# FewerJobs export - 100 curated jobs Generated: 2026-06-18T13:23:34.258Z Source: https://fewerjobs.com ## Filters applied - **q**: Iovance Biotherapeutics Inc - **quality_floor**: default - **match_401k_strict**: true - **parental_strict**: true - **non_birth_strict**: true - **pto_strict**: true - **include_older**: false - **apply_url_verified**: false - **page**: 1 - **per_page**: 100 - **sort**: relevance ## Jobs ### Clinical Trial Manager - Iovance Biotherapeutics Inc - Location: Remote (remote) - Salary: $145K-$165K - Posted: 2026-06-01 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/iovancebiotherapeutics/jobs/5235729008 - Excerpt: Clinical Trial Manager Remote Iovance Biotherapeutics aims to be the global leader in innovating, developing and delivering tumor infiltrating lymphocyte (TIL) therapy for people with cancer. We are pioneering a transformational approach to treating cancer by harnessing the ability of the human immune system to recognize and attack diverse cancer cells in each patient. The Iovance TIL platform has demonstrated promising clinical data across multiple solid tumors. We are committed to continuous innovation in cell therapy, including gene-edited cell therapy, which may be a promising option for patients with cancer. Overview The Clinical Trial Manager has operations experience within the biotech/biopharma arena. This individual has a high level of core competencies and technical skills to be applied within the management of clinical programs leading to registrational submissions of Biologic License Applications (BLAs). The Clinical Trial Manager position is an opportunity for an individual to join a cross-functional clinical team having high-visible and dynamic input in a therapeutic indication of unmet medical need and orphan disease status. Essential Functions and Responsibilities - Support the overall operational execution of clinical studies on one or more clinical programs from initial study synopsis through final project deliverables (ie, database hard-lock, final TLFs, CSR, etc.) - Manage the implementation, on-time execution and conduct of clinical studies; including the development of budget items, milestones and timelines, in addition to scope and management of resources (including vendor selection). All leading to overall quality, safety, and compliance throughout the duration of the clinical studies and program. - Oversight ### AI Strategy Associate - Iovance Biotherapeutics Inc - Location: Remote (remote) - Salary: $100K-$125K - Posted: 2026-05-31 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/iovancebiotherapeutics/jobs/5234975008 - Excerpt: AI Strategy Associate Remote Iovance Biotherapeutics aims to be the global leader in innovating, developing and delivering tumor infiltrating lymphocyte (TIL) therapy for people with cancer. We are pioneering a transformational approach to treating cancer by harnessing the ability of the human immune system to recognize and attack diverse cancer cells in each patient. The Iovance TIL platform has demonstrated promising clinical data across multiple solid tumors. We are committed to continuous innovation in cell therapy, including gene-edited cell therapy, which may be a promising option for patients with cancer. Overview Iovance Biotherapeutics is a commercial-stage cell therapy company focused on developing life-saving cancer immunotherapies. We are building an internal AI Strategy & Operations function to drive measurable cost savings and operational efficiency across the entire organization. We are looking for an AI Strategy Associate to drive process discovery and optimization across Iovance. This role is the analytical engine of our AI program. You will run a comprehensive diagnostic across 15 business functions, build the financial models that translate use cases into P&L savings commitments, and manage stakeholder relationships across the company. Think of this as the operating-side equivalent of a top-tier consulting engagement. You will interview stakeholders, map pain points to savings levers, build controlled comparisons to prove AI impact, and deliver a financial model the CFO can underwrite. In this role, you will own the outcomes, not just the recommendation. Unlike traditional analyst roles, the successful applicant is required to be adept at using AI tools, be able ### AI Product Engineer - Iovance Biotherapeutics Inc - Location: Remote (remote) - Salary: $100K-$125K - Posted: 2026-05-31 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/iovancebiotherapeutics/jobs/5234974008 - Excerpt: AI Product Engineer Remote Iovance Biotherapeutics aims to be the global leader in innovating, developing and delivering tumor infiltrating lymphocyte (TIL) therapy for people with cancer. We are pioneering a transformational approach to treating cancer by harnessing the ability of the human immune system to recognize and attack diverse cancer cells in each patient. The Iovance TIL platform has demonstrated promising clinical data across multiple solid tumors. We are committed to continuous innovation in cell therapy, including gene-edited cell therapy, which may be a promising option for patients with cancer. Overview Iovance Biotherapeutics is a commercial-stage cell therapy company focused on developing life-saving cancer immunotherapies. We are building an internal AI Strategy & Operations function to drive measurable cost savings and operational efficiency across every department in the company. We are hiring an AI Full-Stack Product Engineer to build the first generation of internal AI-enabled tools at Iovance. This is a hands-on full-stack JavaScript engineering role for someone who uses AI-assisted development to ship faster without compromising code quality, security, or maintainability. You will design, build, and deploy micro-applications and workflow automations that solve real business problems. You will work directly with stakeholders across Commercial, Regulatory, Quality, Manufacturing, and R&D to turn validated use cases into tools people use every day. The foundation of this role is engineering. The multiplier is AI fluency. You should be using tools like Claude, Cursor, Copilot to dramatically accelerate your workflow. We want a skilled engineer who produces significantly more output because of how ### Associate Medical Director - Iovance Biotherapeutics Inc - Location: Remote (remote) - Salary: $225K-$265K - Posted: 2026-06-11 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/iovancebiotherapeutics/jobs/5254105008 - Excerpt: Associate Medical Director Remote Iovance Biotherapeutics aims to be the global leader in innovating, developing and delivering tumor infiltrating lymphocyte (TIL) therapy for people with cancer. We are pioneering a transformational approach to treating cancer by harnessing the ability of the human immune system to recognize and attack diverse cancer cells in each patient. The Iovance TIL platform has demonstrated promising clinical data across multiple solid tumors. We are committed to continuous innovation in cell therapy, including gene-edited cell therapy, which may be a promising option for patients with cancer. Overview The Associate Medical Director is primarily responsible for physician-supported clinical trial support and overseeing the direction, planning, execution, and interpretation of IOVANCE clinical trials. Essential Functions and Responsibilities - Primary point of clinical contact for IOVANCE clinical trials. Directs protocol implementation including site identification and communication with Clinical Operations, attendance at investigators' meetings (virtual and live), correspondence with sites regarding patient eligibility and safety considerations, and interaction with US- and Global Medical Affairs teams - Co-manages program development and reports directly to Executive Medical Director. Responsible for cross-functional collaboration with all of the disciplines necessary for successful drug/therapy development (Study Management Team level): clinical, manufacturing, quality assurance, regulatory, medical affairs, legal, biostatistics, global patient safety, data management, pharmacovigilance, and clinical operations - Monitors clinical trials including the oversight of all aspects of trial conduct and safety, contact with investigators and site study staff, and CRO medical monitors - Supports data analysis and assembly, including IDMC meetings, interim analyses, IB ### Senior Accountant - Iovance Biotherapeutics Inc - Location: Philadelphia, PA (unspecified) - Salary: Not disclosed - Posted: 2026-05-06 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/iovancebiotherapeutics/jobs/5211069008 - Excerpt: Senior Accountant Philadelphia, PA Iovance Biotherapeutics aims to be the global leader in innovating, developing and delivering tumor infiltrating lymphocyte (TIL) therapy for people with cancer. We are pioneering a transformational approach to treating cancer by harnessing the ability of the human immune system to recognize and attack diverse cancer cells in each patient. The Iovance TIL platform has demonstrated promising clinical data across multiple solid tumors. We are committed to continuous innovation in cell therapy, including gene-edited cell therapy, which may be a promising option for patients with cancer. Overview The Senior Accountant, reporting to the Senior Director, Finance Plant Controller, is responsible for the maintenance, execution of day-to-day general accounting activities, and oversight of Iovance manufacturing site's (iCTC) monthly, quarterly and annual financial reporting and close process, including analysis and reconciliation of certain General Ledger accounts; these accounts will include Accrued Expenses and Capital Assets, as well as possibly supporting activities in certain Inventory accounts. These roles and responsibilities include frequent engagement with other Business Partners, external vendors and parties to understand the business and operations. The Senior Accountant will also be responsible for SOX controls execution and documentation, performing various financial analysis, assist with the external audit, special projects and process improvement initiatives, and prepare and review certain schedules and information. Specific Responsibilities - Ensure that iCTC GL transactions are accounted for in accordance with U.S. GAAP - Prepare and book journal entries for month-end close, including sub-ledger/ schedule to ledger reconciliations and analysis of reconciling items ### Senior Clinical Trial Manager, Research Alliances - Iovance Biotherapeutics Inc - Location: Remote (remote) - Salary: $165K-$185K - Posted: 2026-04-22 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/iovancebiotherapeutics/jobs/5191029008 - Excerpt: Senior Clinical Trial Manager, Research Alliances Remote Iovance Biotherapeutics aims to be the global leader in innovating, developing and delivering tumor infiltrating lymphocyte (TIL) therapy for people with cancer. We are pioneering a transformational approach to treating cancer by harnessing the ability of the human immune system to recognize and attack diverse cancer cells in each patient. The Iovance TIL platform has demonstrated promising clinical data across multiple solid tumors. We are committed to continuous innovation in cell therapy, including gene-edited cell therapy, which may be a promising option for patients with cancer. Overview The Senior Clinical Trial Manager (CTM) in the Research Alliances team will independently lead and is accountable for the planning, execution, management, and reporting of clinical projects supporting Iovance commercial activities, including Expanded Access Programs (intermediate EAP, single-patient and Ex-US Access Programs) and Phase 4 post marketing studies. In addition, the Sr. CTM/CTM will provide operational leadership for studies within a growing portfolio of Investigator Sponsored collaborations and other non-clinical collaborative research initiatives involving lifileucel and Proleukin. This position works very closely with external vendors, HCPs, as well as multiple Iovance teams: Commercial, Medical Affairs, Regulatory, Safety, Clinical, Biometrics, Quality, Legal, Quality, Supply Chain & Logistics and Manufacturing. The ideal candidate will have clinical operations experience within the pharma/biotech arena, be self-motivated, and able demonstrate the ability to manage complex programs independently while collaborating effectively in a dynamic, agile, and evolving organization. Essential Functions and Responsibilities - Oversee the timely activation, execution, and management of Expanded ### Manager, Regulatory Affairs CMC - Iovance Biotherapeutics Inc - Location: Remote (remote) - Salary: $140K-$160K - Posted: 2026-05-08 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/iovancebiotherapeutics/jobs/5211930008 - Excerpt: Manager, Regulatory Affairs CMC Remote Iovance Biotherapeutics aims to be the global leader in innovating, developing and delivering tumor infiltrating lymphocyte (TIL) therapy for people with cancer. We are pioneering a transformational approach to treating cancer by harnessing the ability of the human immune system to recognize and attack diverse cancer cells in each patient. The Iovance TIL platform has demonstrated promising clinical data across multiple solid tumors. We are committed to continuous innovation in cell therapy, including gene-edited cell therapy, which may be a promising option for patients with cancer. Overview The Manager, Regulatory Affairs CMC, represents Regulatory Affairs on cross-functional teams, working closely with other team members to support corporate and departmental objectives. An important aspect of this role is the planning and management of submissions. Attention to detail in written correspondence, in the maintenance of regulatory files, and ability to work with diverse internal and external stakeholders are also important factors for success in this role. Essential Functions and Responsibilities - Manages the planning, compilation, QC, and submission of Investigational Drug Applications (INDs), Biologics License Applications (BLAs), and their amendments. - Prepares routine IND and CTA amendments. - Work with submission authors and reviewers to ensure that source document planning is complete and that high-quality documents are approved on-schedule. - Represents Regulatory Affairs and provides regulatory expertise to cross-functional teams on specified projects and topics. - Interface with Quality Assurance, clinical manufacturing, commercial manufacturing and other stakeholders to further develop and maintain a robust change control program. ### General Ledger Accountant I [Contract to Hire] - Iovance Biotherapeutics Inc - Location: San Carlos, CA (unspecified) - Salary: $95K-$115K - Posted: 2026-05-06 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/iovancebiotherapeutics/jobs/5211863008 - Excerpt: General Ledger Accountant I [Contract to Hire] San Carlos, CA Iovance Biotherapeutics aims to be the global leader in innovating, developing and delivering tumor infiltrating lymphocyte (TIL) therapy for people with cancer. We are pioneering a transformational approach to treating cancer by harnessing the ability of the human immune system to recognize and attack diverse cancer cells in each patient. The Iovance TIL platform has demonstrated promising clinical data across multiple solid tumors. We are committed to continuous innovation in cell therapy, including gene-edited cell therapy, which may be a promising option for patients with cancer. Overview The General Ledger Accountant I is responsible for the maintenance and reconciliation of assigned General Ledger accounts, including