Grace Linton

Grace Linton, AIA, LEEP AP BD+C is a Director of Process Architecture, SME, and Associate at CRB. She has delivered projects in North America, Europe, and Asia, covering a wide range of facility types, including monoclonal antibodies, vaccines, blood fractionation, active pharmaceutical ingredients, oral solid dosage, medical devices, fill finish, oligonucleotides and cell and gene therapies. As a lead process architect for designing Current Good Manufacturing Practice (CGMP) biopharmaceutical facilities, Grace is responsible for integrating the client’s business goals and programming criteria, regulatory requirements and building codes and standards into a cohesive facility concept. Grace is a contributing member of BioPhorum and ISPE, and served as a chapter lead for ISPE’s Baseline Guide Volume 6: Biopharmaceutical Manufacturing Facilities, 3rd Edition.