Heather Cantwell
Heather Cantwell, Regulatory Affairs Manager, Stryker
Heather Cantwell is a Regulatory Affairs Manager in Stryker, based in Cork. She has worked for Stryker since 2016 with experience spanning across US, EU and emerging markets, with many years focused on the implementation of MDR.
In her current role, Heather is responsible for leading the global ENT regulatory affairs team (based across US, Ireland and Germany) involved in the development and implementation of regulatory strategies and global submissions for new product development as well as product transfers. As part of her role, Heather is dedicated to driving process improvements that support the growth and development of both her team and the organisation.
Prior to joining Stryker, Heather worked in Quality Control with Takeda Pharmaceutical and Clarochem. Heather earned her Bsc. in Pharmaceutical Technology from SETU, Waterford and will be graduating with a H.Dip in Medical Affairs Regulatory Technology this year from NUIG and ATU Sligo.