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Associate Director, Cell Therapy Development Operations Project Lead

Bristol-Myers Squibb

Associate Director, Cell Therapy Development Operations Project Lead

Bristol-Myers Squibb logo

Bristol-Myers Squibb

full-time

Posted: November 26, 2025

Number of Vacancies: 1

Job Description

Development of project plans and ownership of execution from ideation of solutions, endorsement of project strategy, through sustainment or handoff to business owners. Organization and leadership of cross-functional workshops and analyses to ensure clear vision of desired outcomes, actionable output and clear, balanced decision making. Prepare, co-ordinate and lead project communications for peers, senior stakeholders / leadership. Drive and track actions, develop and drive detailed plans, identify critical path and timing, hold team members accountable for due dates. Develop strong relationships with stakeholders across CTDO to understand root causes of gaps in and barriers to organizational flow, enabling incisive problem solving and barrier removal. Foster high performance teamwork and maintain strong relationships with operational and functional leadership. Identify obstacles & remove them, create options and escalate as appropriate to drive response activity in line with key business milestones & budget. Utilize standard project management tools and Scrum methodology for tracking and status reporting. Support establishment of strong, positive, engaged CTDO culture - including focus on safety, engagement, and patient mission focus. Work-life programs include paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility. Supporting People with Disabilities B.S. or B.A. in science and/or engineering (biotechnology, biology, engineering, or related sciences). Prior cell therapy development operations experience is strongly preferred. 5-8 years business experience, with 5+ years in a BioPharma operational or development discipline, including demonstrated 2-3 years of experience managing projects and programs. Demonstrated leadership & collaboration working in, or closely with, Supply Chain, GMP Manufacturing Operations, Manufacturing Science & Technology, Project & Program management, Quality Assurance / Quality Control Operations and related functions. Broad understanding of biologics or cell therapy commercial manufacturing & analytical processes, technology transfer and/or start-up phase experience highly desired Analysis and simplification of complex operational issues Project management execution, expertise in its principles and application, the ability to manage multiple projects simultaneously and evaluation of priorities Effective escalation & communication with multiple levels up to SVP Conflict resolution Understanding and utilization of concepts regarding the roles of - Accountable, responsible, advisor & informed through the changing landscape of rapid response activity

About the Role/Company

  • The company supports people with disabilities
  • Focus on safety, engagement, and patient mission within CTDO culture

Key Responsibilities

  • Develop project plans and own execution from ideation to sustainment or handoff
  • Organize and lead cross-functional workshops and analyses
  • Prepare, coordinate, and lead project communications for peers and senior stakeholders/leadership
  • Drive and track actions, develop and drive detailed plans, identify critical path and timing
  • Hold team members accountable for due dates
  • Develop strong relationships with stakeholders across CTDO to understand root causes and barriers
  • Foster high performance teamwork and maintain strong relationships with operational and functional leadership
  • Identify obstacles, remove them, create options, and escalate as appropriate
  • Utilize standard project management tools and Scrum methodology for tracking and status reporting
  • Support establishment of strong, positive, engaged CTDO culture focusing on safety, engagement, and patient mission

Required Qualifications

  • B.S. or B.A. in science and/or engineering (biotechnology, biology, engineering, or related sciences)
  • -8 years business experience
  • + years in a BioPharma operational or development discipline
  • -3 years of experience managing projects and programs

Preferred Qualifications

  • Prior cell therapy development operations experience
  • Broad understanding of biologics or cell therapy commercial manufacturing & analytical processes
  • Technology transfer and/or start-up phase experience

Skills Required

  • Analysis and simplification of complex operational issues
  • Project management execution and expertise in its principles and application
  • Ability to manage multiple projects simultaneously and evaluate priorities
  • Effective escalation and communication with multiple levels up to SVP
  • Conflict resolution
  • Understanding and utilization of concepts regarding the roles of Accountable, Responsible, Advisor & Informed

Benefits & Perks

  • Paid national holidays and optional holidays
  • Global Shutdown Days between Christmas and New Year's holiday
  • Up to 120 hours of paid vacation
  • Up to two (2) paid days to volunteer
  • Sick time off
  • Summer hours flexibility

Locations

  • Devens MA, United States
  • Summit West NJ, United States
  • Bothell WA, United States

