Catalent · 2 hours ago
Program Manager
Catalent, Inc. is a leading global contract development and manufacturing organization dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers. The Program Manager will lead multiple client Process Development and GMP Manufacturing projects, ensuring programs are delivered on time, within scope, and on budget.
BiotechnologyHealth CareManufacturingPharmaceutical
Responsibilities
Delivers assigned program objectives within agreed time, budget, scope, and quality parameters, applying sound project management principles
Manages cross-functional, multi-site project teams, fostering collaboration and alignment across scientific, operational, and client functions
Oversees overall project scope, budget, and schedule, including tech transfer and other key milestones to ensure timely, high-quality deliverables
Applies strong prioritization and organizational skills to balance multiple, evolving priorities with minimal supervision while maintaining focus on key outcomes
Maintains open, solution-focused communication with clients and internal stakeholders, providing clear updates, progress reports, and issue escalation as needed
Anticipates and troubleshoots issues, developing innovative, flexible solutions as program requirements and scientific data evolve
Builds and maintains strong relationships at all levels of the organization, both internally and externally, fostering trust and resolving conflicts effectively
Leads cross-functional teams without direct authority, promoting accountability, collaboration, and shared ownership of program success
Partners with other program managers to strengthen the overall capabilities, processes, and best practices of the Program Management function
Drives program execution and results by leveraging communication, organization, and leadership skills to overcome challenges and deliver success
Other duties as assigned
Qualification
Required
B.S. in Science or Engineering, or equivalent combination of education and experience required
Minimum of 2 years direct experience in project management within the pharmaceutical, biotechnology, or biopharma industry required
Experience working with Biologics and/or Cell Therapy required
Strong organizational, communication, and analytical skills; proficient in Microsoft Office and SharePoint, with familiarity in project management tools
Demonstrates mathematical reasoning and attention to detail in identifying quality or compliance concerns
Works collaboratively and proactively within cross-functional teams to meet project milestones, effectively addressing challenges, escalating issues, and adapting to a variety of instructions and workflows
Communicates effectively and positively with internal teams, clients, and management at all levels to foster collaboration and strong working relationships
Preferred
Advanced degree (M.S., M.B.A., PhD) is preferred
CDMO experience preferred
Experience with CAR-T and CRISPR human cell cultivation preferred
Professional experience in related fields such as Biologics, Biotechnology, Pharma preferred
Experience with MS Project, Workfront, and Power BI preferred
Benefits
Defined career path and annual performance review and feedback process.
Diverse, inclusive culture.
Potential for career growth on an expanding team.
Cross-functional exposure to other areas within the organization.
152 hours of paid time off annually + 8 paid holidays.
Medical, dental, vision and 401K benefits effective day one of employment.
Tuition Reimbursement.
Company
Catalent
Catalent - Blow-Fill-Seal Sterile CDMO Business is focusing on complex clinical to commercial stage formulation and manufacturing. It is a sub-organization of Catalent Pharma Solutions.
Funding
Current Stage
Late StageTotal Funding
unknown2021-01-06Acquired
Leadership Team
Recent News
2026-01-22
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