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
The Supply Chain Manager will lead warehouse and supply chain operations, including logistics, inventory management, and demand planning. They are responsible for ensuring operational efficiency, managing budgets, and maintaining compliance with cGMP standards.
On-site · Strathroy-Caradoc
The Payroll and HR Coordinator will manage accurate and timely payroll processing while providing administrative support for various Human Resources functions. This role also involves interpreting company policies, assisting with recruitment, and managing employee benefit and disability claims.
On-site · Strathroy-Caradoc
The Production Supervisor will manage daily production objectives and lead a team of hourly employees to ensure efficient, safe, and high-quality pharmaceutical manufacturing. This role involves maintaining strict compliance with GMP and SOPs while driving continuous improvement and resolving operational issues.
On-site · Strathroy-Caradoc
The Quality Assurance Associate will perform in-process document auditing, product quality checks, and final release auditing to ensure compliance with cGMP and standard operating procedures. They will also assist in investigating manufacturing issues and act as a QA representative on shift for decision-making and issue resolution.
On-site · Strathroy-Caradoc
The Director of Quality oversees the planning, implementation, and maintenance of Quality Management Systems at the Zydis Strathroy facility to ensure regulatory and cGMP compliance. This role leads quality functions, manages deviations and CAPA processes, and collaborates with operations to drive systematic process improvements.
On-site · Strathroy-Caradoc
The Lab Analyst coordinates and performs 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 supporting the scientific team.
On-site · Strathroy-Caradoc
The Process Technician will maintain production schedules and ensure equipment availability while upholding strict safety and quality standards. They are responsible for accurately completing batch manufacturing records and supporting continuous improvement initiatives within the facility.
On-site · Strathroy
The Production Supervisor will manage daily production objectives and lead a team of hourly employees to ensure operational efficiency and compliance with GMP standards. They are responsible for troubleshooting production issues, maintaining safety protocols, and driving continuous improvement initiatives within the facility.
On-site · Strathroy-Caradoc
The Quality Management System Specialist maintains quality systems to ensure compliance with Good Manufacturing Practices and regulatory standards. They lead internal audits, manage supplier assessments, and drive continuous improvement initiatives across the facility.
On-site · Strathroy-Caradoc
The Quality Assurance Supervisor oversees daily team priorities and ensures all production processes comply with cGMP standards. They are responsible for managing investigations, approving quality documentation, and collaborating with operations to maintain quality management systems.
On-site · Strathroy
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 quality assurance and control activities while collaborating with operations to drive process improvements and strategic safety leadership.
On-site · Strathroy
The Quality Assurance Associate will perform in-process document auditing, product quality checks, and final release auditing to ensure compliance with cGMP standards. They will also assist in investigating manufacturing deviations and act as the QA representative on shift for issue resolution.
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
The Lab Analyst will perform testing on raw materials, finished products, and stability samples using instrumental and wet chemistry methods. They are also responsible for maintaining laboratory equipment, ensuring compliance with GMP standards, and supporting the scientific team.
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.