prepaids, accruals, and other short- and long-term assets. This role supports the monthly close process, prepares balance sheet reconciliations, and maintains strong internal controls in accordance with U.S. GAAP. The General Ledger Accountant I also serves as the system administrator for the Concur Employee Expense Reporting application and manages the corporate credit card program, including user administration, system modifications, and coordination with Concur auditors. Specific Responsibilities - Ensure all General Ledger (GL) transactions are recorded in accordance with U.S. GAAP. - Process journal entries for month-end close, including subledger-to-ledger reconciliations. - Create accounting schedules and analyses to review additions and deletions, depreciation/amortization, and department expenditures. - Perform monthly bank reconciliations and resolve discrepancies in a timely manner. - Perform balance sheet reconciliations for assigned accounts, including prepaids, accruals, and other short- and long-term assets. - ### Senior Clinical Scientist [Contract] - Iovance Biotherapeutics Inc - Location: San Carlos, CA (unspecified) - Salary: Not disclosed - Posted: 2026-05-31 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/iovancebiotherapeutics/jobs/5235721008 - Excerpt: Senior Clinical Scientist [Contract] San Carlos, CA Iovance Biotherapeutics aims to be the global leader in innovating, developing and delivering tumor infiltrating lymphocyte (TIL) therapy for people with cancer. We are pioneering a transformational approach to treating cancer by harnessing the ability of the human immune system to recognize and attack diverse cancer cells in each patient. The Iovance TIL platform has demonstrated promising clinical data across multiple solid tumors. We are committed to continuous innovation in cell therapy, including gene-edited cell therapy, which may be a promising option for patients with cancer. Overview The Senior Clinical Scientist participates in support of the Clinical Development plans (CDPs) and supports the assigned Medical Director/Clinical Science Physician(s) with various deliverables necessary for effective and efficient CS plan execution for the assigned assets/indication(s). The Senior Clinical Scientist has primary responsibilities for supporting Medical Directors/Clinical Science Physicians with clinical documentation, representing Clinical Science on various teams/sub-teams or other appropriate forums, and supporting training of study site and/or CRO personnel. The Senior Clinical Scientist is expected to perform their responsibilities with independence and are likely to have external interactions with cooperative groups, key opinion leaders (KOLs), and external vendors supporting the work of Clinical Science. Specific Responsibilities - Supports the design and writing of clinical protocols and associated clinical study documents (e.g., ICFs, charters, operational manuals, etc.) - Serves as an expert on the clinical study design (including trial procedures and requirements) and develops training materials to ensure quality execution by the investigational sites. - ### Quality Control Specialist I, Sample Management [Contract to Hire] - Iovance Biotherapeutics Inc - Location: Phildelphia (unspecified) - Salary: Not disclosed - Posted: 2026-06-09 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/iovancebiotherapeutics/jobs/5248785008 - Excerpt: Quality Control Specialist I, Sample Management [Contract to Hire] Phildelphia Iovance Biotherapeutics aims to be the global leader in innovating, developing and delivering tumor infiltrating lymphocyte (TIL) therapy for people with cancer. We are pioneering a transformational approach to treating cancer by harnessing the ability of the human immune system to recognize and attack diverse cancer cells in each patient. The Iovance TIL platform has demonstrated promising clinical data across multiple solid tumors. We are committed to continuous innovation in cell therapy, including gene-edited cell therapy, which may be a promising option for patients with cancer. Overview The Quality Control Specialist I, Sample Management will ensure time-sensitive distribution of quality control samples in support of QC-related activities. They will be responsible for sample inventory management as well as internal and external sample distribution, including storage and shipping under appropriate conditions, for all the iCTC cell therapy asset. Essential Functions and Responsibilities: - Maintain raw material, in-process, and final product samples, including inventory tracking and reconciliation. - Ensures timely sample distribution in support of Quality Control activities, including internal distribution and external shipping. - Ensures proper storage of sample inventory and proper shipping conditions - Support sample receipt and documentation. - Maintain current knowledge base of regulations, corporate policies, and industry best practices, trends, and standards to ensure that the function remains in compliance with applicable requirements. - Packaging of samples using temperature controlled dewars, cold packs, and dry ice. - Perform Quality Control activities - Performs peer review of logbooks ### Director, HTA, Evidence, and Global Access - Iovance Biotherapeutics Inc - Location: Remote (remote) - Salary: $240K-$265K - Posted: 2026-04-30 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/iovancebiotherapeutics/jobs/5206786008 - Excerpt: Director, HTA, Evidence, and Global Access Remote Iovance Biotherapeutics aims to be the global leader in innovating, developing and delivering tumor infiltrating lymphocyte (TIL) therapy for people with cancer. We are pioneering a transformational approach to treating cancer by harnessing the ability of the human immune system to recognize and attack diverse cancer cells in each patient. The Iovance TIL platform has demonstrated promising clinical data across multiple solid tumors. We are committed to continuous innovation in cell therapy, including gene-edited cell therapy, which may be a promising option for patients with cancer. Overview As Iovance prepares to bring AMTAGVI® to patients globally outside the United States, we are seeking an individual who is experienced with HTA, Evidence, and Global Access. This role will be a critical contributor to Iovance's HTA, evidence, and global access strategies and will report to the Senior Director, Global Market Access. The position is responsible for supporting international markets where Iovance is pursuing reimbursement, planning for new indication and products, and support of commercial activities generally. Core responsibilities include end-to-end management of health technology assessment (HTA) submissions, developing Iovance's evidence generation activities, engagement with HTA bodies and payers, development of global value and access materials, and project management across global market access and HEOR activities. The role will also support HEOR-related activities -including research, economic modeling, and publications - and may from time to time engage in activities supporting projects from regulatory, commercial, or other teams. The Director will serve as the internal subject matter ### Senior IT Quality Systems Analyst - Iovance Biotherapeutics Inc - Location: Philadelphia, PA (unspecified) - Salary: Not disclosed - Posted: 2026-03-30 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/iovancebiotherapeutics/jobs/5168519008 - Excerpt: Senior IT Quality Systems Analyst Philadelphia, PA Iovance Biotherapeutics aims to be the global leader in innovating, developing and delivering tumor infiltrating lymphocyte (TIL) therapy for people with cancer. We are pioneering a transformational approach to treating cancer by harnessing the ability of the human immune system to recognize and attack diverse cancer cells in each patient. The Iovance TIL platform has demonstrated promising clinical data across multiple solid tumors. We are committed to continuous innovation in cell therapy, including gene-edited cell therapy, which may be a promising option for patients with cancer. Overview This position reports to the Director IT, Tech Ops and Quality. The Senior Quality Systems Analyst is a hands-on technical and operational lead responsible for the strategy, administration, support, validation, and continuous improvement of Quality and Laboratory systems in a GxP-regulated pharmaceutical manufacturing environment. This role serves as a subject matter expert for enterprise Quality systems, especially the LIMS and QMS platforms, and partners closely with Quality, Manufacturing, QC Laboratories, MSAT, R&D, IT and other departments to deliver compliant, scalable, and efficient digital solutions that support product quality, data integrity, and regulatory commitments. Essential Functions and Responsibilities - Lead the selection, deployment, administration, support, and continuous improvement of computer-based systems supporting 24x7 Manufacturing Operations, Laboratory, and Quality Management processes. - Serve as the subject matter expert and system owner for Quality and Laboratory platforms, including LIMS and QMS solutions. - Perform operational support activities for critical GxP systems, including end-user support, monitoring, troubleshooting, issue resolution, break-fix ### Senior Regulatory Affairs CMC Associate - Iovance Biotherapeutics Inc - Location: Remote (remote) - Salary: $140K-$160K - Posted: 2026-06-02 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/iovancebiotherapeutics/jobs/5238881008 - Excerpt: Senior Regulatory Affairs CMC Associate Remote Iovance Biotherapeutics aims to be the global leader in innovating, developing and delivering tumor infiltrating lymphocyte (TIL) therapy for people with cancer. We are pioneering a transformational approach to treating cancer by harnessing the ability of the human immune system to recognize and attack diverse cancer cells in each patient. The Iovance TIL platform has demonstrated promising clinical data across multiple solid tumors. We are committed to continuous innovation in cell therapy, including gene-edited cell therapy, which may be a promising option for patients with cancer. Overview Iovance seeks a highly motivated Senior Regulatory Affairs Specialist. The successful candidate has experience planning and managing regulatory authority submissions. He / She will coordinate CMC submissions across multiple products, supporting management of the planning, compilation, QC, and submission of CMC dossier content to clinical and commercial applications, and their amendments. This role will be responsible for the preparation and adaptation of submission documents for use in global clinical and commercial submissions following eCTD specifications and market specific requirements and may be responsible for independently planning and preparing routine clinical trial application related amendments and commercial submissions (e.g. Annual reports, DSUR, health authority queries). An important aspect of this role is the planning and management of submissions. Attention to detail in written correspondence, in the maintenance of regulatory files, and ability to work with diverse internal and external stakeholders are also important factors for success in this role. Another important aspect of this role is the capacity ### Cell Therapy Account Management - Michigan - Iovance Biotherapeutics Inc - Location: Michigan (unspecified) - Salary: $200K-$220K - Posted: 2026-05-27 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/iovancebiotherapeutics/jobs/5231791008 - Excerpt: Cell Therapy Account Management - Michigan Michigan Iovance Biotherapeutics aims to be the global leader in innovating, developing and delivering tumor infiltrating lymphocyte (TIL) therapy for people with cancer. We are pioneering a transformational approach to treating cancer by harnessing the ability of the human immune system to recognize and attack diverse cancer cells in each patient. The Iovance TIL platform has demonstrated promising clinical data across multiple solid tumors. We are committed to continuous innovation in cell therapy, including gene-edited cell therapy, which may be a promising option for patients with cancer. Overview Amtagvi™ is the best-in-class cell therapy treatment for advanced melanoma. The Cell Therapy Account Management (CTAM) will be responsible for driving Amtagvi demand by building a robust referral network between community practices and academic centers; enable early patient identification and streamline referral pathways; and collaborate with internal teams to enhance scientific and operational excellence in cell therapy account management. To succeed in this role, you will use prior experience to optimize territory strategy in the oncology rare disease space and have demonstrated experience influencing others and building relationships. Additional competencies include experience with immunotherapy and solid tumor cancer, as well as prior launch experience, demonstrated ability to drive demand, pull through, and sustain the growth of Amtagvi™. Essential Functions and Responsibilities: - Drive Amtagvi TM demand and appropriate pull-through at targeted ATCs and serve as a liaison between community oncology practices and internal stakeholders to align initiatives with business and medical objectives. - Serve as the ### Accounts Payable Specialist [Contract to Hire] - Iovance Biotherapeutics Inc - Location: Hybrid (hybrid) - Salary: Not disclosed - Posted: 2026-05-15 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/iovancebiotherapeutics/jobs/5221444008 - Excerpt: Accounts Payable Specialist [Contract to Hire] Hybrid Iovance Biotherapeutics aims to be the global leader in innovating, developing and delivering tumor infiltrating lymphocyte (TIL) therapy for people with cancer. We are pioneering a transformational approach to treating cancer by harnessing the ability of the human immune system to recognize and attack diverse cancer cells in each patient. The Iovance TIL platform has demonstrated promising clinical data across multiple solid tumors. We are committed to continuous innovation in cell therapy, including gene-edited cell therapy, which may be a promising option for patients with cancer. Overview The Accounts Payable 'AP' Specialist is a frontline accounting position, reporting directly to the Accounts Payable Manager. The AP Specialist is responsible for processing invoices and payments received from vendors and suppliers. This involves reviewing invoices for accuracy and completeness, ensuring they are correctly coded and approved, and entering data into the accounting system. Essential Functions and Responsibilities - Perform day-to-day administration of all payment cycle activities and provide efficient client service. - Manage full AP cycle for assigned vendors, including the related coordination with business process owners. - Ensures correct sorting, general ledger coding, and matching invoices/receipts, where applicable. - Verify that transactions comply with financial policies and procedures established by the Company. - Ensure the Company's authorization matrix approves invoices before payment. - Collaborate with the Procurement team and assist with vendor purchase order inquiries. - Research and resolve invoice discrepancies and issues. - Correspond with vendors and respond to inquiries. - Must adhere ### Supervisor, Aseptic Manufacturing - Night Shift - Iovance Biotherapeutics Inc - Location: Philadelphia, PA (unspecified) - Salary: Not disclosed - Posted: 2026-04-13 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/iovancebiotherapeutics/jobs/5181178008 - Excerpt: Supervisor, Aseptic Manufacturing - Night Shift Philadelphia, PA Iovance Biotherapeutics aims to be the global leader in innovating, developing and delivering tumor infiltrating lymphocyte (TIL) therapy for people with cancer. We are pioneering a transformational approach to treating cancer by harnessing the ability of the human immune system to recognize and attack diverse cancer cells in each patient. The Iovance TIL platform has demonstrated promising clinical data across multiple solid tumors. We are committed to continuous innovation in cell therapy, including gene-edited cell therapy, which may be a promising option for patients with cancer. Overview The Supervisor for Aseptic Manufacturing oversees the production process to ensure that all materials are produced safely and follow the company's standards. This position requires timely document review and ensuring all targets are met. In addition, the supervisor will be responsible for developing staff and implementing an effective "First-time right" program to meet Iovance's growing demands. The successful candidate will also help onboard new team members and manage deviations and CAPAs for the training and learning team. It is crucial that the supervisor has innovative technical knowledge and contributes significantly to the overall manufacturing operation. As a leadership team member for autologous cell therapy manufacturing operations, a background in cell culture and manufacturing in ISO class 5 cleanrooms is necessary. Essential Functions and Responsibilities • Supervision and Development direct reports (operators), mentoring/coaching to motivate and mentor peers/ staff to foster a culture of continuous improvement and operational excellence. • Schedule and coordinate day-to-day activities, ensuring ### Principal AI Systems Engineer - Iovance Biotherapeutics Inc - Location: Remote (remote) - Salary: $175K-$200K - Posted: 2026-05-31 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/iovancebiotherapeutics/jobs/5234960008 - Excerpt: Principal AI Systems Engineer Remote Iovance Biotherapeutics aims to be the global leader in innovating, developing and delivering tumor infiltrating lymphocyte (TIL) therapy for people with cancer. We are pioneering a transformational approach to treating cancer by harnessing the ability of the human immune system to recognize and attack diverse cancer cells in each patient. The Iovance TIL platform has demonstrated promising clinical data across multiple solid tumors. We are committed to continuous innovation in cell therapy, including gene-edited cell therapy, which may be a promising option for patients with cancer. Overview This is a senior role responsible for the hands-on design, build, validation, and deployment of Artificial Intelligence (AI) systems at Iovance Biotherapeutics. This role is focused on execution - turning approved use cases into working, validated, production AI systems that deliver measurable business value. This role directly supports Iovance's strategy to improve overall operational productivity. The ideal candidate is a deeply technical, hands-on senior engineer with demonstrated production experience designing and shipping Large Language Model (LLM) applications, Retrieval-Augmented Generation (RAG) systems, and modern AI integrations. This position works closely with IT leads, business process owners across Manufacturing, Quality, Regulatory Affairs, Clinical, Commercial, G&A, IT Security, Privacy, and Quality Assurance to deliver AI capabilities that respect Iovance's regulated environment. This role executes against a roadmap and prioritized backlog, while contributing technical input to refinement, scoping, and sequencing. Primary Responsibilities - Design, build, and ship AI systems against the approved Iovance AI roadmap, including end-to-end ownership of architecture, retrieval pipelines, ### Cell Therapy Account Management - Western PA/WV - Iovance Biotherapeutics Inc - Location: Pennsylvania (unspecified) - Salary: $200K-$220K - Posted: 2026-05-27 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/iovancebiotherapeutics/jobs/5231805008 - Excerpt: Cell Therapy Account Management - Western PA/WV Pennsylvania Iovance Biotherapeutics aims to be the global leader in innovating, developing and delivering tumor infiltrating lymphocyte (TIL) therapy for people with cancer. We are pioneering a transformational approach to treating cancer by harnessing the ability of the human immune system to recognize and attack diverse cancer cells in each patient. The Iovance TIL platform has demonstrated promising clinical data across multiple solid tumors. We are committed to continuous innovation in cell therapy, including gene-edited cell therapy, which may be a promising option for patients with cancer. Overview Amtagvi™ is the best-in-class cell therapy treatment for advanced melanoma. The Cell Therapy Account Management (CTAM) will be responsible for driving Amtagvi demand by building a robust referral network between community practices and academic centers; enable early patient identification and streamline referral pathways; and collaborate with internal teams to enhance scientific and operational excellence in cell therapy account management. To succeed in this role, you will use prior experience to optimize territory strategy in the oncology rare disease space and have demonstrated experience influencing others and building relationships. Additional competencies include experience with immunotherapy and solid tumor cancer, as well as prior launch experience, demonstrated ability to drive demand, pull through, and sustain the growth of Amtagvi™. Essential Functions and Responsibilities: - Drive Amtagvi TM demand and appropriate pull-through at targeted ATCs and serve as a liaison between community oncology practices and internal stakeholders to align initiatives with business and medical objectives. - Serve as ### Aseptic Manufacturing Technician I - Day Shift B [Contract to Hire] - Iovance Biotherapeutics Inc - Location: Philadelphia, PA (unspecified) - Salary: Not disclosed - Posted: 2026-05-14 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/iovancebiotherapeutics/jobs/5219894008 - Excerpt: Aseptic Manufacturing Technician I - Day Shift B [Contract to Hire] Philadelphia, PA Iovance Biotherapeutics aims to be the global leader in innovating, developing and delivering tumor infiltrating lymphocyte (TIL) therapy for people with cancer. We are pioneering a transformational approach to treating cancer by harnessing the ability of the human immune system to recognize and attack diverse cancer cells in each patient. The Iovance TIL platform has demonstrated promising clinical data across multiple solid tumors. We are committed to continuous innovation in cell therapy, including gene-edited cell therapy, which may be a promising option for patients with cancer. Rotation Schedule: Week 1: Shift B: Thursday to Saturday from 0700 to 1930 Week 2 Shift B: Wednesday to Saturday from 0700 to 1830 Overview Iovance Biotherapeutics is an immuno-oncology company focused on the development and commercialization of novel cancer immunotherapies based on tumor infiltrating lymphocytes (TIL). The Aseptic Manufacturing Technician I, role is crucial for the autologous cell therapy manufacturing program. This position requires a broad understanding of theories, techniques, and principles to support manufacturing processes. As an Aseptic Manufacturing Technician I, you will primarily be responsible for the following tasks: suite preparation for cell processing, material transfer, environmental monitoring, BSC runner duties, final product inspection, and final product cryopreservation in controlled rate freezers, for commercial and clinical use. This position works across different shifts. Depending on your assigned shift, you may be required to work overtime, weekends, and holidays to ensure the manufacturing process is completed. As this person ### Regulatory Affairs CMC Associate II - Iovance Biotherapeutics Inc - Location: Remote (remote) - Salary: $120K-$140K - Posted: 2026-06-02 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/iovancebiotherapeutics/jobs/5238873008 - Excerpt: Regulatory Affairs CMC Associate II Remote Iovance Biotherapeutics aims to be the global leader in innovating, developing and delivering tumor infiltrating lymphocyte (TIL) therapy for people with cancer. We are pioneering a transformational approach to treating cancer by harnessing the ability of the human immune system to recognize and attack diverse cancer cells in each patient. The Iovance TIL platform has demonstrated promising clinical data across multiple solid tumors. We are committed to continuous innovation in cell therapy, including gene-edited cell therapy, which may be a promising option for patients with cancer. Overview Iovance seeks a highly motivated Regulatory Affairs CMC Associate II. The successful candidate has experience planning and managing regulatory authority submissions. This role will coordinate CMC submissions across multiple products, supporting management of the planning, compilation, QC, and submission of CMC dossier content to clinical and commercial applications, and their amendments. This role will be responsible for the preparation and adaptation of submission documents for use in global clinical and commercial submissions following eCTD specifications and market specific requirements and may be responsible for independently planning and preparing routine clinical trial application related amendments and commercial submissions (e.g. Annual reports, DSUR, health authority queries). An important aspect of this role is the planning and management of submissions. Attention to detail in written correspondence, in the maintenance of regulatory files, and ability to work with diverse internal and external stakeholders are also important factors for success in this role. Another important aspect of this role is the capacity ### Senior Director, Total Rewards and Operations - Iovance Biotherapeutics Inc - Location: San Carlos, California (unspecified) - Salary: $260K-$290K - Posted: 2026-03-23 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/iovancebiotherapeutics/jobs/5157424008 - Excerpt: Senior Director, Total Rewards and Operations San Carlos, California Iovance Biotherapeutics aims to be the global leader in innovating, developing and delivering tumor infiltrating lymphocyte (TIL) therapy for people with cancer. We are pioneering a transformational approach to treating cancer by harnessing the ability of the human immune system to recognize and attack diverse cancer cells in each patient. The Iovance TIL platform has demonstrated promising clinical data across multiple solid tumors. We are committed to continuous innovation in cell therapy, including gene-edited cell therapy, which may be a promising option for patients with cancer. Overview Iovance is seeking a Sr. Director, Total Rewards and Operations for leading the global total rewards and HR operations function. Reporting directly to the Executive Vice President of Human Resources (EVP HR), will be responsible for innovating, developing, directing and administering Iovance's total rewards programs encompassing all compensation and benefits programs Ensures our rewards philosophy is competitive, equitable, compliant, and aligned with the company's business strategy, mission, and values, supporting talent attraction and retention globally. Overseeing HRIS and HR Operations administration, driving all HRIS initiatives and with deep collaboration with HR business partners the focus of this position is to optimize and execute the delivery of total rewards programs and services to the business. Essential Functions and Responsibilities - As subject matter expert propose, design and implement industry best practices and lead effective, competitive, compliant and fair total rewards programs. - Ensure all compensation and benefits programs comply with global regulatory requirements (e.g., FLSA, ### Associate Director, Clinical Business Operations Management - Iovance Biotherapeutics Inc - Location: Remote (remote) - Salary: $175K-$195K - Posted: 2026-05-12 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/iovancebiotherapeutics/jobs/5216600008 - Excerpt: Associate Director, Clinical Business Operations Management Remote Iovance Biotherapeutics aims to be the global leader in innovating, developing and delivering tumor infiltrating lymphocyte (TIL) therapy for people with cancer. We are pioneering a transformational approach to treating cancer by harnessing the ability of the human immune system to recognize and attack diverse cancer cells in each patient. The Iovance TIL platform has demonstrated promising clinical data across multiple solid tumors. We are committed to continuous innovation in cell therapy, including gene-edited cell therapy, which may be a promising option for patients with cancer. Essential Functions and Responsibilities - Supports the identification and prioritization of deliverables across clinical departments (i.e., Medical Writing, Biostatistics, Drug Safety, Clinical Science)., organizes cross-functional teams and tracks progress against goals and timelines - Understands and advises on functional priorities within the context of enabling larger organizational success. - Supports business planning, such as budget review, resource forecasting, goals review, etc. - Supports business data collection and analysis, helps track delivery against corporate and department goals and collaborates with Department Heads on Quarterly Business Reviews - Problem solves by leveraging understanding of business and functional relationships to activate right people and solutions. - Spends time connecting individuals and teams within function, across functions and across the organization. - Serves as a thought partner for vision and goal setting and partner with teams to drive functional short-to-long-term business planning and execution. - Keeps Department meetings on track with focused agendas and objectives. Takes minutes and tracks deliverables as ### Quality Assurance Specialist I, Document Control and Training [Contract to Hire] - Iovance Biotherapeutics Inc - Location: Remote (remote) - Salary: Not disclosed - Posted: 2026-05-20 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/iovancebiotherapeutics/jobs/5225558008 - Excerpt: Quality Assurance Specialist I, Document Control and Training [Contract to Hire] Remote Iovance Biotherapeutics aims to be the global leader in innovating, developing and delivering tumor infiltrating lymphocyte (TIL) therapy for people with cancer. We are pioneering a transformational approach to treating cancer by harnessing the ability of the human immune system to recognize and attack diverse cancer cells in each patient. The Iovance TIL platform has demonstrated promising clinical data across multiple solid tumors. We are committed to continuous innovation in cell therapy, including gene-edited cell therapy, which may be a promising option for patients with cancer. Overview This position is responsible for supporting the Quality Document Control and Training program and ensuring compliance to quality objectives and regulatory requirements. Essential Functions and Responsibilities - Independently manage and monitor the processing, review, approval, archival, and distribution of revision- controlled documents in the Electronic Document Management System (eDMS). - Provide user support and guidance on document workflows, processes, and system usage. - Ensure documents meet formatting, content, and compliance standards prior to approval. - Maintain document records to ensure accuracy, completeness, and traceability within the system. - Coordinate