VetJobs
Associate Director, Cell Therapy Dev Operations Project - Summit West
VetJobs, Trenton, New Jersey, United States
Job Description
ATTENTION MILITARY AFFILIATED JOB SEEKERS
– Our organization works with partner companies to source qualified talent for their open roles. This position is available to Veterans, Transitioning Military, National Guard and Reserve Members, Military Spouses, Wounded Warriors, and their Caregivers. If you have the required skill set, education requirements, and experience, please click the submit button and follow the next steps. Unless specifically stated otherwise, this role is "On‑Site" at the location detailed in the job post. Challenging. Meaningful. Life‑changing. Working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, transforming the lives of patients and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high‑achieving teams. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide employees with the resources to pursue their goals, both at work and in their personal lives. Key Responsibilities
Develop project plans and own execution from ideation of solutions through sustainment or handoff to business owners. Organize and lead cross‑functional workshops and analyses to ensure clear vision of desired outcomes and actionable output. Prepare, coordinate and lead project communications for peers, senior stakeholders and leadership. Drive and track actions, develop detailed plans, identify critical path and timing, and hold team members accountable for due dates. Develop strong relationships with stakeholders across CTDO to understand root causes of gaps 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 and 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. Qualifications & Experience
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 and 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 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 and informed through the changing landscape of rapid response activity. If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.
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– Our organization works with partner companies to source qualified talent for their open roles. This position is available to Veterans, Transitioning Military, National Guard and Reserve Members, Military Spouses, Wounded Warriors, and their Caregivers. If you have the required skill set, education requirements, and experience, please click the submit button and follow the next steps. Unless specifically stated otherwise, this role is "On‑Site" at the location detailed in the job post. Challenging. Meaningful. Life‑changing. Working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, transforming the lives of patients and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high‑achieving teams. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide employees with the resources to pursue their goals, both at work and in their personal lives. Key Responsibilities
Develop project plans and own execution from ideation of solutions through sustainment or handoff to business owners. Organize and lead cross‑functional workshops and analyses to ensure clear vision of desired outcomes and actionable output. Prepare, coordinate and lead project communications for peers, senior stakeholders and leadership. Drive and track actions, develop detailed plans, identify critical path and timing, and hold team members accountable for due dates. Develop strong relationships with stakeholders across CTDO to understand root causes of gaps 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 and 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. Qualifications & Experience
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 and 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 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 and informed through the changing landscape of rapid response activity. If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.
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