. * Strong strategic and analytical abilities, diplomacy, and negotiation skills. * Ability to collaboratively influence across multiple functions, and motivate others to accomplish company objectives * Self-motivated and detail oriented with sound judgement and innovative thinking to deal with challenges/opportunities. * Strong verbal, written, and communication skills for effective interaction with internal stakeholders and external regulatory bodies. * Strong leadership collaboration skills with the ability to influence internal/external stakeholders. * High level of integrity and commitment to regulatory compliance in support of patients and healthcare providers. Rewards at Arcellx Our people are our greatest asset, and supporting their well-being is an essential part of delivering on our mission and impacting the lives of patients. Putting this belief into practice means offering strong compensation and benefits. The base salary range for this position is $240,000 - $275,000 per year. Where a candidate falls within that range is determined by factors such as years of experience. Our compensation package also includes an annual bonus based on company goals and an equity (RSU) grant. We do offer relocation assistance for roles if required. Our market-leading benefits package includes: 100% coverage for medical, dental and vision for team members and dependents, unlimited vacation, a 3-day weekend every month, fully-paid parental leave for up to 6 months, tuition reimbursement, 401k employer contribution and more. Join us in our quest to reimagine cell therapy and destroy cancer. For more on our technology, culture, and team, go to **************** #LI-Onsite

Fate Therapeutics is seeking a motivated and execution-driven Manager/Senior Manager to support GMP manufacturing operations of iPSC-derived allogenic cell therapy products. As an integral part of the Manufacturing Team, this role is responsible for overseeing operational execution in addition to managing manufacturing quality events including deviations, CAPAs, and other required change actions. This individual will play a pivotal role in defining and executing the company's operational strategy to enable the execution of a sustainable, scalable and GMP compliant manufacturing process. Accordingly, this role will require proven leadership abilities to drive meaningful communication, collaboration and coordination both internally within the Manufacturing department as well as cross-functionally across all levels of the organization. This is a full-time, exempt position located at our corporate headquarters in San Diego, CA. Responsibilities * Responsible for overseeing end-to-end GMP production of iPSC-based drug product from media preparation and thaw of MCB's through harvest and cryopreservation of drug product. * Work effectively with other groups including Quality Assurance, Supply Chain, Quality Control, MSAT, Process Development, and Facilities. * Coordinate with applicable departments to manage Deviations, CAPAs, Continuous Improvements, Impact Assessments and Change Actions. * Assure manufacturing facility is maintained in an inspection-ready state at all times. * Engage with Materials Management and Planning and Sourcing teams to assure adequate inventory of raw materials to support planned production activities. * Project management utilizing tools including but not limited to SmartSheet and Microsoft Office tools. * Assure manufacturing staff meet and maintain cGMP training requirements. * Develop personnel schedules to allow effective execution of manufacturing activities. * Review and approve applicable manufacturing-related documentation. * Lead authorship and review process of SOPs and GMP BRs. * Identify potential process improvements for Manufacturing and design appropriate experiments to evaluate and implement those changes. * May hire, oversee, train, and motivate team members, ensuring that team goals are met efficiently. Qualifications * Bachelor's or Master's degree in a relevant discipline with 6+ years of Life Science GMP Manufacturing experience is required. * A strong manufacturing administration background specifically related to tech transfer of aseptically produced cell products is preferred. * A strong emphasis on quality event management and process improvement for manufacturing operations * Ability to create, read, review, and edit manufacturing related documents including Batch Records, SOP's, Work Instructions and associated forms. * Self-motivated, flexible, able to prioritize, multi-task, and work in a fast-paced & dynamic environment. * Experience leading projects and managing teams is required. Working Conditions * Subject to extended periods of sitting and standing, vision to monitor, and moderate noise levels. * Will require working with cells and cell lines of human and/or animal origin. * Will require working with hazardous materials. * Will require work in controlled and cGMP Manufacturing environments requiring special gowning. Compensation * The salary offer will be based on a variety of factors, including level, experience, qualifications, internal equity, and location. * Fate offers a competitive employment package that includes an annual bonus, equity, and a generous benefits package. * The anticipated salary range for this role is $110,000 - $150,000. The preceding job description indicates the general nature and level of work performed by employees within this classification. Additional