Program Manager II - Program Management
Catalent
Summary
Catalent's Madison, Wisconsin site is a state-of-the-art biologics development and manufacturing facility supporting customers from research through early- and mid-stage clinical production. The approximately 102,700-square-foot GMP facility specializes in mammalian cell line engineering, drug substance biomanufacturing, and biopharmaceutical development, utilizing flexible single-use systems to enable rapid scale-up and customization.
Job description
Position Summary
- Shift: M-F 8am-5pm
- Location: Madison, WI
- 100% Onsite
Catalent's Madison, Wisconsin site is a state-of-the-art biologics development and manufacturing facility supporting customers from research through early- and mid-stage clinical production. The approximately 102,700-square-foot GMP facility specializes in mammalian cell line engineering, drug substance biomanufacturing, and biopharmaceutical development, utilizing flexible single-use systems to enable rapid scale-up and customization.
Role Overview
We have an opportunity for a Program Manager II - Program Management to join our team. This role is responsible for delivering assigned program objectives within agreed time, budget, scope, and quality. The position involves managing cross-functional, multi-site project teams and maintaining open, solution-focused communication with clients. The successful candidate will monitor progress, ensure high-quality deliverables, and drive program success through collaboration and leadership.
Minimum Requirements
- Bachelor of Science in Science or Engineering, or equivalent combination of education and experience required. Advanced degree (Master of Science, Master of Business Administration, Doctor of Philosophy) is preferred.
- Approximately 5+ years of direct experience in project management and/or the pharmaceutical industry.
- Project Management Professional or Project Management certification or coursework preferred.
- Working knowledge of biologics fermentation, cell culture, purification, and analytics preferred.
- Professional experience in a related field such as biologics, biotechnology, or pharmaceuticals preferred.
Requirements
- Bachelor of Science in Science or Engineering, or equivalent combination of education and experience
- Approximately 5+ years of direct experience in project management and/or the pharmaceutical industry
- Project Management Professional or Project Management certification or coursework preferred
- Working knowledge of biologics fermentation, cell culture, purification, and analytics preferred
- Professional experience in biologics, biotechnology, or pharmaceuticals preferred
Benefits
- Paid Time Off
- 8 Paid Holidays
- Medical, Dental & Vision
- Tuition Reimbursement
- Career Growth
- Annual Performance Reviews
Company overview
Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) that serves as a trusted partner to pharmaceutical, biotech, and consumer health companies worldwide. Founded on a legacy dating back to 1933, Catalent has evolved into a comprehensive drug development and delivery leader with over 40 global sites. The company specializes in providing end-to-end solutions spanning oral dose formulations, biologics, specialty products, and clinical supply services. Catalent's expertise includes formulation development, analytical services, commercial manufacturing, and advanced delivery technologies such as Zydis® fast-dissolve tablets and softgel technologies. With over 1,000 active development programs at any given time, the company launches more than 100 new products and line extensions annually and has supported half of all FDA approvals over the past decade. Catalent produces over 60 billion treatment doses per year, helping approximately 200 million patients annually. Headquartered in Tampa, Florida, the company employs more than 10,000 professionals globally who are dedicated to putting patients first and championing the missions that matter in healthcare innovation.