document periodic reviews of controlled documents to ensure ongoing accuracy and compliance. - Support internal and external inspections by retrieving documentation and ensuring inspection readiness. - Independently manage training assignments and task execution within the Electronic Document Management System (eDMS). - Generate and distribute training compliance reports for management and audit purposes. - Support onboarding training activities and assignment of required curriculum. ### Director, Medical Affairs (Medical Science Liaison) - Mid-Atlantic - Iovance Biotherapeutics Inc - Location: Remote (remote) - Salary: $210K-$245K - Posted: 2026-05-06 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/iovancebiotherapeutics/jobs/5209316008 - Excerpt: Director, Medical Affairs (Medical Science Liaison) - Mid-Atlantic Remote Iovance Biotherapeutics aims to be the global leader in innovating, developing and delivering tumor infiltrating lymphocyte (TIL) therapy for people with cancer. We are pioneering a transformational approach to treating cancer by harnessing the ability of the human immune system to recognize and attack diverse cancer cells in each patient. The Iovance TIL platform has demonstrated promising clinical data across multiple solid tumors. We are committed to continuous innovation in cell therapy, including gene-edited cell therapy, which may be a promising option for patients with cancer. Overview The Director, Medical Affairs (Medical Science Liaison) is a field-based medical leader responsible for shaping and executing regional field medical strategy for Iovances developmental and marketed products through high-impact scientific exchange, generation and communication of actionable medical insights, and cross-functional partnership. This role develops and sustains relationships with regional and national external experts (e.g., key opinion leaders, investigators, and healthcare systems) and leads territory planning and prioritization to support medical objectives, including clinical trial site identification and execution, consistent with applicable laws, regulations, and company policies. The Director operates with a high degree of autonomy and accountability, provides strategic thought leadership within the field medical organization, and helps establish consistent standards, processes, and capability building across the team, including coaching and mentoring as assigned. Essential Functions and Responsibilities - Own and advance the regional field medical strategy within the assigned territory, ensuring impactful, fair-balanced, evidence-based scientific exchange and representing Iovance as a credible, trusted ### Associate Director, Engineering & Technical Services Procurement - Iovance Biotherapeutics Inc - Location: Remote (remote) - Salary: $170K-$195K - Posted: 2026-05-26 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/iovancebiotherapeutics/jobs/5228541008 - Excerpt: Associate Director, Engineering & Technical Services Procurement Remote Iovance Biotherapeutics aims to be the global leader in innovating, developing and delivering tumor infiltrating lymphocyte (TIL) therapy for people with cancer. We are pioneering a transformational approach to treating cancer by harnessing the ability of the human immune system to recognize and attack diverse cancer cells in each patient. The Iovance TIL platform has demonstrated promising clinical data across multiple solid tumors. We are committed to continuous innovation in cell therapy, including gene-edited cell therapy, which may be a promising option for patients with cancer. Overview The Associate Director, Engineering & Technical Services Procurement is responsible for the execution of procurement process as it relates to requests within and across Engineering, Manufacturing, Site MRO Services, Technical Development, and other categories as needed. The Associate Director is accountable for business partnering with senior stakeholders to drive an integrated and aligned category strategy that optimum business value and savings impact through sourcing, strategic planning, and external spend management. The Associate Director has deep knowledge of relevant categories and demonstrated experience in driving end to end sourcing process that delivers breakthrough results. This position needs to balance the dynamic needs of the internal business, evolving market conditions, and supplier capabilities to deliver the best overall procurement benefit. The Associate Director needs to support business stakeholders operationalize both their short and long-term objectives by interfacing with appropriate external vendor networks to implement cost effective solutions that simultaneously reduce supply risk. This position collaborates with Legal ### Associate ATC Operations Liaison - Iovance Biotherapeutics Inc - Location: Ohio Valley Region (unspecified) - Salary: $170K-$200K - Posted: 2026-05-31 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/iovancebiotherapeutics/jobs/5235462008 - Excerpt: Associate ATC Operations Liaison Ohio Valley Region The Ideal candidate will live in Ohio, Indiana, WV, KY, Western PA or Western NY. Iovance Biotherapeutics aims to be the global leader in innovating, developing and delivering tumor infiltrating lymphocyte (TIL) therapy for people with cancer. We are pioneering a transformational approach to treating cancer by harnessing the ability of the human immune system to recognize and attack diverse cancer cells in each patient. The Iovance TIL platform has demonstrated promising clinical data across multiple solid tumors. We are committed to continuous innovation in cell therapy, including gene-edited cell therapy, which may be a promising option for patients with cancer. Overview The Associate ATC Operations Liaison will provide operational and clinical information on establishing TIL as the standard of care to physicians and other healthcare providers. The Associate ATC Operations Liaison will lead the authorization activities of commercial centers and provide operational, quality, and clinical oversite post-launch. The Associate ATC Operations Liaison will also identify and develop relationships with Treatment Center's physicians, nursing, lab, pharmacy, and quality personnel. The successful candidate will have experience working in the cellular therapy field at a treatment center by working within operations, quality, the cell lab, or nursing and bringing practical knowledge and skills as they interact with external teams (physicians, surgeons, nurses, administrators, quality personnel) and work collaboratively with cross-functional internal teams. Understanding the environment and influences impacting the treatment centers' providers and personnel. Essential Functions and Responsibilities - Develop and maintain relationships with key ### Cell Therapy Account Management - Georgia/Eastern TN - Iovance Biotherapeutics Inc - Location: Georgia/Tennessee (unspecified) - Salary: $200K-$220K - Posted: 2026-05-27 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/iovancebiotherapeutics/jobs/5231800008 - Excerpt: Cell Therapy Account Management - Georgia/Eastern TN Georgia/Tennessee Iovance Biotherapeutics aims to be the global leader in innovating, developing and delivering tumor infiltrating lymphocyte (TIL) therapy for people with cancer. We are pioneering a transformational approach to treating cancer by harnessing the ability of the human immune system to recognize and attack diverse cancer cells in each patient. The Iovance TIL platform has demonstrated promising clinical data across multiple solid tumors. We are committed to continuous innovation in cell therapy, including gene-edited cell therapy, which may be a promising option for patients with cancer. Overview Amtagvi™ is the best-in-class cell therapy treatment for advanced melanoma. The Cell Therapy Account Management (CTAM) will be responsible for driving Amtagvi demand by building a robust referral network between community practices and academic centers; enable early patient identification and streamline referral pathways; and collaborate with internal teams to enhance scientific and operational excellence in cell therapy account management. To succeed in this role, you will use prior experience to optimize territory strategy in the oncology rare disease space and have demonstrated experience influencing others and building relationships. Additional competencies include experience with immunotherapy and solid tumor cancer, as well as prior launch experience, demonstrated ability to drive demand, pull through, and sustain the growth of Amtagvi™. Essential Functions and Responsibilities: - Drive Amtagvi TM demand and appropriate pull-through at targeted ATCs and serve as a liaison between community oncology practices and internal stakeholders to align initiatives with business and medical objectives. - Serve as ### Executive Director, Forecasting & Portfolio Analytics - Iovance Biotherapeutics Inc - Location: Remote (remote) - Salary: $280K-$330K - Posted: 2026-04-22 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/iovancebiotherapeutics/jobs/5190715008 - Excerpt: Executive Director, Forecasting & Portfolio Analytics Remote Iovance Biotherapeutics aims to be the global leader in innovating, developing and delivering tumor infiltrating lymphocyte (TIL) therapy for people with cancer. We are pioneering a transformational approach to treating cancer by harnessing the ability of the human immune system to recognize and attack diverse cancer cells in each patient. The Iovance TIL platform has demonstrated promising clinical data across multiple solid tumors. We are committed to continuous innovation in cell therapy, including gene-edited cell therapy, which may be a promising option for patients with cancer. Overview The Executive Director, Forecasting and Portfolio Analytics will serve as the enterprise lead for commercial forecasting, portfolio analytics, and decision support at Iovance Biotherapeutics. As a core member of the Business Analytics & Insights Leadership team, this role is accountable for delivering high‑quality near‑term and long‑term global forecasts, scenario analyses, and enterprise insights that inform commercial strategy, investment decisions, and long‑range planning and governance discussions with Executive Leadership and the Board of Directors. This is a highly hands-on leadership role requiring deep technical expertise and direct ownership of forecasting and analytical work. The Executive Director is expected to be accountable for the design, build and stewardship of core forecasting models and decision-support analyses, ensuring rigorous assumptions, transparency, and confidence in outputs. External partners may be leveraged selectively for supplemental support, but this role retains clear internal ownership and execution responsibility for all critical forecasting and analytics deliverables. This position supports the ongoing commercialization of AMTAGVI® and ### Director US Health Economic Value Access & Strategy (HEVAS) - Iovance Biotherapeutics Inc - Location: Remote (remote) - Salary: $240K-$265K - Posted: 2026-04-23 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/iovancebiotherapeutics/jobs/5199035008 - Excerpt: Director US Health Economic Value Access & Strategy (HEVAS) Remote Iovance Biotherapeutics aims to be the global leader in innovating, developing and delivering tumor infiltrating lymphocyte (TIL) therapy for people with cancer. We are pioneering a transformational approach to treating cancer by harnessing the ability of the human immune system to recognize and attack diverse cancer cells in each patient. The Iovance TIL platform has demonstrated promising clinical data across multiple solid tumors. We are committed to continuous innovation in cell therapy, including gene-edited cell therapy, which may be a promising option for patients with cancer. Overview In the US Cell & Gene (CGT) Marketplace, the payer is not only our Commercial and Government Health Plans, but also the Formulary Decision Makers within our Authorized Treatment Centers (ATCs) who are evaluating the financial viability of our therapies against all other Cell & Gene therapies (CGTs). Iovance is seeking Health Economic Value Access and Strategy (HEVAS) Director as a part of the US Market Access function to develop and translate economic evidence into value-based messaging and will be responsible for developing payer resources, billing & coding guides and patient support in alignment with our value proposition. This individual will understand Payer, hospital and provider clinic evaluation and financial feasibility to support the US Payer field team with pre-approval market readiness (FDAMA 114), cost of care / site of care and cost-effectiveness for our key formulary decision makers. This Market Access leader will partner cross-functionally to identify pricing strategies for our approved ### Cell Therapy Account Management - Missouri/Arkansas - Iovance Biotherapeutics Inc - Location: Kansas / Nebraska / Iowa / Arkansas / Missouri / Arkansas (unspecified) - Salary: $200K-$220K - Posted: 2026-05-04 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/iovancebiotherapeutics/jobs/5209136008 - Excerpt: Cell Therapy Account Management - Missouri/Arkansas Kansas / Nebraska / Iowa / Arkansas / Missouri / Arkansas Iovance Biotherapeutics aims to be the global leader in innovating, developing and delivering tumor infiltrating lymphocyte (TIL) therapy for people with cancer. We are pioneering a transformational approach to treating cancer by harnessing the ability of the human immune system to recognize and attack diverse cancer cells in each patient. The Iovance TIL platform has demonstrated promising clinical data across multiple solid tumors. We are committed to continuous innovation in cell therapy, including gene-edited cell therapy, which may be a promising option for patients with cancer. Overview Amtagvi™ is the best-in-class cell therapy treatment for advanced melanoma. The Cell Therapy Account Management (CTAM) will be responsible for driving Amtagvi demand by building a robust referral network between community practices and academic centers; enable early patient identification and streamline referral pathways; and collaborate with internal teams to enhance scientific and operational excellence in cell therapy account management. To succeed in this role, you will use prior experience to optimize territory strategy in the oncology rare disease space and have demonstrated experience influencing others and building relationships. Additional competencies include experience with immunotherapy and solid tumor cancer, as well as prior launch experience, demonstrated ability to drive demand, pull through, and sustain the growth of Amtagvi™. Essential Functions and Responsibilities: - Drive Amtagvi TM demand and appropriate pull-through at targeted ATCs and serve as a liaison between community oncology practices and internal stakeholders to align ### Cell Therapy Account Management - North Central - Iovance Biotherapeutics Inc - Location: North Central (unspecified) - Salary: $200K-$220K - Posted: 2026-05-27 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/iovancebiotherapeutics/jobs/5231789008 - Excerpt: Cell Therapy Account Management - North Central North Central Iovance Biotherapeutics aims to be the global leader in innovating, developing and delivering tumor infiltrating lymphocyte (TIL) therapy for people with cancer. We are pioneering a transformational approach to treating cancer by harnessing the ability of the human immune system to recognize and attack diverse cancer cells in each patient. The Iovance TIL platform has demonstrated promising clinical