and incidental duties related to the primary duties may be required from time to time. Equal Employment Opportunity Fate Therapeutics, Inc. is an equal opportunity employer. We value diversity and are committed to creating an inclusive environment for all employees. Privacy Notice To learn about how Fate collects and uses job application information, please visit Fate's online Privacy Notice. About Fate Therapeutics, Inc. Fate Therapeutics is a clinical-stage biopharmaceutical company dedicated to bringing a pipeline of induced pluripotent stem cell (iPSC)-derived cellular immunotherapies to patients. Using its proprietary iPSC product platform, the Company has established a leadership position in creating multiplexed-engineered master iPSC lines and in the manufacture and clinical development of off-the-shelf, iPSC-derived cell products. The Company's pipeline includes iPSC-derived T-cell and natural killer (NK) cell product candidates, which are selectively designed, incorporate novel synthetic controls of cell function, and are intended to deliver multiple therapeutic mechanisms to patients. Fate Therapeutics is headquartered in San Diego, CA. For more information, please visit ************************* ️ Recruitment Fraud Alert Recently, we have been made aware of unauthorized individuals falsely presenting themselves as Fate Therapeutics employees or recruiters as part of online scams or phishing attempts. Impersonators may use the Fate Therapeutics name and logo, as well as employee names and job titles, to gain a job seeker's personal or banking information or to request payment as a condition of being considered for a position at the company. Fate Therapeutics and its employees are not involved in these scams. Here are a few things to be aware of to help identify recruitment fraud: * Our Talent Acquisition team only corresponds from ************************* domain. * At no stage in our hiring process will we require payment or ask you to make deposits in your bank account. * We will only ask for personal information when applying for a position via our Careers page or thereafter. * At no stage during our hiring process will we ask you to click a link to begin a one-way video interview. * We do not use Google Hangouts, WhatsApp, or other third-party messaging platforms to recruit candidates or conduct interviews. Please exercise caution. If something feels off about your interactions, we encourage you to contact us at [email protected] to confirm the authenticity of the message. Your security is important to us, and we appreciate your vigilance. We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

Who We Are Arcellx is a public, clinical-stage biotechnology company reimagining cell therapy by engineering innovative immunotherapies for patients with cancer and other incurable diseases. We believe that cell therapies are one of the forward pillars of medicine and our mission is to destroy cancer and advance humanity by developing cell therapies that are safer, more effective, and more broadly accessible. Our team members are made up of talented innovators and dreamers working from our offices in Rockville, Maryland, and Redwood City, California. At Arcellx, we hire exceptional people and create a fun, diverse, supportive, and informal environment that allows everyone to do their best work. What Matters to Us Living our core values is essential to maintaining a work environment that is high-performing, inclusive, and collaborative. We look for candidates who demonstrate strong values alignment and bring different backgrounds, viewpoints, and abilities to the team. Arcellx Core Values * Start with authenticity: We foster an inclusive environment where each person can bring their authentic self to work. * Think 'we' before 'me': We prioritize collective success, collaborating and supporting one another to achieve our shared goals. * Embrace the challenge: We deliver exceptional results by working with shared determination and a commitment to doing what's right. How You'll Make a Difference As a Director, People & Culture supporting our Commercial organization, you will play a critical role in shaping and executing people strategy during a pivotal time in our company's growth-our build to commercial launch. You will partner closely with Commercial leaders and People teammates to develop and execute strategies that drive a highly engaged team, ensure organization effectiveness, effective talent development, and a high-performance culture. The "Fine Print" - What You'll Do * Serve as a strategic advisor to leaders, providing insights and recommendations on talent planning, team design, performance management, and organizational development. * Lead workforce planning and support talent acquisition strategies to build a high-performing sales, marketing, and MSL team prepared for successful market entry. * Support change management initiatives and culture-building efforts as the organization scales to meet the demands of commercialization. * Champion a high-performance, feedback-oriented, and inclusive culture. * Develop and implement talent engagement and retention programs tailored to field-based commercial roles in a dynamic, mission-driven cell therapy environment. * Use data and analytics to monitor organizational health and recommend targeted interventions. Skills and Experience We Look For Our ideal candidate has demonstrated strong business and people results in high-growth