Senior Manager, Project Management, Cell Therapy at Bristol-Myers Squibb

Devens, Massachusetts, United States

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Not SpecifiedCompensation

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

Full TimeJob Type

UnknownVisa

Biotechnology, Pharmaceuticals, Cell TherapyIndustries

Requirements

Ability to lead cross-functional projects and programs at a manufacturing site in cell therapy
Experience managing high complexity projects such as site readiness for new launches, new technologies/materials implementation, information system updates/migrations, plant capability changes, and technical/business process changes
Capability to collaborate with site and global stakeholders across manufacturing, quality, supply chain, IT, facilities, manufacturing science & technology, and other areas
Organized approach to project planning and execution of complex changes in a dynamic environment
Ability to provide structure while adapting quickly to change and advancing project teams
Involvement in maturing site project and portfolio management processes, tools, and methodologies
Reporting through the site’s PMO team

Responsibilities

Manage multiple, high complexity, cross-functional process improvement and/or Technical Commercialization projects and/or programs
Lead project planning, including development of the approach, planning activities, and planning schedule
Identify stakeholders and drive conversations to align on clear project requirements, scope, and deliverables
Ensure project goals and benefit Key Performance Indicators (KPIs) are clearly defined and aligned with site’s strategic objectives; hold team accountable to measure project impact & value delivered once completed
Leverage site and global resources to identify the activities needed to produce the deliverables
Plan and secure resources needed to execute the work; maintain accurate project resource allocations and advise organization of constraints
Develop and maintain project budget and regular reporting (in conjunction with finance and project engineering)
Develop and manage detailed project schedules; coordinate and track execution of project plan activities and action items to ensure deliverables are completed on time and in alignment with Quality standards
Lead the development of integrated timelines, ensuring alignment with Global Project timelines
Develop critical path analyses to understand risks and opportunities within project timelines
Plan and manage project team workshops and meetings; communicate outcomes via meeting

Skills

Key technologies and capabilities for this role

Project ManagementCross-Functional LeadershipCell TherapyManufacturingSite ReadinessTechnology ImplementationSupply ChainInformation SystemsProcess ChangesStakeholder CollaborationQuality AssuranceFacilities Management

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 on-site work?

This information is not specified in the job description.

What are the key responsibilities of this role?

The role involves managing multiple high-complexity cross-functional process improvement and Technical Commercialization projects, leading project planning including approach, activities, and schedule, identifying stakeholders to align on requirements, scope, and deliverables, and ensuring project goals and benefits.

What is the company culture like at Bristol Myers Squibb?

The culture is challenging, meaningful, and life-changing, with uniquely interesting work in cell therapy alongside high-achieving teams, emphasizing balance, flexibility, growth opportunities, and a commitment to transforming patients' lives.

What shifts are available for this position?

Shifts available are Monday through Friday during standard working hours.

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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