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Supervisor, Bulk Manufacturing
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- Establishes & maintains cooperative cross-functional relationships with peers in Quality, Sterile Operations, Process Development, and Supply Chain to meet plant objectives
- Completes final batch record reviews for Bulk formulation and Drug & Chemical.
- Executes Quality Management System assignments (CAPA, Deviation, Change Control, Standard Operating Procedures etc.)
- Obtains knowledge and executes assignments in QMS areas: deviation management and/or change control.
- Desired – 1-3 years in Pharmaceutical Packaging, Operation or Quality Department
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