Jerry Guillorn is a Partner with Validant, based in the Mid-Atlantic region.
A results oriented professional with over 30 years of progressively increasing responsibilities providing consulting and professional services to the Life Science Industry, Jerry has successfully supported Biotech, Pharmaceutical, Start-up/Early Phase and CDMO organizations by providing targeted solutions to achieve or exceed their Quality, Compliance, Regulatory, Operations, Project Management and Capital Project initiatives. He is experienced in delivering results locally, regionally, nationally and globally, either through program, project or individual contributor solutions as appropriate to the scope of the situation and solution.
Prior to joining Validant, Jerry was Group Vice President with Tunnell Consulting’s Life Science Business Unit, where he held several senior leadership responsibilities. He and his technical teams provided a wide variety of support to their clients in achieving their Quality, Compliance, Regulatory and OPEX initiatives. This support included projects for PAI readiness, product launch strategy and implementation, Quality systems assessments and revisions, deviation and CAPA support (project and individual SME support), due diligence and audits, to mention a few. Jerry and his team also provided individual SME support for Regulatory submissions, interim management roles, PIP, Project Management, training roles, as well as numerous Quality and OPEX supporting roles.
Rounding out his Life Science experience, Jerry led Business Development teams providing professional services to achieve capital project objectives locally, nationally and globally. Projects included GMP small molecule, vaccine, biotech and cell therapy manufacturing and GxP R&D facilities, as well as logistic and administrative buildings.