Stuart Campbell

Stuart Campbell

Regulatory Affairs Manager @ Belmont Medical Technologies

About Stuart Campbell

Stuart Campbell is a Regulatory Affairs Manager at Belmont Medical Technologies, where he has worked since 2020. He has extensive experience in regulatory compliance and quality management systems in the medical device and pharmaceutical industries.

Work at Belmont Medical Technologies

Stuart Campbell has served as the Regulatory Affairs Manager at Belmont Medical Technologies since 2020. In this role, he is responsible for conducting regulatory reviews of submitted CE product technical files to ensure compliance with relevant requirements. His position involves navigating the complexities of regulatory standards in the medical device industry, contributing to the company's commitment to quality and compliance.

Previous Experience in Regulatory Affairs

Before joining Belmont Medical Technologies, Stuart Campbell worked at Corning Incorporated as a Regulatory Affairs Manager from 2013 to 2020. His previous roles include serving as a Medical Lead Assessor and certification officer at the National Standards Authority of Ireland from 2006 to 2013. He also held the position of Supervisor QC Microbiology at Wyeth Biotech from 2002 to 2006, and worked as a Senior QC technician at Sigma Aldrich from 1995 to 2002.

Education and Expertise

Stuart Campbell earned a Bachelor of Science (BSc) with honors in Microbiology and Immunology from the University of Paisley, studying from 1992 to 1995. He possesses extensive experience in quality management systems within highly regulated manufacturing facilities, particularly in the medical device, pharmaceutical, and cell culture manufacturing industries. His expertise includes creating and submitting technical documentation for CE Device, EU MDD/MDR, and IVD/IVDR compliance.

Background in Quality Control

Stuart Campbell's career in quality control began at Sigma Aldrich, where he worked as a Senior QC technician for seven years. He then transitioned to Wyeth Biotech, where he supervised the QC Microbiology department. His background in quality control has provided him with a strong foundation in regulatory affairs, particularly in ensuring compliance with industry standards.

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