The Packaging Operator III will be responsible for assembling, operating and monitoring state of the art, inspection and packaging machines in accordance with applicable Standard Operating Procedures and current Good Manufacturing Practices. This position requires extensive amounts of leadership, decision making and coordination with coworkers as subject matter expert. Th

POSITION SUMMARY Aseptic Control Operators are responsible for the cleaning, changeover, setup, startup, operation, and breakdown of production lines. Additionally, they may be assigned tasks related to the general upkeep of the area, such as unloading ovens and sterilizers, performing routine cleaning, and performing minor maintenance. All of these activities are governe

The Packaging Operator III will be responsible for assembling, operating and monitoring state of the art, inspection and packaging machines in accordance with applicable Standard Operating Procedures and current Good Manufacturing Practices. This position requires extensive amounts of leadership, decision making and coordination with coworkers as subject matter expert. Th

The Packaging Operator III will be responsible for assembling, operating and monitoring state of the art, inspection and packaging machines in accordance with applicable Standard Operating Procedures and current Good Manufacturing Practices. This position requires extensive amounts of leadership, decision making and coordination with coworkers as subject matter expert. Th

POSITION SUMMARY Primary Quality Owner of all plant facilities and equipment (critical systems) and associated processes, as well as the quality processes that govern them. Responsible for developing, evaluating, and ensuring compliance and efficient approval of Preventative Maintenance, Metrology, Validation and Qualification activities for all critical systems. Drives t

Responsible for supervising and coordinating the activities of employees engaging in component preparation, filling, capping, autoclaving, terminal sterilization, compounding, and lyophilization production. Ensures the proper systems and resources are in place to meet production schedules on time and that product is manufactured to specification and in accordance with SOP

Responsible for visually inspecting filled product off the filling line following Standard Operating Procedures (SOP) and current Good Manufacturing Processes (cGMP). The production inspector will work in the Capping Department and on the off line inspection area and therefore must be knowledgeable of procedures and equipment in each area. Responsibilities Visually inspec

We hire you at an Entry Level and you advance by demonstrating growing skill levels of operating and maintaining production equipment. Within one year, you will be able to fully operate state of the art equipment through advanced HMI interfaces. For those individuals with Team Leader/Supervisor experience, we offer opportunities to become a technical expert and lead our o

POSITION SUMMARY Performs routine audits of manufacturing areas to ensure product quality and SOP/GMP compliance at the Wilson Manufacturing Facility. Assists in troubleshooting manufacturing problems and inspection defects. Provides plant support for collection of data where needed, while assembling required metrics for review by facility management. Updates controlled d

Responsible for assisting the Cleaning Validation Leader and/ or Supervisor in the coordination of the overall Cleaning Validation Policy from a site and corporate perspective to insure compliance. Performs cleaning validation chemical and sampling/testing as required. This position reports directly to the Cleaning Validation Supervisor or Manager of Product Transfer and

POSITION SUMMARY The Master Technician provides direct engineering and maintenance support for facility and utility processes and equipment to support the manufacturing of pharmaceutical products in a cGMP compliant manner. He/She will collaborate with multiple site functions to implement new equipment and processes. Responsible for repairs, troubleshooting, calibration,

POSITION SUMMARY The Master Technician provides direct engineering and maintenance support for facility and utility processes and equipment to support the manufacturing of pharmaceutical products in a cGMP compliant manner. He/She will collaborate with multiple site functions to implement new equipment and processes. Responsible for repairs, troubleshooting, calibration,

The Project Management Intern will gain experience in a cross functional, matrix environment and be exposed to the project lifecycle including pre evaluation/selection, project initiation, planning, execution, monitoring and controlling, and closing projects. Project types range from strategic to technical and may include new product introductions or continuous improvemen

Responsible for visually inspecting filled product off the filling line following Standard Operating Procedures (SOP) and current Good Manufacturing Processes (cGMP). The production inspector will work in the Capping Department and on the off line inspection area and therefore must be knowledgeable of procedures and equipment in each area Responsibilities Visually inspect

This position will manage implementation of projects related to the manufacturing of terminal sterilized pharmaceutical bags. Will ensure inclusion of existing site operation, facility and engineering team members in the learning and design process for those new systems. This position is responsible for providing process analysis, actively seeks and executes process impro