Nicole Vesce
About Nicole Vesce
Nicole Vesce serves as the Lead Document Control Specialist at Asklepios BioPharmaceutical, Inc. since 2022, bringing extensive experience in document control and quality assurance from previous roles at Taysha Gene Therapies, Dendreon, and Novartis Gene Therapies.
Work at Asklepios BioPharmaceutical
Nicole Vesce serves as the Lead Document Control Specialist at Asklepios BioPharmaceutical, Inc. (AskBio) since 2022. In this role, she is responsible for overseeing the document control processes, ensuring compliance with industry standards, and maintaining the integrity of documentation within the organization. Her position is based in the Raleigh-Durham-Chapel Hill area, where she contributes to the company's mission in the biopharmaceutical sector.
Previous Experience in Document Control
Before joining Asklepios BioPharmaceutical, Nicole Vesce worked at Taysha Gene Therapies as a Sr. Specialist II in Document Control from 2021 to 2022. She also held the position of Sr. Documentation Analyst in Quality Assurance II/Records Management at Dendreon from 2013 to 2019. Additionally, she worked as a QA Documentation Specialist at Novartis Gene Therapies from 2019 to 2021. This extensive experience in document control and quality assurance has equipped her with valuable skills in managing documentation in the pharmaceutical industry.
Education and Expertise
Nicole Vesce studied at Eastwick College, where she focused on Sonography Science and graduated in 2001. Her educational background complements her professional expertise in document control, particularly in the pharmaceutical sector. She possesses a strong working knowledge of Good Documentation Practices, which is essential for maintaining compliance and quality in documentation processes.
Skills in Document Management
Nicole Vesce has demonstrated proficiency in the setup, maintenance, and delivery of both paper and electronic master files. Her experience encompasses various aspects of document management, which is critical in ensuring that all documentation meets regulatory requirements and industry standards. This skill set is fundamental to her roles in the organizations she has worked for in the biopharmaceutical and pharmaceutical industries.