Pfanstiehl, Inc.
Paul S. is an experienced Quality Assurance professional currently serving as QA Manager at Pfanstiehl, Inc. since April 2022. Prior roles include Senior Quality Assurance Manager at Pinnacle Biologics, Inc., where Paul re-developed the Quality Management System Standard Operating Procedures, and Senior Quality Assurance Auditor at Teva Pharmaceuticals, leading global projects to manage vendor compliance and participate in various quality improvement initiatives. Additional experience includes positions at Fresenius Kabi, Hospira, and Deloitte & Touche, where Paul specialized in compliance audits and quality management within the pharmaceutical and healthcare sectors. Paul holds a Bachelor of Science degree in Biology from Elmhurst University.
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Pfanstiehl, Inc.
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Founded in 1919 by Carl A. Pfanstiehl, our company specializes in isolation, purification, custom synthesis and scale-up development of cGMP, high purity and low endotoxin (HPLE) Injectable Formulation Components, Pharmaceutical Intermediates and Active Pharmaceutical Ingredients (API’s), in gram to multi-ton commercial quantities. Tried and true parenteral excipients include trehalose, sucrose, mannitol, maltose, sorbitol, and hydroxypropyl betacyclodextrin. Upstream, high purity media components include animal component free galactose, mannose, and L-arginine. At Pfanstiehl we pride ourselves on being customer focused and are amenable to producing cGMP components on a custom basis to solve formulation challenges for our clients.