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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
Posted 28 days ago
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
Posted 29 days ago
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
Posted 29 days ago
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,
Posted 1 month ago
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,
Posted 1 month ago
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
Posted 1 month ago
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
Posted 1 month ago
Newly expanded and growing Pharmaceutical business
Posted 1 month ago
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