Daniel Miller
About Daniel Miller
Daniel Miller is a Production Technician at QuVa Pharma, Inc. in Bloomsbury, New Jersey, where he ensures compliance with industry standards and manages production processes since 2021.
Work at QuVa Pharma
Daniel Miller has been employed as a Production Technician at QuVa Pharma, Inc. since 2021. He works in Bloomsbury, New Jersey, where he is responsible for conducting and completing line and room clearances in accordance with established procedures. His role includes notifying production management of any deviations from established processes or procedures. Daniel ensures compliance with 503B guidelines, current Good Manufacturing Practices (cGMPs), and company ISO standards during production processes. He also performs equipment calibration checks and troubleshooting to maintain operational efficiency.
Education and Expertise
Daniel Miller studied at Raritan Valley Community College, where he pursued a degree in Registered Nursing/Registered Nurse. He achieved an Associate of Applied Science from 2021 to 2024. His educational background provides him with a solid foundation in healthcare practices, which complements his technical skills in production. Additionally, he completed his high school education at Watchung Regional High School from 2014 to 2018.
Previous Experience at Parexel
Before joining QuVa Pharma, Daniel worked as a Depot Technician at Parexel from 2019 to 2021 in Quakertown, Pennsylvania. In this role, he gained experience in handling various technical tasks related to production and logistics. His time at Parexel contributed to his understanding of the pharmaceutical industry and prepared him for his current responsibilities.
Responsibilities and Compliance
In his current position, Daniel Miller is tasked with ensuring compliance with regulatory guidelines and company standards. He conducts line and room clearances and is vigilant in notifying management of any deviations from established processes. His responsibilities also include the documentation of activities, which involves attaching label specimens and reconciling materials printed with variable data. This attention to detail is essential for maintaining quality and safety in production.