Launch Manager

Bristol-Myers Squibb Co; Seattle (WA); On-site; USD 118,000 - 143,000; Full time

Benefits offered by this job

Flexible Time Off (FTO)

11 paid company holidays

Paid vacation

Job summary

Bristol Myers Squibb is seeking a Launch Project/Program Manager to coordinate cross-functional activities and support manufacturing readiness for commercial and clinical launches in the Seattle area.

The role focuses on developing launch plans, tracking milestones, and communicating status to leadership, while mitigating risks and ensuring alignment with quality and regulatory requirements. Collaboration with the Launch and Lifecycle Management Excellence Team is essential.

Qualifications

• Bachelor's degree in supply chain, engineering, life sciences, business, or related field.
• 2-4 years of project or program management experience.
• Strong organizational, written and verbal communication, meeting facilitation, and relationship-building skills.
• Demonstrated experience coordinating complex projects, launches, technology transfers, or lifecycle transitions; cell therapy is preferred.
• Proficiency in project management tools; experience with OnePlan Portfolio Management and SmartLaunch is a plus.
• Working knowledge of the pharmaceutical product lifecycle and experience operating within a regulated environment.
• Project management training or certification is preferred.

Responsibilities

• Coordinate cross-functional activities to support manufacturing readiness timelines for launches.
• Develop, maintain, and track launch plans with milestones, deliverables, dependencies, and actions.
• Prepare and communicate timely project status, decisions, issues, and risks to stakeholders.
• Identify, assess, document, and elevate launch risks and issues; support mitigation planning.
• Initiate and coordinate global launch change control in the quality system; ensure documentation is complete.
• Support operational excellence by applying launch processes, tools, templates, and best practices.
• Support change management and adoption of new launch processes, tools, and systems.
• Document lessons learned and contribute to improvements for future launches.
• Provide backup coverage for launch activities and knowledge sharing within the team.

Skills

Organizational skills

Communication skills

Meeting facilitation

Relationship-building

Project management tools

Education

Bachelor's degree in supply chain, engineering, life sciences, business, or related field

Tools

OnePlan Portfolio Management

SmartLaunch

Job description

At Bristol Myers Squibb, our employees often ask, \"Who are you working for?\"-a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it.

Key Responsibilities

• Coordinate cross-functional activities to support manufacturing readiness timelines for assigned commercial and clinical launches
• Develop, maintain, and track detailed launch plans, milestones, deliverables, dependencies, and action items utilizing SmartLaunch Plan and facilitate effective meetings with clear agendas, pre-reads, meeting minutes, decisions, and follow-up actions
• Prepare and communicate timely project status, updates, decisions, issues, and risks to stakeholders and leadership
• Identify, assess, document, and elevate launch risks and issues; support mitigation planning while maintaining alignment with schedule and quality/regulatory requirements
• Initiate and coordinate the global launch change control in the BMS quality system, ensuring actions and supporting documentation are completed on schedule
• Support operational excellence by applying standard launch processes, tools, templates, and best practices across assigned launches
• Support change management and adoption of new launch processes, tools, and systems
• Document lessons learned and contribute to the development and implementation of improvements for future launches
• Provide backup coverage for launch activities and support onboarding and knowledge sharing within the Launch and Lifecycle Management Excellence Team

Qualifications & Experience

• Bachelor's degree in supply chain, engineering, life sciences, business, or a related field is required; advanced degree is a plus
• 2-4 years of project or program management experience, preferably supporting complex cross-functional or matrix teams
• Strong organizational, written and verbal communication, meeting facilitation, and relationship-building skills
• Demonstrated experience coordinating complex projects, launches, technology transfers, or lifecycle transitions; experience within Cell Therapy is preferred
• Proficiency in project management tools; experience with OnePlan Portfolio Management and SmartLaunch is a plus
• Working knowledge of the pharmaceutical product lifecycle and experience operating within a regulated environment
• Strong analytical, problem-solving, and critical-thinking skills, with the ability to manage priorities, work independently, and take initiative
• Project management training or certification is preferred

Compensation Overview

Devens - MA - US: $114,880 - $139,205Madison - Giralda - NJ - US: $107,360 - $130,099New Brunswick - NJ - US: $107,360 - $130,099Princeton - NJ - US: $107,360 - $130,099Seattle - WA: $118,100 - $143,108

The starting pay range(s) listed above is for full-time employees (FTE). You may also be eligible for additional discretionary incentive cash and stock opportunities. We determine starting pay thoughtfully - carefully considering the nature of the role, required skills, work location, schedule and the knowledge and experience you bring. Final compensation is guided by pay equity principles and applicable employment laws. Compensation programs are reviewed on an ongoing basis and may be adjusted over time to reflect evolving market factors, and individual, team or Company performance.

Benefits

Subject to the terms and conditions of the applicable plans then in effect, you may be eligible to participate in our comprehensive benefit plans - including wellbeing support, retirement and financial protection benefits, and insurance offerings (medical, dental, vision, life and disability). U.S.-based exempt employees are eligible for Flexible Time Off (FTO), which provides paid time off without a set accrual limit, subject to manager approval, along with 11 paid company holidays each year. Non-exempt employees, RayzeBio employees, and employees located in Puerto Rico receive 160 hours of paid vacation annually for new hires (subject to manager approval), 11 paid company holidays, and 3 optional holidays. Depending on eligibility, employees may also have access to additional time-off benefits, including paid sick leave, up to two paid volunteer days per year, summer hours flexibility, and leaves of absence for medical, personal, parental, caregiver, bereavement, or military needs. Eligible employees also enjoy an annual Global Shutdown between Christmas Day and New Year's Day. U.S.-based job seekers can explore full benefit offerings at https://careers.bms.com/benefits

How We Work

Way you work matters - because collaboration, innovation and patient impact happen in many settings. Our roles are structured across four work models: site-essential, site-by-design, field-based and remote-by-design. The model assigned to this role is based on its core responsibilities. Learn more at https://careers.bms.com/ways-of-working.

Supporting People with Disabilities

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to [e-mail]. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

Candidate Rights

BMS will consider qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. For roles based in Los Angeles County only: If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/

Data Protection

We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection. Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

We’re creating innovative medicines for patients fighting serious diseases. We’re also nurturing our own diverse team with inspiring work and challenging career options. No matter the role, each one of us makes a contribution. And that makes all the difference.