companies, preferably life sciences, and ideally with exposure to commercial launch or new product introduction. They have a good understanding of field-based commercial organizations, including salesforce dynamics, incentive structures, and regional talent strategies. They have demonstrated ability to influence senior leaders and translate business needs into talent strategies, and experience managing organizational change in fast-paced environments. High emotional intelligence and the ability to build meaningful relationships are essential. Rewards at Arcellx Our people are our greatest asset, and supporting their well-being is an essential part of delivering on our mission and impacting the lives of patients. Putting this belief into practice means offering strong compensation and benefits. The estimated base salary range for this position is $180,000-$245,000 per year. Where a candidate falls within that range is determined by factors such as years of experience and location. Our compensation package also includes an annual bonus based on company goals and an equity (RSU) grant. We do offer relocation assistance for roles if required. Our market-leading benefits package includes: 100% coverage for medical, dental and vision for team members and dependents, unlimited vacation, a 3-day weekend every month, fully-paid parental leave for up to 6 months, tuition reimbursement, 401k employer contribution and more. Join us in our quest to reimagine cell therapy and destroy cancer. For more on our technology, culture, and team, go to **************** #LI-Onsite

Fate Therapeutics is seeking a hands-on, service-driven individual to manage general upkeep, cleanliness, and smooth daily operations for our company facilities, focusing on common areas, conference rooms, laboratories and supply management to support a positive and efficient work environment. The successful candidate will have experience managing facility organization and cleanliness for both office and laboratories, including conference room readiness, setting up and breaking down meeting rooms, managing inventory of supplies, biohazardous waste, and reporting maintenance needs to ensure an organized, functional, and safe work environment. This is an entry-level, full-time, non-exempt position located at our corporate headquarters in San Diego, CA.Responsibilities Support operations across the Company facilities: o keep inventory, order, stage and distribute office supplies to office areas, breakroom supplies to break areas, restroom supplies to restrooms, conference room supplies to conference rooms, and consumables to R&D labs.o set up and breakdown of company meetings and events, including arranging tables, chairs, catering and equipment, restoring and cleanup of space afterward.o maintain daily cleanliness, safety, and professional appearance of the Company facilities including the common areas, supply areas, office areas, conference rooms, break areas, and restrooms.o manage centralized waste including trash, paper, plastics, and other recyclable materials. Support Company's hazardous waste program: o collect, transport, segregate, accumulate, and perform initial disposal of hazardous waste for various labs; determine proper method of accumulation and disposal based on hazard classes and compatibility of chemicals. o package, document, and label waste for shipment to appropriate disposal facilities pursuant to disposal facility, state, and federal requirements. o maintain records such as hazardous and non-hazardous waste manifests and associated documents. o respond to hazardous materials spills and non-hazardous spills and implement clean-up plan. Communicate list of activities to facilities personnel for evening janitorial vendor to complete. Work closely with facilities and HR personnel to support daily facilities requests and maintenance needs. Qualifications High school/GED with a minimum of one year's experience providing facilities support to a small to mid-size company; biotech or life science preferred. Experience working in a lab setting preferred. Mechanical knowledge of equipment and tools, including their design, uses, repair, and maintenance such as biosafety cabinets, refrigerators, freezers, and other general laboratory equipment preferred. Able to understand general instructions with proficient problem-solving abilities and detail-orientation. Ability to manage and prioritize end-user facilities requests. Experience using Microsoft Outlook Word and Excel. Strong written and verbal communication and customer service skills. Self-motivated, flexible, able to prioritize, multitask, and work in a professional, fast-paced & dynamic environment. Working Conditions 100% onsite work at corporate headquarters in San Diego, CA from 7:30am - 4:30pm. Subject to extended periods of standing and moving with moderate noise levels. Able to lift up to 35 lbs. on a regular basis. Will require working with hazardous materials. Compensation The salary offer will be based on a variety of factors, including level, experience, qualifications, internal equity, and location. Fate offers a competitive employment package that includes an annual bonus, equity, and a generous benefits package. The anticipated salary range for this role is $28 - $31 per hour. The preceding job description indicates the general nature and level of work performed by employees within this classification. Additional and incidental duties related to the primary duties