Emelia Daniels
About Emelia Daniels
Emelia Daniels is a Senior Biological Process Development Engineer at Teleflex Incorporated in Maple Grove, Minnesota, with a background in pharmaceutical development and a dual degree in Biology and Chemistry.
Company
Emelia Daniels is currently employed at Teleflex Incorporated as a Senior Biological Process Development Engineer. Teleflex Incorporated is a prominent company based in Maple Grove, Minnesota, United States. At Teleflex, she applies her extensive background in chemistry and biology to develop biological processes, ensuring they meet industry standards and regulatory compliance.
Title
Emelia Daniels serves as a Senior Biological Process Development Engineer. In this position, she is responsible for leading pharmaceutical projects from their initiation phase through lab-scale formulation and manufacturing process development scale-up. Her role requires a detailed understanding of biological and chemical processes to enhance product development and achieve successful project outcomes.
Professional Background
Emelia Daniels has an extensive background in pharmaceutical development, having held various positions at Upsher-Smith Laboratories, LLC. She progressed from Associate Scientist I in Pharmaceutical Development (2012-2015) to Associate Scientist II (2015-2017), then to Associate Scientist III (2017-2020), and finally to Scientist-Pharmaceutical Development (2020). She also worked briefly as a Laboratory Analyst at Pace Analytical in 2012 under an Ecolab contract. Additionally, she worked at FedEx Office as a Customer Service Coordinator from 2008 to 2012.
Education and Expertise
Emelia Daniels earned dual Bachelor of Science degrees in Biology and Chemistry from the University of Wisconsin-River Falls, completing her studies in 2011. Her formal education provides a balanced foundation in both disciplines, equipping her with the knowledge necessary for her roles in pharmaceutical product development. Emelia's expertise includes authoring CMC submission documents for FDA approval and leading pharmaceutical projects through various developmental stages.
Achievements
Throughout her career, Emelia Daniels has been instrumental in authoring Chemistry, Manufacturing, and Controls (CMC) submission documents that are crucial for FDA approval during pharmaceutical project development. Her colleagues recognize her for her ethical scientific performance, effective communication skills, and adaptability. These qualities have enabled her to efficiently utilize resources and navigate various roles within the pharmaceutical industry.