Denis Coll
About Denis Coll
Denis Coll is a Co-Op at Boston Scientific in Galway, Ireland, with a background in Biomedical and Pharmaceutical Sciences.
Current Position at Boston Scientific
Denis Coll is currently working as a Co-Op at Boston Scientific in Galway, County Galway, Ireland. His tenure at this role began in 2021. During his time at Boston Scientific, Denis has gained practical experience in process optimization and characterization studies. He is proficient in using statistical analysis tools such as Minitab and Excel. Additionally, he has experience handling medical device documentation and reports, including NCE's, CAPA's, and SOP's. Denis is also familiar with regulatory standards such as 21 CFR 820 and ISO 13485.
Work Experience in the Hospitality Industry
Before joining Boston Scientific, Denis Coll accumulated substantial work experience in various roles within the hospitality industry. From 2020 to 2021, he worked as a Kitchen Assistant at Kasbah Wine Bar in Galway. Prior to that, he served as a Kitchen Porter at the g Hotel & Spa from 2019 to 2020. Denis also held the position of Kitchen Assistant at PEPPER'S DINER in County Donegal, Ireland, from 2015 to 2019.
Educational Background in Biomedical and Pharmaceutical Sciences
Denis Coll pursued his higher education at reputable institutions in Ireland. He studied Biomedical Sciences, General at the National University of Ireland, Galway, achieving a Master's degree from 2020 to 2022. Before that, he attended Galway-Mayo Institute of Technology, where he studied Pharmaceutical Sciences and earned a Bachelor's degree, completing his studies from 2016 to 2020.
Proficiency in Statistical Analysis and Regulatory Standards
Throughout his professional journey, Denis Coll has developed proficiency in various technical skills essential for his role at Boston Scientific. He is skilled in using statistical analysis tools such as Minitab and Excel. Denis is experienced in handling medical device documentation, including Non-Conformance Events (NCE's), Corrective and Preventive Actions (CAPA's), and Standard Operating Procedures (SOP's). Additionally, he is well-versed in regulatory standards applicable to the medical device industry, specifically 21 CFR 820 and ISO 13485.