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Catalent

Global contract drug formulation, manufacturing, packaging

Project Coordinator

Project ManagementPosted on Nov 6
Full-timeManassas, VA, USANo salary listed

About the Job

Requirements

  • A bachelor's degree in Science, Engineering, Business, Project Management, or a related discipline is required; equivalent relevant education and experience may be considered.
  • Experience in project coordination, project administration, operations support, product development, commercialization, or a related environment is required.
  • The role requires regular communication, computer work, sitting, and use of hands and fingers, with occasional standing, walking, reaching, bending, or movement through office, manufacturing, laboratory, and warehouse areas.

Responsibilities

  • Coordinate projects of varying size and complexity from initiation through closeout under the direction of the Project Management team.
  • Create and maintain project plans, schedules, milestone trackers, action logs, decision logs, and other project documentation.
  • Coordinate meetings, prepare agendas and pre-reads, capture decisions and actions, and follow up with owners to support timely completion.
  • Monitor project progress, dependencies, resource needs, and deliverables, and promptly escalate issues or delays.
  • Support project intake, prioritization, governance reviews, stage-gate activities, and project closeout as applicable.
  • Coordinate with Manassas Product Development, Operations, Quality, Regulatory, Supply Chain, Procurement, Engineering, Packaging, Commercial, Finance, and Customer Service teams to advance project deliverables.
  • Partner with site and functional teams, including Operations, Quality, Research and Development, Supply Chain, Procurement, Engineering, Packaging, Regulatory, Commercial, Finance, and other stakeholders as required.
  • Coordinate information and deliverables across Manassas functions and, where required, other Catalent Wellness sites to maintain alignment with project scope, timelines, and business objectives.
  • Support soft chew and lozenge development programs, product launches, reformulations, post-launch changes, packaging and artwork implementation, commercial-readiness activities, and other Manassas portfolio initiatives.
  • Build effective working relationships with internal stakeholders, customers, suppliers, contractors, and consultants, where applicable.
  • Maintain accurate project status, milestone, risk, issue, scope, and change-control information in approved systems and tools.
  • Prepare clear, concise project updates and dashboards for project teams, site leadership, and governance forums.
  • Support tracking of project costs, forecasts, purchase orders, resource requirements, and portfolio data as assigned.
  • Support proactive identification of risks, issues, scope changes, and schedule impacts, and recommend mitigation or contingency actions with the Project Manager and project team.
  • Capture lessons learned and support consistent application and continuous improvement of project management standards, templates, and reporting practices.
  • Perform responsibilities in accordance with company policies, Manassas site procedures, applicable food-safety and quality systems, current Good Manufacturing Practice requirements for dietary supplements, and Environmental Health and Safety standards.
  • Ensure project documentation is complete, current, controlled, and retained in accordance with established requirements.
  • Support audits, inspections, governance reviews, and project documentation requests as needed.
  • Communicate improvement opportunities constructively and contribute to a culture of accountability, collaboration, and continuous improvement.
  • Perform other related duties as assigned.

Desired Qualifications

  • Project management education or certification.
  • Experience in consumer health, dietary supplements, food, pharmaceutical manufacturing, or another regulated environment.
  • Familiarity with current Good Manufacturing Practice manufacturing, food-safety and quality systems, change control, and continuous improvement.
  • Proficiency with Microsoft 365 applications or project management-related tools.

About the Company

Catalent

Global contract drug formulation, manufacturing, packaging

Catalent provides end-to-end contract development and manufacturing services for pharmaceutical, biotechnology, and consumer health products. Its offerings cover drug formulation, large-scale manufacturing, clinical supply, and packaging under long-term partnerships, coordinating through a connected supply chain to move products from development to market. It differentiates itself with a broad, integrated service platform and long-standing customer relationships that help clients accelerate development and ensure reliable supply. The company aims to help clients bring products to market efficiently while balancing quality, cost, and sustainability across the product lifecycle.

Company size
5,001-10,000
Company stage
IPO
Headquarters
Franklin Township, NJ
Founded
1996

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