Daria Wolska
About Daria Wolska
Title
Daria Wolska currently holds the title of Downstream Manufacturing Specialist at Bristol Myers Squibb in Dublin, County Dublin, Ireland.
Professional Experience at Bristol Myers Squibb
Daria Wolska has been working with Bristol Myers Squibb in Dublin, County Dublin, Ireland. She began her career with the company as a Technical Writer - Downstream from 2019 to 2021, where she was responsible for developing and implementing Standard Operating Procedures (SOPs) for large-scale biopharmaceutical manufacturing processes. Currently, she serves as a Downstream Manufacturing Specialist, participating in process optimizations using lean principles and assisting in compliance with cGMP standards by reviewing batch and exception reports.
Previous Roles
Daria Wolska has a diverse work history in various scientific and analytical roles. She worked as a Bio-Analytical Laboratory Technician at APC Ltd from 2018 to 2019 in Cherrywood, Dublin. Prior to that, she was employed by Eurofins Biomnis Ireland as both a Sample Management Officer and a Medical Laboratory Aide, each for 4 months in 2018. Additionally, she served as a Transaction Specialist at Arvato Financial Solutions, operating on behalf of Microsoft from 2017 to 2018 in Sandyford. Earlier in her career, she held the position of Environmental Laboratory Analyst at the Environmental Protection Agency (EPA) Ireland for 6 months in 2015.
Education and Expertise
Daria Wolska has a strong academic background in scientific disciplines. She achieved an Honours Bachelor of Science in Forensic and Environmental Chemistry from Dublin Institute of Technology from 2012 to 2016. She further specialized by earning a Special Award Certificate in Pharmaceutical and Medical Device Manufacturing from Innopharma Education in 2017. Additionally, she completed her Leaving Certificate (LC) from St. Mary's Secondary School from 2006 to 2012. Her education has provided her with a broad scientific foundation and expertise in downstream manufacturing processes.
Contributions to Manufacturing Processes
Throughout her career, Daria Wolska has been actively involved in scientific and engineering investigations aimed at improving manufacturing processes. She has contributed to QA audit activities and provided significant input for related investigations. Her work includes developing and implementing Standard Operating Procedures (SOPs), participating in lean process optimizations, and ensuring compliance with current Good Manufacturing Practices (cGMP). Her roles have enabled her to make substantial advancements in the efficiency and quality of biopharmaceutical manufacturing processes.