Rottendorf Pharma
Marion Bonnemeyer has extensive experience in documentation management and regulatory affairs within the pharmaceutical industry. Currently serving as Process Group Leader for Customer Documentation at Rottendorf Pharma since May 2021, Marion oversees Product Documentation Management and Product Lifecycle Management. Prior to this role, Marion held various managerial positions at Rottendorf Pharma from October 2011 to May 2021, including Manager Documentation and Manager Product Transfer. Marion's career began at STADA as an Assistant in Regulatory Affairs from November 2007 to September 2011, providing a solid foundation in regulatory processes and documentation standards.
Rottendorf Pharma
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A first-class contract development and manufacturing organization (CDMO), Rottendorf Pharma has been manufacturing, packaging, developing formulations and analytical methods for solid oral dosage forms for the global pharmaceutical industry for more than 85 years. The company produces more than 600 originator and generic drug products annually for big, small, virtual, and global pharmaceutical and biotechnology companies. Rottendorf Pharma operates by the philosophy of Total Process Ownership (TPO) and Total Technological Mastering (TTM), in which we work as an extension of clients' organizations. Therefore leveraging our expertise to optimize solid dosage form production for our customers' benefit. Rottendorf Pharma has neither their own product brands in the market nor holds any product licenses, and therefore is never in competition with their clients.