Brian Rowan

Brian Rowan has worked in the field of quality assurance and compliance for over a decade. Brian started their career at Organogenesis in 2008 as a QA Compliance Specialist I, where they reviewed device history records and ensured compliance with established procedures and specifications. Brian later became a QA Compliance Specialist II, where they reviewed and released incoming raw materials, components, and packaging materials. Brian was heavily involved in the development and implementation of the company's ERP system, which included customized quality modules for generating labels and electronically releasing raw materials and final products. Brian then advanced to the role of QA Compliance Specialist III, where they performed duties related to QA review, release of incoming raw materials, and played a key role in maintaining the Active Supplier List. In 2012, Brian became a QA Supervisor, overseeing complex quality activities related to final product disposition and raw material disposition. Brian was responsible for supervising and developing direct reports, conducting performance reviews, and participating in high-level quality system programs. In 2015, Brian joined Celldex Therapeutics as a QA Specialist III and progressed to the roles of QA Specialist IV and Senior QA Compliance Specialist. No end dates are provided for their roles at Celldex Therapeutics.

Brian Rowan attended Bridgewater State University from 2000 to 2004, where they earned a Bachelor of Science (BS) degree. The field of study for their degree is not specified. Additionally, Brian Rowan has obtained a certification as a Certified Quality Process Analyst (CQPA) from ASQ, although the specific month and year of obtaining this certification are not provided.