Sean Wolohan
About Sean Wolohan
Sean Wolohan is a Manufacturing Technology Scientist/Engineer at Bristol Myers Squibb in Dublin with extensive experience in GMP, clinical trials, and molecular biology.
Current Role at Bristol Myers Squibb
Sean Wolohan is currently working as a Manufacturing Technology Scientist/Engineer at Bristol Myers Squibb in Dublin, County Dublin, Ireland. He began his role in December 2020. His responsibilities likely include ensuring compliance with Good Manufacturing Practice (GMP), clinical trials support, and molecular biology tasks. Sean's role involves leveraging his extensive experience in validation processes to maintain high standards in pharmaceutical manufacturing.
Past Experience at STEMCELL Technologies
From 2019 to 2020, Sean Wolohan worked at STEMCELL Technologies in Vancouver as a Process Development Associate. During his one-year tenure, Sean was involved in the development and optimization of manufacturing processes. His role likely included working on molecular biology projects and ensuring the effectiveness of various clinical trials processes.
Operational Role at Pfizer
Sean Wolohan held the role of Operation Technical Support Specialist at Pfizer in Grange Castle from 2015 to 2019. Over his four-year career at Pfizer, Sean gained valuable experience in the pharmaceuticals industry, particularly in GMP practices and validation processes. His responsibilities likely involved support for operations, ensuring compliance, and contributing to the effectiveness of pharmaceutical manufacturing processes.
Short Tenure at Amgen
In 2013, Sean Wolohan worked as a Quality Control Associate at Amgen in Dublin for a two-month period. This brief experience would have given Sean insight into quality control processes within a major biotech company, adding to his comprehensive understanding of GMP and validation within the life sciences sector.
Educational Background at University College Dublin
Sean Wolohan studied at University College Dublin and graduated with a Bachelor of Science (BSc) in Biology - Genetics. He attended from 2011 to 2015. During his four years of university education, Sean developed a strong foundation in Genetics, further bolstering his expertise in molecular biology and clinical trials, which are crucial for his roles in the pharmaceuticals and life sciences fields.
Expertise in GMP and Validation Processes
Sean Wolohan possesses extensive experience in Good Manufacturing Practice (GMP) within the pharmaceuticals industry. Sean's expertise also includes strong skills in clinical trials and molecular biology. His robust background in validation processes is a significant asset in his current and past professional roles, ensuring high standards and compliance in pharmaceutical manufacturing and related activities.