may be required from time to time. Equal Employment OpportunityFate Therapeutics, Inc. is an equal opportunity employer. We value diversity and are committed to creating an inclusive environment for all employees. Privacy NoticeTo learn about how Fate collects and uses job application information, please visit Fate's online Privacy Notice. About Fate Therapeutics, Inc.Fate Therapeutics is a clinical-stage biopharmaceutical company dedicated to bringing a pipeline of induced pluripotent stem cell (iPSC)-derived cellular immunotherapies to patients. Using its proprietary iPSC product platform, the Company has established a leadership position in creating multiplexed-engineered master iPSC lines and in the manufacture and clinical development of off-the-shelf, iPSC-derived cell products. The Company's pipeline includes iPSC-derived T-cell and natural killer (NK) cell product candidates, which are selectively designed, incorporate novel synthetic controls of cell function, and are intended to deliver multiple therapeutic mechanisms to patients. Fate Therapeutics is headquartered in San Diego, CA. For more information, please visit ************************* ⚠️ Recruitment Fraud Alert Recently, we have been made aware of unauthorized individuals falsely presenting themselves as Fate Therapeutics employees or recruiters as part of online scams or phishing attempts. Impersonators may use the Fate Therapeutics name and logo, as well as employee names and job titles, to gain a job seeker's personal or banking information or to request payment as a condition of being considered for a position at the company. Fate Therapeutics and its employees are not involved in these scams. Here are a few things to be aware of to help identify recruitment fraud:- Our Talent Acquisition team only corresponds from our @fatetherapeutics.com domain.- At no stage in our hiring process will we require payment or ask you to make deposits in your bank account.- We will only ask for personal information when applying for a position via our Careers page or thereafter.- At no stage during our hiring process will we ask you to click a link to begin a one-way video interview.- We do not use Google Hangouts, WhatsApp, or other third-party messaging platforms to recruit candidates or conduct interviews. Please exercise caution. If something feels off about your interactions, we encourage you to contact us at **************************** to confirm the authenticity of the message. Your security is important to us, and we appreciate your vigilance. We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

Who We Are Arcellx is a public, clinical-stage biotechnology company reimagining cell therapy by engineering innovative immunotherapies for patients with cancer and other incurable diseases. We believe that cell therapies are one of the forward pillars of medicine and our mission is to destroy cancer and advance humanity by developing cell therapies that are safer, more effective, and more broadly accessible. Our team members are made up of talented innovators and dreamers working from our offices in Rockville, Maryland, and Redwood City, California. At Arcellx, we hire exceptional people and create a fun, diverse, supportive, and informal environment that allows everyone to do their best work. What Matters to Us Living our core values is essential to maintaining a work environment that is high-performing, inclusive, and collaborative. We look for candidates who demonstrate strong values alignment and bring different backgrounds, viewpoints, and abilities to the team. Arcellx Core Values Start with authenticity: We foster an inclusive environment where each person can bring their authentic self to work. Think ‘we' before ‘me': We prioritize collective success, collaborating and supporting one another to achieve our shared goals. Embrace the challenge: We deliver exceptional results by working with shared determination and a commitment to doing what's right. The “Fine Print” - What You'll Do Execute GMP-compliant testing of cell therapy products and in-process samples, with a focus on molecular assays (dd PCR, qPCR), flow cytometry, and functional assays for CAR-T cells. Perform cell culture and expansion of engineered T cells, maintaining aseptic technique and quality standards. Contribute to drafting and updating SOPs, forms, and logbooks governing lab operations, equipment maintenance, and assay procedures. Coordinate preventive maintenance, calibration, and troubleshooting of lab equipment and instruments in collaboration with internal resources and external partners. Manage inventory of cell culture reagents, molecular assay supplies, and lab materials. Support GMP investigations, including out-of-specification results, assay deviations, invalid assays, change controls, and CAPAs, with a focus on molecular and functional testing. Assist in tracking, trending, and reporting QC data for molecular assays, cell culture, and CAR-T functional studies. Skills And Experience We Look For BS or MS in Biological Sciences, Immunology, or a related field. 