John Brennan
About John Brennan
John Brennan is a Quality Assurance Validation professional currently working at Bristol-Myers Squibb in Cruiserath, Dublin, with extensive experience in project management and validation within the pharmaceutical industry.
Company
John Brennan is currently employed at Bristol-Myers Squibb in Cruiserath, Dublin, where he holds the position of Quality Assurance Validation. Bristol-Myers Squibb is a global pharmaceutical company involved in discovering, developing, and delivering innovative medicines.
Previous Positions
Before joining Bristol-Myers Squibb, John Brennan held various positions in several prestigious companies. He worked at Alexion Pharmaceuticals, Inc. as a Validation Engineer for six months in 2015, based in Athlone, Co. Roscommon, Ireland. Prior to that, he was at Intervet International BV, part of Schering-Plough, serving as a Raw Materials Release Officer from 2009 to 2010. John also has significant project management experience from his roles at GSK and SciTech Engineering, among others, demonstrating his extensive background in the pharmaceutical sector.
Educational Background
John Brennan completed his studies at Dublin City University between 1990 and 1994. His education laid a solid foundation for his extensive career in various high-level roles within the pharmaceutical and healthcare industries.
Project Management and Validation Expertise
John Brennan has extensive experience in managing up to 30 validation and continuous improvement projects simultaneously. His diverse project management portfolio includes Validation, Clinical Trial set-up, and Compliance Improvement projects. His expertise extends to audit preparation, training, and professional improvement programs, illustrating his comprehensive skills in maintaining and improving project and operational standards.
Independent Consultant Experience
John Brennan also has a decade of experience working as an independent contractor and consultant. He has provided his expert services to various sectors, including Pharmaceutical, Biotechnological, and Healthcare. His significant involvement in commissioning and qualification projects within the pharmaceutical industry underscores his deep understanding and capability in ensuring compliance and quality standards.