Roy Paul
About Roy Paul
Roy Paul is the Associate Director of Quality Assurance at Bristol Myers Squibb in Summit, NJ, with over 20 years of experience in pharmaceutical analytical R&D, quality control, and quality assurance.
Title
Roy Paul holds the position of Associate Director Quality Assurance at Bristol Myers Squibb in Summit, NJ. In this role, he is responsible for overseeing quality assurance processes within the company.
Professional Experience
Roy Paul has an extensive career spanning over 30 years in the pharmaceutical industry. His previous roles include Fellow at Novartis in East Hanover, NJ (2006-2012), Technical Group Leader at Barr Laboratories in Pomona, NY (2005-2006), and various scientific positions at Purdue Pharma in Ardsley, NY (1991-2005). He began his career as an Analytical Chemist at Geo Chem Laboratories and later worked as an R&D Supervisor at Kedia Chemicals in Bombay, India.
Education and Expertise
Roy Paul has a Master’s degree in Chemistry from Polytechnic University (1995-1997), a Diploma in Industrial Chemistry from Ruia College (1991-1993), and a Bachelor of Science (BSc) in Chemistry from St Albert's College (1980-1985). He possesses over 20 years of experience in Pharmaceutical Analytical R&D, Quality Control, Quality Assurance, CMC, and Metrology, with significant expertise in managing analytical method development and validation.
Industry Knowledge and Skills
Roy Paul is thoroughly knowledgeable about FDA, ICH, and USP guidelines. He possesses a strong background in cGMP’s and their application to pharmaceutical development, and has extensive knowledge in handling Schedule II controlled substances in accordance with DEA regulations. His skills include effective interpersonal communication, technical writing, troubleshooting, and presentation. He is known for his innovative and efficient approach, with sharp analytical and problem-solving capabilities.
Career Goals
Roy Paul aims to achieve a leadership position in Quality Control, Quality Assurance, Regulatory Affairs, or Pharmaceutical Project Management. He seeks to leverage his extensive experience and skills to drive quality excellence and regulatory compliance in the pharmaceutical industry.