Bristol Myers Squibb
Director, Cell Therapy Technical Operations (CTTO) Strategy and Business Service
Bristol Myers Squibb, Seattle, Washington, us, 98127
Overview
Director, Cell Therapy Technical Operations (CTTO) Strategy and Business Services role at Bristol Myers Squibb. This leadership position is responsible for the operational backbone of the CTTO technical support function, owning project management and regulatory support capabilities with a focus on scaling these functions to meet future demands. Responsibilities
Own and evolve the Project Management Framework: take ownership of CTTO's Book of Work, primarily for the Technical Product Team (TPT) and Material Review Committee (MRC) Books of Work, ensuring governance and visibility by refining a standardized, business-enabling project management framework; coordinate the overall project portfolio and provide oversight for major cross-functional projects; lead a team of project managers for comprehensive planning and timely execution. Drive Strategic Planning and Execution: lead CTTO strategy planning through Hoshin Kanri and execution, influence cross-functional execution, contribute to CTTO strategic initiatives, manage portfolio planning (opportunity identification, project prioritization, resource management), and coordinate objectives and KPIs. Own Key Services Business Processes: mature key business processes and initiatives such as annual budget development and workforce planning in partnership with Finance; support CTTO Run the Business activities, including meetings, tier management, and governance. Empower the Team: lead and coach a diverse team of project managers, document submission coordinators, and technical writers, focusing on professional development and adapting to a dynamic environment. Forge and Strengthen Key Partnerships: act as the central hub for collaboration with Global Regulatory Sciences (GRS) and within CTTO; serve as a strategic partner to the department head on CTTO run-the-business activities, including meetings and governance. Ensure Compliance & Business Continuity Management: establish and enhance compliance-related processes and tools to ensure quality records management is compliant within CTTO and with key partners; ensure CTTO business continuity aligns with enterprise needs, escalating issues and risks as appropriate. Qualifications & Experience
Bachelor's degree in Engineering, Life Sciences or related field. Minimum 12 years of experience leading cross-functional teams in cell therapy or biologics operations with a focus on project portfolio management. Strong direct people management experience. Demonstrated experience leading transformational change within a global network. Deep experience managing a broad portfolio of projects of significant complexity and duration across a global network. Experience in developing talent, managing change, engaging and motivating people, and developing organization and work structures. Demonstrated expertise in Operational Excellence and Project/Program Management. Strong organizational skills, ability to multitask, and thrive in a dynamic, fast-paced environment. Experience leading change and delivering results to meet deadlines and commitments. Strong collaboration, delegation and interpersonal communication skills; ability to share critical information with project teams and senior leaders. Analytical and logical thinking with a focus on fact-based decision making. Hands-on operations experience at a manufacturing site; comprehensive understanding of cell therapy manufacturing technology (preferred). Strong financial acumen. Travel: Approximately 10-15% travel may be required domestically and internationally. Compensation & Benefits
Starting compensation: various locations may have different ranges. Example ranges listed include Seattle, WA: $200,330.00–$259,735.00; Devens, MA: $214,340.00–$259,735.00; Madison, NJ: $200,330.00–$242,750.0; other benefits and incentive opportunities (cash and stock) may be available based on eligibility. Eligibility for specific benefits varies by job and location; details at the company's life-at-BMS site and policies. Benefits may include medical, dental, vision, wellbeing programs, 401(k) matching, disability and life insurance, paid holidays, paid time off, volunteer days, parental and caregiver support, tuition reimbursement, and recognition programs, among others as defined by applicable plans. Other
Seniority level: Director. Employment type: Full-time. Job function: Other. Industry: Pharmaceutical Manufacturing.
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Director, Cell Therapy Technical Operations (CTTO) Strategy and Business Services role at Bristol Myers Squibb. This leadership position is responsible for the operational backbone of the CTTO technical support function, owning project management and regulatory support capabilities with a focus on scaling these functions to meet future demands. Responsibilities
Own and evolve the Project Management Framework: take ownership of CTTO's Book of Work, primarily for the Technical Product Team (TPT) and Material Review Committee (MRC) Books of Work, ensuring governance and visibility by refining a standardized, business-enabling project management framework; coordinate the overall project portfolio and provide oversight for major cross-functional projects; lead a team of project managers for comprehensive planning and timely execution. Drive Strategic Planning and Execution: lead CTTO strategy planning through Hoshin Kanri and execution, influence cross-functional execution, contribute to CTTO strategic initiatives, manage portfolio planning (opportunity identification, project prioritization, resource management), and coordinate objectives and KPIs. Own Key Services Business Processes: mature key business processes and initiatives such as annual budget development and workforce planning in partnership with Finance; support CTTO Run the Business activities, including meetings, tier management, and governance. Empower the Team: lead and coach a diverse team of project managers, document submission coordinators, and technical writers, focusing on professional development and adapting to a dynamic environment. Forge and Strengthen Key Partnerships: act as the central hub for collaboration with Global Regulatory Sciences (GRS) and within CTTO; serve as a strategic partner to the department head on CTTO run-the-business activities, including meetings and governance. Ensure Compliance & Business Continuity Management: establish and enhance compliance-related processes and tools to ensure quality records management is compliant within CTTO and with key partners; ensure CTTO business continuity aligns with enterprise needs, escalating issues and risks as appropriate. Qualifications & Experience
Bachelor's degree in Engineering, Life Sciences or related field. Minimum 12 years of experience leading cross-functional teams in cell therapy or biologics operations with a focus on project portfolio management. Strong direct people management experience. Demonstrated experience leading transformational change within a global network. Deep experience managing a broad portfolio of projects of significant complexity and duration across a global network. Experience in developing talent, managing change, engaging and motivating people, and developing organization and work structures. Demonstrated expertise in Operational Excellence and Project/Program Management. Strong organizational skills, ability to multitask, and thrive in a dynamic, fast-paced environment. Experience leading change and delivering results to meet deadlines and commitments. Strong collaboration, delegation and interpersonal communication skills; ability to share critical information with project teams and senior leaders. Analytical and logical thinking with a focus on fact-based decision making. Hands-on operations experience at a manufacturing site; comprehensive understanding of cell therapy manufacturing technology (preferred). Strong financial acumen. Travel: Approximately 10-15% travel may be required domestically and internationally. Compensation & Benefits
Starting compensation: various locations may have different ranges. Example ranges listed include Seattle, WA: $200,330.00–$259,735.00; Devens, MA: $214,340.00–$259,735.00; Madison, NJ: $200,330.00–$242,750.0; other benefits and incentive opportunities (cash and stock) may be available based on eligibility. Eligibility for specific benefits varies by job and location; details at the company's life-at-BMS site and policies. Benefits may include medical, dental, vision, wellbeing programs, 401(k) matching, disability and life insurance, paid holidays, paid time off, volunteer days, parental and caregiver support, tuition reimbursement, and recognition programs, among others as defined by applicable plans. Other
Seniority level: Director. Employment type: Full-time. Job function: Other. Industry: Pharmaceutical Manufacturing.
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