Salary

Salary not disclosed

Estimated Salary Rangemedium confidence

150,000 - 220,000 USD / yearly

Source: ai estimated

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • Analysis and simplification of complex operational issuesintermediate
  • Project management execution and expertise in its principles and applicationintermediate
  • Ability to manage multiple projects simultaneously and evaluate prioritiesintermediate
  • Effective escalation and communication with multiple levels up to SVPintermediate
  • Conflict resolutionintermediate
  • Understanding and utilization of concepts regarding the roles of Accountable, Responsible, Advisor & Informedintermediate

Required Qualifications

  • B.S. or B.A. in science and/or engineering (biotechnology, biology, engineering, or related sciences) (experience)
  • -8 years business experience (experience)
  • + years in a BioPharma operational or development discipline (experience)
  • -3 years of experience managing projects and programs (experience)

Preferred Qualifications

  • Prior cell therapy development operations experience (experience)
  • Broad understanding of biologics or cell therapy commercial manufacturing & analytical processes (experience)
  • Technology transfer and/or start-up phase experience (experience)

Responsibilities

  • Develop project plans and own execution from ideation to sustainment or handoff
  • Organize and lead cross-functional workshops and analyses
  • Prepare, coordinate, and lead project communications for peers and senior stakeholders/leadership
  • Drive and track actions, develop and drive detailed plans, identify critical path and timing
  • Hold team members accountable for due dates
  • Develop strong relationships with stakeholders across CTDO to understand root causes and barriers
  • Foster high performance teamwork and maintain strong relationships with operational and functional leadership
  • Identify obstacles, remove them, create options, and escalate as appropriate
  • Utilize standard project management tools and Scrum methodology for tracking and status reporting
  • Support establishment of strong, positive, engaged CTDO culture focusing on safety, engagement, and patient mission

Benefits

  • general: Paid national holidays and optional holidays
  • general: Global Shutdown Days between Christmas and New Year's holiday
  • general: Up to 120 hours of paid vacation
  • general: Up to two (2) paid days to volunteer
  • general: Sick time off
  • general: Summer hours flexibility

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Bristol-Myers Squibb logo

Associate Director, Cell Therapy Development Operations Project Lead

Bristol-Myers Squibb

Associate Director, Cell Therapy Development Operations Project Lead

Bristol-Myers Squibb logo

Bristol-Myers Squibb

full-time

Posted: November 26, 2025

Number of Vacancies: 1

Job Description

Development of project plans and ownership of execution from ideation of solutions, endorsement of project strategy, through sustainment or handoff to business owners. Organization and leadership of cross-functional workshops and analyses to ensure clear vision of desired outcomes, actionable output and clear, balanced decision making. Prepare, co-ordinate and lead project communications for peers, senior stakeholders / leadership. Drive and track actions, develop and drive detailed plans, identify critical path and timing, hold team members accountable for due dates. Develop strong relationships with stakeholders across CTDO to understand root causes of gaps in and barriers to organizational flow, enabling incisive problem solving and barrier removal. Foster high performance teamwork and maintain strong relationships with operational and functional leadership. Identify obstacles & remove them, create options and escalate as appropriate to drive response activity in line with key business milestones & budget. Utilize standard project management tools and Scrum methodology for tracking and status reporting. Support establishment of strong, positive, engaged CTDO culture - including focus on safety, engagement, and patient mission focus. Work-life programs include paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility. Supporting People with Disabilities B.S. or B.A. in science and/or engineering (biotechnology, biology, engineering, or related sciences). Prior cell therapy development operations experience is strongly preferred. 5-8 years business experience, with 5+ years in a BioPharma operational or development discipline, including demonstrated 2-3 years of experience managing projects and programs. Demonstrated leadership & collaboration working in, or closely with, Supply Chain, GMP Manufacturing Operations, Manufacturing Science & Technology, Project & Program management, Quality Assurance / Quality Control Operations and related functions. Broad understanding of biologics or cell therapy commercial manufacturing & analytical processes, technology transfer and/or start-up phase experience highly desired Analysis and simplification of complex operational issues Project management execution, expertise in its principles and application, the ability to manage multiple projects simultaneously and evaluation of priorities Effective escalation & communication with multiple levels up to SVP Conflict resolution Understanding and utilization of concepts regarding the roles of - Accountable, responsible, advisor & informed through the changing landscape of rapid response activity

About the Role/Company

  • The company supports people with disabilities
  • Focus on safety, engagement, and patient mission within CTDO culture

