Tais Conti
About Tais Conti
Tais Conti is a Senior Manager of Quality Assurance and Compliance at Bristol-Myers Squibb in New York, with over 15 years of experience in the pharmaceutical industry.
Current Title and Role at Bristol-Myers Squibb
Tais Conti is the Senior Manager of Quality Assurance and Compliance at Bristol-Myers Squibb in New York, New York, United States. In her role, she oversees quality assurance processes and ensures compliance with industry standards within the pharmaceutical sector. With over 15 years of experience at Bristol-Myers Squibb, she has contributed to maintaining high standards in quality management across the company.
Education and Academic Background
Tais Conti holds a Master's degree from Escola Politécnica da USP, where she studied from 2003 to 2005. Prior to that, she completed her undergraduate studies at Universidade de São Paulo, from 1998 to 2002. Her education provided a solid foundation in engineering and quality management, which she has effectively applied throughout her career in the pharmaceutical industry.
Professional Experience in Quality Assurance
Specializing in quality assurance and compliance, Tais Conti has accumulated extensive experience managing quality assurance processes on a global scale. Her work ensures that Bristol-Myers Squibb adheres to stringent industry standards and regulations, reflecting her long-term commitment to quality and compliance in the pharmaceutical industry.
Engineering and Quality Management Expertise
Tais Conti possesses a strong background in engineering and quality management, gained through her rigorous education at top Brazilian institutions. Her expertise is foundational to her role in ensuring that quality assurance protocols are meticulously followed, thus supporting the production of high-quality pharmaceuticals at Bristol-Myers Squibb.
Long-Term Commitment to Quality and Compliance
With over 15 years at Bristol-Myers Squibb, Tais Conti has demonstrated a sustained commitment to quality assurance and compliance. Her role involves upholding industry regulations and standards, reflecting her dedication to maintaining excellent quality management practices within the pharmaceutical sector.