data across multiple solid tumors. We are committed to continuous innovation in cell therapy, including gene-edited cell therapy, which may be a promising option for patients with cancer. Overview Amtagvi™ is the best-in-class cell therapy treatment for advanced melanoma. The Cell Therapy Account Management (CTAM) will be responsible for driving Amtagvi demand by building a robust referral network between community practices and academic centers; enable early patient identification and streamline referral pathways; and collaborate with internal teams to enhance scientific and operational excellence in cell therapy account management. To succeed in this role, you will use prior experience to optimize territory strategy in the oncology rare disease space and have demonstrated experience influencing others and building relationships. Additional competencies include experience with immunotherapy and solid tumor cancer, as well as prior launch experience, demonstrated ability to drive demand, pull through, and sustain the growth of Amtagvi™. Essential Functions and Responsibilities: - Drive Amtagvi TM demand and appropriate pull-through at targeted ATCs and serve as a liaison between community oncology practices and internal stakeholders to align initiatives with business and medical objectives. - Serve ### Aseptic Manufacturing Technician I - Day Shift A [Contract to Hire] - Iovance Biotherapeutics Inc - Location: Philadelphia, PA (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/iovancebiotherapeutics/jobs/5254151008 - Excerpt: Aseptic Manufacturing Technician I - Day Shift A [Contract to Hire] Philadelphia, PA Rotation Schedule: Week 1: Shift A: Sunday to Wednesday from 0700 to 1830 Week 2 Shift A: Sunday to Tuesday from 0700 to 1930 Overview Iovance Biotherapeutics is an immuno-oncology company focused on the development and commercialization of novel cancer immunotherapies based on tumor infiltrating lymphocytes (TIL). The Aseptic Manufacturing Technician I, role is crucial for the autologous cell therapy manufacturing program. This position requires a broad understanding of theories, techniques, and principles to support manufacturing processes. As an Aseptic Manufacturing Technician I, you will primarily be responsible for the following tasks: suite preparation for cell processing, material transfer, environmental monitoring, BSC runner duties, final product inspection, and final product cryopreservation in controlled rate freezers, for commercial and clinical use. This position works across different shifts. Depending on your assigned shift, you may be required to work overtime, weekends, and holidays to ensure the manufacturing process is completed. As this person will be a key member of the autologous cell therapy manufacturing program, a background in cell culture, aseptic gowning and qualifications, as well as ISO class 5 (Grade A) cleanroom operations is strongly desired. Aseptic Manufacturing Technicians are required to work their assigned schedule. The first few months of onboarding training for this position will occur during regular work week hours (1 st shift M-F); however, once the technician is trained, they will be assigned to a shift that include weekends, evenings, and holidays, as needed ### Aseptic Manufacturing Technician I - Day Shift B [Contract to Hire] - Iovance Biotherapeutics Inc - Location: Philadelphia, PA (unspecified) - Salary: Not disclosed - Posted: 2026-05-27 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/iovancebiotherapeutics/jobs/5231780008 - Excerpt: Aseptic Manufacturing Technician I - Day Shift B [Contract to Hire] Philadelphia, PA Rotation Schedule: Week 1: Shift B: Thursday to Saturday from 0700 to 1930 Week 2: Shift B: Wednesday to Saturday from 0700 to 1830 Overview Iovance Biotherapeutics is an immuno-oncology company focused on the development and commercialization of novel cancer immunotherapies based on tumor infiltrating lymphocytes (TIL). The Aseptic Manufacturing Technician I, role is crucial for the autologous cell therapy manufacturing program. This position requires a broad understanding of theories, techniques, and principles to support manufacturing processes. As an Aseptic Manufacturing Technician I, you will primarily be responsible for the following tasks: suite preparation for cell processing, material transfer, environmental monitoring, BSC runner duties, final product inspection, and final product cryopreservation in controlled rate freezers, for commercial and clinical use. This position works across different shifts. Depending on your assigned shift, you may be required to work overtime, weekends, and holidays to ensure the manufacturing process is completed. As this person will be a key member of the autologous cell therapy manufacturing program, a background in cell culture, aseptic gowning and qualifications, as well as ISO class 5 (Grade A) cleanroom operations is strongly desired. Aseptic Manufacturing Technicians are required to work their assigned schedule. The first few months of onboarding training for this position will occur during regular work week hours (1 st shift M-F); however, once the technician is trained, they will be assigned to a shift that include weekends, evenings, and holidays, as needed ### Aseptic Manufacturing Technician I - Night Shift A [Contract to Hire] - Iovance Biotherapeutics Inc - Location: Philadelphia, PA (unspecified) - Salary: Not disclosed - Posted: 2026-06-02 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/iovancebiotherapeutics/jobs/5238833008 - Excerpt: Aseptic Manufacturing Technician I - Night Shift A [Contract to Hire] Philadelphia, PA Rotation Schedule: Week 1: Shift A: Sunday to Tuesday from 5:00pm to 5:30am Week 2 Shift A: Sunday to Wednesday from 5:00pm to 4:30am Overview: Iovance Biotherapeutics is an immuno-oncology company focused on the development and commercialization of novel cancer immunotherapies based on tumor infiltrating lymphocytes (TIL). TLead Aseptic Manufacturing Technician - Night Shift A Sun - Wed-5pm - 5:30am role is crucial for the autologous cell therapy manufacturing program. This position requires a broad understanding of theories, techniques, and principles to support manufacturing processes. As an Aseptic Manufacturing Technician I, you will primarily be responsible for the following tasks: suite preparation for cell processing, material transfer, environmental monitoring, BSC runner duties, final product inspection, and final product cryopreservation in controlled rate freezers, for commercial and clinical use. This position works across different shifts. Depending on your assigned shift, you may be required to work overtime, weekends, and holidays to ensure the manufacturing process is completed. As this person will be a key member of the autologous cell therapy manufacturing program, a background in cell culture, aseptic gowning and qualifications, as well as ISO class 5 (Grade A) cleanroom operations is strongly desired. Aseptic Manufacturing Technicians are required to work their assigned schedule. The first few months of onboarding training for this position will occur during regular work week hours (1st shift M-F); however, once the technician is trained, they will be assigned to a shift that ### Aseptic Manufacturing Technician I - Day Shift B [Contract to Hire] - Iovance Biotherapeutics Inc - Location: Philadelphia, PA (unspecified) - Salary: Not disclosed - Posted: 2026-04-22 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/iovancebiotherapeutics/jobs/5190683008 - Excerpt: Aseptic Manufacturing Technician I - Day Shift B [Contract to Hire] Philadelphia, PA Rotation Schedule: Week 1: Shift B: Thursday to Saturday from 0700 to 1930 Week 2 Shift B: Wednesday to Saturday from 0700 to 1830 Overview Iovance Biotherapeutics is an immuno-oncology company focused on the development and commercialization of novel cancer immunotherapies based on tumor infiltrating lymphocytes (TIL). The Aseptic Manufacturing Technician I, role is crucial for the autologous cell therapy manufacturing program. This position requires a broad understanding of theories, techniques, and principles to support manufacturing processes. As an Aseptic Manufacturing Technician I, you will primarily be responsible for the following tasks: suite preparation for cell processing, material transfer, environmental monitoring, BSC runner duties, final product inspection, and final product cryopreservation in controlled rate freezers, for commercial and clinical use. This position works across different shifts. Depending on your assigned shift, you may be required to work overtime, weekends, and holidays to ensure the manufacturing process is completed. As this person will be a key member of the autologous cell therapy manufacturing program, a background in cell culture, aseptic gowning and qualifications, as well as ISO class 5 (Grade A) cleanroom operations is strongly desired. Aseptic Manufacturing Technicians are required to work their assigned schedule. The first few months of onboarding training for this position will occur during regular work week hours (1 st shift M-F); however, once the technician is trained, they will be assigned to a shift that include weekends, evenings, and holidays, as needed ### Sr Scientist Biotherapeutics RD - Johnson & Johnson - Location: Schaffhausen, Switzerland (unspecified) - Salary: Not disclosed - Posted: 2026-05-28 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jj.wd5.myworkdayjobs.com/JJ/job/Schaffhausen-Switzerland/Sr-Scientist-Biotherapeutics-RD_R-077468 - Excerpt: Sr Scientist Biotherapeutics RD Schaffhausen, Switzerland posted: Posted 15 Days Ago ### Sr Scientist Biotherapeutics RD - Johnson & Johnson - Location: Schaffhausen, Switzerland (unspecified) - Salary: Not disclosed - Posted: 2026-06-01 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jj.wd5.myworkdayjobs.com/JJ/job/Schaffhausen-Switzerland/Sr-Scientist-Biotherapeutics-RD_R-079698-1 - Excerpt: Sr Scientist Biotherapeutics RD Schaffhausen, Switzerland posted: Posted 11 Days Ago ### Informatics and AI engineer, Biotherapeutics - Pfizer - Location: United States - Massachusetts - Cambridge (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://pfizer.wd1.myworkdayjobs.com/PfizerCareers/job/United-States---Massachusetts---Cambridge/Informatics-and-AI-engineer--Biotherapeutics_4958820-1 - Excerpt: Informatics and AI engineer, Biotherapeutics United States - Massachusetts - Cambridge posted: Posted 2 Days Ago ### Senior Scientist, Computational Biotherapeutics Engineering - Pfizer - Location: United States - Massachusetts - Cambridge (unspecified) - Salary: Not disclosed - Posted: 2026-05-28 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://pfizer.wd1.myworkdayjobs.com/PfizerCareers/job/United-States---Massachusetts---Cambridge/Senior-Scientist--Computational-Biotherapeutics-Engineering_4956715-2 - Excerpt: Senior Scientist, Computational Biotherapeutics Engineering United States - Massachusetts - Cambridge posted: Posted 15 Days Ago ### Principal Research Scientist I, Biologics Screening - Discovery Biotherapeutics - AbbVie Inc. - Location: San Francisco, CA, United States (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990012912319-principal-research-scientist-i-biologics-screening-discovery-biotherapeutics - Excerpt: Principal Research Scientist I, Biologics Screening - Discovery Biotherapeutics San Francisco, CA, United States Company Description: AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on X , Facebook , Instagram , YouTube , LinkedIn and Tik Tok . Job Description: Discovery Biotherapeutics and Genetic Medicine (BGM) at AbbVie is seeking a highly motivated Principal Scientist to join the Biotherapeutics group at the AbbVie Bay Area (ABA) site based in South San Francisco, CA. This role seeks a skilled and experienced individual to contribute to and lead therapeutic programs, focusing on biophysical screening to advance biotherapeutics from early exploration through lead identification and optimization. Close partnerships with Oncology will be required to drive transformative ideas to the clinic. The ideal candidate must possess expertise in high-throughput biologics screening and characterization methods (e.g. ELISA, FACS, BLI, SPR, etc.) and have a solid foundation in protein sciences and antibody discovery with a proven ability to work effectively on cross-functional teams. Responsibilities Lead from the lab to advance large molecule biologics projects from exploratory to optimization stages and drive Go / No Go decisions. Effectively partner with functional and therapeutic areas to achieve ### Postdoctoral Fellow - Analytical Development & Quality Control, Bouvarel & Camperi Labs - Genentech, Inc. - Location: South San Francisco, California, United States of America (unspecified) - Salary: Not disclosed - Posted: 2026-06-02 - Apply: https://roche.wd3.myworkdayjobs.com/ROG-A2O-GENE/job/South-San-Francisco/Postdoctoral-Fellow---Analytical-Development---Quality-Control--Bouvarel---Camperi-Labs_202606-113861/apply - Excerpt: Postdoctoral Fellow - Analytical Development & Quality Control, Bouvarel & Camperi Labs South San Francisco, California, United States of America Exciting opportunity for a Postdoctoral Fellow to lead next-generation analytical development in advanced liquid chromatography and mass spectrometry. Join our innovative team to drive biotherapeutic research, collaborate internationally, and shape control strategies for complex, high-impact biotherapeutics. Grow your career with cutting-edge science and impactful projects at Genentech. ### Sr. Princ. Process Engineer – DP Aseptic Biotherapeutic Filling Equipment - Johnson & Johnson - Location: Wilson, North Carolina, United States of America (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jj.wd5.myworkdayjobs.com/JJ/job/Wilson-North-Carolina-United-States-of-America/Sr-Princ-Process-Engineer---DP-Aseptic-Biotherapeutic-Filling-Equipment_R-064219-1 - Excerpt: Sr. Princ. Process Engineer – DP Aseptic Biotherapeutic Filling Equipment Wilson, North Carolina, United States of America posted: Posted 30+ Days Ago ### Senior Scientist I - Bioinformatics, Biotherapeutics and Genetic Medicine - AbbVie Inc. - Location: Worcester, MA, United States (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990012920057-senior-scientist-i-bioinformatics-biotherapeutics-and-genetic-medicine - Excerpt: Senior Scientist I - Bioinformatics, Biotherapeutics and Genetic Medicine Worcester, MA, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: Biotherapeutics and Genetic Medicine (BGM), a part of Discovery Research within AbbVie's R&D, is a global organization dedicated to the discovery and optimization of innovative drug candidate molecules for biotherapeutic modalities (monoclonal antibodies, multispecifics, proteins, conjugates, etc.) and genetic medicines (AAV, LNPs, siRNA, etc.) across all therapeutic areas. We are seeking a highly driven and innovative scientist with expertise in bioinformatics to design, develop, and optimize data capture workflows and dynamic visualization dashboards for biologics discovery. Responsibilities: Independently design digital workflows or tools to streamline biologics discovery and evaluate improvements in operational efficiency Identify, champion and test software solutions and that map to the needs of BGM Proactively identify scientist needs that further our digital transformation strategy and propose solutions to meet them Pilot new software and AI tools to evaluate utility for BGM and train others on how to use them Design and implement standard analyses and visualizations that balance customization and increased efficiency ### Senior Scientist I, siRNA Pipeline