Elaine Solano
About Elaine Solano
Elaine Solano is a Quality Manager in Global Quality Regulatory Compliance at Bristol-Myers Squibb, with over 20 years of experience in the pharmaceutical industry.
Current Position
Elaine Solano currently serves as a Quality Manager in Global Quality Regulatory Compliance at Bristol-Myers Squibb in New Jersey, United States. In this role, she oversees regulatory compliance across various projects, ensuring adherence to global quality standards. Her responsibilities include managing compliance activities, conducting internal audits, and implementing quality improvement initiatives.
Work Experience at Bristol-Myers Squibb
Elaine Solano has been with Bristol-Myers Squibb for over 20 years, primarily focusing on global quality regulatory compliance. Her extensive experience in the pharmaceutical industry allows her to contribute significantly to the company's quality management systems. Throughout her tenure, she has handled various critical tasks such as GLP (Good Laboratory Practice), GMP (Good Manufacturing Practice), and technology transfers. Her role requires close collaboration with different departments to maintain high standards of quality control and regulatory adherence.
Previous Experience at Evotec
Prior to her long-standing career at Bristol-Myers Squibb, Elaine Solano worked at Evotec as a chemist from 2002 to 2003. During her time at the company based in Hamburg, Germany, she gained valuable international experience and developed her skills in various analytical techniques. This early experience laid the groundwork for her future roles and helped her build a solid foundation in the pharmaceutical industry.
Educational Background
Elaine Solano completed her undergraduate studies at Dublin City University from 1997 to 2001. Her education provided a strong foundation in the principles of chemistry and the pharmaceutical sciences, equipping her with the knowledge necessary to excel in the industry. Her academic background has been instrumental in her ability to specialize in various aspects of quality management and regulatory compliance throughout her career.
Expertise in Pharmaceutical Quality Management
Elaine Solano possesses over 20 years of experience in the pharmaceutical industry, with a specialization in GLP, validation, verification and validation (V&V), HPLC (High-Performance Liquid Chromatography), technology transfer, change control, GMP, and biotechnology. Her comprehensive expertise in these areas allows her to effectively manage and oversee quality regulatory compliance activities, ensuring that all processes meet stringent global standards. Her skills are vital for maintaining the integrity and quality of pharmaceutical products at Bristol-Myers Squibb.