Will Blackie

Will Blackie is an accomplished professional currently serving as the Director of External Quality for Systems and Process Improvement in the Pharma Supply Chain division of GSK in Europe.

With a rich and varied professional background, Will has held several key roles such as Head of External Supply Quality for AsiaPac & Middle East/Africa, AsiaPac Quality Project Manager, and global Compliance positions within GSK.

His expertise spans across Process Improvement, Regulatory Compliance in areas like Medicinals, devices, and cosmetics, Compliant process engineering design, Lean Manufacturing & 6-Sigma, GMP knowledge, Medical Device certification (ISO 13485), and more.

Education-wise, Will has pursued studies in various fields including B.Technology in Biotechnology and General Management Certificate from the University of Cambridge, showcasing his commitment to continuous learning and professional development.

Throughout his career, Will Blackie has demonstrated strong skills in Supply Chain management, GMP & ISO Auditing, Business Continuity & Crisis Management Planning, and Global Risk Management, making him a valuable asset in the pharmaceutical industry.

His organizational affiliations include key positions at GSK such as the Head of External Supply Quality, Compliance Manager, Validation Manager, and roles in various capacities at other organizations like IRL BioPharm and CSL (NZ) Ltd.

Will's extensive experience in Quality Management Systems, process optimization, and regulatory standards sets him apart as a knowledgeable and skilled professional in the pharmaceutical and healthcare sectors.

With a foundation in Lean Manufacturing and Six Sigma methodologies, coupled with his hands-on experience in engineering roles and global assignments, Will Blackie brings a unique perspective to quality assurance and process enhancement within the industry.