Development & SAR Optimization - AbbVie Inc. - Location: Cambridge, MA, United States (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013524454-senior-scientist-i-sirna-pipeline-development-sar-optimization - Excerpt: Senior Scientist I, siRNA Pipeline Development & SAR Optimization Cambridge, MA, United States Company Description: AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on X , Facebook , Instagram , YouTube , LinkedIn and Tik Tok . Job Description: At AbbVie, we are dedicated to solving some of the world's most complex and serious diseases. Our mission is to develop and deliver advanced therapeutics that change lives. We are looking for talented, passionate, and driven individuals to join our Biotherapeutics and Genetic Medicine (BGM) team. As a Senior Scientist in our siRNA group, you will be part of an innovative team focused on advancing RNA-based therapies that have the potential to revolutionize patient care. AbbVie is looking for a Senior Scientist I to join our siRNA group within the Biotherapeutics and Genetic Medicine (BGM) department. This role will involve designing and executing innovative experimental approaches to address key scientific challenges related to oligonucleotide therapeutics. The successful candidate will drive scientific innovation, identify new methods and techniques, and collaborate across functions to support the development of novel RNA-based therapies. Responsibilities Lead research efforts within a cross-functional team to advance new ### Senior Scientist I, siRNA Pipeline Development & Targeted Delivery - AbbVie Inc. - Location: Cambridge, MA, United States (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013513327-senior-scientist-i-sirna-pipeline-development-targeted-delivery - Excerpt: Senior Scientist I, siRNA Pipeline Development & Targeted Delivery Cambridge, MA, United States Company Description: AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on X , Facebook , Instagram , YouTube , LinkedIn and Tik Tok . Job Description: At AbbVie, we are dedicated to solving some of the world's most complex and serious diseases. Our mission is to develop and deliver advanced therapeutics that change lives. We are looking for talented, passionate, and driven individuals to join our Biotherapeutics and Genetic Medicine (BGM) team. As a Senior Scientist in our siRNA group, you will be part of an innovative team focused on advancing RNA-based therapies that have the potential to revolutionize patient care. AbbVie is looking for a Senior Scientist I to join our siRNA group within the Biotherapeutics and Genetic Medicine (BGM) department. This role will involve designing and executing innovative experimental approaches to address key scientific challenges related to oligonucleotide therapeutics. The successful candidate will drive scientific innovation, identify new methods and techniques, and collaborate across functions to support the development of novel RNA-based therapies. Responsibilities Lead research efforts within a cross-functional team to advance new ### Senior Scientist I, siRNA in vitro Biology - AbbVie Inc. - Location: Cambridge, MA, United States (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990012913220-senior-scientist-i-sirna-in-vitro-biology - Excerpt: Senior Scientist I, siRNA in vitro Biology Cambridge, MA, United States Company Description: AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on X , Facebook , Instagram , YouTube , LinkedIn and Tik Tok . Job Description: At AbbVie, we are dedicated to solving some of the world's most complex and serious diseases. Within AbbVie's Biotherapeutics and Genetic Medicine (BGM) organization, our siRNA team is advancing therapeutic programs from early discovery through development, applying rigorous biology and data-driven decision making to build differentiated RNA medicines. AbbVie is seeking a Senior Scientist I with deep, hands-on expertise in siRNA therapeutic discovery to join the siRNA group within Biotherapeutics and Genetic Medicine (BGM). This role will involve designing and executing innovative experimental approaches to address key scientific challenges related to oligonucleotide therapeutics. The successful candidate will drive scientific innovation, identify new methods and techniques, and collaborate across functions to support the development of novel RNA-based therapies. This role is best suited for candidates with direct, hands-on experience in therapeutic siRNA discovery, where siRNA biology directly informed experimental and program-level decisions. Responsibilities Independently lead in vitro siRNA discovery biology, including experimental strategy, ### Sr. Scientist I- (Biologics Bioanalysis, Characterization and Proteomics Group) - AbbVie Inc. - Location: South San Francisco, CA, United States (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013523525-sr-scientist-i-biologics-bioanalysis-characterization-and-proteomics-group- - Excerpt: Sr. Scientist I- (Biologics Bioanalysis, Characterization and Proteomics Group) South San Francisco, CA, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: The Quantitative, Translational ADME Sciences (QTAS) department at AbbVie is seeking a highly motivated scientist to join the Biologics bioanalysis, characterization, and proteomics group. The main function of this position is to develop and implement LC/MS (liquid chromatography/mass spectrometry)-based bioanalysis and in vitro characterization assays of novel biologics entities. The successful candidate will be experienced in the optimization and implementation of novel and routine LC/MS-based bioanalytical methods to drive in vivo PK, TK, and PK/PD analysis as well as in vitro stability characterization of biotherapeutics. The candidate will be responsible for sample preparation, method development, bioanalytical assay operations, data analysis, report generation, and data presentation. Key tasks and responsibilities: Operate and maintain LC/MS instruments to generate high-quality experimental data. Perform affinity purification of biotherapeutic (including but not limited to monoclonal and multispecific antibody, antibody drug conjugates, antibody-siRNA conjugates, and tLNPs). Analyze data and maintain detailed, accurate and comprehensive study documentation in electronic laboratory ### Associate Scientist - Biotherapeutics - Eurofins Scientific - Location: Saint Charles, MO, United States (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Apply: https://jobs.smartrecruiters.com/Eurofins/744000130885989-associate-scientist-biotherapeutics- - Excerpt: Associate Scientist - Biotherapeutics Saint Charles, MO, United States Company Description: Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies. In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to over 50,000 staff across a network of more than 900 independent companies in over 50 countries and operating more than 800 laboratories. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialized clinical diagnostics testing. In 2021, Eurofins generated total revenues of EUR € 6.7 billion, and has been among the best performing stocks in Europe over the past 20 years. Job Description: The Associate ### Analytical Characterization Scientist - Eurofins Scientific - Location: Andover, MA, United States (unspecified) - Salary: $27-$30/hr - Posted: 2026-06-12 - Apply: https://jobs.smartrecruiters.com/Eurofins/744000131729764-analytical-characterization-scientist - Excerpt: Analytical Characterization Scientist Andover, MA, United States Company Description: The work we do at Eurofins Professional Scientific Services matters-and so do our employees. At Eurofins PSS, we prioritize your professional growth by providing opportunities to break into the biopharmaceutical industry and develop your career from the ground up. Our teams offer a supportive environment, strong mentorship, work-life balance, and a competitive benefits package. Eurofins Scientific is a global life sciences leader providing a broad range of analytical testing services across industries including pharmaceuticals, food, environmental, and clinical research. We partner with leading organizations worldwide to ensure product safety, quality, and authenticity-helping create a safer, healthier, and more sustainable world. Job Description: The Analytical Characterization Scientist plays a key role in supporting the development of biotherapeutic products through advanced analytical testing and molecular characterization. This is a hands-on, laboratory-based position focused on applying analytical chemistry techniques to evaluate biologics across the development lifecycle. This role is responsible for generating high-quality analytical data to assess molecular integrity, purity, and stability using a range of chromatographic, electrophoretic, and biophysical methods. The scientist will collaborate closely with cross-functional teams to support formulation development and candidate progression from early-stage research through commercialization. Key Responsibilities Perform analytical characterization of biotherapeutic molecules using a variety of techniques, including: HPLC-based methods (SE-HPLC, IEX, HIC, RP-HPLC) Capillary electrophoresis (CGE, iCE) Spectroscopic and biophysical characterization techniques Particulate analysis (light obscuration, microflow imaging) Generate, analyze, and interpret complex datasets to assess product quality attributes such as purity, heterogeneity, and stability Support ### Senior Scientist II, Brain Transport Biology - AbbVie Inc. - Location: Cambridge, MA, United States (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013003956-senior-scientist-ii-brain-transport-biology - Excerpt: Senior Scientist II, Brain Transport Biology Cambridge, MA, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: At AbbVie, we are dedicated to solving some of the world's most complex and serious diseases. Our mission is to develop and deliver advanced therapeutics that change lives. The Discovery Neuroscience In Vivo Pharmacology group in Cambridge, Massachusetts, is seeking a highly skilled and self-motivated Senior Scientist to join a dynamic team supporting target identification, validation, and drug transport facilitation over brain barriers. The successful candidate will drive scientific innovation, has experience making tangible contributions to the discovery pipeline, and has people and project management experience. Responsibilities: Responsible for design and implementation of in vivo testing of multispecific biologics, small molecules, and siRNAs to support projects in the areas of Alzheimer's and Parkinson's disease Serve as an in vivo representative in cross-functional teams with Discovery Biotherapeutics, DMPK, and Development Sciences colleagues, providing project updates, analysis, and strategic advice Proactively translate department/project team scientific questions into well-designed experiments, utilizing internal and external resources Identify and solve technical problems independently, ### Senior Scientist I, Analytical Development - Mass Spectrometry tLNP CMC - AbbVie Inc. - Location: North Chicago, IL, United States (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013517326-senior-scientist-i-analytical-development-mass-spectrometry-tlnp-cmc- - Excerpt: Senior Scientist I, Analytical Development - Mass Spectrometry tLNP CMC North Chicago, IL, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: The Analytical Development group within the Targeted LNP (tLNP) CMC Development Team at AbbVie is dedicated to advancing state-of-the-art analytical capabilities for tLNP therapeutics development. Our team provides critical support to tLNP drug substance, drug product, and formulation development. We leverage advanced biophysical, separation, and mass spectrometry techniques to deeply characterize antibodies, mRNA, lipids, and intact LNP particles. We are building a strong team of scientists who will be instrumental in developing and deploying the analytical toolbox needed to deliver high-quality, innovative tLNP medicines to patients. Position Overview: As the mass spectrometry SME within the Analytical Development group of tLNP CMC Development team, you will work in an innovative analytical research and development lab and develop LC-MS method for characterizing biotherapeutic products to support tLNP development, with an emphasis on mRNA and oligonucleotide analysis. The successful candidate will have hands-on analytical method development experience of LC-MS analysis. Additionally, the candidate must foster productive ### Senior Scientist I - Cell Culture Process Development - AbbVie Inc. - Location: Worcester, MA, United States (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013535586-senior-scientist-i-cell-culture-process-development - Excerpt: Senior Scientist I - Cell Culture Process Development Worcester, MA, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: We are seeking an enthusiastic and creative hands-on senior scientist to join the Cell Culture Process Development group within PDS&T Biologics at AbbVie Bioresearch Center in Worcester, MA. As part of the Cell Culture Development organization, you will support process development and technology transfer activities for cell culture processes, contributing to the clinical manufacturing and commercialization of therapeutic proteins in the AbbVie pipeline. Additionally, you will be a part of a team that provides subject matter expertise and experimental support for the production of commercial biologics. The ideal candidate will work effectively both independently and collaboratively within a dynamic team environment. Key Responsibilities: Develop and characterize highly-productive CHO cell culture processes suitable for cGMP biotherapeutic manufacturing within project timelines, performing technical transfer, and manufacturing support activities. Lead and execute scientific research and development initiatives to reduce cost of goods (COGs) by significantly improving platform processes and workflows, deepening scientific understanding, and applying new methods and technologies. ### Principal Research Scientist I, siRNA Synthesis & Analytical Development - AbbVie Inc. - Location: Worcester, MA, United States (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013503219-principal-research-scientist-i-sirna-synthesis-analytical-development - Excerpt: Principal Research Scientist I, siRNA Synthesis & Analytical Development Worcester, MA, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: The Biotherapeutics and Genetic Medicine (BGM) department at AbbVie is seeking a motivated Principal Research Scientist to join the growing siRNA team. In this role, you will work with the genetic medicine teams to establish siRNA synthesis, purification, and analytical capabilities. You will serve as a subject matter expert in oligonucleotide chemistry and siRNA production, with responsibility for generating high-quality siRNA materials to advance genetic medicine studies. Responsibilities: Lead the siRNA synthesis platform to support various stages of siRNA studies. Oversee solid-phase oligonucleotide synthesis, deprotection, purification, desalting, and analytical characterization of siRNA. Troubleshoot synthesis, purification, and analytical challenges to improve yield, purity, and scalability. Partner with cross-functional teams, including the siRNA screening team, the antibody conjugation group, and CMC, to support platform and project objectives. Ensure rigorous documentation, data integrity, and compliance with internal quality standards. Track and evaluate emerging technologies and best practices in oligonucleotide and RNA-based therapeutics. Manage and develop a