Christina Waszak

Christina Waszak has extensive experience in regulatory affairs and quality assurance within the medical device industry. Currently serving as a Pharmacovigilance Quality Assurance Associate at Fidia Pharma USA Inc since March 2016, Christina previously worked at Biomet for over two decades in various roles, including Regulatory Affairs Associate, where responsibilities included maintaining technical files for Class I, II, and III medical devices, managing EU regulatory compliance, and overseeing product labeling changes. Christina also played a critical role in regulatory submissions and audits. Earlier career positions included drafting and documentation roles at Allen-Bradley and US Laser Corp., contributing to the development of manufacturing processes and technical documentation. Christina holds an Associate in Applied Science degree in Visual Communications from Gibbs College and a certificate in Electro-Mechanical Drafting from Passaic School of Drafting.