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-Caradoc
The Quality Assurance Associate performs in-process document auditing and product quality checks to ensure compliance with cGMP and standard operating procedures. They also assist in investigating manufacturing deviations and act as the QA representative on shift for decision-making and issue resolution.
On-site · Strathroy
The Quality Assurance Associate will perform in-process document auditing and product quality checks to ensure compliance with cGMP standards. They will also assist in investigating manufacturing issues and act as the QA representative on shift for decision-making and issue resolution.
On-site · Strathroy-Caradoc
The Process Technician is responsible for minimizing equipment downtime and ensuring adherence to safety and quality standards during pharmaceutical manufacturing. They will accurately complete batch manufacturing records and support continuous improvement initiatives to maintain operational efficiency.
On-site · Strathroy
The Process Technician will maintain production schedules and ensure compliance with safety and quality standards while minimizing equipment downtime. They are responsible for accurately completing batch manufacturing records and supporting continuous improvement initiatives within the facility.
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.
On-site · Windsor
The Fill Compounder is responsible for compounding raw materials according to Master formulas and standard operating procedures while ensuring compliance with Good Manufacturing Practices. They must also maintain equipment, prepare preparation rooms, and accurately complete all required batch documentation.
On-site · Windsor
The Material Prep is responsible for dispensing and compounding raw materials according to master formulas and standard operating procedures. They also perform equipment cleaning and disinfection in strict compliance with Good Manufacturing Practices.
On-site · Windsor
The Lead Production Supervisor is responsible for overseeing manufacturing operations to ensure compliance with safety, quality, and regulatory standards. They also lead and coach shift supervisors and staff to meet organizational objectives and operational excellence goals.
On-site · Strathroy-Caradoc
The Warehouse Supervisor will oversee daily warehouse operations including shipping, receiving, inventory management, and site waste programs. They are responsible for ensuring compliance with safety standards, Good Manufacturing Practices, and regulatory requirements while managing staff and documentation.
On-site · Strathroy-Caradoc
The Quality Assurance Supervisor oversees daily quality team priorities and ensures strict compliance with cGMP standards throughout the production process. They are responsible for leading investigations, managing batch releases, and collaborating with functional areas to resolve quality issues.
On-site · Strathroy-Caradoc
The Director of Quality is responsible for overseeing and maintaining the Quality Management Systems at the Zydis Strathroy facility to ensure regulatory and cGMP compliance. This role leads the quality function, manages commercial quality assurance and control activities, and collaborates with operations to drive process improvements.
On-site · Strathroy-Caradoc
The Lab Analyst will coordinate and perform laboratory activities, including the analysis of raw materials, finished products, and stability samples. They are also responsible for maintaining laboratory equipment, ensuring compliance with SOPs and GMPs, and training laboratory personnel.
On-site · Strathroy
The Lab Analyst will coordinate and perform laboratory activities, including the analysis of raw materials, finished products, and stability samples. They are also responsible for maintaining laboratory equipment, ensuring compliance with SOPs and GMPs, and training laboratory personnel.
On-site · Strathroy-Caradoc
The Operations Manager leads strategic and operational execution across production areas including gel preparation, utilities, compounding, and encapsulation. They are responsible for meeting safety, quality, delivery, and cost metrics while fostering a culture of continuous improvement and GMP compliance.
On-site · Strathroy
The Operations Manager leads strategic and operational execution across production areas including gel preparation, utilities, compounding, and encapsulation. They are responsible for meeting safety, quality, delivery, and cost metrics while fostering a culture of continuous improvement and GMP compliance.
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 · Windsor
The Fill Compounder is responsible for compounding raw materials according to Master formulas and standard operating procedures. They must also maintain equipment, prepare rooms for batch processes, and ensure all documentation is completed accurately.
On-site · Strathroy
The Quality Assurance Associate performs in-process document auditing and product quality checks to ensure compliance with cGMP and SOPs. They also assist in investigating manufacturing deviations and provide coaching to production staff on quality standards.
On-site · Strathroy-Caradoc
The Quality Assurance Associate will perform in-process document auditing and product quality checks to ensure compliance with cGMP and SOPs. They will also assist in investigating manufacturing deviations and provide coaching to production staff to maintain high quality standards.
On-site · Strathroy
The Warehouse Supervisor will oversee daily warehouse operations, including shipping, receiving, inventory management, and site waste programs. They are responsible for maintaining regulatory compliance, managing documentation, and ensuring the facility remains in a state of audit readiness.
