Paul Rohlwing
About Paul Rohlwing
Paul Rohlwing serves as the Director of Quality at Surmodics, Inc., bringing extensive experience from various leadership roles in the medical device, biotech, and pharmaceutical sectors. His background includes significant positions at Cardiovascular Systems, Inc., Cantel Medical, and PDL Biopharma, where he developed expertise in Quality Systems and operations management.
Current Role at SurModics
Paul Rohlwing serves as the Director of Quality at SurModics, Inc. since 2021. His role involves overseeing quality assurance processes and ensuring compliance with industry standards in the medical device sector. He operates from Eden Prairie, Minnesota, and focuses on maintaining high-quality standards within the organization.
Previous Experience in Quality Management
Prior to his current position, Rohlwing held several significant roles in quality management. He worked at Cantel Medical as Sr. Manager Global Quality Systems for 10 months in 2020 to 2021. He also served as Sr. Manager Business Operations IT at Cardiovascular Systems, Inc. from 2015 to 2020, and as Quality Systems Manager from 2011 to 2013. His experience spans various aspects of quality assurance and compliance in the medical device industry.
Background in the Medical Device and Pharmaceutical Industries
Rohlwing has a diverse background in the medical device, biotech, and pharmaceutical industries. His career includes roles at PDL Biopharma, Genmab, and Aventis Behring, where he gained expertise in validation, quality assurance, and operations. This extensive experience contributes to his strategic leadership capabilities.
Educational Qualifications
Paul Rohlwing studied at Bradley University, where he earned a Bachelor of Science degree in Biology. His educational background provides a strong foundation for his career in quality management and compliance within the medical and pharmaceutical sectors.
Expertise in Quality Systems and Compliance
Rohlwing possesses expertise in Quality Systems, Product Lifecycle Management (PLM), Enterprise Resource Planning (ERP), and Customer Relationship Management (CRM). These skills are critical for managing complex projects and ensuring compliance with regulatory standards in the medical device and pharmaceutical industries.