Within this role you will be responsible for enabling chemistry manufacturing and controls (CMC) quality and compliance excellence by ensuring Regeneron IOPS maintains effective systems for monitoring, analyzing, presenting, implementing, and influencing global regulatory and industry trends,
Within this role you will be responsible for the management and leadership of the Technical Operations Quality & Compliance function, providing quality and compliance oversight and support to the Facilities, Engineering and Automation departments under the
Within this role you will be responsible for coordination and completion of manufacturing deviations and change controls. As an Associate / Compliance Specialist a typical day might include, but is not limited to, the following: Coordinating and
Within this role you will be responsible for all aspects of the assigned QA Team; provide leadership and support to direct reports; provides QA oversight to ensure that drug substance manufacturing activities are compliant with Quality
We are currently looking to fill an Associate Manager Quality Compliance position on the Quality Assurance Change Control Team. This role works within the QA Change Control Team to primarily facilitate activities and relationships regarding External Manufacturing
Within this role you will be responsible for providing QA oversight and support to manufacturing activities. Performing and leading activities in support of dispositioning product while ensuring compliance with Quality Assurance (QA) policies and procedures, cGMPs,
Within this role you will lead the Global Laboratory Systems team within the Information Technology function and will be responsible for managing the system lifecycle development, maintenance and compliance activities for laboratory software and process control
This position implements policies and procedures to review and approve validation/qualification documentation for equipment, systems, and processes in accordance with regulatory requirements and company manufacturing standards, and oversees a team of Validation Oversight Specialists. As an Associate Manager
In this role you will provide technical support on the manufacturing process and be a key member in the implementation of large-scale commercial manufacturing production program. You will be heavily involved in technical transfer of processes.
Within this role you will be responsible to perform a variety of chemical or biological analyses on raw materials, products, in-process materials, or stability samples in support of the companys quality program. As a Senior QC