Davina De Cagny
About Davina De Cagny
Davina De Cagny is the Associate Director of CMC Regulatory Affairs at MSD Biotech in Dublin, Ireland, with extensive experience in regulatory and quality assurance roles.
Current Role at MSD Biotech
Davina De Cagny currently serves as the Associate Director of CMC Regulatory Affairs at MSD Biotech in Dublin, County Dublin, Ireland. She has been with the company since July 2020, bringing expertise in regulatory affairs to the biotech industry.
Previous Experience at Generic Specialty Pharma Limited
Before joining MSD Biotech, Davina De Cagny worked at Generic Specialty Pharma Limited as a Regulatory Affairs Team Leader. She held this position for four years, from 2016 to 2020, in County Dublin, Ireland. During this time, she led the regulatory affairs team, ensuring compliance with industry standards and regulatory requirements.
Role at Takeda Ireland Limited
From 2000 to 2005, Davina De Cagny served as a QA Executive at Takeda Ireland Limited in Bray. In this role, she was responsible for quality assurance processes, maintaining compliance with regulatory standards, and supporting the company's manufacturing operations.
Early Career at Bristol-Myers Squibb
Davina De Cagny began her career as a QA Regulatory Chemist at Bristol-Myers Squibb. This role involved ensuring the quality and regulatory compliance of pharmaceutical products. Her experience at Bristol-Myers Squibb laid the foundation for her subsequent roles in quality assurance and regulatory affairs.
Educational Background
Davina De Cagny studied at the National University of Ireland, Galway. She earned a Higher Diploma in Quality Assurance from 1999 to 2000. Prior to that, she completed a degree in Biochemistry at the same university, studying from 1995 to 1999 and achieving an NUIG credential.