Manager, Project Management, Cell Therapy Manufacturing

Bristol Myers SquibbBothell, WA
Onsite

About The Position

Bristol Myers Squibb is seeking a Manager, Project Management for their Cell Therapy Manufacturing facility in Bothell, WA. This role is part of the Project Management Organization (PMO) and is responsible for managing the planning and execution of cross-functional projects and workstreams to support manufacturing operations. Projects may include site readiness for new product trials or launches, implementation of new technologies and materials, information system updates, physical plant layout changes, and technical/business process changes. The position collaborates with various site and global stakeholders across manufacturing, quality, supply chain, IT, facilities, and manufacturing science & technology. The role requires an organized approach to project management, adaptability to change, and active involvement in maturing site project management processes, tools, and methodologies.

Requirements

  • Bachelor’s degree in engineering, science, information technology, business, or related field
  • 5 years of relevant business experience including 3 years of demonstrated project experience, preferably in life sciences.
  • Basic knowledge of financial, operational, and business management principles.
  • Proficient in Microsoft Outlook, Teams, Project, Excel, SharePoint, and PowerPoint.
  • Experience applying predictive/waterfall project management processes and methodologies.
  • Self-starter who can drive small to mid-sized projects forward with minimal direction and meet objectives with a high level of accountability.
  • Exceptional organizational and time management skills.
  • Can efficiently manage a high volume of information.
  • Effective verbal, written and presentation skills.
  • Able to navigate across a global matrix organization to achieve results.
  • Analytical problem solving and critical thinking skills.
  • Understands detailed relationships and can assess the impact of new information.
  • Comfortable working in a rapidly changing environment.
  • Able to prioritize across competing demands.
  • A passion for learning and improvement including a desire to advance project management proficiency.
  • A team player who builds positive relationships and contributes to a collaborative project team and PMO work environment.

Nice To Haves

  • Experience working in biopharma, cell therapy, Good Manufacturing Practices, FDA regulated, or other regulated environments is a plus.
  • Smartsheet is beneficial.
  • PMP or CAPM certification a plus.

Responsibilities

  • Lead project planning activities including development of a project schedule.
  • Identify stakeholders and drive conversations to align on clear project requirements, scope, and deliverables.
  • Leverage site and global resources to identify the activities needed to produce the deliverables.
  • Plan and secure resources needed to execute the work.
  • Support the capital asset request and budget management process where applicable.
  • Develop and manage detailed project schedules.
  • Coordinate and track execution of project plan activities and action items to ensure that deliverables are completed on time and in alignment with Quality standards.
  • Plan and manage project team workshops and meetings.
  • Communicate outcomes via meeting notes, risk and issue logs, and action items logs in alignment with site practices.
  • Identify, document, and manage project risks and issues.
  • Lead mitigation planning or escalation as needed.
  • Control changes to scope and timeline in conjunction with project sponsors and governing bodies.
  • Prepare and deliver presentations and project status updates to project team members, leaders, and other stakeholders to ensure ongoing visibility to project plans, status, decisions, risks, and issues.
  • Capture and share project information electronically using online knowledge management tools.
  • Lead planning and management of communications for cutovers to ensure regulatory and cGMP compliance.
  • Manage operational handoff and project closure activities.
  • Promote excellence in project management capabilities through use of PMO best practices, knowledge sharing, innovation, and process improvements.

Benefits

  • Health Coverage: Medical, pharmacy, dental, and vision care.
  • Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).
  • Financial Well-being and Protection: 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.
  • Work-life benefits include: Paid Time Off US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees) Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays
  • Based on eligibility, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.
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