Darius Crick
About Darius Crick
Darius Crick is a Senior Quality Assurance Specialist at QuVa Pharma, Inc., where he has worked since 2021. He possesses expertise in current Good Manufacturing Practices and 503B Standard Operating Procedures, with experience in batch record review and quality assessments.
Work at QuVa Pharma
Darius Crick has been employed at QuVa Pharma, Inc. since 2020. He started as a Quality Assurance Specialist and transitioned to the role of Senior Quality Assurance Specialist in 2021. His work is based in Bloomsbury, New Jersey, where he has accumulated three years of experience in quality assurance processes. In his current role, he is responsible for ensuring compliance with industry standards and regulations.
Education and Expertise
Darius Crick studied at Northampton Community College from 2013 to 2018, completing a five-year program. He possesses expertise in current Good Manufacturing Practices (cGMP) and 503B Standard Operating Procedures (SOPs). His educational background supports his professional skills in quality assurance within the pharmaceutical industry.
Background
Before becoming a Senior Quality Assurance Specialist, Darius worked at QuVa Pharma, Inc. as a Quality Assurance Specialist for ten months. His experience in this role laid the foundation for his current responsibilities. He has developed a strong understanding of quality assurance protocols and practices in a pharmaceutical setting.
Achievements in Quality Assurance
Darius Crick has demonstrated proficiency in various quality assurance tasks, including batch record review, Acceptable Quality Level (AQL) assessments, and the management of deviations. He is also skilled in implementing Corrective and Preventive Actions (CAPA), which are essential for maintaining product quality and compliance in the pharmaceutical industry.