Program Manager

$118,720 - $163,240/Yr

Catalent - Severn, MD

Full-time - Mid Level

Severn, MD

501-1,000 employees

Chemical Manufacturing

About the position

The Program Manager at Catalent is responsible for leading multiple client Process Development and GMP Manufacturing projects within a global, high-growth organization. This role involves managing client contracts, utilizing project management practices, and collaborating with cross-functional teams to ensure project objectives are met efficiently and effectively. The Program Manager will play a crucial role in delivering high-quality services and products to clients in the pharmaceutical industry, contributing to the mission of improving patient lives.

Responsibilities

• Deliver on assigned program objectives within agreed upon time, budget, scope, and quality.
• Apply sound project management practices within assigned projects.
• Prioritize tasks and balance multiple, often changing priorities with minimal supervision.
• Maintain open, collaborative, and solution-focused communication with clients, providing periodic updates and progress reports.
• Monitor progress of assigned programs to ensure on-time milestone and budget completion while ensuring high-quality deliverables.
• Troubleshoot problems with minimal assistance and seek innovative solutions as requirements evolve.
• Develop project management competencies across the company and strengthen support capabilities of Program Management.
• Drive programs and overcome obstacles with minimal supervision.
• Lead cross-functional teams without direct authority and foster collaborative partnerships.
• Interact with and build relationships at many levels of the organization to accomplish objectives.
• Resolve conflicts effectively.

Requirements

• Bachelor's in Science or Engineering required.
• Advanced degree (M.S., M.B.A., PhD) preferred.
• Knowledge and expertise in project management practices.
• Working knowledge of biological sciences and finance.
• Proficient computer skills required including MS Project.
• Three (3) years direct experience in leading projects in a contract development or manufacturing environment required.
• Working knowledge of Biologics Fermentation, Cell Culture, Purification and Analytics preferred.
• Professional experience in a related field such as Biotechnology or Pharma preferred.

Nice-to-haves

• Experience in a contract development or manufacturing environment.
• Knowledge of GMP practices.

Benefits

• Paid holidays
• Health insurance
• Dental insurance
• Tuition reimbursement
• Vision insurance
• 401(k) matching