Tavaris Avery
Quality Assurance Compliance Specialist @Regeneron
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WORK HISTORY
Quality Assurance Compliance Specialist @Regeneron
NY, US
Developed strategic plans related to change control and the implementation of robust corrective actions to support manufacturing operations by applying function expertise-Crafted business plans to independently advances change control initiatives to implement Corrective and Preventative Actions (CAPA’s) and process improvements in support of manufacturing operation-Assessed sophisticated proposed change controls to evaluate if proposal satisfies company standards-Coordinated and prepared change control documentation that assesses and defines the scope, impact, risk, and regulatory impact associated with the changeReviewed, edited, and revised controlled documentation in accordance with cGMP standards-Coordinated and led cross functional meetings globally with multiple departments to drive implementation-Provided advice and mentorship to cross-functional teams to enable successful and GMP compliant change controls-Presented business critical and regulatory impactful change controls to senior leadership
EDUCATION
University of North Carolina Wilmington
Bachelor's degree, Organic Chemistry
Triton High School
High School Diploma, University Track and AP course study
SKILLS
ABOUT TAVARIS AVERY
As a Quality Assurance Compliance Specialist at Regeneron, I contribute over three years of expertise in quality assurance change and project management, focusing on change control and corrective and preventative actions (CAPAs) to support manufacturing operations. I specialize in quality risk management and Veeva Vault, enabling the development of robust strategies and business plans that align with cGMP standards. My role involves assessing complex proposals, coordinating documentation, and ensuring regulatory compliance to promote operational excellence. My prior experience at Aurobindo Pharma USA strengthened my ability to refine quality systems, lead investigations, and implement quality metrics. By reviewing and approving critical quality documentation and overseeing training initiatives, I supported the development of optimized quality management systems. My dedication centers on driving process improvements and maintaining the highest standards of compliance to ensure quality and safety in manufacturing.
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