Rada Mc Nicholl
About Rada Mc Nicholl
Rada Mc Nicholl is a Regulatory Affairs Specialist at Teleflex Incorporated and Medtronic, with a background in technical documentation and validation in the medical device industry.
Professional Experience at Teleflex Incorporated
Rada Mc Nicholl has been serving as a Regulatory Affairs Specialist at Teleflex Incorporated since April 2019. In this role, she is based in Athlone, where she contributes her extensive expertise in regulatory affairs, technical documentation, and validation within the medical device industry. Her responsibilities likely include ensuring regulatory compliance and managing submissions to regulatory agencies.
Regulatory Affairs Specialist at Medtronic
Rada Mc Nicholl concurrently holds the position of Regulatory Affairs Specialist at Medtronic, based in Tullamore. In this capacity, she utilizes her knowledge in Good Laboratory Practice (GLP) and change control, ensuring that products meet rigorous regulatory standards. Her role is critical in maintaining compliance and supporting product lifecycle management.
Previous Roles in Documentation and Microbiology
Prior to her current positions, Rada Mc Nicholl accumulated valuable experience working at ABBOTT as a Documentation Specialist from 2007 to 2014. Earlier, she worked at Elan Pharmaceuticals as a Microbiology Lab Analyst from 2006 to 2007. These roles provided her with a strong foundation in technical documentation and scientific analysis, which are crucial for her current regulatory affairs responsibilities.
Educational Background and Qualifications
Rada Mc Nicholl has a comprehensive educational background, including a Bachelor's Degree in Honours Biotechnology from Athlone Institute of Technology, completed between 2001 and 2005. She further pursued a Higher Diploma in Education from NUI Galway from 2005 to 2006. Additionally, she holds an Honours Degree in Quality and Regulatory Affairs from the University of Limerick, underscoring her specialized knowledge in regulatory processes.
Expertise in Good Laboratory Practice and Change Control
Rada Mc Nicholl is well-versed in Good Laboratory Practice (GLP) and change control, key aspects of maintaining high standards in the medical device industry. Her expertise in these areas is pivotal in her roles at both Teleflex Incorporated and Medtronic, where compliance with stringent regulatory requirements is essential for product safety and efficacy.