Director, Cell Therapy Development Operations Project Lead at Bristol-Myers Squibb

Seattle, Washington, United States

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Not SpecifiedCompensation

Senior (5 to 8 years), Expert & Leadership (9+ years)Experience Level

Full TimeJob Type

UnknownVisa

Biotechnology, PharmaceuticalsIndustries

Requirements

Strong data management and analytical skills
Experience in process improvement methodologies
Comfort working with and integrating AI and digital tools
Ability to communicate effectively with stakeholders at all levels
Experience analyzing, designing, optimizing, and executing business processes
Ability to work closely with and influence cross-functional senior level CTDO and GPS sponsors, stakeholders, and enabling partners
Ability to lead cross-functional stakeholder teams

Responsibilities

Conduct thorough analysis of existing business processes to identify inefficiencies and areas for improvement
Gather and document detailed business requirements from stakeholders to understand their needs and objectives
Utilize data and process mapping tools to visualize and analyze current processes
Develop and propose optimized business processes that enhance efficiency and effectiveness
Collaborate with cross-functional teams to design and drive implementation of process improvements
Ensure that new processes align with organizational goals and comply with relevant regulations and standards
Collect and analyze data to measure process performance and identify trends and patterns
Develop and maintain performance metrics and KPIs to track the success of process improvement initiatives
Support change management efforts to ensure successful adoption of new processes and systems
Develop and execute communication plans to engage and inform stakeholders about process changes
Provide training and support to teams to facilitate smooth transitions and ensure sustained improvements
Create and maintain comprehensive documentation of business processes, including process maps, workflows, and standard operating procedures (SOPs)
Generate regular reports on process performance, improvement initiatives, and project status
Present findings and recommendations to senior leadership and other stakeholders
Stay current with industry trends and best practices in process improvement methodologies
Serve as the single point of contact and accountability for processes, including how work gets done, performance, optimization efforts, and adoption of changes
In conjunction with the Executive Director, CTDO Chief of Staff, support improved visibility, agility, performance, and scalability while minimizing compliance risks through digitization and automation

Skills

Key technologies and capabilities for this role

Process OptimizationBusiness Process DesignProcess SimplificationStandardizationPerformance MonitoringDigitizationAutomationCross-Functional LeadershipStakeholder ManagementProject ManagementCell Therapy Operations

Questions & Answers

Common questions about this position

What benefits does Bristol Myers Squibb offer?

Bristol Myers Squibb offers a wide variety of competitive benefits, services, and programs that provide employees with resources to pursue their goals both at work and in their personal lives.

Is this a remote position or does it require office work?

This information is not specified in the job description.

What salary or compensation is offered for this role?

This information is not specified in the job description.

What key skills are required for the Director, Cell Therapy Development Operations Project Lead role?

The role requires strong data management and analytical skills, experience in process improvement methodologies, comfort working with and integrating AI and digital tools, and the ability to communicate effectively with stakeholders at all levels.

What is the company culture like at Bristol Myers Squibb?

The culture is challenging, meaningful, and life-changing, with uniquely interesting work, opportunities to grow and thrive alongside high-achieving teams, and a focus on balance and flexibility.

Bristol-Myers Squibb

Develops and delivers biopharmaceutical medicines

About Bristol-Myers Squibb

Bristol Myers Squibb (BMS) develops and delivers medicines aimed at treating serious diseases, focusing on areas like cancer, autoimmune diseases, and heart conditions. The company conducts extensive research and development to create new drugs, which are sold after receiving regulatory approval. BMS also produces generic drugs, offering affordable alternatives that meet the same quality standards as their branded counterparts. What sets BMS apart from competitors is its dual focus on both innovative and generic medicines, enhancing access to healthcare. The company's goal is to improve patient outcomes while maintaining a commitment to sustainability and corporate responsibility.

New York City, New YorkHeadquarters

1887Year Founded

$33,706.1MTotal Funding

IPOCompany Stage

Biotechnology, HealthcareIndustries

10,001+Employees

Benefits

Flexible Work Hours

Hybrid Work Options

Professional Development Budget

Risks

Increased competition in oncology from emerging biotech firms like ArsenalBio.

BMS's lawsuit over the 340B Drug Pricing Program may lead to regulatory challenges.

Rapid AI and digital tech evolution may pose integration challenges for BMS.

Differentiation

BMS focuses on innovative cancer treatments through collaborations like ArsenalBio for T cell therapies.

The company emphasizes digital health technologies, enhancing clinical trial management and patient engagement.

BMS offers both innovative and generic medicines, increasing affordable healthcare solutions.

Upsides

BMS's partnership with Medidata enhances clinical research processes and patient outcomes.

The collaboration with AI Proteins advances novel miniprotein-based therapeutics, expanding therapeutic modalities.

BMS's global license agreement with BioArctic expands its portfolio in neurodegenerative diseases.

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