team of ### Scientist I, Biologics Drug Substance Development, Cell Culture Development - AbbVie Inc. - Location: San Francisco, CA, United States (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013479536-scientist-i-biologics-drug-substance-development-cell-culture-development - Excerpt: Scientist I, Biologics Drug Substance Development, Cell Culture Development San Francisco, CA, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: The Cell Culture Development Group in South San Francisco, CA is seeking a Scientist I to join a talented and collaborative team to develop cell culture processes for GMP applications. In this position, you will perform cell culture process development, scale-up, and technology transfer activities in a well-supported and dynamic environment to help advance novel biotherapeutics into human clinical studies. KEY RESPONSIBILITIES: Perform inoculum expansion and cell bank generation Execute cell culture experiments using Ambr250 and 2L bioreactors Perform pilot scale material generation using 50L, 200L and 500L single use bioreactors Execute small scale and pilot scale depth filtration and centrifugation primary recovery processes Perform tech transfer of Master cell bank generation, cell culture and primary recovery processes to the GMP manufacturing facilities Provide person-in-plant support at the GMP manufacturing facility Perform cell culture experiments to optimize N-1 perfusion processes as well as intensified fed-batch processes Represent the cell culture development group for pipeline ### Principal Research Scientist I, siRNA Platform Automation - AbbVie Inc. - Location: Worcester, MA, United States (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013502644-principal-research-scientist-i-sirna-platform-automation - Excerpt: Principal Research Scientist I, siRNA Platform Automation Worcester, MA, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: AbbVie's Biotherapeutics and Genetic Medicine (BGM) department is seeking a highly motivated Principal Research Scientist to join our expanding siRNA team. In this role, you will partner with genetic medicine teams to establish a high-throughput siRNA screening platform that advances pipeline innovation through next-generation delivery modalities and supports the discovery of therapeutic leads across multiple disease areas. Responsibilities: Establish and implement a high-throughput siRNA screening platform using automated liquid-handling systems. Serve as a subject matter expert in siRNA screening experimental design, execution, and data interpretation. Lead research efforts and mentor scientists to advance siRNA optimization, including sequence design and novel chemical modifications, across multiple programs. Generate new scientific hypotheses and proposals, improve existing screening workflows, and evaluate emerging technologies in the siRNA field. Communicate clearly and effectively with internal siRNA teams and cross-functional collaborators to identify needs and support platform enhancement and program advancement. Manage and develop a team of at least 2-3 scientists, providing technical guidance, ### Sr Scientist - Waters Corporation - Location: Milford, MA, US (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - Apply: https://uscareers-waters.icims.com/jobs/26757/sr-scientist/job - Excerpt: Sr Scientist Milford, MA, US Overview Waters Corporation is seeking a Materials Scientist to help advance biotherapeutics through the research and development of new chemical tools that facilitate the characterization and quantitation of biological molecules. This is an exciting opportunity to join our Bioseparations Portfolio in the Chemistry & Lab Automation Business Unit and develop new chromatographic stationary phase materials. In this Senior Scientist position, you will work with a diverse team of scientists and engineers across the organization, apply yourself as a highly influential individual contributor, and have a major impact on the world's newest therapeutics. Responsibilities Research and develop new inorganic, polymeric, and hybrid materials for diverse chromatographic applications. Functionalize silica and polymer-based materials for the characterization and quantitation of biological molecules. Conduct site-specific modification of constructs to allow orientation directed conjugation. Collaborate with engineers, analytical scientists, and manufacturing teams to ensure product performance requirements and meet development timelines. Monitor scientific advancements and industry trends; identify and pursue intellectual property opportunities. Maintain laboratory equipment and rigorous documentation practices. Comply with environment, safety, health, and quality standards. Qualifications PhD in Chemistry, Biochemistry or related discipline with 1 or more years of relevant experience; or Mast ### Principal Scientist, Biologics Cell Line Development - Asimov - Location: Boston, MA (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Apply: https://jobs.ashbyhq.com/asimov/f27c8759-5ebf-4605-a30c-dd6da318ad97 - Excerpt: Principal Scientist, Biologics Cell Line Development Boston, MA Our mission at Asimov is to advance humanity's ability to design living systems, enabling biotechnologies with outsized benefit to society. We're developing a mammalian synthetic biology platform--from cells to software--to enable the design and manufacture of next-generation therapeutics. We are seeking a Principal Scientist to join our Biologics Cell Line Development team in Boston, MA and help push the boundaries of biotherapeutic cell line development. This role is for a scientific innovator and a manager of junior scientists. The successful candidate will conduct & supervise CHO-based cell line development for biologic therapeutics moving into clinical development. Significant effort designing complex experimental approaches to improve expression systems and workflows through innovation and implementation of new technology is also an important part of this role. The successful candidate will also work cross-functionally with Asimov's synthetic biology, modeling, process development and analytical teams. This is a unique opportunity to work at a nimble, forward-thinking synthetic biology startup and help build the future of biological engineering. About the Role: - You'll perform CHO cell line development processes including transfection, cloning, characterization, and cell banking using state-of-the-art equipment. - You'll drive innovation through the development of improved genetic components, host cell line engineering and cell line development process optimization. - You'll identify emerging practices for biologics cell line development and manufacturing to shape scientific strategies and continued innovation. - You'll represent the cell line development team on cross-functional projects, making decisions for cell line activities and effectively ### Senior Scientist, Biologics Cell Line Development - Asimov - Location: Boston, MA (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Apply: https://jobs.ashbyhq.com/asimov/63faa6b3-f84f-4181-bc2e-8e0c0f885cc8 - Excerpt: Senior Scientist, Biologics Cell Line Development Boston, MA Our mission at Asimov is to advance humanity's ability to design living systems, enabling biotechnologies with outsized benefit to society. We're developing a mammalian synthetic biology platform--from cells to software--to enable the design and manufacture of next-generation therapeutics. We are seeking a Senior Scientist to join our Biologics Cell Line Development team in Boston, MA and help push the boundaries of biotherapeutic cell line development. This role is for a scientific innovator and a manager of junior scientists. The successful candidate will conduct & supervise CHO-based cell line development for biologic therapeutics moving into clinical development. Significant effort designing complex experimental approaches to improve expression systems and workflows through innovation and implementation of new technology is also an important part of this role. The successful candidate will also work cross-functionally with Asimov's synthetic biology, modeling, process development and analytical teams. This is a unique opportunity to work at a nimble, forward-thinking synthetic biology startup and help build the future of biological engineering. About the Role: - You'll perform CHO cell line development processes including transfection, cloning, characterization, and cell banking using state-of-the-art equipment. - You'll drive innovation through the development of improved genetic components, host cell line engineering and cell line development process optimization. - You'll identify emerging practices for biologics cell line development and manufacturing to shape scientific strategies and continued innovation. - You'll represent the cell line development team on cross-functional projects, making decisions for cell line activities and effectively ### Associate Scientist - Analytical Assay - Eurofins Scientific - Location: St. Louis, MO, United States (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Apply: https://jobs.smartrecruiters.com/Eurofins/744000127266254-associate-scientist-analytical-assay - Excerpt: Associate Scientist - Analytical Assay St. Louis, MO, United States Company Description: Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Job Description: The position will be providing analytical support to biotherapeutic process development teams, specifically focusing on large molecules (proteins, polysaccharides, nucleic acids, etc.). Candidates will work in a large diverse team, helping with advancing cutting edge pharmaceutical research. Some to the techniques that our future team members will need to be familiar with are: Ultraviolet and visual light spectroscopy (UV-Vis) Analytical chromatographic separations (HPLC) Small-volume multichannel pipetting skills and plate-based assays pH Appearance Gels, SDS Page, AGE, experience with gel-based assay Qualifications: Minimum Qualifications: Authorization to work in the United States indefinitely without restriction or sponsorship Experience with the following techniques; UV-VIS HPLC, SEC Western Blotting SOLO VPE, pH Appearance SDS Page AGE, CGE, experience with gel-based assay Bachelors or Masters Degree in Biological or Chemical Science. Candidates within a commutable distance of Chesterfield, MO are encouraged to apply Preferred experience: Experience with protein immunoblotting technology and attention to detail. Ability to operate independently after receiving direction Electronic laboratory notebook systems and/or GMP documentation ### PalletOne Inc. Cutting Department - Ufp Industries Inc - Location: Hazlehurst, GA (PalletOne) (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - Apply: https://ufpi.wd503.myworkdayjobs.com/ufpi/job/Hazlehurst-GA-PalletOne/PalletOne-Inc-Cutting-Department_R20948 - Excerpt: PalletOne Inc. Cutting Department Hazlehurst, GA (PalletOne) posted: ### PalletOne Inc. Assembly Department - Ufp Industries Inc - Location: Hazlehurst, GA (PalletOne) (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Apply: https://ufpi.wd503.myworkdayjobs.com/ufpi/job/Hazlehurst-GA-PalletOne/PalletOne-Inc-Assembly-Department_R20452 - Excerpt: PalletOne Inc. Assembly Department Hazlehurst, GA (PalletOne) posted: ### PalletOne Inc. Pallet Assembler I - Ufp Industries Inc - Location: Bartow, FL (529) (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Apply: https://ufpi.wd503.myworkdayjobs.com/ufpi/job/Bartow-FL-529/PalletOne-Inc-Pallet-Assembler-I_R20424-1 - Excerpt: PalletOne Inc. Pallet Assembler I Bartow, FL (529) posted: ### PalletOne Inc. Forklift Operator - Ufp Industries Inc - Location: Bartow, FL (529) (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - Apply: https://ufpi.wd503.myworkdayjobs.com/ufpi/job/Bartow-FL-529/PalletOne-Inc-Forklift-Operator_R20965-1 - Excerpt: PalletOne Inc. Forklift Operator Bartow, FL (529) posted: ### Chief Compliance Officer (CCO) for Truist Investment Services, Inc. and Truist Advisory Services, Inc. - Truist Financial Corporation - Location: 3 Locations (unspecified) - Salary: Not disclosed - Posted: 2026-05-29 - Parental leave: 10 weeks (not source-backed) - Non-birth-parent leave: 10 weeks (not source-backed) - Apply: https://truist.wd1.myworkdayjobs.com/Careers/job/Charlotte-NC/Chief-Compliance-Officer--CCO--for-Truist-Investment-Services--Inc-and-Truist-Advisory-Services--Inc_R0113564 - Excerpt: Chief Compliance Officer (CCO) for Truist Investment Services, Inc. and Truist Advisory Services, Inc. 3 Locations posted: Posted 14 Days Ago ### PalletOne Inc. Electrical Maintenance Tech - Ufp Industries Inc - Location: Bartow, FL (529) (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Apply: https://ufpi.wd503.myworkdayjobs.com/ufpi/job/Bartow-FL-529/PalletOne-Inc-Electrical-Maintenance-Tech_R20244 - Excerpt: PalletOne Inc. Electrical Maintenance Tech Bartow, FL (529) posted: ### Project Manager - Rakuten Wallet, Inc. - Rakuten Inc. - Location: Tokyo, Japan (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - Apply: https://rakuten.wd1.myworkdayjobs.com/RakutenInc/job/Tokyo-Japan/Project-Manager---Rakuten-Wallet--Inc_1031354-155 - Excerpt: Project Manager - Rakuten Wallet, Inc. Tokyo, Japan posted: Posted 30+ Days Ago ### Engineering Manager - Rakuten Wallet, Inc. - Rakuten Inc. - Location: Tokyo, Japan (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - Apply: https://rakuten.wd1.myworkdayjobs.com/RakutenInc/job/Tokyo-Japan/Engineering-Manager---System-Department--Rakuten-Wallet--Inc_1030737-1 - Excerpt: Engineering Manager - Rakuten Wallet, Inc. Tokyo, Japan posted: Posted 30+ Days Ago ### Cloud Engineer - Rakuten Wallet, Inc. - Rakuten Inc. - Location: Tokyo, Japan (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - Apply: https://rakuten.wd1.myworkdayjobs.com/RakutenInc/job/Tokyo-Japan/Cloud-Engineer---Rakuten-Wallet--Inc_1030736 - Excerpt: Cloud Engineer - Rakuten Wallet, Inc. Tokyo, Japan posted: Posted 30+ Days Ago ### Sales planning - MIHA, Inc. (A&M) - Rakuten Inc. - Location: Tokyo, Japan (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - Apply: https://rakuten.wd1.myworkdayjobs.com/RakutenInc/job/Tokyo-Japan/Sales-planning----MIHA--Inc--A-M-_1031856-119 - Excerpt: Sales planning - MIHA, Inc. (A&M) Tokyo, Japan posted: Posted 30+ Days Ago ### Marketing Sales,Influencer Marketing - MIHA, Inc. (A&M) - Rakuten Inc. - Location: Tokyo, Japan (unspecified) - Salary: Not disclosed - Posted: 2026-06-08 - Apply: https://rakuten.wd1.myworkdayjobs.com/RakutenInc/job/Tokyo-Japan/Influencer-Marketing-Account-Planner--MIHA-Business-Department--Commerce---Marketing-Company--A-M-_1028160-150 - Excerpt: Marketing Sales,Influencer Marketing - MIHA, Inc. (A&M) Tokyo, Japan posted: Posted 4 Days Ago ### Producer - Point Card System Development Department, Rakuten Payment, Inc. - Rakuten Inc. - Location: Tokyo, Japan (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - Apply: https://rakuten.wd1.myworkdayjobs.com/RakutenInc/job/Tokyo-Japan/Producer---Point-Card-System-Development-Department--Rakuten-Payment--Inc_1030798-132 - Excerpt: Producer - Point Card System Development Department, Rakuten Payment, Inc. Tokyo, Japan posted: Posted 30+ Days Ago ### Data Scientist - Frontend System Development Department, Rakuten Payment, Inc. - Rakuten Inc. - Location: Tokyo, Japan (unspecified) - Salary: Not disclosed - Posted: 2026-06-08 - Apply: https://rakuten.wd1.myworkdayjobs.com/RakutenInc/job/Tokyo-Japan/Data-Scientist---Frontend-System-Development-Department--Rakuten-Payment--Inc_1033541 - Excerpt: Data Scientist - Frontend System Development Department, Rakuten Payment, Inc. Tokyo, Japan