Cellares Corporation
CMC Program Manager
Cellares Corporation, San Francisco, California, United States, 94199
Cellares is seeking a highly motivated CMC Program Manager who will be responsible for managing CMC specific project timelines and activities related to Cell Therapy Manufacturing. The successful candidate will act as a bridge between CMC cross-functional teams, including Process Development, Analytical Development, Manufacturing, Regulatory Affairs, and Quality. Candidates should focus on successful program coordination and communication, both internally and externally. The successful candidate will be well versed in cell and gene therapy manufacturing, as well as experienced in Technical Operations/CMC project management and client relations.This is a multidisciplinary role and this individual will interface across many parts of the company (with commercial teams, process, analytical, and operational groups) to develop the best solutions possible for our clients. Effective communication, positive relationship building, creative problem solving, and acting with a sense of urgency are essential for this role.Candidates should enjoy working in a fast-paced, mission-driven environment, and be prepared to tackle a broad selection of challenges as the company grows.Responsibilities
Manage and work with cross-functional teams to generate CMC strategies and timelines, identification and removal of project roadblocks, and risk mitigation planningPartner with Finance to manage program budgets and guide resourcing decisions, including forecasting and approval of invoicesSupport inventory management of custom reagents and materials, including drug substancesSupport preparation and planning of regulatory interactions and filings (e.g., FDA Master Files)Track outsourced activities as needed, including management of external vendors from evaluation to closeout, ensuring deliverables are met on time and within budgetContinuous improvement of existing systems as well as implementation of new CMC program management best practices and toolsProvide periodic updates via email, in-person, and/or Zoom with regard to project milestones, schedule, budget, and deliverablesInvestigate and resolve problems, identify root causes, and propose process improvements through clear communication with internal teamsCapture and document requirements from external and internal stakeholdersGenerate program-related documentation, including but not limited to timelines, communication templates, status dashboards, tracking tools, presentation decks, and final reportsWork with internal subject matter experts to assist in and respond to any partner or client questions and ad hoc requests during the duration of the programContinually work to streamline processes by creating more efficient methods of gathering, sorting, and accessing dataInterface and develop strong working relationships with all internal subject matter experts across the organizationDrive overall customer satisfaction and participation in future partnerships or adoption of Cellares’ Technology SolutionsLead cross-functional meetings and facilitate discussions internally and with external partnersRequirements
Bachelor's degree or equivalent experience5+ years of relevant professional experienceExperience with project/program management in a manufacturing environment and interfacing directly with external partnersExperience in a regulated biotech or pharmaceutical setting with proven competency and expertise in the CMC/GMP manufacturing space of cell-based therapies is highly desirable1+ year of experience in client services directly interfacing with partners and/or clientsAbility to understand and communicate scientific and business elements associated with engineered cell therapiesExcellent verbal and written communication, time management, attention to detail, problem-solving, acting with a sense of urgency and enthusiasmHigh level of customer empathy with active listening skillsEnjoys problem-solving in a dynamic and rapidly changing environmentExperience using Google Apps, Project Management Tools (ie SmartSheet or TeamGantt) and CRM applications such as Salesforce$90,000 - $210,000 a year
Cellares total compensation package contains competitive base salaries, highly subsidized Medical, Dental, and Vision Plans, 401(k) Matching, Free EV Charging, Onsite lunches, and Stock options. All displayed pay ranges are approximate, negotiable, and location dependent.#J-18808-Ljbffr
Manage and work with cross-functional teams to generate CMC strategies and timelines, identification and removal of project roadblocks, and risk mitigation planningPartner with Finance to manage program budgets and guide resourcing decisions, including forecasting and approval of invoicesSupport inventory management of custom reagents and materials, including drug substancesSupport preparation and planning of regulatory interactions and filings (e.g., FDA Master Files)Track outsourced activities as needed, including management of external vendors from evaluation to closeout, ensuring deliverables are met on time and within budgetContinuous improvement of existing systems as well as implementation of new CMC program management best practices and toolsProvide periodic updates via email, in-person, and/or Zoom with regard to project milestones, schedule, budget, and deliverablesInvestigate and resolve problems, identify root causes, and propose process improvements through clear communication with internal teamsCapture and document requirements from external and internal stakeholdersGenerate program-related documentation, including but not limited to timelines, communication templates, status dashboards, tracking tools, presentation decks, and final reportsWork with internal subject matter experts to assist in and respond to any partner or client questions and ad hoc requests during the duration of the programContinually work to streamline processes by creating more efficient methods of gathering, sorting, and accessing dataInterface and develop strong working relationships with all internal subject matter experts across the organizationDrive overall customer satisfaction and participation in future partnerships or adoption of Cellares’ Technology SolutionsLead cross-functional meetings and facilitate discussions internally and with external partnersRequirements
Bachelor's degree or equivalent experience5+ years of relevant professional experienceExperience with project/program management in a manufacturing environment and interfacing directly with external partnersExperience in a regulated biotech or pharmaceutical setting with proven competency and expertise in the CMC/GMP manufacturing space of cell-based therapies is highly desirable1+ year of experience in client services directly interfacing with partners and/or clientsAbility to understand and communicate scientific and business elements associated with engineered cell therapiesExcellent verbal and written communication, time management, attention to detail, problem-solving, acting with a sense of urgency and enthusiasmHigh level of customer empathy with active listening skillsEnjoys problem-solving in a dynamic and rapidly changing environmentExperience using Google Apps, Project Management Tools (ie SmartSheet or TeamGantt) and CRM applications such as Salesforce$90,000 - $210,000 a year
Cellares total compensation package contains competitive base salaries, highly subsidized Medical, Dental, and Vision Plans, 401(k) Matching, Free EV Charging, Onsite lunches, and Stock options. All displayed pay ranges are approximate, negotiable, and location dependent.#J-18808-Ljbffr