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 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 · 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 training to production staff.
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 · Windsor
Responsible for installing, maintaining, and repairing electrical systems, HVAC, and control equipment in accordance with Ontario Hydro and CSA standards. The role involves troubleshooting electrical breakdowns and performing equipment set-ups from blueprints in a pharmaceutical manufacturing environment.
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 · 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.
On-site · Windsor
The Production Compliance Associate is responsible for maintaining quality standards and leading quality initiatives within the manufacturing and packaging environment. Key duties include coordinating investigations, implementing CAPA, and ensuring adherence to SOPs and GMPs.
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 · Windsor
The Fill Compounder is responsible for compounding raw materials according to Master formulas and standard operating procedures. This includes maintaining equipment cleanliness, preparing batch processes, and completing all required GMP documentation.
On-site · Windsor
The Electrician is responsible for installing, repairing, and maintaining electrical systems, HVAC, and control equipment in compliance with Ontario Hydro and CSA standards. Key duties include troubleshooting electrical breakdowns and performing equipment set-ups from blueprints and specifications.
On-site · Windsor
The Production Compliance Associate is responsible for implementing and maintaining quality standards within the manufacturing and packaging environment. They lead production investigations, manage CAPA implementation, and ensure compliance with SOPs and GMP regulations.
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 · 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 · Windsor
Accountable for the efficient running of manufacturing operations to meet health, safety, quality, and regulatory objectives. Responsible for leading and coaching shift supervisors and hourly employees while tracking SQDC metrics and managing departmental training.
On-site · Canada
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 · Canada
The coordinator is responsible for receiving, storing, and shipping materials while tracking inventory within the ERP system. They ensure strict compliance with safety policies and Good Manufacturing Practices to support all department material needs.
On-site · Strathroy-Caradoc
The coordinator is responsible for receiving, storing, and shipping materials while tracking inventory within the ERP system. They ensure all warehouse activities comply with safety policies and Good Manufacturing Practices (GMP).
