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 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 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 Fill Compounder is responsible for compounding raw materials according to Master formulas and standard operating procedures. They must also maintain equipment and work areas in a clean, organized condition while ensuring compliance with Good Manufacturing Practices.
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 · 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-Caradoc
Perform maintenance, troubleshooting, and repair of production machinery and supporting equipment to ensure operational efficiency. Maintain compliance with quality standards, Good Manufacturing Practices, and safety protocols while documenting all maintenance activities.
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.
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 · Windsor
The Lead Production Supervisor is accountable for the efficient running of manufacturing operations to meet safety, quality, and regulatory goals. They are responsible for coaching shift supervisors and hourly employees while tracking SQDC metrics and managing departmental training.
On-site · Strathroy
The Director of Quality is accountable for Commercial Quality Assurance and Quality Control activities at the Zydis Strathroy manufacturing site. This role involves implementing and maintaining the Quality Management System to ensure regulatory compliance and meet customer expectations.
On-site · Windsor
Manage day-to-day environmental, health, and safety functions to ensure regulatory compliance and employee safety. Lead the Joint Health and Safety Committee and support sustainability initiatives such as waste and energy reduction.
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 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 · Windsor
The Quality Assurance Associate performs in-process batch reviews and ensures compliance with cGMPs and Standard Operating Procedures. They also act as a quality representative on shift to resolve issues and provide coaching to production staff.
On-site · Windsor
The Fill Compounder is responsible for compounding raw materials according to Master formulas and standard operating procedures. This includes maintaining clean working areas, preparing equipment, and completing all required GMP documentation.
On-site · Strathroy-Caradoc
The Skilled Trades professional performs reactive and preventative maintenance on production and facility equipment to ensure operational excellence. They are responsible for diagnosing mechanical and control system issues while maintaining documentation in accordance with cGMP and regulatory standards.
On-site · Strathroy-Caradoc
The Quality Assurance Supervisor oversees daily team priorities to ensure compliance with cGMP standards and manages product release timelines. They lead investigations, resolve quality issues, and provide guidance on SOPs while maintaining manufacturing batch documentation.
On-site · Canada
The Skilled Trades professional performs reactive, assigned, and preventative maintenance on production and facility equipment. They are responsible for diagnosing mechanical and control issues while ensuring all work complies with cGMP and safety standards.