Key Responsibilities

  • Develop project plans and own execution from ideation to sustainment or handoff
  • Organize and lead cross-functional workshops and analyses
  • Prepare, coordinate, and lead project communications for peers and senior stakeholders/leadership
  • Drive and track actions, develop and drive detailed plans, identify critical path and timing
  • Hold team members accountable for due dates
  • Develop strong relationships with stakeholders across CTDO to understand root causes and barriers
  • Foster high performance teamwork and maintain strong relationships with operational and functional leadership
  • Identify obstacles, remove them, create options, and escalate as appropriate
  • Utilize standard project management tools and Scrum methodology for tracking and status reporting
  • Support establishment of strong, positive, engaged CTDO culture focusing on safety, engagement, and patient mission

Required Qualifications

  • B.S. or B.A. in science and/or engineering (biotechnology, biology, engineering, or related sciences)
  • -8 years business experience
  • + years in a BioPharma operational or development discipline
  • -3 years of experience managing projects and programs

Preferred Qualifications

  • Prior cell therapy development operations experience
  • Broad understanding of biologics or cell therapy commercial manufacturing & analytical processes
  • Technology transfer and/or start-up phase experience

Skills Required

  • Analysis and simplification of complex operational issues
  • Project management execution and expertise in its principles and application
  • Ability to manage multiple projects simultaneously and evaluate priorities
  • Effective escalation and communication with multiple levels up to SVP
  • Conflict resolution
  • Understanding and utilization of concepts regarding the roles of Accountable, Responsible, Advisor & Informed

Benefits & Perks

  • Paid national holidays and optional holidays
  • Global Shutdown Days between Christmas and New Year's holiday
  • Up to 120 hours of paid vacation
  • Up to two (2) paid days to volunteer
  • Sick time off
  • Summer hours flexibility

Locations

  • Devens MA, United States
  • Summit West NJ, United States
  • Bothell WA, United States

Salary

Salary not disclosed

Estimated Salary Rangemedium confidence

150,000 - 220,000 USD / yearly

Source: ai estimated

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • Analysis and simplification of complex operational issuesintermediate
  • Project management execution and expertise in its principles and applicationintermediate
  • Ability to manage multiple projects simultaneously and evaluate prioritiesintermediate
  • Effective escalation and communication with multiple levels up to SVPintermediate
  • Conflict resolutionintermediate
  • Understanding and utilization of concepts regarding the roles of Accountable, Responsible, Advisor & Informedintermediate

Required Qualifications

  • B.S. or B.A. in science and/or engineering (biotechnology, biology, engineering, or related sciences) (experience)
  • -8 years business experience (experience)
  • + years in a BioPharma operational or development discipline (experience)
  • -3 years of experience managing projects and programs (experience)

Preferred Qualifications

  • Prior cell therapy development operations experience (experience)
  • Broad understanding of biologics or cell therapy commercial manufacturing & analytical processes (experience)
  • Technology transfer and/or start-up phase experience (experience)

Responsibilities

  • Develop project plans and own execution from ideation to sustainment or handoff
  • Organize and lead cross-functional workshops and analyses
  • Prepare, coordinate, and lead project communications for peers and senior stakeholders/leadership
  • Drive and track actions, develop and drive detailed plans, identify critical path and timing
  • Hold team members accountable for due dates
  • Develop strong relationships with stakeholders across CTDO to understand root causes and barriers
  • Foster high performance teamwork and maintain strong relationships with operational and functional leadership
  • Identify obstacles, remove them, create options, and escalate as appropriate
  • Utilize standard project management tools and Scrum methodology for tracking and status reporting
  • Support establishment of strong, positive, engaged CTDO culture focusing on safety, engagement, and patient mission

Benefits

  • general: Paid national holidays and optional holidays
  • general: Global Shutdown Days between Christmas and New Year's holiday
  • general: Up to 120 hours of paid vacation
  • general: Up to two (2) paid days to volunteer
  • general: Sick time off
  • general: Summer hours flexibility

Target Your Resume for "Associate Director, Cell Therapy Development Operations Project Lead" , Bristol-Myers Squibb

Get personalized recommendations to optimize your resume specifically for Associate Director, Cell Therapy Development Operations Project Lead. Takes only 15 seconds!

AI-powered keyword optimization
Skills matching & gap analysis
Experience alignment suggestions

Check Your ATS Score for "Associate Director, Cell Therapy Development Operations Project Lead" , Bristol-Myers Squibb

Find out how well your resume matches this job's requirements. Get comprehensive analysis including ATS compatibility, keyword matching, skill gaps, and personalized recommendations.

ATS compatibility check
Keyword optimization analysis
Skill matching & gap identification
Format & readability score

Tags & Categories

PharmaceuticalPharmaceuticalHealthcare

Related Jobs You May Like

No related jobs found at the moment.