posted: Posted 4 Days Ago ### Intellectual Property (Administration for IP Management System), Rakuten Group Inc. - Rakuten Inc. - Location: Tokyo, Japan (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - Apply: https://rakuten.wd1.myworkdayjobs.com/RakutenInc/job/Tokyo-Japan/Administration-for-IP-Management-System---Intellectual-Property-Department--Group-Compliance-Supervisory-Department_1024291-129 - Excerpt: Intellectual Property (Administration for IP Management System), Rakuten Group Inc. Tokyo, Japan posted: Posted 30+ Days Ago ### Intellectual Property (Planning & Administration, Manager Candidate/Member), Rakuten Mobile, Inc. - Rakuten Inc. - Location: Tokyo, Japan (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - Apply: https://rakuten.wd1.myworkdayjobs.com/RakutenInc/job/Tokyo-Japan/Intellectual-Property-Planning---Management-Manager-Candidate---IP-Strategy-Section--Strategic-Business-Compliance-Support-Department--Group-Compliance-Supervisory-Department_1027517-1 - Excerpt: Intellectual Property (Planning & Administration, Manager Candidate/Member), Rakuten Mobile, Inc. Tokyo, Japan posted: Posted 30+ Days Ago ### Operation Engineer, Rakuten Pay - Service Operation Department, Rakuten Payment, Inc. - Rakuten Inc. - Location: Tokyo, Japan (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - Apply: https://rakuten.wd1.myworkdayjobs.com/RakutenInc/job/Tokyo-Japan/Operation-Engineer--Rakuten-Pay--Rakuten-Pay-System-Department---Rakuten-Payment--Inc_1025931-93 - Excerpt: Operation Engineer, Rakuten Pay - Service Operation Department, Rakuten Payment, Inc. Tokyo, Japan posted: Posted 30+ Days Ago ### Product Manager (Advertising Effectiveness Measurement Area) - Rakuten Insight, Inc. (A&M) - Rakuten Inc. - Location: Tokyo, Japan (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - Apply: https://rakuten.wd1.myworkdayjobs.com/RakutenInc/job/Tokyo-Japan/Product-Manager--Advertising-Effectiveness-Measurement-Area----Rakuten-Insight--Inc--A-M-_1027833-60 - Excerpt: Product Manager (Advertising Effectiveness Measurement Area) - Rakuten Insight, Inc. (A&M) Tokyo, Japan posted: Posted 30+ Days Ago ### Business strategic planning - Data Solutions Department, Rakuten Insight, Inc. (A&M) - Rakuten Inc. - Location: Tokyo, Japan (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - Apply: https://rakuten.wd1.myworkdayjobs.com/RakutenInc/job/Tokyo-Japan/Business-strategic-planning---Data-Solutions-Department--Rakuten-Insight--Inc--A-M-_1027834-64 - Excerpt: Business strategic planning - Data Solutions Department, Rakuten Insight, Inc. (A&M) Tokyo, Japan posted: Posted 30+ Days Ago ### Payment Service Implementation Producer - Device Platform Department, Rakuten Payment, Inc. - Rakuten Inc. - Location: Tokyo, Japan (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - Apply: https://rakuten.wd1.myworkdayjobs.com/RakutenInc/job/Tokyo-Japan/Payment-Service-Implementation-Producer----Device-Platform-Department--Rakuten-Payment--Inc_1030492-155 - Excerpt: Payment Service Implementation Producer - Device Platform Department, Rakuten Payment, Inc. Tokyo, Japan posted: Posted 30+ Days Ago ### Web Application Engineer - Pay Online System Development Department, Rakuten Payment, Inc. - Rakuten Inc. - Location: Tokyo, Japan (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - Apply: https://rakuten.wd1.myworkdayjobs.com/RakutenInc/job/Tokyo-Japan/Web-Application-Engineer---Pay-Online-System-Development-Department--Rakuten-Payment--Inc_1027890-145 - Excerpt: Web Application Engineer - Pay Online System Development Department, Rakuten Payment, Inc. Tokyo, Japan posted: Posted 30+ Days Ago ### System Operation/Maintenance Engineer – E-money System Department, Rakuten Edy, Inc. - Rakuten Inc. - Location: Tokyo, Japan (unspecified) - Salary: Not disclosed - Posted: 2026-05-29 - Apply: https://rakuten.wd1.myworkdayjobs.com/RakutenInc/job/Tokyo-Japan/System-Operation-Maintenance-Engineer---E-money-System-Department--System-Division--Rakuten-Cash--Rakuten-Edy--Inc_1025935-55 - Excerpt: System Operation/Maintenance Engineer – E-money System Department, Rakuten Edy, Inc. Tokyo, Japan posted: Posted 14 Days Ago ### Lead Operation Producer - Service Operation Department, Product Development Division, Rakuten Payment, Inc. - Rakuten Inc. - Location: Tokyo, Japan (unspecified) - Salary: Not disclosed - Posted: 2026-06-11 - Apply: https://rakuten.wd1.myworkdayjobs.com/RakutenInc/job/Tokyo-Japan/Operation-Producer---Rakuten-Pay-System-Department--Rakuten-Payment--Inc_1025929-1 - Excerpt: Lead Operation Producer - Service Operation Department, Product Development Division, Rakuten Payment, Inc. Tokyo, Japan posted: Posted Yesterday ### Database Administrator - Platform and Infrastructure Department, Product Development Division, Rakuten Payment, Inc. - Rakuten Inc. - Location: Tokyo, Japan (unspecified) - Salary: Not disclosed - Posted: 2026-06-05 - Apply: https://rakuten.wd1.myworkdayjobs.com/RakutenInc/job/Tokyo-Japan/Database-Administrator---Platform-and-Infrastructure-Department--System-Division--Rakuten-Payment--Inc_1025212-131 - Excerpt: Database Administrator - Platform and Infrastructure Department, Product Development Division, Rakuten Payment, Inc. Tokyo, Japan posted: Posted 7 Days Ago ### Infrastructure Engineer - Platform and Infrastructure Department, Product Development Division, Rakuten Payment, Inc. - Rakuten Inc. - Location: Tokyo, Japan (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - Apply: https://rakuten.wd1.myworkdayjobs.com/RakutenInc/job/Tokyo-Japan/Infrastructure-Engineer----Platform-and-Infrastructure-Department--Product-Development-Division--Rakuten-Payment--Inc_1029533-60 - Excerpt: Infrastructure Engineer - Platform and Infrastructure Department, Product Development Division, Rakuten Payment, Inc. Tokyo, Japan posted: Posted 30+ Days Ago ### DevOps Engineer (Fukuoka Office)- Service Operation Department, Product Development Division, Rakuten Payment, Inc. - Rakuten Inc. - Location: Fukuoka, Japan (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - Apply: https://rakuten.wd1.myworkdayjobs.com/RakutenInc/job/Fukuoka-Japan/DevOps-Engineer---Service-Operation-Department--Product-Development-Division--Rakuten-Payment--Inc_1033210-62 - Excerpt: DevOps Engineer (Fukuoka Office)- Service Operation Department, Product Development Division, Rakuten Payment, Inc. Fukuoka, Japan posted: Posted Today ### Product Manager - Customer Service Development Department, Product Development Division, Rakuten Payment, Inc. - Rakuten Inc. - Location: Tokyo, Japan (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - Apply: https://rakuten.wd1.myworkdayjobs.com/RakutenInc/job/Tokyo-Japan/Product-Manager---Customer-Service-Development-Department--Product-Development-Division--Rakuten-Payment--Inc_1030538-1 - Excerpt: Product Manager - Customer Service Development Department, Product Development Division, Rakuten Payment, Inc. Tokyo, Japan posted: Posted 30+ Days Ago ### Global Member Support Leader Candidate - Membership Strategy Department,Rakuten Insight, Inc. (A&M) - Rakuten Inc. - Location: Tokyo, Japan (unspecified) - Salary: Not disclosed - Posted: 2026-05-14 - Apply: https://rakuten.wd1.myworkdayjobs.com/RakutenInc/job/Tokyo-Japan/Global-Member-Support-Leader-Candidate---Membership-Strategy-Department-Rakuten-Insight--Inc--A-M-_1033529-116 - Excerpt: Global Member Support Leader Candidate - Membership Strategy Department,Rakuten Insight, Inc. (A&M) Tokyo, Japan posted: Posted 29 Days Ago ### Data Scientist - Customer Service Development Department, Product Development Division, Rakuten Payment, Inc. - Rakuten Inc. - Location: Tokyo, Japan (unspecified) - Salary: Not disclosed - Posted: 2026-05-20 - Apply: https://rakuten.wd1.myworkdayjobs.com/RakutenInc/job/Tokyo-Japan/Data-Scientist---FinTech-System-Development-Department--Rakuten-Payment--Inc-FSD-_1025907-24 - Excerpt: Data Scientist - Customer Service Development Department, Product Development Division, Rakuten Payment, Inc. Tokyo, Japan posted: Posted 23 Days Ago ### Producer - Pay Online System Development Department, Product Development Division, Rakuten Payment, Inc. - Rakuten Inc. - Location: Tokyo, Japan (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - Apply: https://rakuten.wd1.myworkdayjobs.com/RakutenInc/job/Tokyo-Japan/Producer---Pay-Online-System-Development-Department--Product-Development-Division--Rakuten-Payment--Inc_1030536-118 - Excerpt: Producer - Pay Online System Development Department, Product Development Division, Rakuten Payment, Inc. Tokyo, Japan posted: Posted 30+ Days Ago ### Cloud Database Administrator - Platform and Infrastructure Department, Product Development Division, Rakuten Payment, Inc. - Rakuten Inc. - Location: Tokyo, Japan (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - Apply: https://rakuten.wd1.myworkdayjobs.com/RakutenInc/job/Tokyo-Japan/Cloud-Database-Administrator---Platform-and-Infrastructure-Department--Product-Development-Division--Rakuten-Payment--Inc_1031204-32 - Excerpt: Cloud Database Administrator - Platform and Infrastructure Department, Product Development Division, Rakuten Payment, Inc. Tokyo, Japan posted: Posted 30+ Days Ago ### Meeting Management/Internal Communication, Internal Communications Group - General Affairs Section, Rakuten Total Solutions, Inc. - Rakuten Inc. - Location: Tokyo, Japan (unspecified) - Salary: Not disclosed - Posted: 2026-06-11 - Apply: https://rakuten.wd1.myworkdayjobs.com/RakutenInc/job/Tokyo-Japan/Meeting-Management-Internal-Communication--Internal-Communications-Group---General-Affairs-Section--Rakuten-Total-Solutions--Inc_1034135-42 - Excerpt: Meeting Management/Internal Communication, Internal Communications Group - General Affairs Section, Rakuten Total Solutions, Inc. Tokyo, Japan posted: Posted Yesterday ### Development PL (Rakuten Edy, Rakuten Cash) - E-money System Department, Rakuten Edy, Inc. - Rakuten Inc. - Location: Tokyo, Japan (unspecified) - Salary: Not disclosed - Posted: 2026-06-11 - Apply: https://rakuten.wd1.myworkdayjobs.com/RakutenInc/job/Tokyo-Japan/Development-PL--Rakuten-Edy--Rakuten-Cash---E-money-System-Department--Rakuten-Edy--Inc_1030346 - Excerpt: Development PL (Rakuten Edy, Rakuten Cash) - E-money System Department, Rakuten Edy, Inc. Tokyo, Japan posted: Posted Yesterday ### Product Manager, Rakuten Pay (Online Payment) - Pay Product Development Department, Rakuten Payment, Inc. - Rakuten Inc. - Location: Tokyo, Japan (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - Apply: https://rakuten.wd1.myworkdayjobs.com/RakutenInc/job/Tokyo-Japan/Product-Manager--Rakuten-Pay--Online-Payment----Pay-Product-Development-Department--Rakuten-Payment--Inc_1033004-48 - Excerpt: Product Manager, Rakuten Pay (Online Payment) - Pay Product Development Department, Rakuten Payment, Inc. Tokyo, Japan posted: Posted 30+ Days Ago ### Project Manager (Operation Kaizen) - Service Operation Department, Product Development Division, Rakuten Payment, Inc. - Rakuten Inc. - Location: Tokyo, Japan (unspecified) - Salary: Not disclosed - Posted: 2026-05-29 - Apply: https://rakuten.wd1.myworkdayjobs.com/RakutenInc/job/Tokyo-Japan/Lead-System-Operation-Maintenance-Engineer---Service-Operation-Department--Product-Development-Division--Rakuten-Payment--Inc_1033209-7 - Excerpt: Project Manager (Operation Kaizen) - Service Operation Department, Product Development Division, Rakuten Payment, Inc. Tokyo, Japan posted: Posted 14 Days Ago ### Digital Marketing Planning Manager for Candidate - Membership Strategy Department, Rakuten Insight Global, Inc.(A&M) - Rakuten Inc. - Location: Tokyo, Japan (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - Apply: https://rakuten.wd1.myworkdayjobs.com/RakutenInc/job/Tokyo-Japan/Digital-Marketing-Planning-Manager-for-Candidate---Membership-Strategy-Department--Rakuten-Insight-Global--Inc-A-M-_1029332-44 - Excerpt: Digital Marketing Planning Manager for Candidate - Membership Strategy Department, Rakuten Insight Global, Inc.(A&M) Tokyo, Japan posted: Posted 30+ Days Ago ### DX Project Manager - Customer Service Development Department, Product Development Division, Rakuten Payment, Inc. - Rakuten Inc. - Location: Tokyo, Japan (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - Apply: https://rakuten.wd1.myworkdayjobs.com/RakutenInc/job/Tokyo-Japan/DX-Project-Manager---Customer-Service-Development-Department--Product-Development-Division--Rakuten-Payment--Inc_1030542 - Excerpt: DX Project Manager - Customer Service Development Department, Product Development Division, Rakuten Payment, Inc. Tokyo, Japan posted: Posted 30+ Days Ago ### Legal Officer - Legal Support Section, Strategic Business Compliance Support Department, Rakuten Symphony, Inc. - Rakuten Inc. - Location: Tokyo, Japan (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - Apply: https://rakuten.wd1.myworkdayjobs.com/RakutenInc/job/Tokyo-Japan/Legal-Officer---Legal-Support-Section--Strategic-Business-Compliance-Support-Department--Rakuten-Symphony--Inc_1031558-160 - Excerpt: Legal Officer - Legal Support Section, Strategic Business Compliance Support Department, Rakuten Symphony, Inc. Tokyo, Japan posted: Posted 30+ Days Ago ### AI Project Manager - Customer Service Development Department, Product Development Division, Rakuten Payment, Inc - Rakuten Inc. - Location: Tokyo, Japan (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - Apply: https://rakuten.wd1.myworkdayjobs.com/RakutenInc/job/Tokyo-Japan/AI-Project-Manager---Customer-Service-Development-Department--Product-Development-Division--Rakuten-Payment--Inc_1030541 - Excerpt: AI Project Manager - Customer Service Development Department, Product Development Division, Rakuten Payment, Inc Tokyo, Japan posted: Posted 30+ Days Ago ### Event Planning & Operation Leader/Manager Candidate - Group Affairs and Facilities Management, Rakuten Symphony, Inc. (GAFMD) - Rakuten Inc. - Location: Tokyo, Japan (unspecified) - Salary: Not disclosed - Posted: 2026-06-05 - Apply: https://rakuten.wd1.myworkdayjobs.com/RakutenInc/job/Tokyo-Japan/Staff-of-Event-Panning---Operation---RM-RTS-General-Affairs-Section--Rakuten-Symphony--Inc--GAFMD-_1032041-101 - Excerpt: Event Planning & Operation Leader/Manager Candidate - Group Affairs and Facilities Management, Rakuten Symphony, Inc. (GAFMD) Tokyo, Japan posted: Posted 7 Days Ago ### Accounting/Business Planning Manager (or Manager Candidate) - Financial Accounting Department, Rakuten Total Solutions, Inc. (FACT) - Rakuten Inc. - Location: Tokyo, Japan (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - Apply: https://rakuten.wd1.myworkdayjobs.com/RakutenInc/job/Tokyo-Japan/Accounting-Business-Planning-Manager--or-Manager-Candidate----Financial-Accounting-Department--Rakuten-Total-Solutions--Inc--FACT-_1032704-43 - Excerpt: Accounting/Business Planning Manager (or Manager Candidate) - Financial Accounting Department, Rakuten Total Solutions, Inc. (FACT) Tokyo, Japan posted: Posted 30+ Days Ago ### Staff of Credit Management ‐ Strategic Business Compliance Support Department, Rakuten Total Solutions, Inc. (SBCSD) - Rakuten Inc. - Location: Tokyo, Japan (unspecified) - Salary: Not disclosed - Posted: 2026-06-04 - Apply: https://rakuten.wd1.myworkdayjobs.com/RakutenInc/job/Tokyo-Japan/Credit-Management-Specialist--Mobile-Corporate-Business-Business-Development----Strategic-Business-Compliance-Support-Department--Group-Compliance-Supervisory-Department--Rakuten-Total-Solutions--Inc_1032574-131 - Excerpt: Staff of Credit Management ‐ Strategic Business Compliance Support Department, Rakuten Total Solutions, Inc. (SBCSD) Tokyo, Japan posted: Posted 8 Days Ago --- Source-backed benefit claims include source links; other benefit values are labeled separately.