Supervisor: QC Supervisor Duties: · Performs routine sampling, analysis and documentation of pharmaceutical samples – raw materials, intermediates, drug products, package materials* · Accurately weighs samples and prepares volumetric solutions* · Performs analytical tests: titration, conductivity, pH, residuals on ignition, specific gravity, loss on drying, etc.* · Generates experimental data according to written SOP, protocol, method, or work instructions* · Follows guidelines when recording
Aurora PharmaceuticalReports to: Regulatory Affairs Director Purpose: The Regulatory Affairs Specialist works with the Regulatory Affairs Director and Quality Department with maintaining controlled documents and creating regulatory submissions in compliance with regulatory standards and guidelines. The Regulatory Affairs Specialist participates in communication with regulatory agencies. Duties and Responsibilities: (*Denotes essential job functions.) · Creates and maintains regulatory timelines and tracks
Aurora PharmaceuticalSupervisor: Production Manager Position Purpose: Manufactures pharmaceutical products according to SOPs, GMP and batch record specifications. Performs the day to day activities of the production process including weighing, blending, filling and packaging products. Collaborates with other production staff and other departments. Job Responsibilities (Essential job functions noted * · Works all areas of production operation: weighing, blending, filling, packaging, cleaning* o Accurately weighs
Aurora Pharmaceutical
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