2+ years in pharmaceutical or biotechnology industry, including cell therapy/CAR-T experience. Hands-on experience with molecular assays and flow cytometry. Experience in cell culture and performing CAR-T functional assays. Familiarity with GMP-compliant lab practices and QC data tracking. Excellent written and oral communication skills. Rewards at Arcellx Our people are our greatest asset, and supporting their well-being is an essential part of delivering on our mission and impacting the lives of patients. Putting this belief into practice means offering strong compensation and benefits. The base salary range for this position is $80,000 - $105,000 per year. Where a candidate falls within that range is determined by factors such as years of experience. Our compensation package also includes an annual bonus based on company goals and an equity (RSU) grant. We do offer relocation assistance for roles if required. Our market-leading benefits package includes: 100% coverage for medical, dental and vision for team members and dependents, unlimited vacation, a 3-day weekend every month, fully-paid parental leave for up to 6 months, tuition reimbursement, 401k employer contribution and more. Join us in our quest to reimagine cell therapy and destroy cancer. For more on our technology, culture, and team, go to **************** #LI-Onsite

Who We Are Arcellx is a public, clinical-stage biotechnology company reimagining cell therapy by engineering innovative immunotherapies for patients with cancer and other incurable diseases. We believe that cell therapies are one of the forward pillars of medicine and our mission is to destroy cancer and advance humanity by developing cell therapies that are safer, more effective, and more broadly accessible. Our team members are made up of talented innovators and dreamers working from our offices in Rockville, Maryland, and Redwood City, California. At Arcellx, we hire exceptional people and create a fun, diverse, supportive, and informal environment that allows everyone to do their best work. What Matters to Us Living our core values is essential to maintaining a work environment that is high-performing, inclusive, and collaborative. We look for candidates who demonstrate strong values alignment and bring different backgrounds, viewpoints, and abilities to the team. Arcellx Core Values * Start with authenticity: We foster an inclusive environment where each person can bring their authentic self to work. * Think 'we' before 'me': We prioritize collective success, collaborating and supporting one another to achieve our shared goals. * Embrace the challenge: We deliver exceptional results by working with shared determination and a commitment to doing what's right. The "Fine Print" - What You'll Do * Serve as the lead Regulatory representative on the Promotional Review and Medical Review Committees * Independently review and approve promotional/non-promotional materials. * Ensure regulatory compliance with the current labeling, applicable regulations, guidance documents, and internal policies/best practices * Collaborate with Medical, Legal and Commercial to execute and approve key Commercial campaigns. * Monitor evolving FDA regulations, enforcement actions, and industry best practices; translate insights into internal training and process improvements. * Develop and implement labeling strategies, including creation, review, and maintenance of prescribing information, patient information, and packaging components. * Serve as primary liaison with FDA's Office of Prescription Drug Promotion (OPDP) and/or Advertising and Promotional Labeling Branch (APLB) on ad promo submissions, inquiries, and regulatory correspondence. * Contribute to broader regulatory strategy and operations as a key leader within a small, agile team preparing for its first product launch. Skills and Experience We Look For * Bachelor's degree in life sciences or related field required. * 10+ years of regulatory affairs experience in the biopharmaceutical industry, with significant expertise in advertising, promotion, and labeling. * In-depth understanding of FDA regulations and guidelines, and other relevant health authority requirements for pharmaceuticals. * Ability to apply regulatory knowledge to develop practical solutions and strategies for complex promotional and labeling issues. * Proven track record of supporting pre-launch through commercial stages, ideally in oncology or specialty pharmaceuticals. * Ability to operate strategically while managing hands-on responsibilities in a small, fast-paced biotech environment. * Strong leadership, verbal/written communication, and collaboration skills with the ability to influence internal/external stakeholders. * High level of integrity and commitment to regulatory compliance in support of patients and healthcare providers. Rewards at Arcellx Our people are our greatest asset, and supporting their well-being is an essential part of delivering on our mission and impacting the lives of patients. Putting this belief into practice means offering strong compensation and benefits. The estimated base salary range for this position is $220,000 - $255,000 per year. Where a candidate falls within that range is determined by factors such as years of experience. Our compensation package also includes an annual bonus based on company goals and an equity (RSU) grant. We do offer relocation assistance for roles if required. Our market-leading benefits package includes: 100% coverage for medical, dental and vision for team members and dependents, unlimited vacation, a 3-day weekend every month, fully-paid parental leave for up to 6 months, tuition reimbursement, 401k employer contribution and more. Join us in our quest to reimagine cell therapy and destroy cancer. For more on our technology, culture, and team, go to **************** #LI-Onsite