Catalent, Inc. is a global leader in contract development and manufacturing, dedicated to advancing healthcare by providing innovative solutions for pharmaceuticals, biotechs, and consumer health markets.
Tampa, Florida
Championing the missions that matter™. Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) and trusted partner to pharma, biotech, and consumer health companies worldwide. We put patients first in everything we do, helping people live better and healthier lives through every product we help develop, manufacture and deliver. With over 1,000 active development programs at any given time, we launch over 100 new products and line extensions annually. Catalent has supported half of all FDA approvals over the past decade, and our teams working at over 40 global sites help us produce over 60 billion doses every year. Our strength lies in our people: teams across our more than 40 sites and thousands of passionate scientists and technicians who bring expertise in development sciences, delivery technologies, and multi-modality manufacturing. What unites us is our commitment to championing our partners’ missions as our own, anticipating customer needs, solving complex challenges and ultimately making a difference in the lives of patients across the globe. At Catalent, you will be able to directly have an impact, solving problems and ensuring excellence for our customers. Our focus on delivering meaningful outcomes alongside our customers means your work directly impacts millions of people around the world. Join us in championing the missions that matter. Catalent is headquartered in Tampa, Florida, with over 40 global sites. Visit www.catalent.com to learn more.
On-site · Strathroy
Lead end-to-end project planning and execution for complex, cross-functional business projects within a cGMP-regulated environment. Manage site capital expenditure budgets, timelines, and stakeholder expectations while ensuring compliance with regulatory and quality standards.
On-site · Strathroy-Caradoc
The Project Manager will lead end-to-end planning and execution for complex, cross-functional projects within a cGMP-regulated pharmaceutical environment. Responsibilities include managing timelines, budgets, and resources while ensuring compliance with regulatory standards and driving project milestones.