Camille C.

Camille C. is a Regulatory Affairs Specialist with extensive experience in the medical device and in vitro diagnostics sectors, currently employed at Hologic, Inc. since June 2021. Camille's responsibilities include planning and executing global regulatory activities for product registration and renewal while staying informed about legislative changes and developing mitigation strategies. Previously, Camille held similar positions at MyAssociates Pte Ltd, where management of multiple client projects was pivotal, and at Oculus Private Limited, where documentation for CE-marketing activities was prepared and submitted. Beginning with an internship at GE Healthcare focused on regulatory documentation for Southeast Asia, Camille's career foundation includes administrative and operational roles in the healthcare sector, supported by a degree from the National University of Singapore.