Associate Director, Cell Therapy Development Operations Project Lead 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, PharmaceuticalsIndustries

Requirements

B.S. or B.A. in science and/or engineering (biotechnology, biology, engineering, or related sciences)
Prior cell therapy development operations experience strongly preferred
5-8 years business experience, with 5+ years in a BioPharma operational or development discipline
Demonstrated 2-3 years of experience managing projects and programs
Demonstrated leadership & 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 its principles and application, the ability to manage multiple projects simultaneously and evaluation of priorities
Effective escalation & communication with multiple levels up to SVP
Conflict resolution
Understanding and utilization of concepts regarding the roles of - Accountable, responsible, advisor & informed through the changing landscape of rapid response activity

Responsibilities

Development of project plans and ownership of execution from ideation of solutions, endorsement of project strategy, through sustainment or handoff to business owners
Organization and leadership of cross-functional workshops and analyses to ensure clear vision of desired outcomes, actionable output and clear, balanced decision making
Prepare, co-ordinate and lead project communications for peers, senior stakeholders / leadership
Drive and track actions, develop and drive detailed plans, identify critical path and timing, hold team members accountable for due dates
Develop strong relationships with stakeholders across CTDO to understand root causes of gaps in 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 & 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

Skills

Key technologies and capabilities for this role

Project ManagementCross-Functional LeadershipStakeholder ManagementProject PlanningRisk ManagementTeam LeadershipProblem SolvingWorkshop FacilitationAction TrackingCell Therapy Operations

Questions & Answers

Common questions about this position

What qualifications and experience are required for this role?

Candidates need a B.S. or B.A. in science and/or engineering (biotechnology, biology, engineering, or related sciences), prior cell therapy development operations experience strongly preferred, 5-8 years business experience with 5+ years in BioPharma operational or development discipline, and 2-3 years managing projects and programs.

Is this a full-time position?

Yes, this is a full-time employment opportunity.

What is the salary range for this position?

This information is not specified in the job description.

What does the company culture at Bristol Myers Squibb emphasize?

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

What makes a strong candidate for this Associate Director role?

Strong candidates have demonstrated leadership and collaboration in BioPharma operations, especially with Supply Chain and GMP Manufacturing, plus experience using project management tools and Scrum methodology.

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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