Cynthia Radcliffe
About Cynthia Radcliffe
Cynthia Radcliffe is a Quality Records Review Specialist with 18 years of experience in packaging and production, currently employed at QuVa Pharma, Inc. and PAREXEL, where she focuses on quality assurance and compliance in the pharmaceutical industry.
Work at QuVa Pharma
Cynthia Radcliffe has been employed at QuVa Pharma, Inc. since 2018. She currently serves as the Lead Quality Assurance Specialist, a position she has held for six years. In this role, she focuses on ensuring the quality and compliance of pharmaceutical products. Additionally, she has worked as a Quality Records Review Specialist at QuVa Pharma since 2021, where she reviews batch records and manufacturing specifications to maintain high standards in quality assurance.
Experience in Pharmaceutical Packaging
With 18 years of experience in packaging and production, Cynthia Radcliffe specializes in batch records and manufacturing specifications. Her extensive background includes supervisory roles within pharmaceutical packaging, where she has developed a strong understanding of quality assurance processes. This experience has equipped her with the skills necessary to oversee quality documentation and compliance in the pharmaceutical industry.
Education and Expertise
Cynthia Radcliffe studied at Northampton Community College from 2006 to 2009, focusing on Business. She also completed her secondary education at Freedom High School. In addition to her formal education, she holds certification as an ISO Internal Auditor, which highlights her expertise in ISO documentation and compliance within the pharmaceutical sector.
Previous Employment History
Before her current roles, Cynthia Radcliffe worked at PAREXEL as a Quality Specialist II LQMO since 2017, accumulating seven years of experience in quality assurance. She briefly held the position of Quality/Documentation Supervisor at Sharp Corporation in 2011 for two months, where she contributed to quality management processes.