Stephen B.
About Stephen B.
Stephen B. is a QC Analyst II at Alkermes with a background in microbiology and health science.
Current Role at Alkermes
Stephen B. holds the position of QC Analyst II at Alkermes. In this role, he deals with quality control tasks and ensures that products meet required standards. Stephen is knowledgeable in cGMP, GDP, GLP, and various other quality standards. His proficiency in sterility testing, LAL endotoxin, and environmental monitoring contributes to his success in maintaining high-quality control standards at Alkermes.
Previous Experience as Microbiologist
Stephen B. has notable experience as a microbiologist. He worked at Pharmaceutical Associates, Inc. in Greenville, South Carolina, from 2020 to 2021, and Stallergenes Greer from 2019 to 2020. In these roles, he focused on microbiological testing and analysis within both sterile and non-sterile pharmaceutical manufacturing environments. His duties included sterility testing, organism identification, and antibiotic assay.
Experience in Fitness Industry
Before transitioning to the pharmaceutical sector, Stephen B. was involved in the fitness industry. He worked at Crossfit Postal as a Head Coach for two months in 2018 and as a Trainer from 2016 to 2018 in Boone, North Carolina. These roles involved designing training programs, coaching clients, and promoting physical fitness.
Education and Degree
Stephen B. completed his undergraduate studies at Appalachian State University, where he earned a Bachelor's degree in Health Science. His time at the university, from 2014 to 2018, provided him with a strong foundation in health and science-related topics, which have been beneficial in his subsequent professional roles.
Technical Skills and Training
Stephen B. is proficient in various technical skills and industry-standard practices. He has administered the MODA system and provided training to coworkers as end users. Additionally, he trained senior department members in EDMS data review. His skills extend to data entry, data review, validation, and the writing and reviewing of official documents. His comprehensive knowledge is further supported by practical experience in both sterile and non-sterile pharmaceutical manufacturing.